Vaccines or candidate vaccines used to prevent infection with Japanese B encephalitis virus (ENCEPHALITIS VIRUS, JAPANESE).
A mosquito-borne encephalitis caused by the Japanese B encephalitis virus (ENCEPHALITIS VIRUS, JAPANESE) occurring throughout Eastern Asia and Australia. The majority of infections occur in children and are subclinical or have features limited to transient fever and gastrointestinal symptoms. Inflammation of the brain, spinal cord, and meninges may occur and lead to transient or permanent neurologic deficits (including a POLIOMYELITIS-like presentation); SEIZURES; COMA; and death. (From Adams et al., Principles of Neurology, 6th ed, p751; Lancet 1998 Apr 11;351(9109):1094-7)
A species of FLAVIVIRUS, one of the Japanese encephalitis virus group (ENCEPHALITIS VIRUSES, JAPANESE), which is the etiological agent of Japanese encephalitis found in Asia, southeast Asia, and the Indian subcontinent.
A subgroup of the genus FLAVIVIRUS which comprises a number of viral species that are the etiologic agents of human encephalitis in many different geographical regions. These include Japanese encephalitis virus (ENCEPHALITIS VIRUS, JAPANESE), St. Louis encephalitis virus (ENCEPHALITIS VIRUS, ST. LOUIS), Murray Valley encephalitis virus (ENCEPHALITIS VIRUS, MURRAY VALLEY), and WEST NILE VIRUS.
Vaccines in which the infectious microbial nucleic acid components have been destroyed by chemical or physical treatment (e.g., formalin, beta-propiolactone, gamma radiation) without affecting the antigenicity or immunogenicity of the viral coat or bacterial outer membrane proteins.
Suspensions of attenuated or killed viruses administered for the prevention or treatment of infectious viral disease.
A collection of single-stranded RNA viruses scattered across the Bunyaviridae, Flaviviridae, and Togaviridae families whose common property is the ability to induce encephalitic conditions in infected hosts.
Immunoglobulins produced in response to VIRAL ANTIGENS.
Inflammation of the BRAIN due to infection, autoimmune processes, toxins, and other conditions. Viral infections (see ENCEPHALITIS, VIRAL) are a relatively frequent cause of this condition.
Inflammation of brain parenchymal tissue as a result of viral infection. Encephalitis may occur as primary or secondary manifestation of TOGAVIRIDAE INFECTIONS; HERPESVIRIDAE INFECTIONS; ADENOVIRIDAE INFECTIONS; FLAVIVIRIDAE INFECTIONS; BUNYAVIRIDAE INFECTIONS; PICORNAVIRIDAE INFECTIONS; PARAMYXOVIRIDAE INFECTIONS; ORTHOMYXOVIRIDAE INFECTIONS; RETROVIRIDAE INFECTIONS; and ARENAVIRIDAE INFECTIONS.
Stable cobalt atoms that have the same atomic number as the element cobalt, but differ in atomic weight. Co-59 is a stable cobalt isotope.
A group of ALPHAVIRUS INFECTIONS which affect horses and man, transmitted via the bites of mosquitoes. Disorders in this category are endemic to regions of South America and North America. In humans, clinical manifestations vary with the type of infection, and range from a mild influenza-like syndrome to a fulminant encephalitis. (From Joynt, Clinical Neurology, 1996, Ch26, pp8-10)
Infections of the brain caused by arthropod-borne viruses (i.e., arboviruses) primarily from the families TOGAVIRIDAE; FLAVIVIRIDAE; BUNYAVIRIDAE; REOVIRIDAE; and RHABDOVIRIDAE. Life cycles of these viruses are characterized by ZOONOSES, with birds and lower mammals serving as intermediate hosts. The virus is transmitted to humans by the bite of mosquitoes (CULICIDAE) or TICKS. Clinical manifestations include fever, headache, alterations of mentation, focal neurologic deficits, and COMA. (From Clin Microbiol Rev 1994 Jan;7(1):89-116; Walton, Brain's Diseases of the Nervous System, 10th ed, p321)
Suspensions of killed or attenuated microorganisms (bacteria, viruses, fungi, protozoa), antigenic proteins, synthetic constructs, or other bio-molecular derivatives, administered for the prevention, amelioration, or treatment of infectious and other diseases.
A genus of FLAVIVIRIDAE containing several subgroups and many species. Most are arboviruses transmitted by mosquitoes or ticks. The type species is YELLOW FEVER VIRUS.
Infections with viruses of the genus FLAVIVIRUS, family FLAVIVIRIDAE.
The measurement of infection-blocking titer of ANTISERA by testing a series of dilutions for a given virus-antiserum interaction end-point, which is generally the dilution at which tissue cultures inoculated with the serum-virus mixtures demonstrate cytopathology (CPE) or the dilution at which 50% of test animals injected with serum-virus mixtures show infectivity (ID50) or die (LD50).
Live vaccines prepared from microorganisms which have undergone physical adaptation (e.g., by radiation or temperature conditioning) or serial passage in laboratory animal hosts or infected tissue/cell cultures, in order to produce avirulent mutant strains capable of inducing protective immunity.
A genus of mosquitoes (CULICIDAE) commonly found in tropical regions. Species of this genus are vectors for ST. LOUIS ENCEPHALITIS as well as many other diseases of man and domestic and wild animals.
A species of FLAVIVIRUS, one of the Japanese encephalitis virus group (ENCEPHALITIS VIRUSES, JAPANESE), which is the etiologic agent of ST. LOUIS ENCEPHALITIS in the United States, the Caribbean, and Central and South America.
A family of the order DIPTERA that comprises the mosquitoes. The larval stages are aquatic, and the adults can be recognized by the characteristic WINGS, ANIMAL venation, the scales along the wing veins, and the long proboscis. Many species are of particular medical importance.
A species of ALPHAVIRUS that is the etiologic agent of encephalomyelitis in humans and equines. It is seen most commonly in parts of Central and South America.
A paraneoplastic syndrome marked by degeneration of neurons in the LIMBIC SYSTEM. Clinical features include HALLUCINATIONS, loss of EPISODIC MEMORY; ANOSMIA; AGEUSIA; TEMPORAL LOBE EPILEPSY; DEMENTIA; and affective disturbance (depression). Circulating anti-neuronal antibodies (e.g., anti-Hu; anti-Yo; anti-Ri; and anti-Ma2) and small cell lung carcinomas or testicular carcinoma are frequently associated with this syndrome.
A viral encephalitis caused by the St. Louis encephalitis virus (ENCEPHALITIS VIRUS, ST. LOUIS), a FLAVIVIRUS. It is transmitted to humans and other vertebrates primarily by mosquitoes of the genus CULEX. The primary animal vectors are wild birds and the disorder is endemic to the midwestern and southeastern United States. Infections may be limited to an influenza-like illness or present as an ASEPTIC MENINGITIS or ENCEPHALITIS. Clinical manifestations of the encephalitic presentation may include SEIZURES, lethargy, MYOCLONUS, focal neurologic signs, COMA, and DEATH. (From Adams et al., Principles of Neurology, 6th ed, p750)
Recombinant DNA vectors encoding antigens administered for the prevention or treatment of disease. The host cells take up the DNA, express the antigen, and present it to the immune system in a manner similar to that which would occur during natural infection. This induces humoral and cellular immune responses against the encoded antigens. The vector is called naked DNA because there is no need for complex formulations or delivery agents; the plasmid is injected in saline or other buffers.
Small synthetic peptides that mimic surface antigens of pathogens and are immunogenic, or vaccines manufactured with the aid of recombinant DNA techniques. The latter vaccines may also be whole viruses whose nucleic acids have been modified.
An acute (or rarely chronic) inflammatory process of the brain caused by SIMPLEXVIRUS infections which may be fatal. The majority of infections are caused by human herpesvirus 1 (HERPESVIRUS 1, HUMAN) and less often by human herpesvirus 2 (HERPESVIRUS 2, HUMAN). Clinical manifestations include FEVER; HEADACHE; SEIZURES; HALLUCINATIONS; behavioral alterations; APHASIA; hemiparesis; and COMA. Pathologically, the condition is marked by a hemorrhagic necrosis involving the medial and inferior TEMPORAL LOBE and orbital regions of the FRONTAL LOBE. (From Adams et al., Principles of Neurology, 6th ed, pp751-4)
## I'm sorry for any confusion, but "Japan" is not a medical term or concept. It is a country located in Asia, known as Nihon-koku or Nippon-koku in Japanese, and is renowned for its unique culture, advanced technology, and rich history. If you have any questions related to medical topics, I would be happy to help answer them!
Two or more vaccines in a single dosage form.
Suspensions of attenuated or killed bacteria administered for the prevention or treatment of infectious bacterial disease.
Administration of vaccines to stimulate the host's immune response. This includes any preparation intended for active immunological prophylaxis.
A species of FLAVIVIRUS, one of the Japanese encephalitis virus group (ENCEPHALITIS VIRUSES, JAPANESE), found in Australia and New Guinea. It causes a fulminating viremia resembling Japanese encephalitis (ENCEPHALITIS, JAPANESE).
A species of FLAVIVIRUS, one of the Japanese encephalitis virus group (ENCEPHALITIS VIRUSES, JAPANESE). It can infect birds and mammals. In humans, it is seen most frequently in Africa, Asia, and Europe presenting as a silent infection or undifferentiated fever (WEST NILE FEVER). The virus appeared in North America for the first time in 1999. It is transmitted mainly by CULEX spp mosquitoes which feed primarily on birds, but it can also be carried by the Asian Tiger mosquito, AEDES albopictus, which feeds mainly on mammals.
Vaccines or candidate vaccines containing inactivated HIV or some of its component antigens and designed to prevent or treat AIDS. Some vaccines containing antigens are recombinantly produced.
A species of ALPHAVIRUS causing encephalomyelitis in Equidae and humans. The virus ranges along the Atlantic seaboard of the United States and Canada and as far south as the Caribbean, Mexico, and parts of Central and South America. Infections in horses show a mortality of up to 90 percent and in humans as high as 80 percent in epidemics.

Molecular basis for attenuation of neurovirulence of a yellow fever Virus/Japanese encephalitis virus chimera vaccine (ChimeriVax-JE). (1/81)

A yellow fever virus (YFV)/Japanese encephalitis virus (JEV) chimera in which the structural proteins prM and E of YFV 17D are replaced with those of the JEV SA14-14-2 vaccine strain is under evaluation as a candidate vaccine against Japanese encephalitis. The chimera (YFV/JEV SA14-14-2, or ChimeriVax-JE) is less neurovirulent than is YFV 17D vaccine in mouse and nonhuman primate models (F. Guirakhoo et al., Virology 257:363-372, 1999; T. P. Monath et al., Vaccine 17:1869-1882, 1999). Attenuation depends on the presence of the JEV SA14-14-2 E protein, as shown by the high neurovirulence of an analogous YFV/JEV Nakayama chimera derived from the wild JEV Nakayama strain (T. J. Chambers, A. Nestorowicz, P. W. Mason, and C. M. Rice, J. Virol. 73:3095-3101, 1999). Ten amino acid differences exist between the E proteins of ChimeriVax-JE and the YFV/JEV Nakayama virus, four of which are predicted to be neurovirulence determinants based on various sequence comparisons. To identify residues that are involved in attenuation, a series of intratypic YFV/JEV chimeras containing either single or multiple amino acid substitutions were engineered and tested for mouse neurovirulence. Reversions in at least three distinct clusters were required to restore the neurovirulence typical of the YFV/JEV Nakayama virus. Different combinations of cluster-specific reversions could confer neurovirulence; however, residue 138 of the E protein (E(138)) exhibited a dominant effect. No single amino acid reversion produced a phenotype significantly different from that of the ChimeriVax-JE parent. Together with the known genetic stability of the virus during prolonged cell culture and mouse brain passage, these findings support the candidacy of this experimental vaccine as a novel live-attenuated viral vaccine against Japanese encephalitis.  (+info)

Analysis of Japanese encephalitis epidemic in Western Nepal in 1997. (2/81)

We conducted an epidemiological study of a Japanese encephalitis (JE) outbreak in the southwestern part of Nepal in 1997. A high density of JE infections was found and it was estimated that 27.9% the total population were infected with JE virus in the study area. The fatality rate was 13.2% and there was no difference in the fatality rate between males and females over 5 years old. However, the case fatality rate was 2.1 times higher in females than in males (14.6% vs. 6.9%) among children under 5 years of age. Fifty-three blood samples were collected from suspected JE cases during the epidemic period in 1998. Findings for JE specific IgM revealed that clinical diagnoses of JE were serologically confirmed in an average 78% (70-93%) of patients in three collaborating hospitals. These studies demonstrated that JE was highly prevalent in the area and clinical diagnoses were reliable. Effective preventive measures should be taken against this vaccine-preventable disease.  (+info)

Suppression of immune response and protective immunity to a Japanese encephalitis virus DNA vaccine by coadministration of an IL-12-expressing plasmid. (3/81)

IL-12 plays a central role in both innate and acquired immunity and has been demonstrated to potentiate the protective immunity in several experimental vaccines. However, in this study, we show that IL-12 can be detrimental to the immune responses elicited by a plasmid DNA vaccine. Coadministration of the IL-12-expressing plasmid (pIL-12) significantly suppressed the protective immunity elicited by a plasmid DNA vaccine (pE) encoding the envelope protein of Japanese encephalitis virus. This suppressive effect was associated with marked reduction of specific T cell proliferation and Ab responses. A single dose of pIL-12 treatment with plasmid pE in initial priming resulted in significant immune suppression to subsequent pE booster immunization. The pIL-12-mediated immune suppression was dose dependent and evident only when the IL-12 gene was injected either before or coincident with the pE DNA vaccine. Finally, using IFN-gamma gene-disrupted mice, we showed that the suppressive activity of the IL-12 plasmid was dependent upon endogenous production of IFN-gamma. These results demonstrate that coexpression of the IL-12 gene can sometimes produce untoward effects to immune responses, and thus its application as a vaccine adjuvant should be carefully evaluated.  (+info)

Travel vaccines and elderly persons: review of vaccines available in the United States. (4/81)

Aging is associated with alterations in immune responses and may lead to clinically significant changes in the safety, immunogenicity, and protective efficacy of certain vaccines. This review summarizes published data regarding the effects of age on responses after immunization with vaccines generally administered before travel. The specific vaccines discussed in detail include hepatitis A, typhoid, yellow fever, Japanese encephalitis, and rabies vaccines. There is some evidence of diminished serological responses to hepatitis A and rabies vaccines in older individuals. In addition, increased toxic effects following yellow fever vaccination in elderly recipients have recently been reported. However, many travel-related vaccines have never been studied specifically in elderly populations. Consideration of potential age-related differences in responses to travel vaccines is becoming increasingly important as elderly persons more frequently venture to exotic destinations.  (+info)

Plasmid DNA immunization against Japanese encephalitis virus: immunogenicity of membrane-anchored and secretory envelope protein. (5/81)

Plasmid DNA synthesizing membrane-anchored or secretory Japanese encephalitis virus (JEV) envelope (E) protein and premembrane protein was delivered to mice by intramuscular injection or gene gun. Intramuscular plasmid immunization induced anti-E antibody responses similar to those associated with commercial JEV vaccine. The gene gun induced less antibody response. The 2 forms of the E protein induced similar antibody titers when administered by the same delivery mode. Both plasmids generated high titers of JEV-neutralizing antibodies, although the titers were lower than those induced by the vaccine. Intramuscular DNA immunization induced T helper 1 (Th1) immune responses, and the gene gun induced Th2 responses. Compared with secretory E protein, the membrane-anchored protein heavily skewed the immune response toward either Th1 or Th2, depending on the route of immunization. In an intracerebral JEV challenge model, plasmid-immunized mice had approximately 60% protection; this was not affected by the form of the E protein or by immunization route.  (+info)

Single mutation in the flavivirus envelope protein hinge region increases neurovirulence for mice and monkeys but decreases viscerotropism for monkeys: relevance to development and safety testing of live, attenuated vaccines. (6/81)

A chimeric yellow fever (YF) virus/Japanese encephalitis (JE) virus vaccine (ChimeriVax-JE) was constructed by insertion of the prM-E genes from the attenuated JE virus SA14-14-2 vaccine strain into a full-length cDNA clone of YF 17D virus. Passage in fetal rhesus lung (FRhL) cells led to the emergence of a small-plaque virus containing a single Met-->Lys amino acid mutation at E279, reverting this residue from the SA14-14-2 to the wild-type amino acid. A similar virus was also constructed by site-directed mutagenesis (J. Arroyo, F. Guirakhoo, S. Fenner, Z.-X. Zhang, T. P. Monath, and T. J. Chambers, J. Virol. 75:934-942, 2001). The E279 mutation is located in a beta-sheet in the hinge region of the E protein that is responsible for a pH-dependent conformational change during virus penetration from the endosome into the cytoplasm of the infected cell. In independent transfection-passage studies with FRhL or Vero cells, mutations appeared most frequently in hinge 4 (bounded by amino acids E266 to E284), reflecting genomic instability in this functionally important region. The E279 reversion caused a significant increase in neurovirulence as determined by the 50% lethal dose and survival distribution in suckling mice and by histopathology in rhesus monkeys. Based on sensitivity and comparability of results with those for monkeys, the suckling mouse is an appropriate host for safety testing of flavivirus vaccine candidates for neurotropism. After intracerebral inoculation, the E279 Lys virus was restricted with respect to extraneural replication in monkeys, as viremia and antibody levels (markers of viscerotropism) were significantly reduced compared to those for the E279 Met virus. These results are consistent with the observation that empirically derived vaccines developed by mouse brain passage of dengue and YF viruses have increased neurovirulence for mice but reduced viscerotropism for humans.  (+info)

Dengue-specific T cell responses in peripheral blood mononuclear cells obtained prior to secondary dengue virus infections in Thai schoolchildren. (7/81)

Children who experience secondary dengue virus (DV) infections are at increased risk for dengue hemorrhagic fever. To study the effect of preexisting T cell responses to DV on the severity of secondary virus infection, peripheral blood mononuclear cells (PBMC) from 10 subsequently hospitalized and 12 nonhospitalized Thai schoolchildren were stimulated with inactivated dengue antigens, and proliferation of interferon (IFN)-gamma or tumor necrosis factor (TNF)-alpha responses of the preinfection PBMC were measured. Proliferation responses were observed in 11 subjects, and IFN-gamma responses were seen in 12 subjects, 6 of whom showed broad serotype cross-reactive IFN-gamma responses. TNF-alpha responses were detected exclusively in 4 hospitalized subjects. Four PBMC samples that showed neither proliferation nor cytokine responses to any dengue antigen were from nonhospitalized subjects. This study, thought to be the first to investigate T cell responses to DV in preinfection PBMC, suggests that the pattern of preexisting T cell responses influences the risk for severe disease.  (+info)

Japanese encephalitis vaccine for travelers: exploring the limits of risk. (8/81)

The prevention of Japanese encephalitis in travelers presents the juxtaposition of 4 factors: a disease that is widespread throughout Asia, a disease with a low incidence in travelers, a vaccine about which there are safety concerns, and a clinical course that can result in death or permanent disability in two-thirds of symptomatic cases. Travel medicine practitioners often seem to be polarized into 2 groups: a group that gives more weight to the severity of the disease (and therefore often recommend vaccination) and another group that is more persuaded by the low occurrence of cases in travelers (and therefore rarely recommend vaccination). This review assesses the known risks of contracting Japanese encephalitis and the risks associated with the vaccine and tries to develop an appropriate way to recommend this vaccine to travelers who may be at significant risk.  (+info)

Japanese Encephalitis (JE) vaccines are immunobiological preparations used for active immunization against Japanese Encephalitis, a viral infection transmitted through the bite of infected mosquitoes. The vaccines contain inactivated or live attenuated strains of the JE virus. They work by stimulating the immune system to produce antibodies and T-cells that provide protection against the virus. There are several types of JE vaccines available, including inactivated Vero cell-derived vaccine, live attenuated SA14-14-2 vaccine, and inactivated mouse brain-derived vaccine. These vaccines have been shown to be effective in preventing JE and are recommended for use in individuals traveling to or living in areas where the disease is endemic.

Japanese encephalitis is a viral inflammation of the brain (encephalitis) caused by the Japanese encephalitis virus (JEV). It is transmitted to humans through the bite of infected Culex mosquitoes, particularly in rural and agricultural areas. The majority of JE cases occur in children under the age of 15. Most people infected with JEV do not develop symptoms, but some may experience mild symptoms such as fever, headache, and vomiting. In severe cases, JEV can cause high fever, neck stiffness, seizures, confusion, and coma. There is no specific treatment for Japanese encephalitis, and care is focused on managing symptoms and supporting the patient's overall health. Prevention measures include vaccination and avoiding mosquito bites in endemic areas.

Japanese Encephalitis Virus (JEV) is a type of flavivirus that is the causative agent of Japanese encephalitis, a mosquito-borne viral infection of the brain. The virus is primarily transmitted to humans through the bite of infected Culex species mosquitoes, particularly Culex tritaeniorhynchus and Culex gelidus.

JEV is endemic in many parts of Asia, including China, Japan, Korea, India, Nepal, Thailand, and Vietnam. It is estimated to cause around 68,000 clinical cases and 13,000-20,000 deaths each year. The virus is maintained in a transmission cycle between mosquitoes and vertebrate hosts, primarily pigs and wading birds.

Most JEV infections are asymptomatic or result in mild symptoms such as fever, headache, and muscle aches. However, in some cases, the infection can progress to severe encephalitis, which is characterized by inflammation of the brain, leading to neurological symptoms such as seizures, tremors, paralysis, and coma. The case fatality rate for Japanese encephalitis is estimated to be 20-30%, and around half of those who survive have significant long-term neurological sequelae.

Prevention of JEV infection includes the use of insect repellent, wearing protective clothing, and avoiding outdoor activities during peak mosquito feeding times. Vaccination is also an effective means of preventing Japanese encephalitis, and vaccines are available for travelers to endemic areas as well as for residents of those areas.

Japanese Encephalitis Viruses (JEV) are part of the Flaviviridae family and belong to the genus Flavivirus. JEV is the leading cause of viral encephalitis in Asia, resulting in significant morbidity and mortality. The virus is primarily transmitted through the bite of infected Culex mosquitoes, particularly Culex tritaeniorhynchus and Culex vishnui complex.

JEV has a complex transmission cycle involving mosquito vectors, amplifying hosts (primarily pigs and wading birds), and dead-end hosts (humans). The virus is maintained in nature through a enzootic cycle between mosquitoes and amplifying hosts. Humans become infected when bitten by an infective mosquito, but they do not contribute to the transmission cycle.

The incubation period for JEV infection ranges from 5 to 15 days. Most infections are asymptomatic or result in mild symptoms such as fever, headache, and malaise. However, a small percentage of infected individuals develop severe neurological manifestations, including encephalitis, meningitis, and acute flaccid paralysis. The case fatality rate for JEV-induced encephalitis is approximately 20-30%, with up to half of the survivors experiencing long-term neurological sequelae.

There are no specific antiviral treatments available for Japanese encephalitis, and management primarily focuses on supportive care. Prevention strategies include vaccination, personal protective measures against mosquito bites, and vector control programs. JEV vaccines are available and recommended for travelers to endemic areas and for residents living in regions where the virus is circulating.

Inactivated vaccines, also known as killed or non-live vaccines, are created by using a version of the virus or bacteria that has been grown in a laboratory and then killed or inactivated with chemicals, heat, or radiation. This process renders the organism unable to cause disease, but still capable of stimulating an immune response when introduced into the body.

Inactivated vaccines are generally considered safer than live attenuated vaccines since they cannot revert back to a virulent form and cause illness. However, they may require multiple doses or booster shots to maintain immunity because the immune response generated by inactivated vaccines is not as robust as that produced by live vaccines. Examples of inactivated vaccines include those for hepatitis A, rabies, and influenza (inactivated flu vaccine).

A viral vaccine is a biological preparation that introduces your body to a specific virus in a way that helps your immune system build up protection against the virus without causing the illness. Viral vaccines can be made from weakened or inactivated forms of the virus, or parts of the virus such as proteins or sugars. Once introduced to the body, the immune system recognizes the virus as foreign and produces an immune response, including the production of antibodies. These antibodies remain in the body and provide immunity against future infection with that specific virus.

Viral vaccines are important tools for preventing infectious diseases caused by viruses, such as influenza, measles, mumps, rubella, polio, hepatitis A and B, rabies, rotavirus, chickenpox, shingles, and some types of cancer. Vaccination programs have led to the control or elimination of many infectious diseases that were once common.

It's important to note that viral vaccines are not effective against bacterial infections, and separate vaccines must be developed for each type of virus. Additionally, because viruses can mutate over time, it is necessary to update some viral vaccines periodically to ensure continued protection.

Encephalitis viruses are a group of viruses that can cause encephalitis, which is an inflammation of the brain. Some of the most common encephalitis viruses include:

1. Herpes simplex virus (HSV) type 1 and 2: These viruses are best known for causing cold sores and genital herpes, but they can also cause encephalitis, particularly in newborns and individuals with weakened immune systems.
2. Varicella-zoster virus (VZV): This virus causes chickenpox and shingles, and it can also lead to encephalitis, especially in people who have had chickenpox.
3. Enteroviruses: These viruses are often responsible for summertime meningitis outbreaks and can occasionally cause encephalitis.
4. Arboviruses: These viruses are transmitted through the bites of infected mosquitoes, ticks, or other insects. Examples include West Nile virus, St. Louis encephalitis virus, Eastern equine encephalitis virus, and Western equine encephalitis virus.
5. Rabies virus: This virus is transmitted through the bite of an infected animal and can cause encephalitis in its later stages.
6. Measles virus: Although rare in developed countries due to vaccination, measles can still cause encephalitis as a complication of the infection.
7. Mumps virus: Like measles, mumps is preventable through vaccination, but it can also lead to encephalitis as a rare complication.
8. Cytomegalovirus (CMV): This virus is a member of the herpesvirus family and can cause encephalitis in people with weakened immune systems, such as those with HIV/AIDS or organ transplant recipients.
9. La Crosse virus: This arbovirus is primarily transmitted through the bites of infected eastern treehole mosquitoes and mainly affects children.
10. Powassan virus: Another arbovirus, Powassan virus is transmitted through the bites of infected black-legged ticks (also known as deer ticks) and can cause severe encephalitis.

It's important to note that many of these viruses are preventable through vaccination or by avoiding exposure to infected animals or mosquitoes. If you suspect you may have been exposed to one of these viruses, consult a healthcare professional for proper diagnosis and treatment.

Antibodies, viral are proteins produced by the immune system in response to an infection with a virus. These antibodies are capable of recognizing and binding to specific antigens on the surface of the virus, which helps to neutralize or destroy the virus and prevent its replication. Once produced, these antibodies can provide immunity against future infections with the same virus.

Viral antibodies are typically composed of four polypeptide chains - two heavy chains and two light chains - that are held together by disulfide bonds. The binding site for the antigen is located at the tip of the Y-shaped structure, formed by the variable regions of the heavy and light chains.

There are five classes of antibodies in humans: IgA, IgD, IgE, IgG, and IgM. Each class has a different function and is distributed differently throughout the body. For example, IgG is the most common type of antibody found in the bloodstream and provides long-term immunity against viruses, while IgA is found primarily in mucous membranes and helps to protect against respiratory and gastrointestinal infections.

In addition to their role in the immune response, viral antibodies can also be used as diagnostic tools to detect the presence of a specific virus in a patient's blood or other bodily fluids.

Encephalitis is defined as inflammation of the brain parenchyma, which is often caused by viral infections but can also be due to bacterial, fungal, or parasitic infections, autoimmune disorders, or exposure to toxins. The infection or inflammation can cause various symptoms such as headache, fever, confusion, seizures, and altered consciousness, ranging from mild symptoms to severe cases that can lead to brain damage, long-term disabilities, or even death.

The diagnosis of encephalitis typically involves a combination of clinical evaluation, imaging studies (such as MRI or CT scans), and laboratory tests (such as cerebrospinal fluid analysis). Treatment may include antiviral medications, corticosteroids, immunoglobulins, and supportive care to manage symptoms and prevent complications.

Viral encephalitis is a medical condition characterized by inflammation of the brain caused by a viral infection. The infection can be caused by various types of viruses, such as herpes simplex virus, enteroviruses, arboviruses (transmitted through insect bites), or HIV.

The symptoms of viral encephalitis may include fever, headache, stiff neck, confusion, seizures, and altered level of consciousness. In severe cases, it can lead to brain damage, coma, or even death. The diagnosis is usually made based on clinical presentation, laboratory tests, and imaging studies such as MRI or CT scan. Treatment typically involves antiviral medications, supportive care, and management of complications.

Cobalt isotopes are variants of the chemical element Cobalt (Co) that have different numbers of neutrons in their atomic nuclei. This results in the different isotopes having slightly different masses and varying levels of stability.

The most naturally occurring stable cobalt isotope is Co-59, which contains 27 neutrons in its nucleus. However, there are also several radioactive isotopes of cobalt, including Co-60, which is a commonly used medical and industrial radioisotope.

Co-60 has 30 neutrons in its nucleus and undergoes beta decay, emitting gamma rays and becoming Nickel-60. It has a half-life of approximately 5.27 years, making it useful for a variety of applications, including cancer treatment, industrial radiography, and sterilization of medical equipment.

Other radioactive isotopes of cobalt include Co-57, which has a half-life of 271.8 days and is used in medical imaging, and Co-56, which has a half-life of just 77.2 seconds and is used in research.

Equine encephalomyelitis is a viral disease that affects the central nervous system (CNS) of horses and other equids such as donkeys and mules. The term "encephalomyelitis" refers to inflammation of both the brain (encephalitis) and spinal cord (myelitis). There are three main types of equine encephalomyelitis found in North America, each caused by a different virus: Eastern equine encephalomyelitis (EEE), Western equine encephalomyelitis (WEE), and Venezuelan equine encephalomyelitis (VEE).

EEE is the most severe form of the disease. It is transmitted to horses through the bite of infected mosquitoes, primarily Culiseta melanura and Coquillettidia perturbans. The virus multiplies in the horse's bloodstream and then spreads to the brain and spinal cord, causing inflammation and damage to nerve cells. Clinical signs of EEE include high fever, depression, loss of appetite, weakness, unsteady gait, muscle twitching, paralysis, and potentially death within 2-3 days after the onset of symptoms. The mortality rate for horses with EEE is approximately 75-90%.

WEE is less severe than EEE but can still cause significant illness in horses. It is also transmitted to horses through mosquito bites, primarily Culex tarsalis. Clinical signs of WEE include fever, depression, loss of appetite, muscle twitching, weakness, and unsteady gait. The mortality rate for horses with WEE is around 20-50%.

VEE is the least severe form of equine encephalomyelitis in horses, but it can still cause significant illness. It is primarily transmitted to horses through mosquito bites, mainly Culex (Melanoconion) spp., and also by direct contact with infected animals or their secretions. Clinical signs of VEE include fever, depression, loss of appetite, muscle twitching, weakness, and unsteady gait. The mortality rate for horses with VEE is around 5-20%.

Prevention measures for equine encephalomyelitis include vaccination, mosquito control, and avoiding exposure to infected animals or their secretions. There are vaccines available for EEE and WEE, which can provide protection against these diseases in horses. Mosquito control measures such as removing standing water, using insect repellents, and installing screens on windows and doors can help reduce the risk of mosquito-borne illnesses. Additionally, avoiding contact with infected animals or their secretions can help prevent the spread of VEE.

Arbovirus encephalitis is a type of encephalitis (inflammation of the brain) caused by a group of viruses that are transmitted through the bite of infected arthropods, such as mosquitoes or ticks. The term "arbovirus" stands for "arthropod-borne virus."

There are many different types of arboviruses that can cause encephalitis, including:

* La Crosse virus
* St. Louis encephalitis virus
* West Nile virus
* Eastern equine encephalitis virus
* Western equine encephalitis virus
* Venezuelan equine encephalitis virus

The symptoms of arbovirus encephalitis can vary, but may include fever, headache, stiff neck, seizures, confusion, and weakness. In severe cases, it can lead to coma or death. Treatment typically involves supportive care to manage symptoms, as there is no specific antiviral treatment for most types of arbovirus encephalitis. Prevention measures include avoiding mosquito and tick bites, using insect repellent, and eliminating standing water where mosquitoes breed.

A vaccine is a biological preparation that provides active acquired immunity to a particular infectious disease. It typically contains an agent that resembles the disease-causing microorganism and is often made from weakened or killed forms of the microbe, its toxins, or one of its surface proteins. The agent stimulates the body's immune system to recognize the agent as a threat, destroy it, and "remember" it, so that the immune system can more easily recognize and destroy any of these microorganisms that it encounters in the future.

Vaccines can be prophylactic (to prevent or ameliorate the effects of a future infection by a natural or "wild" pathogen), or therapeutic (to fight disease that is already present). The administration of vaccines is called vaccination. Vaccinations are generally administered through needle injections, but can also be administered by mouth or sprayed into the nose.

The term "vaccine" comes from Edward Jenner's 1796 use of cowpox to create immunity to smallpox. The first successful vaccine was developed in 1796 by Edward Jenner, who showed that milkmaids who had contracted cowpox did not get smallpox. He reasoned that exposure to cowpox protected against smallpox and tested his theory by injecting a boy with pus from a cowpox sore and then exposing him to smallpox, which the boy did not contract. The word "vaccine" is derived from Variolae vaccinae (smallpox of the cow), the term devised by Jenner to denote cowpox. He used it in 1798 during a conversation with a fellow physician and later in the title of his 1801 Inquiry.

Flavivirus is a genus of viruses in the family Flaviviridae. They are enveloped, single-stranded, positive-sense RNA viruses that are primarily transmitted by arthropod vectors such as mosquitoes and ticks. Many flaviviruses cause significant disease in humans, including dengue fever, yellow fever, Japanese encephalitis, West Nile fever, and Zika fever. The name "flavivirus" is derived from the Latin word for "yellow," referring to the yellow fever virus, which was one of the first members of this genus to be discovered.

Flavivirus infections refer to a group of diseases caused by various viruses belonging to the Flaviviridae family, specifically within the genus Flavivirus. These viruses are primarily transmitted to humans through the bites of infected arthropods, such as mosquitoes and ticks.

Some well-known flavivirus infections include:

1. Dengue Fever: A mosquito-borne viral infection that is prevalent in tropical and subtropical regions worldwide. It can cause a wide range of symptoms, from mild flu-like illness to severe complications like dengue hemorrhagic fever and dengue shock syndrome.
2. Yellow Fever: A viral hemorrhagic disease transmitted by the Aedes and Haemagogus mosquitoes, primarily in Africa and South America. It can cause severe illness, including jaundice, bleeding, organ failure, and death.
3. Japanese Encephalitis: A mosquito-borne viral infection that is endemic to Southeast Asia and the Western Pacific. While most infections are asymptomatic or mild, a small percentage of cases can lead to severe neurological complications, such as encephalitis (inflammation of the brain) and meningitis (inflammation of the membranes surrounding the brain and spinal cord).
4. Zika Virus Infection: A mosquito-borne viral disease that has spread to many regions of the world, particularly in tropical and subtropical areas. Most Zika virus infections are mild or asymptomatic; however, infection during pregnancy can cause severe birth defects, such as microcephaly (abnormally small head size) and other neurological abnormalities in the developing fetus.
5. West Nile Virus Infection: A mosquito-borne viral disease that is endemic to North America, Europe, Africa, Asia, and Australia. Most infections are mild or asymptomatic; however, a small percentage of cases can lead to severe neurological complications, such as encephalitis, meningitis, and acute flaccid paralysis (sudden weakness in the arms and legs).

Prevention measures for these diseases typically involve avoiding mosquito bites through the use of insect repellent, wearing long sleeves and pants, staying indoors during peak mosquito hours, and removing standing water from around homes and businesses. Additionally, vaccines are available for some of these diseases, such as Japanese encephalitis and yellow fever, and should be considered for individuals traveling to areas where these diseases are common.

Neutralization tests are a type of laboratory assay used in microbiology and immunology to measure the ability of a substance, such as an antibody or antitoxin, to neutralize the activity of a toxin or infectious agent. In these tests, the substance to be tested is mixed with a known quantity of the toxin or infectious agent, and the mixture is then incubated under controlled conditions. After incubation, the mixture is tested for residual toxicity or infectivity using a variety of methods, such as cell culture assays, animal models, or biochemical assays.

The neutralization titer is then calculated based on the highest dilution of the test substance that completely neutralizes the toxin or infectious agent. Neutralization tests are commonly used in the diagnosis and evaluation of immune responses to vaccines, as well as in the detection and quantification of toxins and other harmful substances.

Examples of neutralization tests include the serum neutralization test for measles antibodies, the plaque reduction neutralization test (PRNT) for dengue virus antibodies, and the cytotoxicity neutralization assay for botulinum neurotoxins.

Attenuated vaccines consist of live microorganisms that have been weakened (attenuated) through various laboratory processes so they do not cause disease in the majority of recipients but still stimulate an immune response. The purpose of attenuation is to reduce the virulence or replication capacity of the pathogen while keeping it alive, allowing it to retain its antigenic properties and induce a strong and protective immune response.

Examples of attenuated vaccines include:

1. Sabin oral poliovirus vaccine (OPV): This vaccine uses live but weakened polioviruses to protect against all three strains of the disease-causing poliovirus. The weakened viruses replicate in the intestine and induce an immune response, which provides both humoral (antibody) and cell-mediated immunity.
2. Measles, mumps, and rubella (MMR) vaccine: This combination vaccine contains live attenuated measles, mumps, and rubella viruses. It is given to protect against these three diseases and prevent their spread in the population.
3. Varicella (chickenpox) vaccine: This vaccine uses a weakened form of the varicella-zoster virus, which causes chickenpox. By introducing this attenuated virus into the body, it stimulates an immune response that protects against future infection with the wild-type virus.
4. Yellow fever vaccine: This live attenuated vaccine is used to prevent yellow fever, a viral disease transmitted by mosquitoes in tropical and subtropical regions of Africa and South America. The vaccine contains a weakened form of the yellow fever virus that cannot cause the disease but still induces an immune response.
5. Bacillus Calmette-Guérin (BCG) vaccine: This live attenuated vaccine is used to protect against tuberculosis (TB). It contains a weakened strain of Mycobacterium bovis, which does not cause TB in humans but stimulates an immune response that provides some protection against the disease.

Attenuated vaccines are generally effective at inducing long-lasting immunity and can provide robust protection against targeted diseases. However, they may pose a risk for individuals with weakened immune systems, as the attenuated viruses or bacteria could potentially cause illness in these individuals. Therefore, it is essential to consider an individual's health status before administering live attenuated vaccines.

'Culex' is a genus of mosquitoes that includes many species that are vectors for various diseases, such as West Nile virus, filariasis, and avian malaria. They are often referred to as "house mosquitoes" because they are commonly found in urban environments. These mosquitoes typically lay their eggs in standing water and have a cosmopolitan distribution, being found on all continents except Antarctica. The life cycle of Culex mosquitoes includes four stages: egg, larva, pupa, and adult. Both male and female adults feed on nectar, but only females require blood meals to lay eggs.

St. Louis Encephalitis Virus (SLEV) is a type of arbovirus (arthropod-borne virus) from the family Flaviviridae and genus Flavivirus. It is the causative agent of St. Louis encephalitis (SLE), a viral disease characterized by inflammation of the brain (encephalitis). The virus is primarily transmitted to humans through the bite of infected mosquitoes, particularly Culex spp.

The SLEV infection in humans is often asymptomatic or may cause mild flu-like symptoms such as fever, headache, nausea, and vomiting. However, in some cases, the virus can invade the central nervous system, leading to severe neurological manifestations like meningitis, encephalitis, seizures, and even coma or death. The risk of severe disease increases in older adults and people with weakened immune systems.

There is no specific antiviral treatment for SLE; management typically focuses on supportive care to alleviate symptoms and address complications. Prevention measures include avoiding mosquito bites, using insect repellents, and eliminating breeding sites for mosquitoes. Vaccines are not available for SLEV, but they have been developed and tested in the past, with potential for future use in high-risk populations during outbreaks.

'Culicidae' is the biological family that includes all species of mosquitoes. It consists of three subfamilies: Anophelinae, Culicinae, and Toxorhynchitinae. Mosquitoes are small, midge-like flies that are known for their ability to transmit various diseases to humans and other animals, such as malaria, yellow fever, dengue fever, and Zika virus. The medical importance of Culicidae comes from the fact that only female mosquitoes require blood meals to lay eggs, and during this process, they can transmit pathogens between hosts.

Venezuelan Equine Encephalitis Virus (VEEV) is a type of alphavirus that can cause encephalitis (inflammation of the brain) in horses and humans. It is primarily transmitted through the bite of infected mosquitoes, although it can also be spread through contact with contaminated food or water, or by aerosolization during laboratory work or in bioterrorism attacks.

VEEV infection can cause a range of symptoms in humans, from mild flu-like illness to severe encephalitis, which may result in permanent neurological damage or death. There are several subtypes of VEEV, some of which are more virulent than others. The virus is endemic in parts of Central and South America, but outbreaks can also occur in other regions, including the United States.

VEEV is considered a potential bioterrorism agent due to its ease of transmission through aerosolization and its high virulence. There are no specific treatments for VEEV infection, although supportive care can help manage symptoms. Prevention measures include avoiding mosquito bites in endemic areas, using personal protective equipment during laboratory work with the virus, and implementing strict biocontainment procedures in research settings.

Limbic encephalitis is a rare type of inflammatory autoimmune disorder that affects the limbic system, which is a part of the brain involved in emotions, behavior, memory, and sense of smell. It is characterized by inflammation of the limbic system, leading to symptoms such as memory loss, confusion, seizures, changes in behavior and mood, and problems with autonomic functions.

Limbic encephalitis can be caused by a variety of factors, including viral infections, cancer, or autoimmune disorders. In some cases, the cause may remain unknown. Diagnosis typically involves a combination of clinical evaluation, imaging studies (such as MRI), and analysis of cerebrospinal fluid. Treatment usually involves immunosuppressive therapy to reduce inflammation, as well as addressing any underlying causes if they can be identified.

It is important to note that limbic encephalitis is a serious condition that requires prompt medical attention and treatment. If you or someone else experiences symptoms such as sudden confusion, memory loss, or seizures, it is essential to seek medical care immediately.

St. Louis Encephalitis (SLE) is a type of viral brain inflammation caused by the St. Louis Encephalitis virus. It is transmitted to humans through the bite of infected mosquitoes, primarily Culex species. The virus breeds in warm, stagnant water and is more prevalent in rural and suburban areas.

Most people infected with SLE virus do not develop symptoms or only experience mild flu-like illness. However, some individuals, particularly the elderly, can develop severe illness characterized by sudden onset of fever, headache, neck stiffness, disorientation, coma, seizures, and spastic paralysis. There is no specific treatment for SLE, and management is focused on supportive care, including hydration, respiratory support, and prevention of secondary infections. Vaccination against SLE is not available, and prevention measures include using insect repellent, wearing protective clothing, and eliminating standing water around homes to reduce mosquito breeding sites.

I could not find a specific medical definition for "Vaccines, DNA." However, I can provide you with some information about DNA vaccines.

DNA vaccines are a type of vaccine that uses genetically engineered DNA to stimulate an immune response in the body. They work by introducing a small piece of DNA into the body that contains the genetic code for a specific antigen (a substance that triggers an immune response). The cells of the body then use this DNA to produce the antigen, which prompts the immune system to recognize and attack it.

DNA vaccines have several advantages over traditional vaccines. They are relatively easy to produce, can be stored at room temperature, and can be designed to protect against a wide range of diseases. Additionally, because they use DNA to stimulate an immune response, DNA vaccines do not require the growth and culture of viruses or bacteria, which can make them safer than traditional vaccines.

DNA vaccines are still in the experimental stages, and more research is needed to determine their safety and effectiveness. However, they have shown promise in animal studies and are being investigated as a potential tool for preventing a variety of infectious diseases, including influenza, HIV, and cancer.

Synthetic vaccines are artificially produced, designed to stimulate an immune response and provide protection against specific diseases. Unlike traditional vaccines that are derived from weakened or killed pathogens, synthetic vaccines are created using synthetic components, such as synthesized viral proteins, DNA, or RNA. These components mimic the disease-causing agent and trigger an immune response without causing the actual disease. The use of synthetic vaccines offers advantages in terms of safety, consistency, and scalability in production, making them valuable tools for preventing infectious diseases.

Herpes simplex encephalitis (HSE) is a severe and potentially life-thingening inflammation of the brain caused by the herpes simplex virus (HSV), most commonly HSV-1. It is a rare but serious condition that can cause significant neurological damage if left untreated.

The infection typically begins in the temporal or frontal lobes of the brain and can spread to other areas, causing symptoms such as headache, fever, seizures, confusion, memory loss, and personality changes. In severe cases, it can lead to coma or death.

Diagnosis of HSE is often made through a combination of clinical presentation, imaging studies (such as MRI), and laboratory tests, including polymerase chain reaction (PCR) analysis of cerebrospinal fluid (CSF) to detect the presence of the virus.

Treatment typically involves antiviral medications, such as acyclovir, which can help reduce the severity of the infection and prevent further neurological damage. In some cases, corticosteroids may also be used to reduce inflammation in the brain. Prompt treatment is critical for improving outcomes and reducing the risk of long-term neurological complications.

I'm sorry for any confusion, but "Japan" is not a medical term. Japan is the name of a country, officially known as Nippon-koku or Nihon-koku in Japanese, and is located in East Asia. It is an island nation in the Pacific Ocean with a population of about 126 million people.

If you have any medical questions or terms that you would like me to define, please let me know!

Combined vaccines are defined in medical terms as vaccines that contain two or more antigens from different diseases, which are given to provide protection against multiple diseases at the same time. This approach reduces the number of injections required and simplifies the immunization schedule, especially during early childhood. Examples of combined vaccines include:

1. DTaP-Hib-IPV (e.g., Pentacel): A vaccine that combines diphtheria, tetanus, pertussis (whooping cough), Haemophilus influenzae type b (Hib) disease, and poliovirus components in one injection to protect against these five diseases.
2. MMRV (e.g., ProQuad): A vaccine that combines measles, mumps, rubella, and varicella (chickenpox) antigens in a single injection to provide immunity against all four diseases.
3. HepA-HepB (e.g., Twinrix): A vaccine that combines hepatitis A and hepatitis B antigens in one injection, providing protection against both types of hepatitis.
4. MenACWY-TT (e.g., MenQuadfi): A vaccine that combines four serogroups of meningococcal bacteria (A, C, W, Y) with tetanus toxoid as a carrier protein in one injection for the prevention of invasive meningococcal disease caused by these serogroups.
5. PCV13-PPSV23 (e.g., Vaxneuvance): A vaccine that combines 13 pneumococcal serotypes with PPSV23, providing protection against a broader range of pneumococcal diseases in adults aged 18 years and older.

Combined vaccines have been thoroughly tested for safety and efficacy to ensure they provide a strong immune response and an acceptable safety profile. They are essential tools in preventing various infectious diseases and improving overall public health.

Bacterial vaccines are types of vaccines that are created using bacteria or parts of bacteria as the immunogen, which is the substance that triggers an immune response in the body. The purpose of a bacterial vaccine is to stimulate the immune system to develop protection against specific bacterial infections.

There are several types of bacterial vaccines, including:

1. Inactivated or killed whole-cell vaccines: These vaccines contain entire bacteria that have been killed or inactivated through various methods, such as heat or chemicals. The bacteria can no longer cause disease, but they still retain the ability to stimulate an immune response.
2. Subunit, protein, or polysaccharide vaccines: These vaccines use specific components of the bacterium, such as proteins or polysaccharides, that are known to trigger an immune response. By using only these components, the vaccine can avoid using the entire bacterium, which may reduce the risk of adverse reactions.
3. Live attenuated vaccines: These vaccines contain live bacteria that have been weakened or attenuated so that they cannot cause disease but still retain the ability to stimulate an immune response. This type of vaccine can provide long-lasting immunity, but it may not be suitable for people with weakened immune systems.

Bacterial vaccines are essential tools in preventing and controlling bacterial infections, reducing the burden of diseases such as tuberculosis, pneumococcal disease, meningococcal disease, and Haemophilus influenzae type b (Hib) disease. They work by exposing the immune system to a harmless form of the bacteria or its components, which triggers the production of antibodies and memory cells that can recognize and fight off future infections with that same bacterium.

It's important to note that while vaccines are generally safe and effective, they may cause mild side effects such as pain, redness, or swelling at the injection site, fever, or fatigue. Serious side effects are rare but can occur, so it's essential to consult with a healthcare provider before receiving any vaccine.

Vaccination is a simple, safe, and effective way to protect people against harmful diseases, before they come into contact with them. It uses your body's natural defenses to build protection to specific infections and makes your immune system stronger.

A vaccination usually contains a small, harmless piece of a virus or bacteria (or toxins produced by these germs) that has been made inactive or weakened so it won't cause the disease itself. This piece of the germ is known as an antigen. When the vaccine is introduced into the body, the immune system recognizes the antigen as foreign and produces antibodies to fight it.

If a person then comes into contact with the actual disease-causing germ, their immune system will recognize it and immediately produce antibodies to destroy it. The person is therefore protected against that disease. This is known as active immunity.

Vaccinations are important for both individual and public health. They prevent the spread of contagious diseases and protect vulnerable members of the population, such as young children, the elderly, and people with weakened immune systems who cannot be vaccinated or for whom vaccination is not effective.

Murray Valley Encephalitis Virus (MVEV) is a type of arbovirus (arthropod-borne virus) that is primarily transmitted to humans through the bite of an infected mosquito. The virus is named after the Murray Valley region in Australia where it was first identified.

MVEV is the causative agent of Murray Valley encephalitis, a serious illness that can affect the brain and cause inflammation (encephalitis). The virus is found primarily in Australia, Papua New Guinea, and parts of Southeast Asia.

The transmission cycle of MVEV involves mosquitoes serving as vectors that transmit the virus between birds and mammals, including humans. Infection with MVEV can cause a range of symptoms, from mild fever and headache to severe neurological complications such as seizures, coma, and permanent brain damage. There is no specific treatment for Murray Valley encephalitis, and prevention efforts focus on reducing mosquito populations and avoiding mosquito bites in areas where the virus is known to be present.

West Nile Virus (WNV) is an Flavivirus, which is a type of virus that is spread by mosquitoes. It was first discovered in the West Nile district of Uganda in 1937 and has since been found in many countries throughout the world. WNV can cause a mild to severe illness known as West Nile fever.

Most people who become infected with WNV do not develop any symptoms, but some may experience fever, headache, body aches, joint pain, vomiting, diarrhea, or a rash. In rare cases, the virus can cause serious neurological illnesses such as encephalitis (inflammation of the brain) or meningitis (inflammation of the membranes surrounding the brain and spinal cord). These severe forms of the disease can be fatal, especially in older adults and people with weakened immune systems.

WNV is primarily transmitted to humans through the bite of infected mosquitoes, but it can also be spread through blood transfusions, organ transplants, or from mother to baby during pregnancy, delivery, or breastfeeding. There is no specific treatment for WNV, and most people recover on their own with rest and supportive care. However, hospitalization may be necessary in severe cases. Prevention measures include avoiding mosquito bites by using insect repellent, wearing long sleeves and pants, and staying indoors during peak mosquito activity hours.

An AIDS vaccine is a type of preventive vaccine that aims to stimulate the immune system to produce an effective response against the human immunodeficiency virus (HIV), which causes acquired immunodeficiency syndrome (AIDS). The goal of an AIDS vaccine is to induce the production of immune cells and proteins that can recognize and eliminate HIV-infected cells, thereby preventing the establishment of a persistent infection.

Despite decades of research, there is still no licensed AIDS vaccine available. This is due in part to the unique challenges posed by HIV, which has a high mutation rate and can rapidly evolve to evade the immune system's defenses. However, several promising vaccine candidates are currently being tested in clinical trials around the world, and researchers continue to explore new approaches and strategies for developing an effective AIDS vaccine.

Eastern equine encephalitis virus (EEEV) is a single-stranded RNA virus that belongs to the family Togaviridae and the genus Alphavirus. It is the causative agent of Eastern equine encephalitis (EEE), a rare but serious viral disease that can affect humans, horses, and some bird species.

EEEV is primarily transmitted through the bite of infected mosquitoes, particularly those belonging to the Culiseta and Coquillettidia genera. The virus is maintained in a transmission cycle between mosquitoes and wild birds, primarily passerine birds. Horses and humans are considered dead-end hosts, meaning they do not develop high enough levels of viremia to infect feeding mosquitoes and perpetuate the transmission cycle.

EEE is most commonly found in the eastern and Gulf Coast states of the United States, as well as in parts of Canada, Central and South America, and the Caribbean. The disease can cause severe neurological symptoms, including inflammation of the brain (encephalitis), meningitis, and neuritis. In severe cases, EEE can lead to seizures, coma, and death. There is no specific treatment for EEE, and prevention efforts focus on reducing mosquito populations and avoiding mosquito bites.

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Japanese Encephalitis Vaccine: learn about side effects, dosage, special precautions, and more on MedlinePlus ... Japanese encephalitis (JE) is a serious infection caused by the Japanese encephalitis virus. ... Japanese encephalitis vaccine is approved for people 2 months of age and older. It is recommended for travelers to Asia who:. * ... Japanese Encephalitis Vaccine Information Statement. U.S. Department of Health and Human Services/Centers for Disease Control ...
Japanese encephalitis vaccine is a vaccine that protects against Japanese encephalitis. The vaccines are more than 90% ... "Japanese Encephalitis Vaccine". Drug Information Portal. U.S. National Library of Medicine. "Japanese Encephalitis Vaccine ... Japanese encephalitis vaccines first became available in the 1930s. One of them was an inactivated mouse brain-derived vaccine ... "New Japanese encephalitis vaccines: alternatives to production in mouse brain". Expert Review of Vaccines. 10 (3): 355-364. doi ...
Japanese Encephalitis Vaccine - Travel Vaccination. Book your Travel Vaccinations for either Pleasure of Business with Pall ... What is Japanese Encephalitis?. Japanese encephalitis is a viral disease which is passed from animals or birds to humans via ... How much does a private Japanese Encephalitis vaccination cost?. Japanese Encephalitis vaccination. *. £100 for vaccination + £ ... The vaccine is given as two injections, with the second dose given 28 days after the first. A booster dose is required after 12 ...
"Japanese Encephalitis (JE) Vaccine" 201703, no. 020304 (2017). Walter, Emmanuel B. "Japanese Encephalitis (JE) Vaccine" vol. ... Title : Japanese Encephalitis (JE) Vaccine Personal Author(s) : Walter, Emmanuel B. Corporate Authors(s) : United States. ... Epidemiology and risk of Japanese encephalitis in U.S. travelers Cite CITE. Title : Epidemiology and risk of Japanese ... Meeting (2018 June 20-21 : Atlanta, GA) Published Date : 08/14/2018 Series : ACIP meeting Japanese Encephalitis Vaccine URL : ...
... launched today investigating the effectiveness of intradermal administration of the existing TGA-approved Japanese encephalitis ... Japanese encephalitis vaccine delivery study - subcutaneous injection versus intradermal injection Researchers are calling for ... JE is a rare but serious illness caused by the Japanese encephalitis virus (JEV) and is spread to humans by infected mosquitoes ... The Imojev® vaccine being administered in the study has been used extensively across the world for more than a decade and is ...
... and interchangeability of JENVAC to an SA 14-14-2 strain derived vaccine has found JENVAC offers statistically higher ... IXIARO is an inactivated cell-derived vaccine based on the same SA 14-14-2 strain of Japanese Encephalitis as CD.JEVAX. ... There are currently 15 Japanese Encephalitis vaccines in use worldwide. The most widely administered of these is the live ... No participant in either group had an illness associated with Japanese Encephalitis during the 3 years of study. ...
Vaccines against Japanese encephalitis. In: Jong EC, Zuckerman JN, editors. Travelers vaccines. Hamilton (Canada): B.C. Decker ... Japanese encephalitis: development of new candidate vaccines. Expert Rev Anti Infect Ther. 2006;4:313-24. DOIPubMedGoogle ... Immunization against Japanese encephalitis in China: a policy analysis. Vaccine. 2006;24:5178-82. DOIPubMedGoogle Scholar ... Japanese encephalitis vaccines-needs, flaws and achievements. Biol Chem. 2008;389:547-50. DOIPubMedGoogle Scholar ...
Factors associated with the administration of rabies PrEP and Japanese encephalitis vaccine to pediatric international ... Factors associated with the administration of rabies PrEP and Japanese encephalitis vaccine to pediatric international ... Long-term pediatric travel can be associated with higher risk of infections, like Japanese encephalitis (JE) and rabies. This ... Sufficient time to complete JE vaccine series (aOR= 8.03; 95%CI 1.25, 51.75) was significantly associated with JE vaccine ...
... represents the most significant etiology of arboviral encephalitis worldwide. Japanese encephalitis is a neurologic infection ... Japanese encephalitis virus (JEV), a flavivirus (single-stranded ribonucleic acid [RNA]), ... Japanese Encephalitis Vaccines: WHO position paper, February 2015 - Recommendations. Vaccine. 2016 Jan 12. 34(3):302-3. [QxMD ... The main genotypic variants of Japanese encephalitis virus include the following [3] :. * Japanese encephalitis virus genotype ...
... www.healthrising.org/blog/2023/03/17/japanese-encephalitis-vaccine-long-covid/,Can the Japanese Encephalitis Vaccine Reduce ... Could similar vaccines hold clues to fighting Long COVID? … Continue reading Can the Japanese Encephalitis Vaccine Reduce ... Can the Japanese Encephalitis Vaccine Reduce Symptoms of Long COVID? As a researcher in international development, travel ... But I never expected that once I developed Long COVID, a travel vaccine for Japanese encephalitis might help me make a rapid ...
Abstract The live attenuated Japanese encephalitis (JE) vaccine SA14-14-2 was licensed decades ago and now approved for ... Large-scale clinical trials demonstrate ideal safety and efficacy profile of this Chinese vaccine. The SA14-14-2 vaccine was ... In the present study, to study the in vitro and in vivo genetic and attenuation stability of the vaccine virus, SA14-14-2 was ... These findings are important for quality control and evaluation of live JE vaccines and will help understand the attenuation ...
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First, the vaccine is the only Japanese encephalitis vaccine to be prequalified for use in children by the WHO. Prior to this, ... There is no specific treatment for Japanese encephalitis.. Infection and severe disease from Japanese encephalitis are most ... Japanese Encephalitis Vaccine Prequalified by WHO. October 11, 2013. January 25, 2023. Sheryl Gordon ... Not all vaccines live, attenuated. Some vaccines include a killed pathogen (inactivated vaccines) and some include only a ...
Japanese Encephalitis Virus Vaccine. Most other Common Side Effects - Headache, muscle pain, injection site pain and tenderness ... Influenza Virus Vaccine Most other Common Side Effects: Dizziness, headache, fatigue, tingling, impotence and sleep ... Anthrax Vaccine Adsorbed. Most other Common Side Effects: Injection site tenderness, pain, warmth, muscle pain, arm motion ...
Vector-Borne Diseases (Lyme disease, Japanese Encephalitis, Yellow Fever); 1991:08:01. Japanese Encephalitis Vaccines; 1990:01: ... Topic: Japanese Encephalitis. (Please note that the documents listed below are sorted by date.). Health Information for ...
ATAGI clinical guidance on Japanese encephalitis virus vaccines. For further information on JEV, including background on ... regarding the administration of Japanese encephalitis virus (JEV) vaccines.​ These recommendations follow on from earlier ... The Melbourne Vaccine Education Centre (MVEC) is an educational website, developed with the aim of providing up-to-date ... Updated monovalent mRNA COVID-19 vaccines approved by FDA September 21, 2023 ...
Safety profile of the Vero cell-derived Japanese encephalitis virus (JEV) vaccine IXIARO(®).. ... Safety profile of the Vero cell-derived Japanese encephalitis virus (JEV) vaccine IXIARO(®).. ... Produits Focusing on vaccines for infectious diseases with major unmet needs En savoir plus ...
SciTech Europa Vaccines for zoonoses: a one Health paradigm - Pages 227-229 (Read PDF) "One of the One Health Initiative teams ... Vaccines for zoonoses: a One Health paradigm SciTech Europa Quarterly (March 2018) - Issue 26 ...
Japanese encephalitis (vaccine available). Top of Page. L. La Crosse virus. Lyme disease (Borrelia burgdorferi) ... Tick-borne encephalitis virus (vaccine available). Tickborne relapsing fever (Borrelia hermsii, B. turicatae, and B. parkerii) ... Only a few mosquito-borne viruses can be prevented with vaccines. In most cases, people need to protect themselves from ...
A Large Outbreak of Japanese Encephalitis in Rakhine State, Myanmar: Implication for Vaccine Policy Article Sidebar. ... A Large Outbreak of Japanese Encephalitis in Rakhine State, Myanmar: Implication for Vaccine Policy. OSIR Journal, [S.l.], v. 9 ... Japanese Encephalitis is endemic in Rakhine State, western Myanmar. In July 2014, 27 patients were admitted to Sittwe General ... Few patients died and some patients were confirmed as having Japanese Encephalitis (JE) infection. An outbreak investigation ...
The incidence of Japanese Encephalitis (JE) in Bali Province remains high, and is one among the highest in Indonesia. The ... Cost-effectiveness analysis of Japanese Encephalitis (JE) vaccination program in Bali Province, Indonesia. ... Cost-effectiveness analysis of Japanese Encephalitis (JE) vaccination program in Bali Prov ... Vaccine Ano de publicação: 2023 Tipo de documento: Artigo ... Vaccine Ano de publicação: 2023 Tipo de documento: Artigo ...
p,Recombinant Japanese encephalitis (JE) vaccine candidates based on a highly attenuated vaccinia virus (NYVAC-JEV) and a ... Poxvirus-based Japanese encephalitis vaccine candidates induce JE virus-specific CD8+ cytotoxic T lymphocytes in mice. ... Recombinant Japanese encephalitis (JE) vaccine candidates based on a highly attenuated vaccinia virus (NYVAC-JEV) and a ... Poxvirus-based Japanese encephalitis vaccine candidates induce JE virus-specific CD8+ cytotoxic T lymphocytes in mice. ...
Results for Intercells Japanese Encephalitis virus vaccine in the pivotal Phase III safety trial, which included 2,683 ... Intercell AG said a safety analysis of its Japanese Encephalitis vaccine showed no serious side effects, moving the Austrian ... First analyses of this trial show that Intercells investigational Japanese Encephalitis vaccine was systemically and locally ... Japanese Encephalitis is a virus spread by mosquitoes that affects the nervous system.. ...
SLU researcher discovered worlds first dengue vaccine A vaccine to prevent dengue fever discovered by a Saint Louis University ... Japanese Encephalitis News and Research. RSS Japanese encephalitis (previously known as Japanese B encephalitis to distinguish ... is a disease caused by the mosquito-borne Japanese encephalitis virus. The Japanese encephalitis virus is a virus from the ... Japanese Encephalitis (JE) virus causes serious inflammation of the brain in people and fertility problems in pigs. Mosquitoes ...
Japanese Encephalitis - Why You Should Get the Vaccine in Tamworth. *Japanese Encephalitis - Why You Should Get the Vaccine in ... Japanese Encephalitis - Why You Should Get the Vaccine in Birmingham. *Home. *Japanese Encephalitis - Why You Should Get the ... Japanese Encephalitis - Why You Should Get the Vaccine in Birmingham. Japanese encephalitis is a serious viral infection with ... Side effects of Japanese encephalitis vaccine in Birmingham. Up to 40% of individuals who get the vaccine may experience mild ...
Persistence of IgM Antibodies after Vaccination with Live Attenuated Japanese Encephalitis Vaccine ... Hospital-Based Surveillance for Japanese Encephalitis at Four Sites in Bangladesh, 2003-2005 ...
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