*  Monitoring Epstein-Barr Virus (EBV) Load in Rheumatoid Arthritis Patients Treated With New Immunosuppressive Drugs - Tabular...
Current treatment of RA routinely includes potentially immunosuppressive medications like methotrexate and TNFa inhibitors. New immunosuppressive drugs are at disposal, Orencia* (abatacept) which is a T cell co-stimulation modulator (CTLA4Ig) and RoActemra* (tocilizumab), an antibody against IL6 receptor. In solid organ transplant recipients under immunosuppressants, emergence of lymphoma can be predicted by monitoring EBV load in peripheral blood mononuclear cells (PBMNCs). EBV load above 1000 copies per 500 ng PBMNC DNA is considered a limit above which patients will develop EBV associated post transplant lymphoproliferative disorder, a condition characterized by polyclonal EBV positive B lymphocyte proliferation which can evolve into EBV positive B cell lymphoma .. In a first study, we showed that Rheumatoid arthritis patients have 10 fold systemic EBV overload, very similar to that observed in healthy organ transplant recipients. More recently, we showed that methotrexate tended to ...
  https://clinicaltrials.gov/ct2/show/record/NCT00947492
*  CellCept (Mycophenolate Mofetil) - Side Effects, Dosage, Interactions - Drugs
Use CellCept exactly as prescribed by your doctor. Mycophenolate mofetil is reported to have a pKa values of 5. Study April 26, Baseball Great Rod Carew Owes His Life to NFL Player's Transplanted Organs April 17, Before taking mycophenolate mofetil , tell your doctor or pharmacist if you are allergic to it; or to mycophenolic acid; or to mycophenolate sodium; or if you have any other allergies. Cases of pure red cell aplasia PRCA have been reported in patients treated with CellCept in combination with other immunosuppressive agents. Do not take any new medicine without talking with your doctor. CellCept Intravenous infusion solution must be prepared in two steps: The genotoxic potential of mycophenolate hearts game was determined in five assays. The highest dose tested was 0. CellCept has been administered in combination with the following agents in clinical trials: No data are kostenlos zocken online on the slotmaschinen gratis ohne anmeldung spielen of long-term exposure to this level of MPAG. ...
  http://businessinvietnam.eu/stargames/another-name-for-cellcept.php
*  A novel immunosuppressive agent FTY720 induced Akt dephosphorylation in leukemia cells.
Abstract 1. Our previous studies revealed that the immunosuppressive agent, FTY720, mainly induces mitochondria-involved apoptosis in some types of cancer cells, since Bcl-2 overex..
  https://www.omicsonline.org/references/a-novel-immunosuppressive-agent-fty720-induced-akt-dephosphorylation-in-leukemia-cells-951394.html
*  Immunosuppressive compounds - Vertex Pharmaceuticals, Inc.
This invention relates to a novel class of immunosuppressive compounds having an affinity for the FK-506 binding protein (FKBP). Once bound to this protein, the immunosuppressive compounds inhibit the
  http://www.freepatentsonline.com/5192773.html
*  DailyMed - MYCOPHENOLATE MOFETIL - mycophenolate mofetil tablet, film coated MYCOPHENOLATE MOFETIL - mycophenolate mofetil...
Pregnancy Category D. See WARNINGS section.. Use of MMF during pregnancy is associated with an increased risk of first trimester pregnancy loss and an increased risk of congenital malformations, especially external ear and other facial abnormalities including cleft lip and palate, and anomalies of the distal limbs, heart, esophagus, kidney, and nervous system. In animal studies, congenital malformations and pregnancy loss occurred when pregnant rats and rabbits received mycophenolic acid at dose multiples similar to and less than clinical doses. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to the fetus.. Risks and benefits of mycophenolate mofetil should be discussed with the patient. When appropriate, consider alternative immunosuppressants with less potential for embryofetal toxicity. In certain situations, the patient and her healthcare practitioner may decide that ...
  https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9f84ea84-2d8b-4d91-a33f-7dfb5df937dc
*  Reduction of immunosuppressant therapy requirement in heart transplantation by calcitriol - Garvan Institute of Medical Research
Calcitriol has been shown to have immunomodulatory effects. We examined whether heart transplant recipients, randomly assigned to receive calcitriol to reduce bone loss, required less immunosuppressive therapy or demonstrated different rejection and survival outcomes. Patients receiving low-dose calcitriol required substantially lower cumulative doses of cyclosporin (29% [95% confidence interval; 8%-50%] and 28% [7%-50%] for 1 and 2 years, respectively) for organ rejection without any detectable change in episodes of rejection, infection, or deaths. This major reduction of oral cyclosporine requirement, in addition to the skeletal benefits of calcitriol in those receiving immunosuppressive therapy, indicates a potential role for co-therapy with calcitriol or its analogues in the management of patients with solid-organ transplantation.
  https://www.garvan.org.au/research/publications/1633
*  "Immunosuppressive strategies to avoid complications: The Achilles' hee" by Gregory Smallwood
PURPOSE OF REVIEW: The goal of solid organ transplantation has now evolved into minimizing the long-term consequences of immunosuppression. The consequences of immunosuppression include an increased risk of developing diabetes, renal insufficiency, osteoporosis, malignancies, and viral infections, to name but a few. RECENT FINDINGS: Immunosuppressive protocols that avoid or minimize the use of calcineurin inhibitors hold the promise of better long-term patient outcomes, especially with patients who progress on to dialysis or renal transplantation after organ transplantation. New, aggressive induction protocols have been used in patients with chronic viral infections, such as hepatitis C, without untoward effects on outcomes. SUMMARY: It is important to appreciate that the long-term benefits of new immunosuppressive strategies have yet to stand the test of time when considering long-term graft survival. Follow-ups to these ...
  https://digitalcommons.pcom.edu/scholarly_papers/1191/
*  Conventional Immunosuppression is Compatible with Costimulation Blockade-Based, Mixed Chimerism Tolerance Induction - Adams -...
Clinical trials to test the safety and efficacy of costimulation-based strategies in clinical solid organ transplantation will likely involve the concomitant use of conventional immunosuppressive agents. For example, the clinical trial currently in progress to test blockade of the CD28/B7 pathway in renal transplant patients includes concurrent treatment with MMF, steroids, and an anti-CD25 mAb. The design of clinical trials to include conventional agents provides an adequate margin of safety against allograft rejection thus permitting the testing of new, exciting agents in an ethically acceptable manner. As a result, a more basic understanding of the interactions between these agents and costimulation blockade strategies is critical for the design of preclinical nonhuman primate studies and clinical trials.. Blockade of the CD40 and CD28 pathways effectively inhibits rejection responses in rodent and nonhuman primate allograft models. However, when this strategy is combined with calcineurin ...
  http://onlinelibrary.wiley.com/doi/10.1034/j.1600-6143.2003.00155.x/full
*  A PHARMACOKINETIC POPULATION MODEL FOR CYCLOSPORIN A IN RENAL TRANSPLANT RECIPIENTS : Development of a model for whole blood-...
ABSTRACT. Background: Cyclosporine A (CsA) has since its introduction in the 1980's played a substantial part of the success in solid organ transplantation. Like many other immunosuppressive drugs, CsA has a narrow therapeutic window and a large inter-individual variability. Drug exposure above the therapeutic window is associated with adverse events like nephrotoxicity, infection and cancer while drug exposure below will yield a lack of effect and increased risk for acute rejection episodes. Obtaining an optimal drug concentration will prevent acute organ rejections and optimize survival of the grafts and ultimately the patients.. The primary aim of this study is to implement a T-cell compartment to an already existing whole blood model. Another goal was to further develop the basic whole blood model after the inclusion of 20 new patients followed for at least 8 weeks, by re-evaluating for relevant covariates and include estimation of ...
  https://www.duo.uio.no/handle/10852/12276
*  Renal Function Optimization With Mycophenolate Mofetil (MMF) Immunosuppressor Regimes (ALHAMBRA) - Full Text View -...
The study population characteristics raise the need to establish a treatment regime that assures suitable intensity immunosuppression to avoid the appearance of rejection episodes, but minimizes the doses to prevent over-immunosuppression in a population with a theoretic minor immune response.. On the other hand, the delay in the introduction of calcineurin inhibitors will prevent increasing the risk of early graft dysfunction allowing the highest post-transplant renal recovery in organs with less operative mass and greater sensibility to the nephrotoxic effect of these drugs.. The results of several studies confirm the goodness of regimes that include low doses of calcineurin inhibitors, delay their introduction or avoid them.. Nevertheless, although it is standard practice to evaluate the effectiveness of the regimes for a time to assure, with certainty, the response to the treatments, these follow-ups are still relatively ...
  https://clinicaltrials.gov/ct2/show/NCT00290069
*  Cellcept: A Promising New Immunosuppressive Drug | Pemphigus Pemphigoid Foundation (IPPF)
By Grant J. Anhalt, M.D. and Hossein Nousari, M.D.Johns Hopkins University, School of Medicine In February 1997, the FDA approved a new drug, mycophenolate
  http://www.pemphigus.org/cellcept-a-promising-new-immunosuppressive-drug-2/
*  Immunosuppressive Medications for Participants in ITN005CT (NCT00014911) - Full Text View - ClinicalTrials.gov
Study acronym: EXIIST - Extended Immunosuppression in Islet Transplantation. Islet transplantation is an experimental therapy in people with difficult to control Type 1 diabetes (T1D). Insulin producing cells (islets) are isolated from a pancreas. After the cells are prepared, the islets are put into the subject's liver. These transplanted islets may produce insulin that the subject's islets can no longer make. In order to help keep up the function of the transplanted islets, immunosuppressive medications must be given indefinitely or for as long as the study doctor determines is necessary. The medications serve to modify the immune system that normally tries to destroy (reject) new islets.. Participants in this study have received up to three islet cell infusions as a previous participant in the ITN005CT (NIS01) protocol. They also received a maintenance immunosuppressive treatment regimen consisting of a combination of orally administered ...
  https://clinicaltrials.gov/ct2/show/NCT01309022?term=NIAID&recr=Open&no_unk=Y&sntx=
*  Immunosuppressive Medications for Participants in ITN005CT (NCT00014911) - Full Text View - ClinicalTrials.gov
Study acronym: EXIIST - Extended Immunosuppression in Islet Transplantation. Islet transplantation is an experimental therapy in people with difficult to control Type 1 diabetes (T1D). Insulin producing cells (islets) are isolated from a pancreas. After the cells are prepared, the islets are put into the subject's liver. These transplanted islets may produce insulin that the subject's islets can no longer make. In order to help keep up the function of the transplanted islets, immunosuppressive medications must be given indefinitely or for as long as the study doctor determines is necessary. The medications serve to modify the immune system that normally tries to destroy (reject) new islets.. Participants in this study have received up to three islet cell infusions as a previous participant in the ITN005CT (NIS01) protocol. They also received a maintenance immunosuppressive treatment regimen consisting of a combination of orally administered ...
  https://clinicaltrials.gov/ct2/show/NCT01309022?type=Expn&rank=36
*  Renal Fellow Network: How to best design RCTs for new transplant immunosuppressives
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  http://renalfellow.blogspot.com/2009/10/how-to-best-design-rcts-for-new.html
*  Phase 1/2 Safety and Efficacy of PLX3397 in Adults With Relapsed or Refractory Acute Myeloid Leukemia (AML) - Tabular View -...
For both Parts 1 and 2, receipt of HSCT within 60 days of the first dose of PLX3397 is an exclusion criterion. Patients on immunosuppressive therapy post HSCT, or with clinically significant graft-versus-host disease are excluded from Part 1. (Use of topical steroids for ongoing skin GVHD is permitted). Patients for Part 1 must have a wash-out period of ≥2 weeks or at least 4 half-lives from their last systemic immunosuppressive treatment for GVHD. Patients for Part 2 may be receiving systemic immunosuppressive treatment for management of GVHD at the time of screening and ...
  https://clinicaltrials.gov/ct2/show/record/NCT01349049
*  Sirolimus for rescue and primary immunosuppression in transpla...
Sirolimus for rescue and primary immunosuppression in transplanted children receiving tacrolimus.: SRL and reduced-dose TAC may achieve adequate immunosuppressi
  https://www.mysciencework.com/publication/show/sirolimus-rescue-primary-immunosuppression-transplanted-children-receiving-tacrolimus-e93a8435
*  It has become evident that tumor-induced immuno-suppressive elements in the growth | COX-2 contributes to the maintenance of...
It has become evident that tumor-induced immuno-suppressive elements in the growth microenvironment play a main part in suppressing normal features of effector Capital t cells. can promote antitumor results by re-establishing T-cell defenses (for review, discover ref. 6767).65, 68 1MT is anticipated to possess no serious side effects since it prevents IDO while sparing tryptophan dioxygenase, a hepatic enzyme that regulates body tryptophan amounts.69 Style and advancement of more effective IDO inhibitors is underway (for examine, discover ref. 60, 67, 70).60, 67, 70 Arginase and nitric-oxide synthase Change in the path involving the catabolism of L-arginine is linked to the reductions of T-cell expansion. Two essential digestive enzymes included in arginine rate of metabolism are arginase and inducible nitric oxide synthase (iNOS).9 Arginine is used by iNOS as a precursor for the production of nitric oxide (NO). Consequently, raised amounts of arginase and iNOS deplete arginine, an important ...
  http://lifescienceexec.com/it-has-become-evident-that-tumor-induced-immuno-suppressive-elements-in-the-growth/
*  Plus it
The recognition that immune suppression is crucial to promote tumor progression, which might explain the failure of some cancer vaccines, has resulted in a paradigm shift regarding approaches to cancer immunotherapy. It indeed becomes clear that successful cancer immunotherapy will only be achieved when associated with the elimination of suppressive cells (31-33). Two major immunosuppressive cell types are mainly involved in tumor-induced immunosuppression: Tregs and MDSC. The elimination of Treg cells using a low dosage of cyclophosphamide as a metronomic regimen proved its efficacy in many rodent models as well as in humans (25, 26, 30, 34-37). Many strategies have been tested to dampen the immunosuppressive actions of MDSC, including treatments designed to favor their differentiation, or to inhibit their expansion or their inhibitory function (13, 38). However, the most promising results have been obtained with the selective depletion of these cells. Some groups tested ...
  http://cancerres.aacrjournals.org/content/70/8/3052
*  Peptides - LIFE SCIENCES - Products
Find here a selection of peptides of various nature such as toxins, immunosuppressives, antibiotics or chromogenic diagnostic peptides.
  https://www.iris-biotech.de/de/products/life-sciences/peptides.html
*  glucocorticoid | hormone | Britannica.com
glucocorticoid: Any steroid hormone that is produced by the adrenal gland and known particularly for its anti-inflammatory and immunosuppressive actions. The adrenal gland is an organ situated...
  https://www.britannica.com/science/glucocorticoid
*  "Immunosuppressive properties of purified immune t-interferon." by M A. Lucero, J Wietzerbin et al.
Lucero, M A.; Wietzerbin, J; Stefanos, S; Billardon, C; Falcoff, R; and Fridman, W H., "Immunosuppressive properties of purified immune t-interferon." (1980). Subject Strain Bibliography 1980. 3146 ...
  https://mouseion.jax.org/ssbb1980/3146/
*  Composition for the prevention and/or treatment of the cytotoxic effects induced by the use of immunosuppressive agents - Sigma...
A composition is disclosed which is suitable for the prevention and/or treatment of cell and tissue abnormalities of exogenous, toxic or metabolic origin and suitable for reducing the toxic effects of
  http://www.freepatentsonline.com/7897641.html
*  JoVE Author Search: Sfriso P
Anakinra, Arthritis, Corticosteroids, Dermatitis, Disease, Eye, Eyes, Family, Gene, Genetics, Immunosuppressive Agents, Joint, Morbidity, Patients, Skin, Syndrome, Therapeutic, Treatment, Uveitis
  http://labindex.jove.com/author/Sfriso-P
*  Basiliximab (Professional Patient Advice) - Drugs.com
Professional guide for Basiliximab. Includes: pharmacology, pharmacokinetics, contraindications, interactions, adverse reactions and more.
  https://www.drugs.com/ppa/basiliximab.html
*  Idogen
... develops tolerogenic vaccines which re-program the immune system. The company's technology has the potential to develop long-acting treatment of anti-drug antibodies as well as autoimmune diseases that currently can not be cured. In addition, Idogen has the potential to change the transplantation market by reducing the need for immunosuppressive therapy after transplantation. Idogen was founded in 2008 based on a fundamental immunological discovery at Lund University.
  http://news.cision.com/idogen