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JAK3 inhibition: what potential for the future?

JAK3 inhibition with the CP-690,550 compound has an immunosuppressive potency in murine models, nonhuman primates and humans. This drug blocks STAT5 activation in most T-cell subpopulations but less effectively in T-regulator cells. In low to moderate risk human kidney transplant recipients, combine...

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Autor principal: Legendre, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834527/
https://www.ncbi.nlm.nih.gov/pubmed/24565406
http://dx.doi.org/10.1186/2047-1440-2-S1-S6
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author Legendre, Christophe
author_facet Legendre, Christophe
author_sort Legendre, Christophe
collection PubMed
description JAK3 inhibition with the CP-690,550 compound has an immunosuppressive potency in murine models, nonhuman primates and humans. This drug blocks STAT5 activation in most T-cell subpopulations but less effectively in T-regulator cells. In low to moderate risk human kidney transplant recipients, combined with mycophenolate mofetil, steroids and an induction with basiliximab, CP-690,550 proved as effective as calcineurin inhibitors with regard to prevention of acute rejection but better than calcineurin inhibitors with regard to preservation of kidney function and histology. However, at the same time, an increased incidence of overimmunosuppression consequences (cytomegalovirus, BK virus and lymphoproliferation) was observed and led to discontinuation of this specific drug development in kidney transplantation.
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spelling pubmed-38345272013-11-21 JAK3 inhibition: what potential for the future? Legendre, Christophe Transplant Res Review JAK3 inhibition with the CP-690,550 compound has an immunosuppressive potency in murine models, nonhuman primates and humans. This drug blocks STAT5 activation in most T-cell subpopulations but less effectively in T-regulator cells. In low to moderate risk human kidney transplant recipients, combined with mycophenolate mofetil, steroids and an induction with basiliximab, CP-690,550 proved as effective as calcineurin inhibitors with regard to prevention of acute rejection but better than calcineurin inhibitors with regard to preservation of kidney function and histology. However, at the same time, an increased incidence of overimmunosuppression consequences (cytomegalovirus, BK virus and lymphoproliferation) was observed and led to discontinuation of this specific drug development in kidney transplantation. BioMed Central 2013-11-20 /pmc/articles/PMC3834527/ /pubmed/24565406 http://dx.doi.org/10.1186/2047-1440-2-S1-S6 Text en Copyright © 2014 Legendre; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Legendre, Christophe
JAK3 inhibition: what potential for the future?
title JAK3 inhibition: what potential for the future?
title_full JAK3 inhibition: what potential for the future?
title_fullStr JAK3 inhibition: what potential for the future?
title_full_unstemmed JAK3 inhibition: what potential for the future?
title_short JAK3 inhibition: what potential for the future?
title_sort jak3 inhibition: what potential for the future?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834527/
https://www.ncbi.nlm.nih.gov/pubmed/24565406
http://dx.doi.org/10.1186/2047-1440-2-S1-S6
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