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IL-12 unmasks latent autoimmune disease in resistant mice

Inbred mice exhibit a spectrum of susceptibility to induction of experimental allergic encephalomyelitis (EAE). We have compared the immune responses of the susceptible SJL (H-2s) and resistant B10.S (H- 2s) strains to determine factors other than the MHC background which control resistance/suscepti...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192714/
https://www.ncbi.nlm.nih.gov/pubmed/8786337
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collection PubMed
description Inbred mice exhibit a spectrum of susceptibility to induction of experimental allergic encephalomyelitis (EAE). We have compared the immune responses of the susceptible SJL (H-2s) and resistant B10.S (H- 2s) strains to determine factors other than the MHC background which control resistance/susceptibility to EAE. The resistance of the B10.S strain was found to be secondary to an antigen-specific defect in the generation of Th 1 cells that produce IFN gamma. This defect in IFN gamma production could be restored by exposure of the myelin basic protein (MBP)-reactive T cells to IL-12 with the subsequent induction of the ability to transfer EAE to naive recipients. These findings have important implications for the therapeutic use of IL-12 and IL-12 antagonists and may explain the association between relapses/exacerbation of autoimmune disease and infectious diseases.
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spelling pubmed-21927142008-04-16 IL-12 unmasks latent autoimmune disease in resistant mice J Exp Med Articles Inbred mice exhibit a spectrum of susceptibility to induction of experimental allergic encephalomyelitis (EAE). We have compared the immune responses of the susceptible SJL (H-2s) and resistant B10.S (H- 2s) strains to determine factors other than the MHC background which control resistance/susceptibility to EAE. The resistance of the B10.S strain was found to be secondary to an antigen-specific defect in the generation of Th 1 cells that produce IFN gamma. This defect in IFN gamma production could be restored by exposure of the myelin basic protein (MBP)-reactive T cells to IL-12 with the subsequent induction of the ability to transfer EAE to naive recipients. These findings have important implications for the therapeutic use of IL-12 and IL-12 antagonists and may explain the association between relapses/exacerbation of autoimmune disease and infectious diseases. The Rockefeller University Press 1996-08-01 /pmc/articles/PMC2192714/ /pubmed/8786337 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
IL-12 unmasks latent autoimmune disease in resistant mice
title IL-12 unmasks latent autoimmune disease in resistant mice
title_full IL-12 unmasks latent autoimmune disease in resistant mice
title_fullStr IL-12 unmasks latent autoimmune disease in resistant mice
title_full_unstemmed IL-12 unmasks latent autoimmune disease in resistant mice
title_short IL-12 unmasks latent autoimmune disease in resistant mice
title_sort il-12 unmasks latent autoimmune disease in resistant mice
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192714/
https://www.ncbi.nlm.nih.gov/pubmed/8786337