Infectious tolerance. NLM AIDSLINE Important note: Information in this article was accurate in 1999. The state of the art may have changed since the publication date.

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Infectious tolerance.

Curr Opin Immunol. 1998 Oct;10(5):518-24. Unique Identifier : AIDSLINE MED/99014155
Cobbold S; Waldmann H; Sir William Dunn School of Pathology, South Parks Road, Oxford,; OX1 3RE, UK. stephen.cobbold@pathology.ox.ac.uk


Abstract: Infectious tolerance can be induced in many ways, does not require a thymus or clonal deletion and can spread to third-party antigens linked on the same antigen-presenting cell-the process being variously described as linked-, bystanderor epitope-suppression. We here review the evidence concerning the mechanisms involved and attempt to make a consistent hypothesis, that during tolerance induction in the Th1-mediated autoimmune diseases and transplantation systems there would seem to be a phase of immune deviation towards Th2 cytokines, like IL-4 and IL-10; however, this may lead to an IL-10-induced form of anergy or nonresponsiveness and generation of the recently characterized Th3/T-regulatory-1 CD4+ T cell subset which is thought to downregulate the antigen-presenting cell, possibly via transforming growth factor beta.
Keywords: JOURNAL ARTICLE REVIEW REVIEW, TUTORIAL Animal Human *Immune Tolerance Infection/*IMMUNOLOGY Th1 Cells/IMMUNOLOGY Th2 Cells/IMMUNOLOGY Transforming Growth Factor beta/PHYSIOLOGYKWDjournalarticlereviewreview,tutorialanimalhumanKWDimmunetoleranceinfection/KWDimmunologyth1cells/immunologyth2cells/immunologytransforminggrowthfactorbeta/physiology
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Copyright © 1999 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

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