CD4+ T Cell Help Impairs CD8+ T Cell Deletion Induced by Cross-presentation of Self-Antigens and Favors Autoimmunity

Author:

Kurts Christian1,Carbone Francis R.1,Barnden Megan1,Blanas Effrossini1,Allison Janette1,Heath William R.1,Miller Jacques F.A.P.1

Affiliation:

1. From the Immunology Division, The Walter and Eliza Hall Institute of Medical Research, Victoria 3050; and The Department of Pathology and Immunology, Monash Medical School, Prahran 3181, Victoria, Australia

Abstract

Self-antigens expressed in extrathymic tissues such as the pancreas can be transported to draining lymph nodes and presented in a class I–restricted manner by bone marrow-derived antigen-presenting cells. Such cross-presentation of self-antigens leads to CD8+ T cell tolerance induction via deletion. In this report, we investigate the influence of CD4+ T cell help on this process. Small numbers of autoreactive OVA-specific CD8+ T cells were unable to cause diabetes when adoptively transferred into mice expressing ovalbumin in the pancreatic β cells. Coinjection of OVA-specific CD4+ helper T cells, however, led to diabetes in a large proportion of mice (68%), suggesting that provision of help favored induction of autoimmunity. Analysis of the fate of CD8+ T cells indicated that CD4+ T cell help impaired their deletion. These data indicate that control of such help is critical for the maintenance of CD8+ T cell tolerance induced by cross-presentation.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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