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

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 deletio...

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Detalles Bibliográficos
Autores principales: Kurts, Christian, Carbone, Francis R., Barnden, Megan, Blanas, Effrossini, Allison, Janette, Heath, William R., Miller, Jacques F.A.P.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2199175/
https://www.ncbi.nlm.nih.gov/pubmed/9396776
Descripción
Sumario: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.