The Journal of Experimental Medicine · 1997 · 316 citations · 23 references
Life SciencesCell BiologyImmunologyAutoimmunityCellular ImmunologyImmunoregulationAntigen RecognitionAutoantigensAutoimmune Disease PathogenesisAutoimmune DiseasesCell-mediated ImmunityT Cell BiologyAntigen Presenting CellsBone Marrow - Derived CellsCd4 Positive T CellsCd8 Positive T CellsSelf-reactive T Cell DeletionT Helper CellsT-cell Mediated AutoimmunityT-cell Mediated Immunity
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 beta 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.
23