Kurts C, Carbone F R, Barnden M, Blanas E, Allison J, Heath W R, Miller J F
Immunology Division, The Walter and Eliza Hall Institute of Medical Research, Victoria 3050, Australia.
J Exp Med. 1997 Dec 15;186(12):2057-62. doi: 10.1084/jem.186.12.2057.
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.
在胸腺外组织(如胰腺)中表达的自身抗原可被转运至引流淋巴结,并由骨髓来源的抗原呈递细胞以I类限制性方式呈递。这种自身抗原的交叉呈递通过细胞凋亡导致CD8 + T细胞耐受诱导。在本报告中,我们研究了CD4 + T细胞辅助对此过程的影响。少量自身反应性卵清蛋白特异性CD8 + T细胞在过继转移到胰腺β细胞中表达卵清蛋白的小鼠体内时,无法引发糖尿病。然而,共注射卵清蛋白特异性CD4 +辅助性T细胞会导致很大比例的小鼠(68%)患糖尿病,这表明提供辅助有利于自身免疫的诱导。对CD8 + T细胞命运的分析表明,CD4(+) T细胞辅助会损害它们的凋亡。这些数据表明,控制这种辅助对于维持由交叉呈递诱导的CD8 + T细胞耐受至关重要。