Kurts C, Kosaka H, Carbone F R, Miller J F, Heath W R
Thymus Biology Unit, The Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Parkville 3050, Victoria, Australia.
J Exp Med. 1997 Jul 21;186(2):239-45. doi: 10.1084/jem.186.2.239.
In this report, we show that cross-presentation of self-antigens can lead to the peripheral deletion of autoreactive CD8(+) T cells. We had previously shown that transfer of ovalbumin (OVA)-specific CD8(+) T cells (OT-I cells) into rat insulin promoter-membrane-bound form of OVA transgenic mice, which express the model autoantigen OVA in the proximal tubular cells of the kidneys, the beta cells of the pancreas, the thymus, and the testis of male mice, led to the activation of OT-I cells in the draining lymph nodes. This was due to class I-restricted cross-presentation of exogenous OVA on a bone marrow-derived antigen presenting cell (APC) population. Here, we show that adoptively transferred or thymically derived OT-I cells activated by cross-presentation are deleted from the peripheral pool of recirculating lymphocytes. Such deletion only required antigen recognition on a bone marrow-derived population, suggesting that cells of the professional APC class may be tolerogenic under these circumstances. Our results provide a mechanism by which the immune system can induce CD8(+) T cell tolerance to autoantigens that are expressed outside the recirculation pathway of naive T cells.
在本报告中,我们表明自身抗原的交叉提呈可导致自身反应性CD8⁺ T细胞在外周被清除。我们之前曾表明,将卵清蛋白(OVA)特异性CD8⁺ T细胞(OT-I细胞)转移至表达模型自身抗原OVA的大鼠胰岛素启动子-膜结合形式的OVA转基因小鼠中,该抗原在雄性小鼠的肾近端小管细胞、胰腺β细胞、胸腺和睾丸中表达,并导致引流淋巴结中OT-I细胞的活化。这是由于外源性OVA在骨髓来源的抗原呈递细胞(APC)群体上进行I类限制性交叉提呈所致。在此,我们表明通过交叉提呈激活的过继转移或胸腺来源的OT-I细胞从外周循环淋巴细胞池中被清除。这种清除仅需要在骨髓来源的群体上进行抗原识别,这表明在这些情况下,专职APC类细胞可能具有致耐受性。我们的结果提供了一种机制,通过该机制免疫系统可诱导CD8⁺ T细胞对在初始T细胞再循环途径之外表达的自身抗原产生耐受性。