Swat W, Ignatowicz L, von Boehmer H, Kisielow P
Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wroclaw, Poland.
Nature. 1991 May 9;351(6322):150-3. doi: 10.1038/351150a0.
One mechanism ensuring self tolerance of T cells is the clonal deletion of thymocytes bearing alpha beta T-cell receptors. The stage of thymocyte development at which the interaction with antigen-presenting cells (APCs) leads to deletion, however, has not been determined directly. Indirect evidence suggests that intrathymic APCs induce deletion of CD4+8+ thymocytes (which die by apoptosis) but deletion at less and more mature developmental stages has also been implied. It is also not clear if clonal elimination of thymocytes can be triggered by peripheral antigens carried on extrathymic APCs migrating through the thymus. Here we show antigen-specific induction of apoptosis in CD4+8+ thymocytes cultured in suspension, by thymic as well as splenic APCs. Thus the recognition of antigen by CD4+8+ thymocytes may lead to deletion, suggesting that this is the central mechanism of tolerance induction, which is not limited by the antigen-presenting ability of the thymic stroma.
确保T细胞自身耐受性的一种机制是克隆清除带有αβT细胞受体的胸腺细胞。然而,胸腺细胞发育过程中与抗原呈递细胞(APC)相互作用导致清除的阶段尚未直接确定。间接证据表明,胸腺内的APC可诱导CD4+8+胸腺细胞的清除(这些细胞通过凋亡死亡),但在较不成熟和较成熟的发育阶段也有清除的情况。胸腺外APC携带的外周抗原穿过胸腺时能否触发胸腺细胞的克隆清除也不清楚。在这里,我们展示了胸腺和脾脏APC在悬浮培养的CD4+8+胸腺细胞中诱导抗原特异性凋亡。因此,CD4+8+胸腺细胞对抗原的识别可能导致清除,这表明这是诱导耐受性的核心机制,不受胸腺基质抗原呈递能力的限制。