Kruisbeek A M, Mond J J, Fowlkes B J, Carmen J A, Bridges S, Longo D L
J Exp Med. 1985 May 1;161(5):1029-47. doi: 10.1084/jem.161.5.1029.
In an effort to elucidate the role of intrathymic Ia-bearing antigen-presenting cells (APC) on the development of the class II-restricted T cell repertoire, we examined the effect of neonatal anti-I-A treatment on both intrathymic and splenic APC function; on the generation of Lyt-2-,L3T4+, Lyt-2+,L3T4-, and Lyt-2+,L3T4+ T cells; and on the development of class I- and class II-specific T cell functions. Both the thymus and the spleen are completely devoid of Lyt-2-,L3T4+ T cells in young mice treated from birth with anti-I-A, and also lack functions associated with this subset, i.e., alloantigen-specific interleukin 2 production (present report), allo-class II-specific and self-class II-restricted T cell proliferative responses, and helper cell function for the generation of cytotoxic T lymphocyte responses (18). Development of the Lyt-2+,L3T4- subset proceeds undisturbed in these mice, in accord with the previously reported normal levels of cytotoxic T lymphocyte precursors (18). The thymus contains normal numbers of the immature cortical Lyt-2+,L3T4+ cells, indicating that acquisition of the L3T4 marker, in and of itself, is not influenced by anti-I-A treatment. This striking absence of the lineage of T cells responsible for class II-specific T cell functions is correlated with absence of thymic APC function for class II-restricted T cell clones. When anti-I-A-treated mice are allowed to recover from the antibody treatment, splenic and thymic APC function return to normal in 2-3 wk, and thymic Lyt-2-,L3T4+ T cell numbers and functions reappear before such cells are detectable in the spleen. Collectively, these findings suggest that development of the Lyt-2-,L3T4+ lineage of class II-specific T cells is entirely dependent on functional I-A-bearing APC cells in the thymus. In addition, the presence of normal levels of Lyt-2+,L3T4-T cells argues that generation of the two major subsets of T cells (i.e., Lyt-2+,L3T4- and Lyt-2-,L3T4+) occurs through separate events, involving unique sites of interactions between precursor T cells and nonlymphoid major histocompatibility complex-bearing thymus cells.
为了阐明胸腺内表达Ia的抗原呈递细胞(APC)在II类限制性T细胞库发育中的作用,我们研究了新生期抗I-A治疗对胸腺内和脾内APC功能的影响;对Lyt-2-、L3T4+、Lyt-2+、L3T4-和Lyt-2+、L3T4+ T细胞生成的影响;以及对I类和II类特异性T细胞功能发育的影响。在出生时用抗I-A治疗的幼鼠中,胸腺和脾脏完全缺乏Lyt-2-、L3T4+ T细胞,并且也缺乏与该亚群相关的功能,即同种异体抗原特异性白细胞介素2的产生(本报告)、同种II类特异性和自身II类限制性T细胞增殖反应,以及产生细胞毒性T淋巴细胞反应的辅助细胞功能(18)。在这些小鼠中,Lyt-2+、L3T4-亚群的发育不受干扰,这与先前报道的细胞毒性T淋巴细胞前体的正常水平一致(18)。胸腺中含有正常数量的未成熟皮质Lyt-2+、L3T4+细胞,这表明L3T4标记的获得本身不受抗I-A治疗的影响。负责II类特异性T细胞功能的T细胞谱系的这种显著缺失与II类限制性T细胞克隆的胸腺APC功能缺失相关。当抗I-A治疗的小鼠从抗体治疗中恢复时,脾和胸腺的APC功能在2 - 3周内恢复正常,并且胸腺Lyt-2-、L3T4+ T细胞的数量和功能在脾脏中可检测到此类细胞之前重新出现。总的来说,这些发现表明II类特异性T细胞的Lyt-2-、L3T4+谱系的发育完全依赖于胸腺中具有功能的表达I-A的APC细胞。此外,Lyt-2+、L3T4- T细胞正常水平的存在表明,T细胞的两个主要亚群(即Lyt-2+、L3T4-和Lyt-2-、L3T4+)的产生是通过独立的事件发生的,涉及前体T细胞与携带主要组织相容性复合体的非淋巴细胞胸腺细胞之间独特的相互作用位点。