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同种抗原反应性T淋巴细胞的极限稀释分析。III. 启动对前体细胞频率的影响。

Limiting dilution analysis of alloantigen-reactive T lymphocytes. III. Effect of priming on precursor frequencies.

作者信息

Ryser J E, MacDonald H R

出版信息

J Immunol. 1979 Jul;123(1):128-32.

PMID:156230
Abstract

The effect of specific priming with alloantigens on the frequency of cytolytic T lymphocyte precursors (CTL-P) has been investigated. Alloimmune lymphoid cells were obtained from the spleen of C57BL/6 (H-2b) mice primed with DBA/2 (H-2d) tumor cells or from 14-day unidirectional mixed leukocyte cultures (C57BL/6 anti-DBA/2). CTL-P frequencies directed against H-2d alloantigens were estimated by limiting dilution analysis in a sensitive micro MLC system. Under these conditions, an apparent increase of 3 to 4-fold in CTL-P frequency was observed in alloimmune (as compared with normal) C57BL/6 spleen cells. Evidence was obtained suggesting that this increase was specific for the priming alloantigens. A much greater increase in CTL-P frequency (25 to 100-fold) was observed after alloimmunization of C57BL/6 spleen cells in unidirectional MLC. Under the latter conditions, 5 to 20% of the surviving splenic MLC cells could be identified operationally as CTL-P. A similar enrichment in CTL-P frequency was obtained when lymph node, peripheral blood, or thymus cells were cultured for 14 days in MLC. These studies provide direct evidence that the pool of specific CTL-P can be expanded after alloimmunization. Furthermore, the very high frequencies observed after in vitro priming indicate that this system should be particularly useful for future studies of the progeny of individual CTL-P.

摘要

已对同种异体抗原特异性启动对细胞毒性T淋巴细胞前体(CTL-P)频率的影响进行了研究。同种免疫淋巴细胞取自用DBA/2(H-2d)肿瘤细胞启动的C57BL/6(H-2b)小鼠的脾脏,或取自14天单向混合淋巴细胞培养物(C57BL/6抗DBA/2)。在灵敏的微量混合淋巴细胞培养(MLC)系统中,通过有限稀释分析来估计针对H-2d同种异体抗原的CTL-P频率。在这些条件下,与正常C57BL/6脾细胞相比,同种免疫的C57BL/6脾细胞中CTL-P频率明显增加了3至4倍。有证据表明这种增加是针对启动的同种异体抗原特异性的。在单向MLC中对C57BL/6脾细胞进行同种免疫后,观察到CTL-P频率有更大幅度的增加(25至100倍)。在后一种条件下,5%至20%存活的脾MLC细胞在操作上可被鉴定为CTL-P。当淋巴结、外周血或胸腺细胞在MLC中培养14天时,也获得了类似的CTL-P频率富集。这些研究提供了直接证据,表明同种免疫后特异性CTL-P库可以扩大。此外,体外启动后观察到的非常高的频率表明,该系统对于未来对单个CTL-P后代的研究应该特别有用。

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