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在抗体应答中协同作用的雄性抗原特异性辅助性T细胞的MHC限制

MHC restriction of male-antigen-specific T helper cells collaborating in antibody responses.

作者信息

Pettersson S, Pobor G, Coutinho A

出版信息

Immunogenetics. 1982;15(2):129-38. doi: 10.1007/BF00621946.

Abstract

By priming female C57BL/6 mice with syngeneic male spleen cells and enriching inguinal and paraaortic lymph node cells in long-term culture (LTC) by repeated restimulations, H-Y-specific T helper cells can be produced. In response to male spleen cells carrying I-Ab antigens these cells activate "antigen-expressing" B cells to secrete polyclonal antibody. Before the end of the second week in LTC it was impossible to detect any helper activity. Induction of plaque-forming cells (PFC) also requires simultaneous recognition of antigen and I-A-encoded determinants in the "stimulator-responder" spleen-cell population. The testing of spleen cells from H-2 recombinant strains as "stimulator-responders" to anti-H-Y helper T cells of C57BL/6 origin also revealed that other genes, telomeric to I-A, control the magnitude of both specific T-cell proliferation and helper-dependent B-cell activation.

摘要

通过用同基因雄性脾细胞对雌性C57BL/6小鼠进行致敏,并通过反复刺激在长期培养(LTC)中富集腹股沟和主动脉旁淋巴结细胞,可产生H-Y特异性辅助性T细胞。这些细胞对携带I-Ab抗原的雄性脾细胞作出反应,激活“表达抗原的”B细胞分泌多克隆抗体。在LTC培养的第二周结束前,无法检测到任何辅助活性。形成噬斑细胞(PFC)的诱导还需要在“刺激-反应”脾细胞群体中同时识别抗原和I-A编码的决定簇。对来自H-2重组品系的脾细胞作为C57BL/6来源的抗H-Y辅助性T细胞的“刺激-反应细胞”进行检测,结果还表明,位于I-A端粒的其他基因控制着特异性T细胞增殖和辅助依赖性B细胞活化的程度。

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