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名义抗原和Ia抗原在抗原特异性T淋巴细胞与巨噬细胞结合中的作用。

Role of nominal antigen and Ia antigen in the binding of antigen-specific T lymphocytes to macrophages.

作者信息

Werdelin O, Shevach E M

出版信息

J Immunol. 1979 Dec;123(6):2779-84.

PMID:91645
Abstract

We have previously demonstrated that when primed T lymphocytes were repeatedly incubated on monolayers of antigen-pulsed macrophages (M phi), the cells that failed to adhere to the monolayer demonstrated a marked depletion of their proliferative response that was specific both for the antigen used for pulsing the M phi and for Ia determinants on the M phi. In order to further analyze the contribution of the nominal antigen and Ia antigens to the physical binding of T lymphocytes to M phi, we have attempted to block the absorption of T lymphocytes to M phi with a large excess of soluble antigen and with anti-Ia sera. Our results demonstrate that anti-Ia sera inhibit but that soluble antigen augments the binding of specific T lymphocytes to M phi. The implications of these findings for "dual recognition" and "linked recognition" models of T lymphocyte receptors are discussed.

摘要

我们之前已经证明,当致敏的T淋巴细胞反复在抗原脉冲巨噬细胞(M phi)单层上孵育时,未能黏附于单层的细胞其增殖反应显著降低,这种降低对于用于脉冲M phi的抗原以及M phi上的Ia决定簇均具有特异性。为了进一步分析名义抗原和Ia抗原对T淋巴细胞与M phi物理结合的贡献,我们尝试用大量过量的可溶性抗原和抗Ia血清来阻断T淋巴细胞对M phi的吸附。我们的结果表明,抗Ia血清具有抑制作用,而可溶性抗原则增强特异性T淋巴细胞与M phi的结合。本文讨论了这些发现对T淋巴细胞受体“双重识别”和“连锁识别”模型的意义。

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