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T4分子可能参与T细胞对II类HLA抗原的识别:来自对SB抗原增殖反应研究的证据。

Possible involvement of the T4 molecule in T cell recognition of class II HLA antigens: evidence from studies of proliferative responses to SB antigens.

作者信息

Biddison W E, Rao P E, Talle M A, Goldstein G, Shaw S

出版信息

J Immunol. 1983 Jul;131(1):152-7.

PMID:6190904
Abstract

The T4 molecule has been identified as a marker of human T cell differentiation, but the function of this molecule remains to be defined. We have investigated its possible functional involvement in T cell proliferative responses to class II HLA antigens encoded by the recently described SB locus. The responses of SB-primed cells (specific for each of four different SB antigens) were studied with the use of two proliferation-inducing stimuli, SB antigen or TCGF. The proliferative responses to both stimuli were found to be mediated by T4+, T8- cells. Monoclonal antibodies against some epitopes on the T4 molecule (OKT4A and OKT4B) substantially blocked antigen-stimulated proliferative responses; antibodies against other epitopes of the T4 molecule (OKT4, T4C, T4D) blocked less well. Inhibition of SB-specific proliferation by antibodies to the T4 molecule was maximal only when the antibodies were incubated with the responder cells before the addition of stimulator cells. Proliferative responses of SB-primed cells stimulated with TCGF alone were not inhibited by any of the OKT4-related antibodies, but were completely inhibited by the anti-Tac monoclonal antibody, which reacts with the TCGF receptor. These results lend further support for the hypothesis that the T4 molecule is involved in T cell recognition of and/or activation by class II HLA antigens. We suggest that 1) the T4 molecule binds a nonpolymorphic epitope on class II HLA molecules, and 2) this interaction may facilitate, but not be an obligate requirement for, T cell activation by class II antigens.

摘要

T4分子已被确定为人类T细胞分化的标志物,但其功能仍有待明确。我们研究了它在对最近描述的SB基因座编码的II类HLA抗原的T细胞增殖反应中可能的功能参与情况。使用两种增殖诱导刺激物,即SB抗原或TCGF,研究了经SB致敏的细胞(对四种不同的SB抗原中的每一种都具有特异性)的反应。发现对这两种刺激物的增殖反应均由T4 +、T8 - 细胞介导。针对T4分子上某些表位的单克隆抗体(OKT4A和OKT4B)能显著阻断抗原刺激的增殖反应;针对T4分子其他表位的抗体(OKT4、T4C、T4D)阻断效果较差。只有在加入刺激细胞之前将抗T4分子抗体与应答细胞一起孵育时,该抗体对SB特异性增殖的抑制作用才最大。单独用TCGF刺激的经SB致敏细胞的增殖反应不受任何OKT4相关抗体的抑制,但被与TCGF受体反应的抗Tac单克隆抗体完全抑制。这些结果进一步支持了T4分子参与T细胞对II类HLA抗原的识别和/或激活的假说。我们认为:1)T4分子结合II类HLA分子上的一个非多态性表位;2)这种相互作用可能促进II类抗原对T细胞的激活,但并非其激活的必要条件。

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