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LFA-1膜分子在人B淋巴细胞同型黏附中的调节作用。

LFA-1 membrane molecule in the regulation of homotypic adhesions of human B lymphocytes.

作者信息

Mentzer S J, Gromkowski S H, Krensky A M, Burakoff S J, Martz E

出版信息

J Immunol. 1985 Jul;135(1):9-11.

PMID:3889159
Abstract

We report here that MAb to human LFA-1 inhibit spontaneous homotypic adhesions of human B lymphocytes. This is, to our knowledge, the first report of a MAb that inhibits human homotypic intercellular adhesions for any cell type. LFA-1 has previously been recognized as a molecule capable of regulating specific immunologic adhesions between T lymphocytes and antigen-bearing target cells. The present findings show that the role of LFA-1 is not limited to adhesions initiated by specific immunologic recognition. The results indicate that the LFA-1 molecule is capable of regulating lymphocyte adhesions, possibly because it is a direct participant in adhesion formation.

摘要

我们在此报告,针对人类淋巴细胞功能相关抗原-1(LFA-1)的单克隆抗体(MAb)可抑制人类B淋巴细胞的自发性同型黏附。据我们所知,这是关于一种单克隆抗体抑制任何细胞类型的人类同型细胞间黏附的首次报道。LFA-1此前已被认为是一种能够调节T淋巴细胞与携带抗原的靶细胞之间特异性免疫黏附的分子。目前的研究结果表明,LFA-1的作用并不局限于由特异性免疫识别引发的黏附。这些结果表明,LFA-1分子能够调节淋巴细胞黏附,可能是因为它是黏附形成的直接参与者。

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