Hamann A, Jablonski-Westrich D, Thiele H G
Eur J Immunol. 1986 Jul;16(7):847-50. doi: 10.1002/eji.1830160721.
When lymphocytes are activated in vitro, discrete cell-cell contacts are initiated which result in cluster formation. This contact interaction is found in syngeneic or allogeneic mixed leukocyte reactions as well as in mitogen-stimulated cultures (concanavalin A, periodate, lipopolysaccharide). T cells as well as B cells display the binding phenomenon. This activation-dependent lymphocyte-lymphocyte adhesion involves LFA-1, since monoclonal antibodies (including Fab fragments) against this molecule inhibit adhesion between clustering lymphocytes in a dose-dependent manner, whereas antibodies directed to several other cell surface antigens are inactive. Since a wide variety of functional interactions are inhibited by antibodies to LFA-1, it may be concluded that LFA-1-mediated cell contact is a discrete and essential step between a recognition event and the generation of functional activities by lymphocytes in general.
当淋巴细胞在体外被激活时,会启动离散的细胞间接触,进而导致细胞簇的形成。这种接触相互作用在同基因或异基因混合白细胞反应以及有丝分裂原刺激的培养物(刀豆球蛋白A、高碘酸盐、脂多糖)中均有发现。T细胞和B细胞都表现出这种结合现象。这种依赖于激活的淋巴细胞-淋巴细胞黏附涉及淋巴细胞功能相关抗原-1(LFA-1),因为针对该分子的单克隆抗体(包括Fab片段)以剂量依赖的方式抑制聚集淋巴细胞之间的黏附,而针对其他几种细胞表面抗原的抗体则无此作用。由于针对LFA-1的抗体可抑制多种功能相互作用,因此可以得出结论,LFA-1介导的细胞接触通常是淋巴细胞识别事件与功能活动产生之间一个离散且必不可少的步骤。