Watzl C, Peterson M, Long E O
Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland 20852, USA.
Tissue Antigens. 2000 Sep;56(3):240-7. doi: 10.1034/j.1399-0039.2000.560306.x.
The activity of human natural killer (NK) cells is in part regulated by the expression of killer cell immunoglobulin (Ig)-like receptors (KIR) that recognize major histocompatibility complex (MHC) class I and can inhibit NK cell cytotoxicity. A monoclonal anti-KIR antibody was established and designated Lig1. Lig1 was shown to be specific for KIR in cell-surface staining and to react with all KIR2D, except KIR2DL4 which lacks a D1 domain, but not with KIR3D molecules in an enzyme-linked immunoadsorbent assay (ELISA) and Western blotting. Unlike other anti-KIR antibodies, Lig1 did not inhibit binding of KIR-Ig-fusion proteins to MHC-class I expressing cells nor did it interfere with KIR-mediated inhibition of NK cell cytotoxicity in a functional assay. Lig1 reacted with all NK cells in polyclonal NK populations from different donors, demonstrating that all NK cells express at least one KIR2D receptor.
人类自然杀伤(NK)细胞的活性部分受杀伤细胞免疫球蛋白(Ig)样受体(KIR)表达的调节,KIR可识别主要组织相容性复合体(MHC)I类分子并能抑制NK细胞的细胞毒性。一种单克隆抗KIR抗体被制备出来并命名为Lig1。在细胞表面染色中,Lig1显示对KIR具有特异性,可与所有KIR2D反应,但不包括缺乏D1结构域的KIR2DL4;在酶联免疫吸附测定(ELISA)和蛋白质免疫印迹法中,Lig1不与KIR3D分子反应。与其他抗KIR抗体不同,Lig1不抑制KIR-Ig融合蛋白与表达MHC-I类分子的细胞的结合,在功能试验中也不干扰KIR介导的对NK细胞细胞毒性的抑制作用。Lig1与来自不同供体的多克隆NK细胞群体中的所有NK细胞反应,表明所有NK细胞至少表达一种KIR2D受体。