Dougherty G J, Selvendran Y, Murdoch S, Palmer D G, Hogg N
Macrophage Laboratory, Imperial Cancer Research Fund, Lincoln's Inn Fields, London, GB.
Eur J Immunol. 1987 Oct;17(10):1453-9. doi: 10.1002/eji.1830171011.
The properties of the mononuclear phagocyte (Mph) high-affinity Fc receptor, FcRI, were investigated using a novel monoclonal antibody (mAb) designated 10.1. This receptor was shown to be a protein of 71 kDa, presented chiefly on monocytes and the myeloid cell lines U937 and HL60. mAb 10.1 inhibited the binding to Mph of erythrocytes opsonized with rabbit IgG or human IgG3. It also blocked T cell proliferation induced by murine CD3 mAb of the IgG2a but not the IgG1 subclass. These results suggest that rabbit IgG, human IgG3 and murine IgG2a all bind to FcRI in a similar manner and that mAb 10.1 reacts with an epitope on FcRI near to the binding site for the Fc region of IgG. In addition, although it is well known that FcRI has a high affinity for both monomeric human IgG1 and IgG3, we show in this study that while erythrocytes opsonized with human IgG3 bind to Mph, equivalent cells opsonized with IgG1 surprisingly do not. These results define further the nature of the constraints on the interaction between Mph FcRI and particular IgGs.
利用一种名为10.1的新型单克隆抗体(mAb)对单核吞噬细胞(Mph)高亲和力Fc受体FcRI的特性进行了研究。该受体被证明是一种71 kDa的蛋白质,主要存在于单核细胞以及髓系细胞系U937和HL60上。单克隆抗体10.1抑制了用兔IgG或人IgG3调理的红细胞与Mph的结合。它还阻断了由IgG2a亚类而非IgG1亚类的鼠CD3单克隆抗体诱导的T细胞增殖。这些结果表明,兔IgG、人IgG3和鼠IgG2a均以相似的方式与FcRI结合,并且单克隆抗体10.1与FcRI上靠近IgG Fc区域结合位点的一个表位发生反应。此外,尽管众所周知FcRI对单体人IgG1和IgG3均具有高亲和力,但我们在本研究中表明,用人IgG3调理的红细胞可与Mph结合,而用IgG1调理的同等细胞却出人意料地不能结合。这些结果进一步明确了Mph FcRI与特定IgG之间相互作用的限制性质。