Geffner J R, Serebrinsky G, Isturiz M A
Immunology. 1986 Oct;59(2):239-43.
A progressive inhibition of both antibody-dependent cellular cytotoxicity (ADCC) and Fc gamma R expression was observed when peripheral blood mononuclear cells (PBMC) were incubated with soluble immune complexes (IC) at 37 degrees. Treatment of these IC-blocked PBMC with normal human serum (NHS) reversed both effects and increased the release of attached IC from the cell surface when compared to heat-inactivated serum (HI-NHS) or culture medium (TCM) treatments. Immunofluorescence studies demonstrated a redistribution of IC, predominantly in the form of caps in IC-blocked cells treated with HI-NHS (56%) or TCM (51%). However, when these IC-blocked cells were treated with NHS, only 11% of them showed caps redistribution. We propose that NHS regulation of Fc gamma R expression may be a physiological way of modulating the different immunological events triggered by IC.
当外周血单个核细胞(PBMC)在37℃下与可溶性免疫复合物(IC)孵育时,观察到抗体依赖性细胞毒性(ADCC)和FcγR表达均出现进行性抑制。与热灭活血清(HI-NHS)或培养基(TCM)处理相比,用正常人血清(NHS)处理这些被IC阻断的PBMC可逆转这两种效应,并增加细胞表面附着的IC的释放。免疫荧光研究表明IC发生了重新分布,在用HI-NHS(56%)或TCM(51%)处理的IC阻断细胞中,主要以帽状形式存在。然而,当用NHS处理这些被IC阻断的细胞时,只有11%的细胞显示帽状重新分布。我们提出,NHS对FcγR表达的调节可能是一种调节由IC触发的不同免疫事件的生理方式。