Katz J D, Mitsuyasu R, Gottlieb M S, Lebow L T, Bonavida B
J Immunol. 1987 Jul 1;139(1):55-60.
Our studies and other investigations have shown that NK effector cells can also mediate antibody-dependent cellular cytotoxicity (ADCC) through the use of the Fc gamma receptor on the NK cell membrane. Peripheral blood lymphocytes (PBL) derived from patients with acquired immunodeficiency syndrome (AIDS) and AIDS-related complex exhibit a poor NK activity due to a defective "trigger" required for activation in the lethal hit stage of the NK lytic pathway. Consequently, it was important to delineate whether the defect in AIDS NK cells affected the ADCC function. By using the 51Cr-release assay, the ADCC cytotoxic activity of AIDS PBL was found to be within the normal range, despite the absence of significant NK activity. Several experiments corroborated that the same effector cells mediate both NK CMC and ADCC. Depletion of Fc gamma R-bearing cells resulted in elimination of both the ADCC and NK cytotoxic functions. Single cell analyses, using one- and two-target cell conjugates, revealed that the frequency of ADCC effector:target conjugates and the frequency of killer cells from AIDS PBL were comparable to the frequencies seen in the normal controls. However, when mixtures of NK and ADCC targets were used to form mixed two-target conjugates, the AIDS effector cells lysed only the bound ADCC target, whereas the normal effector cells lysed both the bound NK and ADCC targets. These results demonstrate clearly that the same NK/K effector cells from AIDS PBL, defective in NK activity, are not impaired in mediating ADCC activity. These findings were supported by the demonstration that AIDS PBL stimulated with ADCC targets, but not with NK targets, released NK cytotoxic factors, postulated mediators of the NK CMC reaction. These findings indicate that the NK/K cells in AIDS are triggered normally for ADCC activity but are not triggered for NK activity. Furthermore, the results indicate that the lytic machinery is not impaired in the AIDS NK/K cells.
我们的研究及其他调查表明,自然杀伤(NK)效应细胞也可通过利用NK细胞膜上的Fcγ受体来介导抗体依赖性细胞毒性作用(ADCC)。获得性免疫缺陷综合征(AIDS)患者及AIDS相关综合征患者外周血淋巴细胞(PBL)表现出较差的NK活性,这是由于NK细胞溶解途径致死性打击阶段激活所需的“触发”存在缺陷。因此,明确AIDS患者NK细胞的缺陷是否影响ADCC功能很重要。通过使用51Cr释放试验,发现尽管AIDS患者PBL缺乏显著的NK活性,但其ADCC细胞毒性活性仍在正常范围内。多项实验证实,相同的效应细胞介导NK细胞介导的细胞毒作用(NK CMC)和ADCC。去除携带FcγR的细胞会导致ADCC和NK细胞毒性功能均消失。使用单靶细胞和双靶细胞结合物进行的单细胞分析显示,AIDS患者PBL中ADCC效应细胞与靶细胞结合物的频率以及杀伤细胞的频率与正常对照组相当。然而,当使用NK靶细胞和ADCC靶细胞的混合物形成混合双靶细胞结合物时,AIDS效应细胞仅裂解结合的ADCC靶细胞,而正常效应细胞则裂解结合的NK靶细胞和ADCC靶细胞。这些结果清楚地表明,AIDS患者PBL中NK活性有缺陷的相同NK/K效应细胞在介导ADCC活性方面并未受损。这些发现得到了以下证据的支持:用ADCC靶细胞而非NK靶细胞刺激AIDS患者PBL会释放NK细胞毒性因子,推测其为NK CMC反应的介质。这些发现表明,AIDS患者的NK/K细胞在ADCC活性方面能正常被触发,但在NK活性方面未被触发。此外,结果表明AIDS患者的NK/K细胞中的溶解机制并未受损。