Petrie H T, Klassen L W, Kay H D
J Immunol. 1985 Jan;134(1):230-4.
Peripheral blood granulocytes from normal healthy donors were found to reproducibly inhibit the cytolytic effector function of specifically sensitized cytotoxic T lymphocytes in vitro when co-incubated with these effector cells and target cells in 8 hr 51Cr release assays. Inhibition required intact granulocytes, was proportional to the number of granulocytes present, and was independent of granulocyte adherence, phagocytic function, and viability. Equivalent numbers of enriched normal or leukemic peripheral T lymphocytes did not cause inhibition of 51Cr release, and preincubation of granulocytes with effectors did not significantly alter viability or cytotoxic function. Because granulocytes can inhibit natural killer cell function in vitro, these data indicate that granulocytes can regulate diverse antigen-specific and spontaneous cytotoxic functions in vitro, suggesting that circulating granulocytes may have the potential for in vivo regulation of these cytotoxic effectors.
在8小时的51Cr释放试验中,当将正常健康供体的外周血粒细胞与这些效应细胞和靶细胞共同孵育时,发现其可在体外反复抑制特异性致敏细胞毒性T淋巴细胞的溶细胞效应功能。抑制作用需要完整的粒细胞,与存在的粒细胞数量成正比,并且与粒细胞的黏附、吞噬功能和活力无关。等量富集的正常或白血病外周T淋巴细胞不会导致51Cr释放的抑制,并且粒细胞与效应细胞的预孵育不会显著改变活力或细胞毒性功能。由于粒细胞可在体外抑制自然杀伤细胞功能,这些数据表明粒细胞可在体外调节多种抗原特异性和自发细胞毒性功能,提示循环粒细胞可能具有在体内调节这些细胞毒性效应器的潜力。