Poutsiaka D D, Taylor D D, Levy E M, Black P H
J Immunol. 1985 Jan;134(1):145-50.
The expression of immune region-associated (Ia) antigens by macrophages is a prerequisite for antigen presentation, which is necessary for the activation of T helper cell function. A decrease in macrophage Ia expression is associated with a decrease in immune function in vitro. However, the effect of diseases accompanied by immunosuppression, such as cancer, on macrophage Ia expression has not been studied. The expression of Ia antigen was induced by the culture of murine peritoneal macrophages with recombinant interferon-gamma (IFN). Maximal expression was achieved after 4 days of culture. Membrane vesicles shed from the murine B16 F10 melanoma cell line inhibited the in vitro induction of Ia expression by 40 to 90% in allogeneic and syngeneic systems. Inhibition was not due to toxicity, a reduction in IFN activity, phagocytosis or contamination of the vesicle preparation with endotoxin, which is an inhibitor of Ia expression. Inhibition exerted by vesicles was prostaglandin-dependent and was over-come by increasing concentrations of IFN. It is possible that the reduction of macrophage Ia antigen expression by tumor cell products, such as shed membrane vesicles, contributes to the immunosuppression of tumor-bearing hosts. Employing IFN to reverse the inhibition provides a strategy for improving the therapy of patients with cancer.
巨噬细胞表达免疫区域相关(Ia)抗原是抗原呈递的前提条件,而抗原呈递是激活T辅助细胞功能所必需的。体外实验中,巨噬细胞Ia表达的降低与免疫功能的下降有关。然而,诸如癌症等伴有免疫抑制的疾病对巨噬细胞Ia表达的影响尚未得到研究。用重组干扰素-γ(IFN)培养小鼠腹腔巨噬细胞可诱导Ia抗原的表达。培养4天后达到最大表达量。从小鼠B16 F10黑色素瘤细胞系脱落的膜泡在同种异体和同基因系统中可使体外Ia表达的诱导降低40%至90%。抑制作用并非由于毒性、IFN活性降低、吞噬作用或膜泡制剂被内毒素污染(内毒素是Ia表达的抑制剂)所致。膜泡产生的抑制作用依赖于前列腺素,并且可通过增加IFN浓度来克服。肿瘤细胞产物(如脱落的膜泡)导致巨噬细胞Ia抗原表达降低,这可能是荷瘤宿主免疫抑制的原因之一。使用IFN来逆转这种抑制作用为改善癌症患者的治疗提供了一种策略。