Gabrilovich D I, Shepeleva G K, Serebrovskaya L V, Avdeeva L A, Pokrovsky V V
Laboratory of AIDS Epidemiology and Prevention, Central Institute for Epidemiology, Moscow, Russia.
Scand J Immunol. 1993 Apr;37(4):459-67. doi: 10.1111/j.1365-3083.1993.tb03319.x.
The aim of this study was to determine whether polymorphonuclear neutrophils (PMN) can modify the immune response in HIV cases. Supernatants of PMN (PMNS) from 33 HIV-infected patients (16 with lymphoadenopathy syndrome, 17 with AIDS-related complex) were tested for their influence on the functional activity of lymphocytes and monocytes from 6 healthy donors. PMNS from another 6 healthy donors comprised a control group. It was found that PMNS from HIV-infected patients, but not from healthy donors, induced suppression of lymphocyte proliferative response and down-regulation of CD8 receptor expression on lymphocytes. Decrease of NK-cell cytotoxicity in the presence of PMNS from HIV-infected patients was the same as that from healthy donors. PMNS did not influence the production of anti-HIV antibody by lymphocytes from HIV-infected patients, as well as non-specific IgG by lymphocytes from healthy donors. PMNS effect on functional activity of lymphocytes was blocked completely after treatment of PMN by catalase and superoxide dismutase. At the same time PMNS from HIV-infected patients but not from healthy donors induced increased production of TNF-alpha by monocytes and up-regulation of monocyte phagocytosis. These effects were independent of catalase and superoxide dismutase and were not abrogated by antibody against IL-1, IL-8, TNF-alpha, IFN-gamma or IFN-alpha.
本研究的目的是确定多形核中性粒细胞(PMN)是否能够改变HIV病例中的免疫反应。检测了33例HIV感染患者(16例患有淋巴结病综合征,17例患有艾滋病相关综合征)的PMN上清液(PMNS)对6名健康供体的淋巴细胞和单核细胞功能活性的影响。另外6名健康供体的PMNS组成了对照组。结果发现,HIV感染患者的PMNS可诱导淋巴细胞增殖反应受抑制以及淋巴细胞上CD8受体表达下调,而健康供体的PMNS则无此作用。HIV感染患者的PMNS存在时NK细胞细胞毒性的降低程度与健康供体的相同。PMNS不影响HIV感染患者淋巴细胞产生抗HIV抗体,也不影响健康供体淋巴细胞产生非特异性IgG。用过氧化氢酶和超氧化物歧化酶处理PMN后,PMNS对淋巴细胞功能活性的作用被完全阻断。同时,HIV感染患者的PMNS可诱导单核细胞产生TNF-α增加以及单核细胞吞噬作用上调,而健康供体的PMNS则无此作用。这些作用与过氧化氢酶和超氧化物歧化酶无关,且不被抗IL-1、IL-8、TNF-α、IFN-γ或IFN-α抗体消除。