Rich E A, Toossi Z, Fujiwara H, Hanigosky R, Lederman M M, Ellner J J
Department of Medicine, University Hospitals, Cleveland, OH 44106-5000.
J Lab Clin Med. 1988 Aug;112(2):174-81.
It is not clear whether the accessory function of monocytes from subjects with human immunodeficiency virus (HIV)-related diseases such as acquired immunodeficiency syndrome (AIDS) and persistent generalized lymphadenopathy (PGL) is intact. In this study, the accessory function of monocytes from healthy subjects (n = 9) and subjects with AIDS (n = 4) and PGL (n = 5) was assessed by adding graded numbers of monocytes to lymphocytes stimulated with either tetanus toxoid or phytohemagglutinin. By nonparametric analysis, it was determined that a significantly greater number of monocytes was required for half-maximal responses of lymphocytes from subjects with PGL (for tetanus toxid but not phytohemagglutinin) and from those with AIDS, compared with healthy subjects. To address whether this observed difference was a result of a defect in accessory function of monocytes or a result of altered responsiveness of lymphocytes, a mixing experiment was performed between monocytes and lymphocytes obtained from a patient with PGL but without symptoms and an HLA-D-matched healthy sib. Dysfunction of both monocytes and lymphocytes was evident. Thus, this report provides data that monocytes in HIV infection are defective in accessory function for lymphocyte responses to soluble stimuli. We speculate that such dysfunction of monocytes may contribute to the progressive disturbance of the immune response that occurs during HIV infection.
目前尚不清楚来自患有人类免疫缺陷病毒(HIV)相关疾病(如获得性免疫缺陷综合征(AIDS)和持续性全身性淋巴结病(PGL))患者的单核细胞的辅助功能是否完整。在本研究中,通过向用破伤风类毒素或植物血凝素刺激的淋巴细胞中添加不同数量的单核细胞,评估了健康受试者(n = 9)、AIDS患者(n = 4)和PGL患者(n = 5)的单核细胞的辅助功能。通过非参数分析确定,与健康受试者相比,PGL患者(针对破伤风类毒素而非植物血凝素)和AIDS患者的淋巴细胞达到半数最大反应所需的单核细胞数量明显更多。为了确定观察到的差异是单核细胞辅助功能缺陷的结果还是淋巴细胞反应性改变的结果,对一名无症状的PGL患者和与其HLA - D匹配的健康同胞的单核细胞和淋巴细胞进行了混合实验。单核细胞和淋巴细胞的功能障碍均很明显。因此,本报告提供的数据表明,HIV感染中的单核细胞在淋巴细胞对可溶性刺激的反应的辅助功能方面存在缺陷。我们推测,单核细胞的这种功能障碍可能导致HIV感染期间发生的免疫反应的进行性紊乱。