Krohn K J, Antonen J, Valle S L, Kazakevicius R, Saxinger C, Gallo R C, Ranki A
Cancer Res. 1985 Sep;45(9 Suppl):4612s-4615s.
Clinical, immunological, microbiological, virological, and lifestyle parameters were followed in 200 homosexual men living in Finland. The subjects were seen at 3- to 6-month intervals starting in summer 1983. Human T-cell lymphotropic virus III (HTLV-III) antibodies detected by enzyme immunoassay and confirmed by Western blotting were seen in 18 (9%) of the cases. Initially two cases had acquired immunodeficiency syndrome, three had acquired immunodeficiency syndrome-related complex, three had lymphadenopathy syndrome, and ten were asymptomatic. During the follow-up two asymptomatic cases developed lymphadenopathy syndrome and three developed enlarged lymph nodes. Immunological studies revealed decreased T-helper cell values and/or T-helper/suppressor ratios in all clinical categories, the findings being more severe and progressive in the symptomatic cases. The finding most clearly distinguishing HTLV-III antibody positive cases from the antibody negative ones was a decreased response to a specific recall antigen, purified protein derivative of tuberculoprotein. Responses to mitogens phytohemagglutinin and pokeweed mitogen were also decreased, but to a lesser extent. The primary immunological defect associated with helper T-cell infection by HTLV-III thus seems to be loss of antigen specific immune responses. It is suggested that this is the result of previous antigenic stimulation of HTLV-III infected T-helper cells and that the cellular destruction is associated with initial mitotic activity.
对居住在芬兰的200名同性恋男性的临床、免疫学、微生物学、病毒学和生活方式参数进行了跟踪研究。从1983年夏季开始,每隔3至6个月对这些受试者进行一次检查。通过酶免疫测定法检测并经蛋白质印迹法确认的人类T细胞嗜淋巴细胞病毒III型(HTLV-III)抗体在18例(9%)病例中被发现。最初,2例患有获得性免疫缺陷综合征,3例患有与获得性免疫缺陷综合征相关的综合征,3例患有淋巴结病综合征,10例无症状。在随访期间,2例无症状病例发展为淋巴结病综合征,3例出现淋巴结肿大。免疫学研究显示,所有临床类型的辅助性T细胞值和/或辅助性T细胞/抑制性T细胞比值均降低,有症状的病例中这些发现更为严重且呈进行性发展。最能明确区分HTLV-III抗体阳性病例和抗体阴性病例的发现是对一种特定回忆抗原——结核蛋白纯化蛋白衍生物的反应降低。对有丝分裂原植物血凝素和商陆有丝分裂原的反应也降低,但程度较轻。因此,与HTLV-III感染辅助性T细胞相关的主要免疫缺陷似乎是抗原特异性免疫反应的丧失。有人认为,这是HTLV-III感染的辅助性T细胞先前受到抗原刺激的结果,并且细胞破坏与初始有丝分裂活动有关。