Katzenstein D A, Latif A S, Grace S A, Basset M, Mashu A, de Villiers D M, Carrow E W, Hendry R M, Marowa E, Emmanuel J C
Division of Virology, Food and Drug Administration, Bethesda, Maryland.
J Acquir Immune Defic Syndr (1988). 1990;3(7):701-7.
To define the impact of human immunodeficiency virus (HIV) infection in Africa, clinical and laboratory investigations were conducted on 265 HIV-seropositive outpatients in Zimbabwe. Twenty-four of the study subjects were asymptomatic (ASX), 124 had persistent generalized lymphadenopathy (PGL), and 117 had AIDS-related complex (ARC). HIV infection was assessed by commercial ELISA, Western blots, synthetic peptide ELISA, and measurement of p24 antigen. Serum immunoglobulins, lymphocyte mitogen responses, and CD4+ cell numbers were obtained in 54 sequential patients. Compared to seronegative subjects, mean CD4+ cell numbers were decreased and serum immunoglobulins, particularly IgM and IgG, were increased in all groups of seropositive subjects. Lymphocyte proliferative responses to phytohemagglutinin and concanavalin A decreased progressively in ASX, PGL, and ARC patients and were significantly lower in PGL and ARC patients compared to seronegative controls. Generalized lymphadenopathy was present in 234/265 (88%) of patients. Lymph node biopsies in 100 patients demonstrated follicular hyperplasia in 97 and Mycobacterium tuberculosis in 3. Of 165 patients followed for a median of 6 months, 5 developed the acquired immune deficiency syndrome (AIDS). Symptoms of ARC, low CD4+ cell number, and p24 antigen were predictive of the development of AIDS in Zimbabwe.
为确定人类免疫缺陷病毒(HIV)感染在非洲的影响,对津巴布韦的265名HIV血清阳性门诊患者进行了临床和实验室调查。研究对象中24人无症状(ASX),124人有持续性全身性淋巴结肿大(PGL),117人有艾滋病相关综合征(ARC)。通过商用ELISA、免疫印迹法、合成肽ELISA以及p24抗原检测评估HIV感染情况。对54例连续患者测定了血清免疫球蛋白、淋巴细胞丝裂原反应以及CD4+细胞数量。与血清阴性受试者相比,所有血清阳性受试者组的平均CD4+细胞数量均减少,血清免疫球蛋白,尤其是IgM和IgG增加。ASX、PGL和ARC患者对植物血凝素和刀豆球蛋白A的淋巴细胞增殖反应逐渐降低,与血清阴性对照相比,PGL和ARC患者的反应显著更低。234/265(88%)的患者有全身性淋巴结肿大。100例患者的淋巴结活检显示97例有滤泡增生,3例有结核分枝杆菌。在165例中位随访6个月的患者中,5例发展为获得性免疫缺陷综合征(AIDS)。在津巴布韦,ARC症状、低CD4+细胞数量和p24抗原可预测AIDS的发展。