Daul C B, deShazo R D, Andes W A
Tulane/Louisiana State Universities, AIDS Treatment Evaluation Unit, New Orleans.
Am J Med. 1988 May;84(5):801-9. doi: 10.1016/0002-9343(88)90056-3.
Thirty-seven heterosexual hemophiliac patients underwent prospective evaluation with clinical examinations, serologic studies for antibody to human immunodeficiency virus (HIV), and tests of immune function for an average of 37 months. At the time of entry into the study in 1982 to 1983, 18 subjects (49 percent) were already seropositive for HIV and 11 (30 percent) had persistent generalized lymphadenopathy. Seventy percent of the total population were clinically asymptomatic. In nine subjects, seroconversion occurred during the study such that 81 percent of the population was seropositive at the conclusion. During the same period, lymphadenopathy developed in six subjects, there was progression to AIDS-related complex (ARC) in four, and acquired immunodeficiency syndrome (AIDS) developed in one patient. Thus, at the end of the study, 54 percent were clinically asymptomatic, 32 percent had persistent lymphadenopathy, and 11 percent had ARC. Subjects who remained seronegative had received less factor concentrate than seropositive subjects, remained asymptomatic, and had normal results on tests of immune function. In those who had experienced seroconversion, there were decreased absolute numbers of CD4+ lymphocytes prior to seroconversion, and abnormalities of lymphocyte function developed after seroconversion. The development of persistent generalized lymphadenopathy was associated temporally with seroconversion. The presence of persistent generalized lymphadenopathy did not appear to be associated with an increased risk for AIDS in seropositive persons, since the condition of most hemophiliac patients with persistent generalized lymphadenopathy at the time of initial evaluation remained clinically and immunologically stable. In contrast to patients with persistent generalized lymphadenopathy, asymptomatic seropositive subjects had progressive abnormalities of lymphocyte function over time that were independent of the numbers of CD4+ cells in the peripheral blood.
37名异性恋血友病患者接受了前瞻性评估,包括临床检查、针对人类免疫缺陷病毒(HIV)抗体的血清学研究以及免疫功能测试,平均随访37个月。在1982年至1983年进入研究时,18名受试者(49%)已为HIV血清阳性,11名(30%)有持续性全身性淋巴结肿大。总人群中有70%临床无症状。在9名受试者中,研究期间发生了血清转化,因此在研究结束时81%的人群为血清阳性。同期,6名受试者出现淋巴结肿大,4名进展为艾滋病相关综合征(ARC),1名患者发展为获得性免疫缺陷综合征(AIDS)。因此,在研究结束时,54%临床无症状,32%有持续性淋巴结肿大,11%有ARC。血清学仍为阴性的受试者接受的凝血因子浓缩物比血清阳性受试者少,仍无症状,免疫功能测试结果正常。在经历血清转化的受试者中,血清转化前CD4+淋巴细胞绝对数量减少,血清转化后淋巴细胞功能出现异常。持续性全身性淋巴结肿大的出现与血清转化在时间上相关。持续性全身性淋巴结肿大的存在似乎与血清阳性者患艾滋病的风险增加无关,因为大多数初始评估时有持续性全身性淋巴结肿大的血友病患者的病情在临床和免疫方面保持稳定。与持续性全身性淋巴结肿大的患者不同,无症状血清阳性受试者随着时间推移淋巴细胞功能出现进行性异常,且与外周血中CD4+细胞数量无关。