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艾滋病相关的良性淋巴结病和恶性淋巴瘤:临床方面及病毒学相互作用

AIDS-related benign lymphadenopathy and malignant lymphoma: clinical aspects and virologic interactions.

作者信息

Abrams D I, Kaplan L D, McGrath M S, Volberding P A

出版信息

AIDS Res. 1986 Dec;2 Suppl 1:S131-40.

PMID:3828009
Abstract

Infection with the human immunodeficiency virus (HIV) leads to selective depletion of the helper/inducer lymphocyte subset and a subsequent state of acquired cellular immunodeficiency. Simultaneously, evidence of B-cell hyper-activity may exist. A subset of patients infected with HIV demonstrates a syndrome of persistent generalized lymphadenopathy (PGL). Lymph node biopsies reveal benign reactive changes with a pattern of florid follicular hyperplasia. A polyclonal hypergammaglobulinemia reflects humoral immune dysfunction. Patients with PGL are similar to those with full-blown AIDS with regards to demographics, immune and virologic studies. Our prospective natural history study of PGL patients initiated in November 1981 reveals a 15% rate of evolution to AIDS in the 200 patient cohort. Factors associated with increased risk of transformation to AIDS include severity of constitutional symptoms, shrinking adenopathy, oral candidiasis or viral hairy leukoplakia, peripheral cytopenias, elevated erythrocyte sedimentation rate or an antecedent episode of herpes zoster. Therapeutic interventions to prevent evolution to AIDS in high risk subsets of lymphadenopathy patients have been investigated. In addition to benign B-cell proliferation associated with HIV infection, malignant lymphomas have also been diagnosed in 29 patients in AIDS risk groups in our clinic population. All patients were male; 26 homosexuals, 2 IV drug abusers and 1 multiply transfused sickle cell anemia patient. Seven patients had antecedent PGL. Non-Hodgkin's lymphoma was diagnosed in 19 patients. Histologies were predominantly diffuse undifferentiated or large cell. Eleven patients were Stage IV at diagnosis. Of 10 patients with mixed cellularity Hodgkin's disease, 7 were Stage IV-B at presentation. Extranodal disease was frequent in patients with lymphomas. Fourteen patients lacked peripheral lymphadenopathy. Response to chemotherapy was good, but complicated by prolonged marrow suppression and development of AIDS-related opportunistic infections. Median survival was 7 months. Laboratory studies investigating the possible role of lymphotropic retroviruses in the development of AIDS-related lymphomas revealed that serum from all patients with high grade non-Hodgkin's lymphoma contained antibodies to HIV and that the majority also expressed antibodies to HTLV-I. This degree of seroreactivity to HTLV-I and HIV was characteristic only of lymphoma patients as sera from only 10 - 15% of AIDS and ARC patients in San Francisco had similar findings.

摘要

人类免疫缺陷病毒(HIV)感染导致辅助/诱导淋巴细胞亚群选择性耗竭,进而出现获得性细胞免疫缺陷状态。同时,可能存在B细胞过度活跃的证据。一部分感染HIV的患者表现出持续性全身性淋巴结病(PGL)综合征。淋巴结活检显示为良性反应性改变,伴有明显的滤泡增生。多克隆高丙种球蛋白血症反映了体液免疫功能障碍。在人口统计学、免疫和病毒学研究方面,PGL患者与艾滋病患者相似。我们于1981年11月启动的PGL患者前瞻性自然史研究显示,在200例患者队列中,发展为艾滋病的比例为15%。与转化为艾滋病风险增加相关的因素包括全身症状的严重程度、淋巴结病缩小、口腔念珠菌病或病毒性毛状白斑、外周血细胞减少、红细胞沉降率升高或带状疱疹既往发作史。已对在淋巴结病患者高危亚组中预防发展为艾滋病的治疗干预措施进行了研究。除了与HIV感染相关的良性B细胞增殖外,在我们临床人群中的艾滋病风险组中,还有29例患者被诊断出患有恶性淋巴瘤。所有患者均为男性;26例为同性恋者,2例为静脉注射毒品者,1例为多次输血的镰状细胞贫血患者。7例患者有PGL病史。19例患者被诊断为非霍奇金淋巴瘤。组织学类型主要为弥漫性未分化或大细胞型。11例患者诊断时为IV期。在淋巴瘤患者中,结外病变很常见。14例患者无外周淋巴结病。化疗反应良好,但伴有骨髓抑制延长和艾滋病相关机会性感染的发生。中位生存期为7个月。研究亲淋巴逆转录病毒在艾滋病相关淋巴瘤发生中可能作用的实验室研究表明,所有高级别非霍奇金淋巴瘤患者的血清均含有抗HIV抗体,且大多数患者还表达抗HTLV-I抗体。这种对HTLV-I和HIV的血清反应程度仅在淋巴瘤患者中具有特征性,因为在旧金山只有10 - 15%的艾滋病和艾滋病相关综合征(ARC)患者的血清有类似发现。

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