Pahwa S, Chirmule N, Leombruno C, Lim W, Harper R, Bhalla R, Pahwa R, Nelson R P, Good R A
Department of Pediatrics, North Shore University Hospital, Cornell University Medical College, Manhasset, NY 11030.
Proc Natl Acad Sci U S A. 1989 Oct;86(19):7532-6. doi: 10.1073/pnas.86.19.7532.
An assay system was developed for the analysis of antibodies secreted in vitro against human immunodeficiency virus (HIV) by cultured peripheral blood lymphocytes of HIV-infected individuals. Cultures of peripheral blood lymphocytes were established with medium alone or with medium containing Epstein-Barr virus (EBV) or pokeweed mitogen. HIV antibodies were determined by an ELISA performed with commercial kits in which a whole virus extract served as antigen. Optimal antibody secretion was detected in 7-day peripheral blood lymphocyte cultures to which EBV had been added to provide polyclonal B-cell activation. Pokeweed mitogen-induced antibody secretion and spontaneous antibody secretion were less consistent. With EBV as a stimulus, the sensitivity and specificity of this assay for determining HIV infection status were each 100% in adults. When the assay was applied to infants and children, 23 of 24 symptomatic HIV-seropositive children (class P-2) and 11 of 33 asymptomatic seropositive infants aged less than or equal to 15 months (class P-0) tested positive for EBV-induced antibody secretion. Six of the 11 P-0 patients who tested positive have progressed to develop symptomatic disease, while the remainder are still seropositive at ages 2-15 months. Of the infants who were negative in this assay, all have remained asymptomatic. Treatment with 3'-azido-3'-deoxythymidine in infected adults and children has resulted in transient suppression of the in vitro antibody response in some instances. Thus EBV-induced synthesis of HIV-specific antibodies in vitro is a sensitive and specific indicator of HIV infection and is of help in determining infection status of asymptomatic seropositive infants who are classified as having "indeterminate" infection.
开发了一种检测系统,用于分析HIV感染个体培养的外周血淋巴细胞体外分泌的抗人类免疫缺陷病毒(HIV)抗体。外周血淋巴细胞培养物单独用培养基建立,或用含有爱泼斯坦-巴尔病毒(EBV)或商陆有丝分裂原的培养基建立。HIV抗体通过使用商业试剂盒进行的ELISA测定,其中全病毒提取物用作抗原。在添加了EBV以提供多克隆B细胞活化的7天外周血淋巴细胞培养物中检测到最佳抗体分泌。商陆有丝分裂原诱导的抗体分泌和自发抗体分泌不太一致。以EBV作为刺激物,该检测用于确定HIV感染状态的敏感性和特异性在成人中均为100%。当该检测应用于婴儿和儿童时,24例有症状的HIV血清阳性儿童(P-2类)中有23例,33例年龄小于或等于15个月的无症状血清阳性婴儿(P-0类)中有11例,检测到EBV诱导的抗体分泌呈阳性。11例检测呈阳性的P-0患者中有6例已发展为有症状疾病,其余患者在2至15个月时仍为血清阳性。在该检测中呈阴性的婴儿均保持无症状。在感染的成人和儿童中用3'-叠氮-3'-脱氧胸苷治疗在某些情况下导致体外抗体反应的短暂抑制。因此,EBV在体外诱导合成HIV特异性抗体是HIV感染的敏感和特异性指标,有助于确定被归类为“不确定”感染的无症状血清阳性婴儿的感染状态。