Shimamura Masako, Mach Michael, Britt William J
Department of Pediatrics, University of Alabama at Birmingham, 1600 6th Avenue South, CHB107, Birmingham, Alabama 35233, USA.
J Virol. 2006 May;80(9):4591-600. doi: 10.1128/JVI.80.9.4591-4600.2006.
Human cytomegalovirus (HCMV) is a ubiquitous human pathogen that infects 40 to 90% of adult human populations. HCMV infections are often asymptomatic in healthy individuals but can cause severe organ and life-threatening disease in immunocompromised patients. The antiviral antibody response to HCMV infection is complex and is known to include virus-neutralizing antibody production against surface glycoproteins encoded by HCMV. We have investigated the human antibody response to a complex of HCMV surface glycoproteins composed of glycoprotein M (gM)/gN, the gene products of the UL100 and UL73 open reading frames. Mouse monoclonal antibodies generated against gM/gN have previously been shown to neutralize HCMV infection of human fibroblasts in vitro. To determine whether human antibodies reactive with the gM/gN complex possess virus-neutralizing properties, we isolated human antibodies reactive with gM/gN from pooled human HCMV hyperimmune globulin by affinity purification using recombinant gM/gN. The affinity-purified human anti-gM/gN antibodies reacted specifically by immunofluorescence with HCMV-infected human fibroblasts and with cells transiently expressing gM/gN, but not with cells transfected with plasmids encoding other immunogenic HCMV proteins. The anti-gM/gN antibodies also reacted specifically only with gM/gN in immunoblot assays using lysates of transfected cells expressing specific HCMV proteins. Last, human anti-gM/gN antibodies efficiently neutralized infectious HCMV in vitro with a capacity comparable to that of human anti-gB antibodies. These data indicated that gM/gN can elicit a virus-neutralizing antibody response in humans infected with HCMV and therefore should be considered a potential candidate for inclusion in prophylactic CMV vaccines.
人巨细胞病毒(HCMV)是一种普遍存在的人类病原体,感染40%至90%的成年人群。HCMV感染在健康个体中通常无症状,但在免疫功能低下的患者中可导致严重器官疾病和危及生命的疾病。针对HCMV感染的抗病毒抗体反应很复杂,已知包括针对HCMV编码的表面糖蛋白产生病毒中和抗体。我们研究了人类对由糖蛋白M(gM)/gN组成的HCMV表面糖蛋白复合物的抗体反应,gM/gN是UL100和UL73开放阅读框的基因产物。先前已证明,针对gM/gN产生的小鼠单克隆抗体可在体外中和人成纤维细胞的HCMV感染。为了确定与gM/gN复合物反应的人类抗体是否具有病毒中和特性,我们使用重组gM/gN通过亲和纯化从合并的人HCMV高免疫球蛋白中分离出与gM/gN反应的人类抗体。亲和纯化的人抗gM/gN抗体通过免疫荧光与HCMV感染的人成纤维细胞以及瞬时表达gM/gN的细胞特异性反应,但与转染了编码其他免疫原性HCMV蛋白的质粒的细胞不反应。在使用表达特定HCMV蛋白的转染细胞裂解物进行的免疫印迹分析中,抗gM/gN抗体也仅与gM/gN特异性反应。最后,人抗gM/gN抗体在体外有效中和感染性HCMV,其能力与人抗gB抗体相当。这些数据表明,gM/gN可在感染HCMV的人类中引发病毒中和抗体反应,因此应被视为预防性CMV疫苗的潜在候选成分。