Spiller O B, Morgan B P, Tufaro F, Devine D V
Department of Pathology, University of British Columbia, Vancouver, Canada.
Eur J Immunol. 1996 Jul;26(7):1532-8. doi: 10.1002/eji.1830260719.
Human cytomegalovirus (HCMV)-infected cells persist in the presence of anti-HCMV antibody, suggesting that HCMV has evolved mechanisms to evade host immune defenses. Insofar as no virus-encoded complement inhibitors have been identified for HCMV, we hypothesized that HCMV infection may alter the expression of host-encoded cell surface complement inhibitors. Herein, we report that cell surface expression of two complement regulator proteins, CD55 and CD46, which are members of the regulators of complement activation (RCA) gene cluster, increased up to eightfold following infection of fibroblasts or glioblastoma cells with HCMV, but not after infection with HSV-1 or adenovirus. However, the cell surface expression of a third complement regulator, CD59, which is not a member of the RCA gene cluster, was not altered during HCMV infection. Functional studies using purified complement components demonstrated that up-regulation of CD55 suppressed the activity of cell-associated C3 convertases on HCMV-infected cells. Furthermore, increased CD55 expression protected infected cells from complement-mediated lysis, an effect which directly correlated with the length of HCMV infection. Increased expression of host-encoded complement regulator proteins may provide protection of HCMV-infected cells from the host immune response in vivo, through increasing the resistance of infected cells to complement-mediated lysis and decreasing the deposition of C3-derived products on the cell surface.
人巨细胞病毒(HCMV)感染的细胞在抗HCMV抗体存在的情况下仍能持续存在,这表明HCMV已经进化出逃避宿主免疫防御的机制。鉴于尚未鉴定出HCMV的病毒编码补体抑制剂,我们推测HCMV感染可能会改变宿主编码的细胞表面补体抑制剂的表达。在此,我们报告,补体激活调节因子(RCA)基因簇成员补体调节蛋白CD55和CD46的细胞表面表达,在成纤维细胞或胶质母细胞瘤细胞被HCMV感染后增加了多达八倍,但在被单纯疱疹病毒1型(HSV-1)或腺病毒感染后未增加。然而,第三种补体调节蛋白CD59(它不是RCA基因簇的成员)的细胞表面表达在HCMV感染期间未发生改变。使用纯化补体成分的功能研究表明,CD55的上调抑制了HCMV感染细胞上细胞相关C3转化酶的活性。此外,CD55表达的增加保护感染细胞免受补体介导的裂解,这一效应与HCMV感染的持续时间直接相关。宿主编码的补体调节蛋白表达的增加可能通过增加感染细胞对补体介导裂解的抵抗力以及减少C3衍生产物在细胞表面的沉积,在体内为HCMV感染的细胞提供对宿主免疫反应的保护。