Kushnir N, Bos N A, Zuercher A W, Coffin S E, Moser C A, Offit P A, Cebra J J
Department of Biology, University of Pennsylvania, Philadelphia 19104-6018, USA.
J Virol. 2001 Jun;75(12):5482-90. doi: 10.1128/JVI.75.12.5482-5490.2001.
Studies utilizing various immunodeficient mouse models of rotavirus (RV) infection demonstrated significant roles of RV-specific secretory immunoglobulin A (IgA), CD4+ T cells, and CD8+ T cells in the clearance of RV and protection from secondary infection. Secretion of small but detectable amounts of IgA in RV-infected alphabeta T-cell receptor knockout mice (11) and distinctive anatomical localization and physiology of B1 cells suggested that B1 cells might be capable of producing RV-specific intestinal IgA in a T-cell-independent fashion and, therefore, be responsible for ablation of RV shedding. We investigated the role of B1 cells in the resolution of primary RV infection using a SCID mouse model. We found that the adoptive transfer of unseparated peritoneal exudate cells ablates RV shedding and leads to the production of high levels of RV-specific intestinal IgA. In contrast, purified B1 cells do not ablate RV shedding and do not induce a T-cell-independent or T-cell-dependent, RV-specific IgA response but do secrete large amounts of polyclonal (total) intestinal IgA. Cotransfer of mixtures of purified B1 cells and B1-cell-depleted peritoneal exudate cells differing in IgA allotypic markers also demonstrated that B2 cells (B1-cell-depleted peritoneal exudate cells) and not B1 cells produced RV-specific IgA. To our knowledge, this is the first observation that B1 cells are unable to cooperate with CD4+ T cells and produce virus-specific intestinal IgA antibody. We also observed that transferred CD4+ T cells alone are capable of resolving RV shedding, although no IgA is secreted. These data suggest that RV-specific IgA may not be obligatory for RV clearance but may protect from reinfection and that effector CD4+ T cells alone can mediate the resolution of primary RV infection. Reconstitution of RV-infected SCID mice with B1 cells results in the outgrowth of contaminating, donor CD4+ T cells that are unable to clear RV, possibly because their oligoclonal specificities may be ineffective against RV antigens.
利用各种轮状病毒(RV)感染的免疫缺陷小鼠模型进行的研究表明,RV特异性分泌型免疫球蛋白A(IgA)、CD4⁺ T细胞和CD8⁺ T细胞在RV清除及预防二次感染中发挥着重要作用。在感染RV的αβ T细胞受体敲除小鼠中可分泌少量但可检测到的IgA(11),以及B1细胞独特的解剖定位和生理学特性表明,B1细胞可能能够以不依赖T细胞的方式产生RV特异性肠道IgA,因此,负责消除RV shedding。我们使用SCID小鼠模型研究了B1细胞在原发性RV感染消退中的作用。我们发现,未分离的腹腔渗出细胞的过继转移可消除RV shedding,并导致产生高水平的RV特异性肠道IgA。相比之下,纯化的B1细胞不能消除RV shedding,也不能诱导不依赖T细胞或依赖T细胞的RV特异性IgA反应,但会分泌大量多克隆(总)肠道IgA。对具有不同IgA同种异型标记的纯化B1细胞和不含B1细胞的腹腔渗出细胞混合物的共转移也表明,产生RV特异性IgA的是B2细胞(不含B1细胞的腹腔渗出细胞)而非B1细胞。据我们所知,这是首次观察到B1细胞无法与CD4⁺ T细胞合作并产生病毒特异性肠道IgA抗体。我们还观察到,单独转移的CD4⁺ T细胞能够解决RV shedding问题,尽管不分泌IgA。这些数据表明,RV特异性IgA可能不是清除RV所必需的,但可能预防再次感染,并且单独的效应CD4⁺ T细胞可以介导原发性RV感染的消退。用B1细胞重建感染RV的SCID小鼠会导致污染的供体CD4⁺ T细胞生长,这些细胞无法清除RV,可能是因为它们的寡克隆特异性对RV抗原可能无效。