Nahill S R, Welsh R M
Department of Pathology, University of Massachusetts Medical Center, Worcester 01655.
J Exp Med. 1993 Feb 1;177(2):317-27. doi: 10.1084/jem.177.2.317.
Polyclonal stimulation of CD8+ cytotoxic T lymphocytes (CTL) occurs during infection with many viruses including those not known to transform CTL or encode superantigens. This polyclonal CTL response includes the generation of high levels of allospecific CTL directed against many class I haplotypes. In this report we investigated whether the allospecific CTL generated during an acute lymphocytic choriomeningitis virus (LCMV) infection of C57BL/6 mice were stimulated specifically by antigen recognition or nonspecifically by polyclonal mechanisms possibly involving lymphokines or superantigens. An examination of the ability of different strains of mice to induce high levels of CTL specific for a given alloantigen showed that most, but not all, strains generated high levels of allospecific CTL, and that their abilities to generate them mapped genetically to the major histocompatibility complex locus, exclusive of the class II region. This indicated that the virus-induced allospecific CTL generation was independent of the class II allotype, and mice depleted of CD4+ cells generated allospecific CTL, indicating independence of class II-CD4+ cell interactions and resulting CD4+ cell-secreted lymphokines. FACS staining with a variety of V beta-binding antibodies did not show a superantigen-like depletion or enrichment of any tested V beta + subset during infection. Several experiments provided evidence in support of direct stimulation of CD8+ cells via the T cell receptor: (a) both virus- and allo-specific killing were enriched within a given V beta subpopulation; (b) relative CTL precursor frequencies against different class I alloantigens changed during the course of virus infection; (c) the relative levels of virus-induced, allospecific CTL-mediated lysis at day 8 after infection did not parallel the CTL precursor frequencies before infection; and (d) limiting dilution analyses of day 8 LCMV-infected spleen cells stimulated by virus-infected syngeneic peritoneal exudate cells (PEC) revealed not only the expected virus-specific CTL clones, but also a high frequency of clones that were cross-reactive with allogeneic and virus-infected syngeneic targets. In addition to the virus cross-reactive allospecific CTL clones, virus-infected PEC also stimulated the generation of some allospecific clones that did not lyse virus-infected fibroblasts. Surprisingly, LCMV-infected PEC were much more efficient at stimulating allospecific CTL clones from day 8 LCMV-infected splenocytes than were allogeneic stimulators. These results indicate that at least part of the polyclonal allospecific CTL response elicited by acute virus infection is a consequence of the selective expansion of many clones of allospecific CTL which cross-react with virus-infected cells.(ABSTRACT TRUNCATED AT 400 WORDS)
在包括那些未知可转化细胞毒性T淋巴细胞(CTL)或编码超抗原的多种病毒感染期间,CD8 + 细胞毒性T淋巴细胞会发生多克隆刺激。这种多克隆CTL反应包括产生针对许多I类单倍型的高水平同种特异性CTL。在本报告中,我们研究了C57BL / 6小鼠急性淋巴细胞性脉络丛脑膜炎病毒(LCMV)感染期间产生的同种特异性CTL是通过抗原识别被特异性刺激,还是通过可能涉及淋巴因子或超抗原的多克隆机制被非特异性刺激。对不同品系小鼠诱导针对给定同种抗原的高水平CTL能力的检查表明,大多数(但不是全部)品系产生高水平的同种特异性CTL,并且它们产生这些CTL的能力在遗传上定位于主要组织相容性复合体基因座,不包括II类区域。这表明病毒诱导的同种特异性CTL产生与II类同种异型无关,并且耗尽CD4 + 细胞的小鼠产生同种特异性CTL,表明II类 - CD4 + 细胞相互作用以及由此产生的CD4 + 细胞分泌的淋巴因子无关。用多种Vβ结合抗体进行的FACS染色在感染期间未显示任何测试的Vβ + 亚群有超抗原样的耗竭或富集。几个实验提供了支持通过T细胞受体直接刺激CD8 + 细胞的证据:(a)病毒特异性和同种特异性杀伤在给定的Vβ亚群中均有富集;(b)针对不同I类同种抗原的相对CTL前体频率在病毒感染过程中发生变化;(c)感染后第8天病毒诱导的、同种特异性CTL介导的裂解相对水平与感染前的CTL前体频率不平行;(d)对受病毒感染的同基因腹膜渗出细胞(PEC)刺激的感染第8天LCMV的脾细胞进行有限稀释分析,不仅揭示了预期的病毒特异性CTL克隆,还发现了与同种异体和受病毒感染的同基因靶标交叉反应的高频率克隆。除了病毒交叉反应性同种特异性CTL克隆外,受病毒感染的PEC还刺激产生了一些不裂解受病毒感染的成纤维细胞的同种特异性克隆。令人惊讶的是,受LCMV感染的PEC在刺激来自感染第8天LCMV的脾细胞的同种特异性CTL克隆方面比同种异体刺激物效率高得多。这些结果表明,急性病毒感染引发的多克隆同种特异性CTL反应至少部分是许多与受病毒感染细胞交叉反应的同种特异性CTL克隆选择性扩增的结果。(摘要截短至400字)