O'Neill H C, Brenan M
Department of Experimental Pathology, John Curtin School of Medical Research, Australian National University, Canberra, ACT.
J Gen Virol. 1987 Oct;68 ( Pt 10):2669-73. doi: 10.1099/0022-1317-68-10-2669.
Ectromelia virus-specific cytotoxic T (Tc) cell precursors were present in the draining popliteal lymph node of all strains of mice tested at 2 to 3 days after footpad inoculation of a high dose (10(5) p.f.u.) of the virulent Moscow strain of ectromelia virus. To detect this response it was necessary to culture lymph node cells from infected mice in the presence of T cell growth factors and to use the more sensitive neutral red assay for measuring cytotoxicity. Cells with lytic activity were virus-specific, major histocompatibility complex-restricted TC cells. C57BL/6J resistant mice, which express a single dominant gene conferring innate resistance had virus-specific TC cell precursors 1 to 2 days sooner than did susceptible BALB/b mice. This TC cell-mediated immune response early after infection could account for the barrier to virus dissemination known to operate 1 to 2 days after infection to slow virus passage into the lymphoreticular system.
在用高剂量(10⁵ 蚀斑形成单位)的强毒力莫斯科株埃可病毒足垫接种小鼠后2至3天,在所有测试品系小鼠引流的腘窝淋巴结中均存在埃可病毒特异性细胞毒性T(Tc)细胞前体。为检测这种反应,有必要在T细胞生长因子存在的情况下培养感染小鼠的淋巴结细胞,并使用更灵敏的中性红试验来测定细胞毒性。具有裂解活性的细胞是病毒特异性的、主要组织相容性复合体限制的Tc细胞。表达单个赋予先天抗性的显性基因的C57BL/6J抗性小鼠,比易感的BALB/b小鼠早1至2天出现病毒特异性Tc细胞前体。感染后早期这种由Tc细胞介导的免疫反应,可以解释已知在感染后1至2天起作用以减缓病毒进入淋巴网状系统的病毒传播屏障。