Rabinowitz S G, Lipton H L
J Immunol. 1976 Aug;117(2):357-63.
After (IC) inoculation of the DA strain of TMEV, SJL/J mice develop chronic CNS infection with marked mononuclear cell infiltration of spinal cord leptomeninges and white matter and concomitant demyelination. In the present study the temporal course of cell-mediated and humoral immune responses to virus were measured in this infection. It was shown that chronic TMEV infection is associated with the development of immunologically specific spleen cell reactivity as judged by in vitro incorporation of 3H-TdR into DNA in response to inactivated TMEV antigen. Spleen cell reactivity is first detectable about 2 months after infection, persists for at least 1 year, and correlates with the temporal development of serum-neutralizing antibody. The late development of sensitized spleen cells is not the result of an immunosuppressive effect of this virus infection since infected mice exhibit normal spleen cell proliferative responses to T cell mitogens and produce normal antibody responses to a heterologous protein antigen, sheep red blood cells. In addition, anti-viral antibody inhibits virus-induced spleen cell reactivity. Finally, the antigen-reactive lymphocyte subpopulation within the spleen responsible for proliferation to TMEV antigen are T cells and not B cells.
接种TMEV的DA毒株后,SJL/J小鼠会发生慢性中枢神经系统感染,脊髓软脑膜和白质有明显的单核细胞浸润并伴有脱髓鞘。在本研究中,检测了该感染中针对病毒的细胞介导免疫反应和体液免疫反应的时间进程。结果表明,根据体外3H-TdR掺入DNA以响应灭活的TMEV抗原的情况判断,慢性TMEV感染与免疫特异性脾细胞反应性的发展有关。脾细胞反应性在感染后约2个月首次可检测到,持续至少1年,并与血清中和抗体的时间发展相关。致敏脾细胞的晚期出现不是这种病毒感染免疫抑制作用的结果,因为感染的小鼠对T细胞有丝分裂原表现出正常的脾细胞增殖反应,并对异源蛋白抗原绵羊红细胞产生正常的抗体反应。此外,抗病毒抗体抑制病毒诱导的脾细胞反应性。最后,脾内负责对TMEV抗原增殖的抗原反应性淋巴细胞亚群是T细胞而非B细胞。