Niewiesk S, Götzelmann M, ter Meulen V
Institute of Virology and Immunobiology, University of Wurzburg, Versbacher Strasse 7, 97078 Wurzburg, Germany.
Proc Natl Acad Sci U S A. 2000 Apr 11;97(8):4251-5. doi: 10.1073/pnas.060012097.
During and after measles virus (MV) infection humans are highly susceptible to opportunistic infections because of a marked immunosuppressive effect of the virus. The mechanisms by which the virus induces this phenomenon is not well understood. In particular, detailed information is missing on the targets of suppression in relation to antigen-specific T and B cell responses. Because such studies require animal experiments, we used the cotton rat model, in which the MV causes a respiratory tract infection. Primary as well as secondary T cell responses were impaired in vivo and ex vivo by MV infection. The proliferation of T cells was greatly reduced, but their effector functions, such as cytolysis or cytokine secretion, were not. In contrast, primary and secondary B cell responses in vivo as measured by the frequency of antigen-specific plasma cells in an enzyme-linked immunospot (ELISPOT) assay were not altered by MV infection. Only the secretion of immunoglobulins was reduced slightly in animals primarily infected with MV after 2 weeks. These data demonstrate that MV-induced immunosuppression acts primarily on the T cell responses in vivo.
在麻疹病毒(MV)感染期间及之后,由于该病毒具有显著的免疫抑制作用,人类极易受到机会性感染。病毒诱发这种现象的机制尚不清楚。特别是,关于与抗原特异性T细胞和B细胞反应相关的抑制靶点,缺少详细信息。由于此类研究需要进行动物实验,我们使用了棉鼠模型,在该模型中MV会引发呼吸道感染。MV感染在体内和体外均损害了原发性以及继发性T细胞反应。T细胞的增殖大幅减少,但其效应功能,如细胞溶解或细胞因子分泌,并未受到影响。相比之下,通过酶联免疫斑点(ELISPOT)测定法检测抗原特异性浆细胞频率来衡量,体内原发性和继发性B细胞反应并未因MV感染而改变。仅在初次感染MV的动物中,2周后免疫球蛋白的分泌略有减少。这些数据表明,MV诱导的免疫抑制主要作用于体内的T细胞反应。