Peck R, Brown A, Wust C J
J Immunol. 1979 Oct;123(4):1763-6.
An in vitro correlate of cell-mediated cross-protection among alpha-viruses was demonstrated by cytotoxicity of Sindbis-immune spleen cells from mice to both Sindbis and Semliki Forest virus (SFV)-infected target cells. This cytotoxicity was shown to be mediated by the T cell population of the spleen and was independent of the presence of macrophages or B cells. The time when the level of the lymphocyte-mediated cytotoxicity (LMC) to SFV-infected cells was maximal coincides with the time when immunity to SFV is maximal in vivo, as reported previously, and when adoptive immunity to SFV can be transferred. After one i.p. injection of Sindbis virus, the level of homologous LMC was higher than the level of heterologous LMC. However, following a second injection of Sindbis virus as immunogen, at a time when the mice are cross-protected to SFV, the heterologous LMC was considerably higher than homologous LMC. We propose that there is suppression of the effector T cells specific for Sindbis-infected cells after the second immunizing injection, probably by homologous antibody. In contrast, there appears to be an anamnestic cell-mediated response to SFV.
小鼠辛德毕斯免疫脾细胞对辛德毕斯病毒和塞姆利基森林病毒(SFV)感染的靶细胞具有细胞毒性,这证明了α病毒之间细胞介导的交叉保护在体外具有相关性。这种细胞毒性由脾脏的T细胞群体介导,且与巨噬细胞或B细胞的存在无关。淋巴细胞介导的对SFV感染细胞的细胞毒性(LMC)水平达到最大值的时间,与体内对SFV的免疫力达到最大值的时间一致,如先前报道,此时对SFV的过继免疫也可以转移。腹腔注射一次辛德毕斯病毒后,同源LMC水平高于异源LMC水平。然而,在第二次注射辛德毕斯病毒作为免疫原后,当小鼠对SFV具有交叉保护作用时,异源LMC远高于同源LMC。我们认为,第二次免疫注射后,可能是同源抗体抑制了针对辛德毕斯感染细胞的效应T细胞。相比之下,似乎存在对SFV的回忆性细胞介导反应。