Brody B A, Hunter E, Kluge J D, Lasarow R, Gardner M, Marx P A
Department of Microbiology, University of Alabama, Birmingham 35294.
J Virol. 1992 Jun;66(6):3950-4. doi: 10.1128/JVI.66.6.3950-3954.1992.
Rhesus macaques were immunized with live vaccinia virus recombinants expressing the envelope glycoproteins (gp70 and gp22) of simian type D retrovirus (SRV), serotype 1 or 3. All of the animals immunized with either the SRV-1 env or the SRV-3 env vaccinia virus recombinant developed neutralizing antibodies against the homologous SRV. In addition, both groups developed cross-reactive antibodies and were protected against an intravenous live-virus challenge with SRV-1. The four control animals immunized with a vaccinia virus recombinant expressing the G protein of respiratory syncytial virus were not protected against the same SRV-1 challenge. Although SRV-1 and SRV-3 immune sera showed cross-neutralization, they failed to neutralize a separate, more distantly related serotype, SRV-2, in an in vitro assay. These findings are consistent with the known degree of serologic and genetic relatedness of these three SRV strains.
恒河猴用表达猿猴D型逆转录病毒(SRV)1型或3型包膜糖蛋白(gp70和gp22)的活痘苗病毒重组体进行免疫。用SRV-1 env或SRV-3 env痘苗病毒重组体免疫的所有动物均产生了针对同源SRV的中和抗体。此外,两组均产生了交叉反应性抗体,并对SRV-1的静脉内活病毒攻击具有抵抗力。用表达呼吸道合胞病毒G蛋白的痘苗病毒重组体免疫的四只对照动物对相同的SRV-1攻击没有抵抗力。尽管SRV-1和SRV-3免疫血清显示出交叉中和作用,但在体外试验中它们未能中和另一种亲缘关系更远的血清型SRV-2。这些发现与这三种SRV毒株已知的血清学和遗传相关性程度一致。