Berman P W, Murthy K K, Wrin T, Vennari J C, Cobb E K, Eastman D J, Champe M, Nakamura G R, Davison D, Powell M F, Bussiere J, Francis D P, Matthews T, Gregory T J, Obijeski J F
Department of Immunology, Genentech, Inc., South San Francisco, California 94080, USA.
J Infect Dis. 1996 Jan;173(1):52-9. doi: 10.1093/infdis/173.1.52.
Three chimpanzees immunized with recombinant gp120 from human immunodeficiency virus type 1 (HIV-1) strain MN and 1 control animal were challenged intravenously with a primary isolate of HIV-1SF2. Viral infection was detected in the control animal by viral culture, polymerase chain reaction, and multiple serologic assays beginning 2 weeks after infection. Markers of HIV-1 infection were not detected in any of the gp120-vaccinated animals during 12 months of follow-up. Antisera from the gp120-immunized chimpanzees were unable to neutralize the challenge virus cultured in peripheral blood mononuclear cells (PBMC). These studies demonstrate that immunization with recombinant gp120 derived from a T cell-adapted isolate prevented infection by a heterologous primary isolate of HIV-1. The results suggest that in vitro virus neutralization assays utilizing primary isolates cultured in PBMC may be imperfect indicators of protection in vivo.
用来自1型人类免疫缺陷病毒(HIV-1)MN株的重组gp120免疫的3只黑猩猩和1只对照动物,静脉内接种了HIV-1 SF2的原始分离株。在感染后2周开始,通过病毒培养、聚合酶链反应和多种血清学检测在对照动物中检测到病毒感染。在12个月的随访期间,在任何接种gp120的动物中均未检测到HIV-1感染的标志物。来自接种gp120的黑猩猩的抗血清无法中和在外周血单核细胞(PBMC)中培养的攻击病毒。这些研究表明,用源自T细胞适应株的重组gp120免疫可预防HIV-1异源原始分离株的感染。结果表明,利用在PBMC中培养的原始分离株进行的体外病毒中和试验可能不是体内保护的完美指标。