Shibata R, Siemon C, Cho M W, Arthur L O, Nigida S M, Matthews T, Sawyer L A, Schultz A, Murthy K K, Israel Z, Javadian A, Frost P, Kennedy R C, Lane H C, Martin M A
Laboratory of Molecular Microbiology, Division of AIDS, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, USA.
J Virol. 1996 Jul;70(7):4361-9. doi: 10.1128/JVI.70.7.4361-4369.1996.
To test whether the protective effects of attenuated simian immunodeficiency virus vaccines in macaques were applicable to the human immunodeficiency virus type 1 (HIV-1)-chimpanzee system, two groups of animals, previously infected with HIV-1(IIIB) or HIV-1(SF2) were each challenged with a heterologous clade B virus, HIV-1(DH12). Following challenge, the parameters measured included virus isolation (from plasma, peripheral blood mononuclear cells, and lymph node tissue); quantitative DNA PCR using primers capable of distinguishing HIV-1(IIIB), HIV-1(SF2), and HIV-1(DH12) from one another; and serologic assays to monitor changes in binding and neutralizing antibodies. In contrast to an HIV-1-naive chimpanzee that rapidly became infected following the inoculation of HIV-1(DH12), the two chimpanzees previously infected with HIV-1(IIIB) resisted repeated and escalating inoculations of HIV-1(DH12), as monitored by virus isolation and PCR. The two animals previously infected with HIV-1(SF2) became infected with HIV-1(DH12) but in contrast to the case with the HIV-1-naive chimpanzee, no cell-free viral RNA was detected in the plasma by the branched DNA procedure and levels of peripheral blood mononuclear cell-associated viral DNA were reduced 35- to 50-fold.
为了测试减毒猿猴免疫缺陷病毒疫苗在猕猴中的保护作用是否适用于人类免疫缺陷病毒1型(HIV-1)-黑猩猩系统,两组先前感染了HIV-1(IIIB)或HIV-1(SF2)的动物分别用一种异源B亚型病毒HIV-1(DH12)进行攻击。攻击后,所测量的参数包括病毒分离(从血浆、外周血单核细胞和淋巴结组织中);使用能够区分HIV-1(IIIB)、HIV-1(SF2)和HIV-1(DH12)的引物进行定量DNA PCR;以及监测结合抗体和中和抗体变化的血清学检测。与接种HIV-1(DH12)后迅速被感染的未感染HIV-1的黑猩猩不同,通过病毒分离和PCR监测发现,两只先前感染HIV-1(IIIB)的黑猩猩抵抗了HIV-1(DH12)的反复和递增接种。两只先前感染HIV-1(SF2)的动物感染了HIV-1(DH12),但与未感染HIV-1的黑猩猩的情况不同,通过分支DNA方法在血浆中未检测到无细胞病毒RNA,外周血单核细胞相关病毒DNA水平降低了35至50倍。