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重组亚单位疫苗对猕猴猿猴免疫缺陷病毒感染的保护效力评估。

Evaluation of protective efficacy of recombinant subunit vaccines against simian immunodeficiency virus infection of macaques.

作者信息

Hu S L, Abrams K, Misher L, Stallard V, Moran P, Zarling J M, Langlois A J, Kuller L, Morton W R, Benveniste R E

机构信息

Bristol-Myers Squibb Pharmaceutical Research Institute, Seattle, WA 98121.

出版信息

J Med Primatol. 1992 Feb-May;21(2-3):119-25.

PMID:1433262
Abstract

Simian immunodeficiency virus (SIV) was used as a model to study the protective efficacy of an immunization regimen currently being evaluated as candidate vaccines against HIV in human subjects. Four Macaca fascicularis were first immunized with recombinant vaccinia virus expressing the envelope glycoprotein gp160 of SIVmne and then boosted with subunit gp160. Both cell-mediated and humoral immune responses against SIV, including neutralizing antibodies, were elicited. The macaques were shown to be protected from a homologous virus infection as determined by serology, lymphocyte cocultivation, polymerase chain reactions and in vivo transmission analyses. Four unimmunized control animals were readily infected. However, viremia in infected control animals could decrease substantially following the initial phase of infection so that persistent infection might not be readily detectable.

摘要

猿猴免疫缺陷病毒(SIV)被用作模型,以研究一种免疫方案的保护效果,该方案目前正在作为针对人类受试者的HIV候选疫苗进行评估。首先用表达SIVmne包膜糖蛋白gp160的重组痘苗病毒对4只食蟹猴进行免疫,然后用亚单位gp160进行加强免疫。引发了针对SIV的细胞介导免疫反应和体液免疫反应,包括中和抗体。通过血清学、淋巴细胞共培养、聚合酶链反应和体内传播分析确定,这些猕猴受到保护,免受同源病毒感染。4只未免疫的对照动物很容易被感染。然而,感染的对照动物中的病毒血症在感染初始阶段后可能会大幅下降,因此可能不容易检测到持续性感染。

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