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用于评估抗逆转录病毒疗法的小鼠模型。

Murine models for evaluating antiretroviral therapy.

作者信息

Ruprecht R M, Bernard L D, Gama Sosa M A, Sosa M A, Fazely F, Koch J, Sharma P L, Mullaney S

机构信息

Division of Cancer Pharmacology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115.

出版信息

Cancer Res. 1990 Sep 1;50(17 Suppl):5618S-5627S.

PMID:2167158
Abstract

The pandemic of the acquired immunodeficiency syndrome (AIDS), caused by the human immunodeficiency virus type 1 (HIV-1), requires rapid development of effective therapy and prevention. Analysis of candidate anti-HIV-1 drugs in animals is problematic since no ideal animal model for HIV-1 infection and disease exists. For many reasons, including small size, availability of inbred strains, immunological reagents, and lymphokines, murine systems have been used for in vivo analysis of antiretroviral agents. Here we review currently available murine models involving HIV-1 in transgenic mice and in chimeric mice reconstituted with human cells, as well as murine systems using retroviruses of the subfamily Oncovirinae rather than Lentivirinae. We report our results on various antiretroviral treatment strategies, including chemoprophylaxis after acute retroviral exposure, therapy of chronic viremia, quantitative analysis of combination therapy, and therapy during pregnancy and in the neonatal period aimed at preventing viremia in the offspring. Due to our highly effective postexposure treatment protocols with 3'-azido-3'-deoxythymidine (zidovudine) combined with recombinant human interferon-alpha A/D, retrovirus-inoculated mice developed immunity to the virus to which they were exposed, which will allow us to determine the nature of protective antiretroviral immunity in inbred mice.

摘要

由1型人类免疫缺陷病毒(HIV-1)引起的获得性免疫缺陷综合征(艾滋病)大流行,需要迅速开发有效的治疗方法和预防措施。由于不存在用于HIV-1感染和疾病的理想动物模型,因此在动物中分析候选抗HIV-1药物存在问题。出于多种原因,包括体型小、近交系的可获得性、免疫试剂和淋巴因子等,小鼠系统已被用于抗逆转录病毒药物的体内分析。在此,我们综述了目前可用的小鼠模型,包括转基因小鼠和用人细胞重建的嵌合小鼠中涉及HIV-1的模型,以及使用嗜肿瘤病毒亚科而非慢病毒亚科逆转录病毒的小鼠系统。我们报告了我们在各种抗逆转录病毒治疗策略方面的结果,包括急性逆转录病毒暴露后的化学预防、慢性病毒血症的治疗、联合治疗的定量分析,以及旨在预防子代病毒血症的孕期和新生儿期治疗。由于我们采用3'-叠氮-3'-脱氧胸苷(齐多夫定)与重组人干扰素-α A/D联合使用的高效暴露后治疗方案,接种逆转录病毒的小鼠对其所暴露的病毒产生了免疫力,这将使我们能够确定近交小鼠中保护性抗逆转录病毒免疫的性质。

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