首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Merck Ad5/HIV induces broad innate immune activation that predicts CD8~+ T-cell responses but is attenuated by preexisting Ad5 immunity
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Merck Ad5/HIV induces broad innate immune activation that predicts CD8~+ T-cell responses but is attenuated by preexisting Ad5 immunity

机译:默克Ad5 / HIV诱导广泛的先天免疫活化,该活化可预测CD8〜+ T细胞反应,但会因预先存在的Ad5免疫而减弱

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摘要

A highly efficacious HIV vaccine offers the greatest hope for halting the AIDS pandemic, but it remains unclear what type of immune response an HIV vaccine must induce to be effective. Modest but encouraging results from two recent clinical trials have provided some insights. The RV144 study in Thailand used an engineered poxvirus expressing HIV proteins in conjunction with an HIV envelope protein and demonstrated 31% efficacy in reducing HIV-1 infection (1). MRKAd5/HIV, an adenovirus serotype 5 (Ad5)-based HIV vaccine expressing HIV proteins, and the focus of the present study, did not show efficacy but exerted selective pressure on infecting viruses, forcing them to evolve in response to the HIV proteins it expressed (2, 3).
机译:高效的HIV疫苗为遏制AIDS大流行提供了最大希望,但目前尚不清楚HIV疫苗必须诱导哪种免疫反应才能有效。最近两项临床试验得出的适度但令人鼓舞的结果提供了一些见识。在泰国进行的RV144研究中,使用了一种工程病毒来表达HIV蛋白和HIV包膜蛋白,并证明其减少HIV-1感染的功效为31%(1)。 MRKAd5 / HIV是一种表达HIV蛋白的基于腺病毒血清型5(Ad5)的HIV疫苗,也是本研究的重点,它没有显示出功效,但对感染病毒施加了选择性压力,迫使它们响应其HIV蛋白而进化。表示(2,3)。

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    Seattle Biomedical Research Institute, Seattle, WA 98109;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;

    Seattle Biomedical Research Institute, Seattle, WA 98109;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109,HIV Vaccine Trials Network, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109,HIV Vaccine Trials Network, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109,HIV Vaccine Trials Network, Fred Hutchinson Cancer Research Center, Seattle, WA 98109,Department of Laboratory Medicine, University of Washington, Seattle, WA 98195;

    Seattle Biomedical Research Institute, Seattle, WA 98109,Department of Immunology, University of Washington, Seattle, WA 98195;

    Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109,HIV Vaccine Trials Network, Fred Hutchinson Cancer Research Center, Seattle, WA 98109,Department of Medicine, University of Washington, Seattle, WA 98195;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 00:40:35

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