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首页> 外文期刊>AIDS Research and Human Retroviruses >Delaying a Treatment Switch in Antiretroviral-Treated HIV Type 1-Infected Patients with Detectable Drug-Resistant Viremia Does Not Have a Profound Effect on Immune Parameters: AIDS Clinical Trials Group Study A5115
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Delaying a Treatment Switch in Antiretroviral-Treated HIV Type 1-Infected Patients with Detectable Drug-Resistant Viremia Does Not Have a Profound Effect on Immune Parameters: AIDS Clinical Trials Group Study A5115

机译:延迟抗逆转录病毒治疗的HIV 1型感染可检测抗药性病毒血症患者的治疗转换不会对免疫参数产生深远影响:A​​IDS临床试验小组研究A5115

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摘要

Some patients are unable to achieve and maintain an undetectable plasma HIV-1 RNA level with combination antiretroviral therapy (ART) and are therefore maintained on a partially suppressive regimen. To determine the immune consequences of continuing ART despite persistent viremia, we randomized 47 ART-treated individuals with low to moderate plasma HIV-1 RNA levels (200–9999 copies/ml) to either an immediate switch in therapy or a delayed switch (when plasma HIV-1 RNA became ≥10,000 copies/ml). After 48 weeks of follow-up, naive and memory CD4+ T cell percents were comparable in the two groups. The proportion of subjects with a lymphocyte proliferative response to Candida, Mycobacterium avium- intracellulare complex, or HIV-gag was also not significantly different at week 48. Delaying a treatment switch in patients with partial virologic suppression and stable CD4+ T cells does not have profound effects on immune parameters.
机译:一些患者无法通过联合抗逆转录病毒疗法(ART)达到和维持无法检测到的血浆HIV-1 RNA水平,因此被维持在部分抑制方案下。为了确定尽管存在持续的病毒血症而继续进行抗逆转录病毒疗法的免疫后果,我们将47名接受低抗中度血浆HIV-1 RNA水平(200–9999拷贝/ ml)的抗逆转录病毒疗法的患者随机分为治疗方案或延迟方案(当血浆HIV-1 RNA≥10,000拷贝/ ml)。随访48周后,两组的幼稚和记忆CD4 + T细胞百分比相当。在48周时,对念珠菌,鸟分枝杆菌-细胞内复合物或HIV-gag产生淋巴细胞增殖反应的受试者比例也没有显着差异。在部分病毒学抑制和CD4 +稳定的患者中延迟治疗切换sup> T细胞对免疫参数没有深远的影响。

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  • 来源
    《AIDS Research and Human Retroviruses》 |2009年第2期|135-139|共5页
  • 作者单位

    Department of Medicine, Rush Medical College, Chicago, Illinois 60612.;

    Department of Biostatistics, Statistical and Data Analysis Center, Harvard School of Public Health, Boston, Massachusetts 02319.;

    Department of Biostatistics, Statistical and Data Analysis Center, Harvard School of Public Health, Boston, Massachusetts 02319.;

    Social & Scientific Systems, Inc., Silver Spring, Maryland 20910.;

    Section of Retroviral Therapeutics, Brigham and Women's Hospital and Division of AIDS, Harvard Medical School, Boston, Massachusetts 02319.;

    Department of Medicine, Duke University Medical Center, Durham, North Carolina 27706.;

    Department of Medicine, University of California–San Francisco and San Francisco General Hospital, San Francisco, California 94143.;

    Department Immunology and Microbiology, Rush Medical College, Chicago, Illinois 60612.;

    Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15260.;

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