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首页> 外文期刊>Journal of Infectious Diseases >No Evidence for Decay of the Latent Reservoir in HIV-1—Infected Patients Receiving Intensive Enfuvirtide-Containing Antiretroviral Therapy
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No Evidence for Decay of the Latent Reservoir in HIV-1—Infected Patients Receiving Intensive Enfuvirtide-Containing Antiretroviral Therapy

机译:没有证据表明HIV-1感染的接受Enfuvirtide强化抗逆转录病毒治疗的患者体内潜伏性水库的衰变

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摘要

Human immunodeficiency virus type 1 (HIV-1) persists in a latent reservoir of infected resting memory CD4 cells in patients receiving antiretroviral therapy.We assessed whether multitarget therapy with enfuvirtide, 2 reverse-transcriptase inhibitors, and a ritonavir-boosted protease inhibitor leads to decay of this reservoir. Nineteen treatment-naive patients initiated this regimen; 9 experienced virologic suppression and continued enfuvirtide-containing therapy for at least 48 weeks. In enfuvirtide-treated patients with virological suppression, there was no decay of the latent reservoir (95% confidence interval for half-life, 11 months to infinity). The stability of the latent reservoir despite intensive therapy suggests that new strategies are needed to eradicate HIV-1 from this reservoir. (ClinicalTrials.gov identifier: NCT00051831.)
机译:在接受抗逆转录病毒治疗的患者中,人类免疫缺陷病毒1型(HIV-1)仍保留在感染的静息记忆CD4细胞的潜在库中。我们评估了恩夫韦肽,2种逆转录酶抑制剂和利托那韦增强蛋白酶抑制剂的多靶点治疗是否导致该储层的衰变。 19名未接受过治疗的患者开始了该治疗方案。 9位患者受到病毒抑制,并持续接受恩夫韦肽治疗至少48周。在用恩夫韦肽治疗的病毒学抑制的患者中,潜伏储库没有衰减(半衰期为95%置信区间,无穷11个月)。尽管进行了强化治疗,但潜在水库的稳定性表明需要采取新的策略从该水库中清除HIV-1。 (ClinicalTrials.gov标识符:NCT00051831。)

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  • 来源
    《Journal of Infectious Diseases》 |2010年第2期|p.293-296|共4页
  • 作者单位

    Massachusetts General Hospital, Boston, Massachusetts;

    Harvard School of Public Health, Boston, Massachusetts;

    Harvard School of Public Health, Boston, Massachusetts;

    Beth Israel Deaconess Medical Center, Boston, Massachusetts;

    University of Rochester School of Medicine and Dentistry, Rochester, New York;

    University of Rochester School of Medicine and Dentistry, Rochester, New York;

    Social and Scientific Systems, Silver Spring, Maryland;

    Ohio State University, Colombus;

    Johns Hopkins School of Medicine, Baltimore, Maryland;

    Johns Hopkins School of Medicine, Baltimore, Maryland|Howard Hughes Medical Institute, Baltimore, Maryland;

    Johns Hopkins School of Medicine, Baltimore, Maryland;

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