Brief Report: Low-Dose Methotrexate Does Not Affect Measures of HIV-1 Persistence in Individuals With Chronically Treated HIV-1 Infection.

IF 2.9 3区 医学 Q3 IMMUNOLOGY JAIDS Journal of Acquired Immune Deficiency Syndromes Pub Date : 2024-08-15 DOI:10.1097/qai.0000000000003453
Joshua C Cyktor,Eunice Yeh,Heather Ribaudo,Dianna Hoeth,Asma Naqvi,Tanvir Bell,Paul M Ridker,Carl Fichtenbaum,Eric S Daar,Diane Havlir,Ahmed Tawakol,Michael M Lederman,James H Stein,Steven G Deeks,Judith S Currier,Priscilla Y Hsue,John W Mellors,
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Abstract

BACKGROUND People with HIV-1 often have chronic inflammation leading to severe non-AIDS morbidity and mortality. The AIDS Clinical Trials Group Study A5314 sought to lower inflammation with low-dose methotrexate (LDMTX). The primary study outcomes were reported previously but here we present the impact of LDMTX on multiple measures of HIV-1 persistence. METHODS A5314 was a phase 2 randomized, double-blind, multicenter trial in 176 adult people with HIV-1 on virally suppressive antiretroviral therapy. LDMTX (5-15 mg/wk) was administered for 24 weeks with an additional 12 weeks of participant follow-up. The current analyses of HIV-1 persistence were restricted to 60 participants (30 LDMTX and 30 placebo) randomly selected from the total population. Plasma HIV-1 RNA, total HIV-1 DNA, and cell-associated HIV-1 RNA (CA HIV-1 RNA) were measured by sensitive quantitative PCR assays. RESULTS LDMTX treatment had no significant effect on sensitive measures of plasma HIV-1 RNA, HIV-1 DNA, CA HIV-1 RNA, or CA HIV-1 RNA/DNA ratio at any time point or from baseline to week 24. As observed in the main study, absolute peripheral CD4+ and CD8+ T-cell numbers decreased from baseline to week 24 among the 30 participants receiving LDMTX compared with placebo (median decrease of -31.5 CD4+ T cells/µL, -83.5 CD8+ T cells/µL). CONCLUSIONS LDMTX had no significant effect on any measure of HIV-1 persistence in plasma or peripheral blood mononuclear cells. Further studies are needed to determine whether other immunosuppressive and/or immunoreductive interventions are safe and capable of affecting HIV-1 persistence.
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简要报告:小剂量甲氨蝶呤不会影响长期治疗的 HIV-1 感染者的 HIV-1 持久性。
背景HIV-1感染者通常患有慢性炎症,导致严重的非艾滋病发病率和死亡率。艾滋病临床试验小组 A5314 研究试图用低剂量甲氨蝶呤 (LDMTX) 降低炎症反应。该研究的主要结果已在之前报道过,但在此我们要介绍的是 LDMTX 对 HIV-1 持续性的多种测量指标的影响。LDMTX(5-15 毫克/周)用药 24 周,并对参与者进行了为期 12 周的随访。目前的 HIV-1 持久性分析仅限于从全部人群中随机抽取的 60 名参与者(30 名 LDMTX 患者和 30 名安慰剂患者)。结果LDMTX治疗对任何时间点或从基线到第24周的血浆HIV-1 RNA、HIV-1 DNA、CA HIV-1 RNA或CA HIV-1 RNA/DNA比值的敏感指标均无显著影响。正如在主要研究中观察到的那样,与安慰剂相比,接受LDMTX治疗的30名参与者的外周CD4+和CD8+T细胞绝对数量从基线到第24周均有所下降(CD4+T细胞/µL的中位下降率为-31.5,CD8+T细胞/µL的中位下降率为-83.5)。还需要进一步研究,以确定其他免疫抑制和/或免疫调节干预措施是否安全,是否能够影响 HIV-1 的持续存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.80
自引率
5.60%
发文量
490
审稿时长
3-6 weeks
期刊介绍: JAIDS: Journal of Acquired Immune Deficiency Syndromes​ seeks to end the HIV epidemic by presenting important new science across all disciplines that advance our understanding of the biology, treatment and prevention of HIV infection worldwide. JAIDS: Journal of Acquired Immune Deficiency Syndromes is the trusted, interdisciplinary resource for HIV- and AIDS-related information with a strong focus on basic and translational science, clinical science, and epidemiology and prevention. Co-edited by the foremost leaders in clinical virology, molecular biology, and epidemiology, JAIDS publishes vital information on the advances in diagnosis and treatment of HIV infections, as well as the latest research in the development of therapeutics and vaccine approaches. This ground-breaking journal brings together rigorously peer-reviewed articles, reviews of current research, results of clinical trials, and epidemiologic reports from around the world.
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