Differences in HIV-1 reservoir size, landscape characteristics, and decay dynamics in acute and chronic treated HIV-1 Clade C infection.

IF 6.4 1区 生物学 Q1 BIOLOGY eLife Pub Date : 2025-02-20 DOI:10.7554/eLife.96617
Kavidha Reddy, Guinevere Q Lee, Nicole Reddy, Tatenda J B Chikowore, Kathy Baisley, Krista L Dong, Bruce D Walker, Xu G Yu, Mathias Lichterfeld, Thumbi Ndung'u
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Abstract

Persisting HIV reservoir viruses in resting CD4 T cells and other cellular subsets are a barrier to cure efforts. Early antiretroviral therapy (ART) enables post-treatment viral control in some cases, but mechanisms remain unclear. We hypothesised that ART initiated before peak viremia impacts HIV-1 subtype C reservoirs. We studied 35 women at high risk of infection from Durban, South Africa, identified with hyperacute HIV by twice-weekly HIV-RNA testing. Participants included 11 starting ART at a median of 456 (297-1203) days post-onset of viremia (DPOV) and 24 at 1 (1-3) DPOV. Peripheral blood mononuclear cells (PBMCs) were used to measured total HIV-1 DNA by droplet digital PCR (ddPCR) and sequence viral reservoir genomes by full-length proviral sequencing (FLIP-seq). ART during hyperacute infection blunted peak viremia (p<0.0001), but contemporaneous total HIV-1 DNA did not differ (p=0.104). Over 1 year, a decline of total HIV-1 DNA was observed in early treated persons (p=0.0004), but not late treated. Among 697 viral genome sequences, the proviral genetic landscape differed between untreated, late treated, and early treated groups. Intact genomes after 1 year were higher in untreated (31%) versus late treated (14%) and early treated (0%). Treatment in both late and early infection caused more rapid decay of intact (13% and 51% per month) versus defective (2% and 35%) viral genomes. However, intact genomes persisted 1 year post chronic treatment but were undetectable with early ART. Early ART also reduced phylogenetic diversity of intact genomes and limited cytotoxic T lymphocyte immune escape variants in the reservoir. Overall, ART initiated in hyperacute HIV-1 subtype C infection did not impact reservoir seeding but was associated with rapid intact viral genome decay, reduced genetic complexity, and limited immune escape, which may accelerate reservoir clearance in combination with other interventional strategies.

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急性和慢性治疗的HIV-1进化支C感染中HIV-1病毒库大小、景观特征和衰变动力学的差异
在静止的CD4 T细胞和其他细胞亚群中持续存在的HIV库病毒是治疗努力的障碍。在某些情况下,早期抗逆转录病毒治疗(ART)能够在治疗后控制病毒,但机制尚不清楚。我们假设ART是在病毒血症高峰影响HIV-1亚型C储库之前启动的。我们研究了来自南非德班的35名感染高危妇女,通过每周两次的HIV- rna检测确诊为超急性HIV。参与者包括11名在病毒血症(DPOV)发病后456(297-1203)天开始ART治疗的患者和24名在1 (1-3)DPOV开始ART治疗的患者。用外周血单核细胞(PBMCs)检测HIV-1总DNA,用液滴数字PCR (ddPCR)测定病毒库基因组,用全长前序列测序(FLIP-seq)测定病毒库基因组序列。在超急性感染期间抗逆转录病毒治疗使峰值病毒血症钝化(p
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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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