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Author Notes:

Correspondence: M. A. Price, PhD, International AIDS Vaccine Initiative, 125 Broad St, 9th Floor, NY, NY 10004 (mprice@iavi.org).

See publication for full list of author contributions.

See publication for full list of author acknowledgments.

The contents of this article are the responsibility of the authors and do not necessarily reflect the views of the US Agency for International Development or the US government.

This article is published with permission of the Director of the Kenya Medical Research Institute. IAVI donors (ie, the study funders) played no role in study design, conduct, analysis, or manuscript preparation.

In the role of sponsor, International AIDS Vaccine Initiative (IAVI) staff in collaboration with research partners wrote the study protocol, monitored study progress, conducted study analysis, and the primary author of this article (M. A. P.) is an IAVI employee.

All other authors report no potential conflicts.

All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest.

Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

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Research Funding:

This study was sponsored by the International AIDS Vaccine Initiative (IAVI), which in turn is funded by many donors, including the Bill and Melinda Gates Foundation, the Ministry of Foreign Affairs of Denmark, Irish Aid, the Ministry of Finance of Japan in partnership with The World Bank, the Ministry of Foreign Affairs of the Netherlands, the Norwegian Agency for Development Cooperation, the United Kingdom Department for International Development, and the US Agency for International Development (the full list of IAVI donors is available at: http://www.iavi.org).

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Immunology
  • Infectious Diseases
  • Microbiology
  • HIV
  • AIDS
  • Africa
  • epidemiology
  • HIV subtype
  • IMMUNODEFICIENCY-VIRUS TYPE-1
  • DISEASE PROGRESSION
  • VIREMIC CONTROLLERS
  • TRANSMISSION
  • HOST
  • DETERMINANTS
  • ELITE

Control of the HIV-1 Load Varies by Viral Subtype in a Large Cohort of African Adults With Incident HIV-1 Infection

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Journal Title:

Journal of Infectious Diseases

Volume:

Volume 220, Number 3

Publisher:

, Pages 432-441

Type of Work:

Article | Final Publisher PDF

Abstract:

Few human immunodeficiency virus (HIV)-infected persons can maintain low viral levels without therapeutic intervention. We evaluate predictors of spontaneous control of the viral load (hereafter, "viral control") in a prospective cohort of African adults shortly after HIV infection. Viral control was defined as ≥2 consecutively measured viral loads (VLs) of ≤10 000 copies/mL after the estimated date of infection, followed by at least 4 subsequent measurements for which the VL in at least 75% was ≤10 000 copies/mL in the absence of ART. Multivariable logistic regression characterized predictors of viral control. Of 590 eligible volunteers, 107 (18.1%) experienced viral control, of whom 25 (4.2%) maintained a VL of 51-2000 copies/mL, and 5 (0.8%) sustained a VL of ≤50 copies/mL. The median ART-free follow-up time was 3.3 years (range, 0.3-9.7 years). Factors independently associated with control were HIV-1 subtype A (reference, subtype C; adjusted odds ratio [aOR], 2.1 [95% confidence interval {CI}, 1.3-3.5]), female sex (reference, male sex; aOR, 1.8 [95% CI, 1.1-2.8]), and having HLA class I variant allele B∗57 (reference, not having this allele; aOR, 1.9 [95% CI, 1.0-3.6]) in a multivariable model that also controlled for age at the time of infection and baseline CD4+ T-cell count. We observed strong associations between infecting HIV-1 subtype, HLA type, and sex on viral control in this cohort. HIV-1 subtype is important to consider when testing and designing new therapeutic and prevention technologies, including vaccines.

Copyright information:

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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