Activation of CXCR3 <sup>+</sup> Tfh cells and B cells in lymph nodes during acute HIV-1 infection correlates with HIV-specific antibody development

Early initiation of antiretroviral therapy (ART) is important to limit the seeding of the long-lasting HIV-1 reservoir; however, it also precludes the development of HIV-specific antibodies that can help control the virus if ART is stopped. Antibody development occurs within germinal centers in the lymph node and requires activation of both antigen-specific B cells and T follicular helper cells (Tfh), a specialized CD4<sup>+</sup> cell that provides B cell help. To understand how early ART initiation may prohibit antibody development, we analyzed the frequencies and activation status of Tfh and B cells in lymph node biopsies collected in the different stages of acute HIV-1 infection. Our data suggest that decreased antibody development after early ART initiation may be due to limited germinal center development at the time of treatment and that new interventions that target activation of CXCR3<sup>+</sup> Tfh may be beneficial to increase long-term HIV-specific antibody levels.

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Publication Details

Journal
Journal of Virology
Published
2025-02-11
DOI
https://doi.org/10.1128/jvi.01532-24
Citations
3
Primary Topic
HIV Research and Treatment
Type
article
Field-Weighted Citation Impact
3.11

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article

Activation of CXCR3 + Tfh cells and B cells in lymph nodes during acute HIV-1 infection correlates with HIV-specific antibody development

Julie L. Mitchell, Justin Pollara, Roshell Muir, Bessara Nuntapinit et al.
3 citations
Journal of Virology
HIV Research and Treatment
3.11
article

Activation of CXCR3 + Tfh cells and B cells in lymph nodes during acute HIV-1 infection correlates with HIV-specific antibody development

Julie L. Mitchell, Justin Pollara, Roshell Muir, Bessara Nuntapinit, Nicha Tulmethakaan, Dominic Paquin‐Proulx, Hiroshi Takata, Sopark Manasnayakorn, Kenneth A. Dietze, Sandhya Vasan, Suthat Chottanapund, Pierre Gantner, Guido Ferrari, Suwanna Puttamaswin, Nittaya Phanuphak, Suteeraporn Pinyakorn, Carlo Sacdalan, Junsuke Nohara, Kombo F. N’Guessan, Eugène Kroon, Lydie Trautmann, Supranee Buranapraditkun, Peeriya Prueksakaew, Nicolas Chomont, Denise C. Hsu, Elias K. Haddad, Praphan Phanuphak, Pattarawat Thantiworasit, Nisakorn Ratnaratorn, Jintanat Ananworanich, Lawrence Fox
article en
3 citations

Abstract

Early initiation of antiretroviral therapy (ART) is important to limit the seeding of the long-lasting HIV-1 reservoir; however, it also precludes the development of HIV-specific antibodies that can help control the virus if ART is stopped. Antibody development occurs within germinal centers in the lymph node and requires activation of both antigen-specific B cells and T follicular helper cells (Tfh), a specialized CD4<sup>+</sup> cell that provides B cell help. To understand how early ART initiation may prohibit antibody development, we analyzed the frequencies and activation status of Tfh and B cells in lymph node biopsies collected in the different stages of acute HIV-1 infection. Our data suggest that decreased antibody development after early ART initiation may be due to limited germinal center development at the time of treatment and that new interventions that target activation of CXCR3<sup>+</sup> Tfh may be beneficial to increase long-term HIV-specific antibody levels.

Journal of VirologyVol. 99(3)
Henry M. Jackson Foundation (US), National Institutes of Health (US), Chulalongkorn University (TH), Oregon Health & Science University (US), Armed Forces Research Institute of Medical Science (TH), HIV Netherlands Australia Thailand Research Collaboration (TH), Amsterdam Institute for Global Health and Development (NL), Duke Medical Center (US), National Institute of Allergy and Infectious Diseases (US), Centre Hospitalier de l’Université de Montréal (CA), Institut de Recherche et d’Innovation (FR), Amsterdam University Medical Centers (NL), Drexel University (US), University of Amsterdam (NL), Walter Reed Army Institute of Research (US)
U.S. Department of Defense, Henry M. Jackson Foundation, Gilead Sciences, ViiV Healthcare, Chulalongkorn University, National Institutes of Health, Faculty of Medicine, Chulalongkorn University, National Institute of Allergy and Infectious Diseases, U.S. Military HIV Research Program
Good health and well-being
Openalex Percentile: Top 11%
HIV Research and Treatment
3.11
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