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Vedolizumab and ART in recent HIV-1 infection unveil the role of α4β7 in reservoir size
Maria Reyes Jimenez-Leon, … , Luis F. Lopez-Cortes, Ezequiel Ruiz-Mateos
Maria Reyes Jimenez-Leon, … , Luis F. Lopez-Cortes, Ezequiel Ruiz-Mateos
Published July 9, 2024
Citation Information: JCI Insight. 2024;9(16):e182312. https://doi.org/10.1172/jci.insight.182312.
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Clinical Research and Public Health AIDS/HIV Immunology

Vedolizumab and ART in recent HIV-1 infection unveil the role of α4β7 in reservoir size

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Abstract

BACKGROUND We evaluated the safety and viral rebound, after analytical treatment interruption (ATI), of vedolizumab and ART in recent HIV-1 infection. We used this model to analyze the effect of α4β7 on the HIV-1 reservoir size.METHODS Participants started ART with monthly vedolizumab infusions, and ATI was performed at week 24. Biopsies were obtained from ileum and cecum at baseline and week 24. Vedolizumab levels, HIV-1 reservoir, flow cytometry, and cell-sorting and antibody competition experiments were assayed.RESULTS Vedolizumab was safe and well tolerated. No participant achieved undetectable viremia off ART 24 weeks after ATI. Only a modest effect on the time to achieve more than 1,000 HIV-1 RNA copies/mL and the proportion of participants off ART was observed, being higher in the vedolizumab group compared with historical controls. Just before ATI, α4β7 expression was associated with HIV-1 DNA and RNA in peripheral blood and with PD1 and TIGIT levels. Importantly, a complete blocking of α4β7 was observed on peripheral CD4+ T cells but not in gut (ileum and cecum), where α4β7 blockade and vedolizumab levels were inversely associated with HIV-1 DNA.CONCLUSION Our findings support α4β7 as an important determinant in HIV-1 reservoir size, suggesting the complete α4β7 blockade in tissue as a promising tool for HIV-cure combination strategies.TRIAL REGISTRATION ClinicalTrials.gov NCT03577782.FUNDING This work was supported by the Instituto de Salud Carlos III (Fondo Europeo de Desarrollo Regional, “a way to make Europe,” research contracts FI17/00186 and FI19/00083 and research projects PI18/01532, PI19/01127, PI22/01796), Conserjería de Economía, Conocimiento, Empresas y Universidad, Junta de Andalucía (research projects P20/00906), the Red Temática de Investigación Cooperativa en SIDA (RD16/0025/0020), and the Spanish National Research Council.

Authors

Maria Reyes Jimenez-Leon, Carmen Gasca-Capote, Cristina Roca-Oporto, Nuria Espinosa, Salvador Sobrino, Maria Fontillon-Alberdi, Ce Gao, Isabelle Roseto, Gregory Gladkov, Inmaculada Rivas-Jeremias, Karin Neukam, Jose German Sanchez-Hernandez, Raul Rigo-Bonnin, Antonio J. Cervera-Barajas, Rosario Mesones, Federico García, Ana Isabel Alvarez-Rios, Sara Bachiller, Joana Vitalle, Alberto Perez-Gomez, María Inés Camacho-Sojo, Isabel Gallego, Christian Brander, Ian McGowan, Beatriz Mothe, Pompeyo Viciana, Xu Yu, Mathias Lichterfeld, Luis F. Lopez-Cortes, Ezequiel Ruiz-Mateos

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Figure 2

Plasma viral load, proportion of participants off ART, and time to viral load rebound after ATI.

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Plasma viral load, proportion of participants off ART, and time to viral...
(A) Longitudinal plasma viremia evolution after ATI. Four participants restarted ART (gray area) because of an increase of viral load (>105 HIV-1 RNA copies/mL). The horizontal red line indicates the limit of detection (20 HIV-1 RNA copies/mL). (B) Kaplan-Meier analysis of the proportion of participants off ART after ATI compared with the historical control group. (C) Kaplan-Meier analysis between the vedolizumab and historical control groups of the time to first viral load of more than 1,000 HIV-1 RNA copies/mL. (D and E) Kaplan-Meier analysis considering only participants without protective alleles (HLA-B*27 and HLA-B*57). In this analysis, participants 36, 16, and 17 from the historical control cohort and participant 4 from the vedolizumab group were excluded. Wilcoxon’s test, log-rank, and Kaplan-Meier curves were used to assess differences during the follow-up period. BL, baseline; W, week; ATI, analytic treatment interruption.

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