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Vedolizumab and ART in recent HIV-1 infection unveil the role of α4β7 in reservoir size
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
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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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 6

Immune checkpoint molecules are associated with α4β7 and HIV-1 reservoir levels.

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Immune checkpoint molecules are associated with α4β7 and HIV-1 reservoir...
(A) Dynamic of PD1 and TIGIT expression on CD4+ T cells during the follow-up period in PBMCs. (B) Correlation between total HIV-1 DNA levels assayed by FLIP-Seq and the expression of PD1 and TIGIT on peripheral CD4+ T cells before ATI. (C) Correlation between the expression of α4β7 integrin and immune checkpoint molecules (PD1 and TIGIT) on peripheral CD4+T cells before ATI. (D) Correlation between the expression of α4β7 integrin and total HIV-1 DNA in PBMCs assayed by FLIP-Seq and the simultaneous expression of α4β7, LAG3, PD1, and TIM3 on peripheral CD4+ T cells just before ATI. (E) Plasma soluble biomarkers levels, hsCRP, D-dimer, and B2M during the follow-up period. (F) Correlation matrix representing negative (blue shading) and positive (red shading) association between soluble biomarkers and HIV-1 DNA in PBMCs and the expression of α4β7 and immune checkpoint molecules on CD4+ T cells. (G) Dynamic of PD1 expression on CD4+ T cells in ileum and cecum at BL and before ATI (week 24). (H) Dynamic of CD4+ Tfh cells in ileum and cecum at BL and before ATI (week 24). (I) Association between Tfh cells and CD4+α4β7+ T cells and HIV-1 DNA at ileum before ATI (week 24). P values were computed using Friedman’s test with Dunn’s multiple comparisons test correction, Wilcoxon’s, and Spearman’s test. P values are shown within the graphs. BL, baseline; W, week; ATI, analytic treatment interruption; Tfh, T follicular helper cells.

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