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Neutrophil Expression of T and B Immunomodulatory Molecules in HIV Infection

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URI: http://hdl.handle.net/10498/26419

DOI: 10.3389/fimmu.2021.670966

ISSN: 1664-3224

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2022_024.pdf (1.205Mb)
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Author/s
Márquez Coello, María de las MercedesAuthority UCA; Ruiz Sánchez, Cristina; Martín Aspas, AndrésAuthority UCA; Fernández-Gutiérrez del Álamo, Clotilde; Illanes Álvarez, Francisco; Cuesta Sancho, Sara; Girón González, José AntonioAuthority UCA
Date
2021-12
Department
Biomedicina, Biotecnología y Salud Pública; Medicina
Source
Front. Immunol. 12:670966
Abstract
ObjectiveEvaluate the expression of B and T cell immunomodulatory molecules in polymorphonuclear neutrophils (PMN) in HIV-infected patients. MethodsHIV load, bacterial translocation and neutrophils' expression of T [programmed death ligand, interleukin-10+, arginase 1+] and B [BAFF, APRIL] molecules were analyzed in different cohorts and time points: a control group of 25 healthy individuals and two groups of HIV-infected patients. Group 1 of patients included 35 untreated patients, studied at baseline and after antiretroviral therapy (ART). Group 2 was composed of 25 patients with undetectable viral load after a median of 101 months of ART prior to inclusion in the study. ResultsCompared with the control group, group 1 patients showed increased bacterial translocation and their PMN had a significantly higher expression of T and B-cell immunomodulatory molecules, both at baseline and after 12 months of ART. Group 2 patients showed reduced bacterial translocation levels when compared with group 1 patients after 12 months of treatment. PMN expression of B-cell modulators was similar between group 2 patients and healthy controls, although the expression of T-cell modulators remained increased. ConclusionIn HIV-infected patients, the expression of B-cell stimulatory and T-cell suppressive molecules by neutrophils was increased at baseline and after a limited time of therapy. After a prolonged period of ART, only PMNs expression of T-cell immunosuppressive molecules remained elevated.
Subjects
HIV; neutrophils; BAFF; APRIL; bacterial translocation; interleukins; arginase-1; PDL-1
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