Open AccessAnalysis of the dysregulation between regulatory B and T cells (Breg and Treg) in human immunodeficiency virus (HIV)-infected patients
Author(s) -
Carolina Gutiérrez,
Jacobo LópezAbente,
Verónica Astrid Pérez-Fernández,
Adrián Prieto-Sanchez,
Rafael CorreaRocha,
Santiago Moreno-Guillén,
María Ángeles MuñozFernández,
Marjorie Pion
Publication year - 2019
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0213744
Subject(s) - regulatory b cells , immunology , immune dysregulation , context (archaeology) , immune system , flow cytometry , homeostasis , human immunodeficiency virus (hiv) , interleukin 10 , t cell , biology , medicine , paleontology
This study examines the relationship between regulatory B (Breg) and T (Treg) compartments, which play crucial roles in the maintenance of immune homeostasis in the context of HIV. Using flow cytometry, the phenotypes of different Breg and Treg subsets from HIV-infected and healthy individuals were analyzed, along with the suppressive capacity of Breg. Peripheral blood samples of thirteen HIV + treatment-naïve individuals, fourteen treated-HIV + individuals with undetectable viral load and twelve healthy individuals were analyzed. The absolute counts of Breg and Treg subsets were decreased in HIV + treatment-naïve individuals in comparison to treated-HIV + and healthy individuals. Interestingly, correlations between Breg subsets (CD24 hi CD27 + and PD-L1 + B cells) and IL-10-producing Breg observed in healthy individuals were lost in HIV + treatment-naïve individuals. However, a correlation between frequencies of CD24 hi CD38 hi or TIM-1 + -Breg subsets and Treg was observed in HIV + treatment-naïve individuals and not in healthy individuals. Therefore, we hypothesized that various Breg subsets might have different functions during B and T-cell homeostasis during HIV-1 infection. In parallel, stimulated Breg from HIV-infected treatment-naïve individuals presented a decreased ability to suppress CD4 + T-cell proliferation in comparison to the stimulated Breg from treated-HIV + or healthy individuals. We demonstrate a dysregulation between Breg and Treg subsets in HIV-infected individuals, which might participate in the hyper-activation and exhaustion of the immune system that occurs in such patients.