Specific Antibody Production by Blood B Cells is Retained in Late Stage Drug-naïve HIV-infected Africans

Unseparated peripheral blood mononuclear cells (PBMCs) obtained from drug-naïve African individuals living in a context of multi-infections and presenting with high viral load (VL), were cultured in vitro and tested for their ability to produce antibodies (Abs)...

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Main Authors: Lydie Béniguel, Evelyne Bégaud, Fabrice Cognasse, Philippe Gabrié, Christophe D. Mbolidi, Mary A. Marovich, Céline Cazorla, Frédéric Lucht, Christian Genin, Olivier Garraud
Format: Article
Language:English
Published: Wiley 2004-01-01
Series:Clinical and Developmental Immunology
Online Access:http://dx.doi.org/10.1080/10446670410001722104
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author Lydie Béniguel
Evelyne Bégaud
Fabrice Cognasse
Philippe Gabrié
Christophe D. Mbolidi
Mary A. Marovich
Céline Cazorla
Frédéric Lucht
Christian Genin
Olivier Garraud
author_facet Lydie Béniguel
Evelyne Bégaud
Fabrice Cognasse
Philippe Gabrié
Christophe D. Mbolidi
Mary A. Marovich
Céline Cazorla
Frédéric Lucht
Christian Genin
Olivier Garraud
author_sort Lydie Béniguel
collection DOAJ
description Unseparated peripheral blood mononuclear cells (PBMCs) obtained from drug-naïve African individuals living in a context of multi-infections and presenting with high viral load (VL), were cultured in vitro and tested for their ability to produce antibodies (Abs) reacting with HIV-1 antigens. Within these PBMCs, circulating B cells were differentiated in vitro and produced IgG Abs against not only ENV, but also GAG and POL proteins. Under similar experimental conditions, HAART treated patients produced Abs to ENV proteins only. The in vitro antibody production by drug-naïve individuals' PBMCs depended on exogenous cytokines (IL-2 and IL-10) but neither on the re-stimulation of reactive cells in cultures by purified HIV-1-gp 160 antigen nor on the re-engagement of CD40 surface molecules. Further, it was not abrogated by the addition of various monoclonal Abs (mAbs) to co-stimulatory molecules. This suggests that the in vitro antibody production by drug-naïve individuals' PBMCs resulted from the maturation of already envelope and core antigen-primed, differentiated B cells, presumably pre-plasma cells, which are not known to circulate at homeostasy. As in vitro produced Abs retained the capacity of binding antigen and forming complexes, this study provides pre-clinical support for functional humoral responses despite major HIV- and other tropical pathogen-induced B cell perturbations.
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spelling doaj-art-0e1ea0ae1a0746bd85b739f5dd210df22025-02-03T05:48:07ZengWileyClinical and Developmental Immunology1740-25221740-25302004-01-0111212112710.1080/10446670410001722104Specific Antibody Production by Blood B Cells is Retained in Late Stage Drug-naïve HIV-infected AfricansLydie Béniguel0Evelyne Bégaud1Fabrice Cognasse2Philippe Gabrié3Christophe D. Mbolidi4Mary A. Marovich5Céline Cazorla6Frédéric Lucht7Christian Genin8Olivier Garraud9GIMAP EA3064, Faculté de Médecine, Université J. Monnet, St-Etienne, France Institut Pasteur de Bangui, Bangui, Central African RepublicGIMAP EA3064, Faculté de Médecine, Université J. Monnet, St-Etienne, FranceHôpital Communautaire, Bangui, Central African RepublicHôpital Communautaire, Bangui, Central African RepublicCombined US Military HIV Research Program, Rockville, MD, USAService des Maladies Infectieuses, CHU. St-Etienne, FranceService des Maladies Infectieuses, CHU. St-Etienne, FranceGIMAP EA3064, Faculté de Médecine, Université J. Monnet, St-Etienne, FranceGIMAP EA3064, Faculté de Médecine, Université J. Monnet, St-Etienne, FranceUnseparated peripheral blood mononuclear cells (PBMCs) obtained from drug-naïve African individuals living in a context of multi-infections and presenting with high viral load (VL), were cultured in vitro and tested for their ability to produce antibodies (Abs) reacting with HIV-1 antigens. Within these PBMCs, circulating B cells were differentiated in vitro and produced IgG Abs against not only ENV, but also GAG and POL proteins. Under similar experimental conditions, HAART treated patients produced Abs to ENV proteins only. The in vitro antibody production by drug-naïve individuals' PBMCs depended on exogenous cytokines (IL-2 and IL-10) but neither on the re-stimulation of reactive cells in cultures by purified HIV-1-gp 160 antigen nor on the re-engagement of CD40 surface molecules. Further, it was not abrogated by the addition of various monoclonal Abs (mAbs) to co-stimulatory molecules. This suggests that the in vitro antibody production by drug-naïve individuals' PBMCs resulted from the maturation of already envelope and core antigen-primed, differentiated B cells, presumably pre-plasma cells, which are not known to circulate at homeostasy. As in vitro produced Abs retained the capacity of binding antigen and forming complexes, this study provides pre-clinical support for functional humoral responses despite major HIV- and other tropical pathogen-induced B cell perturbations.http://dx.doi.org/10.1080/10446670410001722104
spellingShingle Lydie Béniguel
Evelyne Bégaud
Fabrice Cognasse
Philippe Gabrié
Christophe D. Mbolidi
Mary A. Marovich
Céline Cazorla
Frédéric Lucht
Christian Genin
Olivier Garraud
Specific Antibody Production by Blood B Cells is Retained in Late Stage Drug-naïve HIV-infected Africans
Clinical and Developmental Immunology
title Specific Antibody Production by Blood B Cells is Retained in Late Stage Drug-naïve HIV-infected Africans
title_full Specific Antibody Production by Blood B Cells is Retained in Late Stage Drug-naïve HIV-infected Africans
title_fullStr Specific Antibody Production by Blood B Cells is Retained in Late Stage Drug-naïve HIV-infected Africans
title_full_unstemmed Specific Antibody Production by Blood B Cells is Retained in Late Stage Drug-naïve HIV-infected Africans
title_short Specific Antibody Production by Blood B Cells is Retained in Late Stage Drug-naïve HIV-infected Africans
title_sort specific antibody production by blood b cells is retained in late stage drug naive hiv infected africans
url http://dx.doi.org/10.1080/10446670410001722104
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