Dengue Virus Directly Stimulates Polyclonal B Cell Activation.

Dengue infection is associated to vigorous inflammatory response, to a high frequency of activated B cells, and to increased levels of circulating cross-reactive antibodies. We investigated whether direct infection of B cells would promote activation by culturing primary human B lymphocytes from hea...

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Main Authors: Arturo Ramon Vargas Correa, Ana Carolina Egypto Rosa Berbel, Michelle Premazzi Papa, Ana Theresa Silveira de Morais, Ligia Maria Torres Peçanha, Luciana Barros de Arruda
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4675537?pdf=render
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spelling doaj-c8f36b11200644f7a50a7d7c159ae53f2020-11-25T01:22:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-011012e014339110.1371/journal.pone.0143391Dengue Virus Directly Stimulates Polyclonal B Cell Activation.Arturo Ramon Vargas CorreaAna Carolina Egypto Rosa BerbelMichelle Premazzi PapaAna Theresa Silveira de MoraisLigia Maria Torres PeçanhaLuciana Barros de ArrudaDengue infection is associated to vigorous inflammatory response, to a high frequency of activated B cells, and to increased levels of circulating cross-reactive antibodies. We investigated whether direct infection of B cells would promote activation by culturing primary human B lymphocytes from healthy donors with DENV in vitro. B cells were susceptible, but poorly permissive to infection. Even though, primary B cells cultured with DENV induced substantial IgM secretion, which is a hallmark of polyclonal B cell activation. Notably, DENV induced the activation of B cells obtained from either DENV immune or DENV naïve donors, suggesting that it was not dependent on DENV-specific secondary/memory response. B cell stimulation was dependent on activation of MAPK and CD81. B cells cultured with DENV also secreted IL-6 and presented increased expression of CD86 and HLA-DR, which might contribute to B lymphocyte co-stimulatory function. Indeed, PBMCs, but not isolated B cells, secreted high amounts of IgG upon DENV culture, suggesting that interaction with other cell types in vivo might promote Ig isotype switching and IgG secretion from different B cell clones. These findings suggest that activation signaling pathways triggered by DENV interaction with non-specific receptors on B cells might contribute to the exacerbated response observed in dengue patients.http://europepmc.org/articles/PMC4675537?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Arturo Ramon Vargas Correa
Ana Carolina Egypto Rosa Berbel
Michelle Premazzi Papa
Ana Theresa Silveira de Morais
Ligia Maria Torres Peçanha
Luciana Barros de Arruda
spellingShingle Arturo Ramon Vargas Correa
Ana Carolina Egypto Rosa Berbel
Michelle Premazzi Papa
Ana Theresa Silveira de Morais
Ligia Maria Torres Peçanha
Luciana Barros de Arruda
Dengue Virus Directly Stimulates Polyclonal B Cell Activation.
PLoS ONE
author_facet Arturo Ramon Vargas Correa
Ana Carolina Egypto Rosa Berbel
Michelle Premazzi Papa
Ana Theresa Silveira de Morais
Ligia Maria Torres Peçanha
Luciana Barros de Arruda
author_sort Arturo Ramon Vargas Correa
title Dengue Virus Directly Stimulates Polyclonal B Cell Activation.
title_short Dengue Virus Directly Stimulates Polyclonal B Cell Activation.
title_full Dengue Virus Directly Stimulates Polyclonal B Cell Activation.
title_fullStr Dengue Virus Directly Stimulates Polyclonal B Cell Activation.
title_full_unstemmed Dengue Virus Directly Stimulates Polyclonal B Cell Activation.
title_sort dengue virus directly stimulates polyclonal b cell activation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Dengue infection is associated to vigorous inflammatory response, to a high frequency of activated B cells, and to increased levels of circulating cross-reactive antibodies. We investigated whether direct infection of B cells would promote activation by culturing primary human B lymphocytes from healthy donors with DENV in vitro. B cells were susceptible, but poorly permissive to infection. Even though, primary B cells cultured with DENV induced substantial IgM secretion, which is a hallmark of polyclonal B cell activation. Notably, DENV induced the activation of B cells obtained from either DENV immune or DENV naïve donors, suggesting that it was not dependent on DENV-specific secondary/memory response. B cell stimulation was dependent on activation of MAPK and CD81. B cells cultured with DENV also secreted IL-6 and presented increased expression of CD86 and HLA-DR, which might contribute to B lymphocyte co-stimulatory function. Indeed, PBMCs, but not isolated B cells, secreted high amounts of IgG upon DENV culture, suggesting that interaction with other cell types in vivo might promote Ig isotype switching and IgG secretion from different B cell clones. These findings suggest that activation signaling pathways triggered by DENV interaction with non-specific receptors on B cells might contribute to the exacerbated response observed in dengue patients.
url http://europepmc.org/articles/PMC4675537?pdf=render
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