Plasmablasts During Acute Dengue Infection Represent a Small Subset of a Broader Virus-specific Memory B Cell Pool
Author(s) -
Ramapraba Appanna,
Srinivasan KG,
Mei Xu,
Ying-Xiu Toh,
Sumathy Velumani,
Daniel Carbajo,
Chia Yin Lee,
Roland Zuest,
Thavamalar Balakrishnan,
Weili Xu,
Bernett Lee,
Michael Poidinger,
Francesca Zolezzi,
YeeSin Leo,
Tun-Linn Thein,
ChengI Wang,
Katja Fink
Publication year - 2016
Publication title -
ebiomedicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.596
H-Index - 63
ISSN - 2352-3964
DOI - 10.1016/j.ebiom.2016.09.003
Subject(s) - dengue virus , dengue fever , immunology , serotype , virology , convalescence , virus , antibody , memory b cell , antibody dependent enhancement , biology , immunity , medicine , b cell , immune system , pathology
Dengue is endemic in tropical countries worldwide and the four dengue virus serotypes often co-circulate. Infection with one serotype results in high titers of cross-reactive antibodies produced by plasmablasts, protecting temporarily against all serotypes, but impairing protective immunity in subsequent infections. To understand the development of these plasmablasts, we analyzed virus-specific B cell properties in patients during acute disease and at convalescence. Plasmablasts were unrelated to classical memory cells expanding in the blood during early recovery. We propose that only a small subset of memory B cells is activated as plasmablasts during repeat infection and that plasmablast responses are not representative of the memory B cell repertoire after dengue infection.
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