EBioMedicine (Oct 2016)

Plasmablasts During Acute Dengue Infection Represent a Small Subset of a Broader Virus-specific Memory B Cell Pool

  • Ramapraba Appanna,
  • Srinivasan KG,
  • Mei Hui Xu,
  • Ying-Xiu Toh,
  • Sumathy Velumani,
  • Daniel Carbajo,
  • Chia Yin Lee,
  • Roland Zuest,
  • Thavamalar Balakrishnan,
  • Weili Xu,
  • Bernett Lee,
  • Michael Poidinger,
  • Francesca Zolezzi,
  • Yee Sin Leo,
  • Tun Linn Thein,
  • Cheng-I Wang,
  • Katja Fink

DOI
https://doi.org/10.1016/j.ebiom.2016.09.003
Journal volume & issue
Vol. 12, no. C
pp. 178 – 188

Abstract

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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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