Publication: Dengue virus infection induces expansion of a CD14<sup>+</sup>CD16<sup>+</sup>monocyte population that stimulates plasmablast differentiation
Issued Date
2014-07-09
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ISSN
19346069
19313128
19313128
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2-s2.0-84904161011
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Mahidol University
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SCOPUS
Bibliographic Citation
Cell Host and Microbe. Vol.16, No.1 (2014), 115-127
Suggested Citation
Marcin Kwissa, Helder I. Nakaya, Nattawat Onlamoon, Jens Wrammert, Francois Villinger, Guey Chuen Perng, Sutee Yoksan, Kovit Pattanapanyasat, Kulkanya Chokephaibulkit, Rafi Ahmed, Bali Pulendran Dengue virus infection induces expansion of a CD14<sup>+</sup>CD16<sup>+</sup>monocyte population that stimulates plasmablast differentiation. Cell Host and Microbe. Vol.16, No.1 (2014), 115-127. doi:10.1016/j.chom.2014.06.001 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/33960
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Title
Dengue virus infection induces expansion of a CD14<sup>+</sup>CD16<sup>+</sup>monocyte population that stimulates plasmablast differentiation
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Abstract
Dengue virus (DENV) infection induces the expansion of plasmablasts, which produce antibodies that can neutralize DENV but also enhance disease upon secondary infection with another DENV serotype. To understand how these immune responses are generated, we used a systems biological approach to analyze immune responses to dengue in humans. Transcriptomic analysis of whole blood revealed that genes encoding proinflammatory mediators and type I interferon-related proteins were associated with high DENV levels during initial symptomatic disease. Additionally, CD14+CD16+monocytes increased in the blood. Similarly, in a nonhuman primate model, DENV infection boosted CD14+CD16+monocyte numbers in the blood and lymph nodes. Upon DENV infection in vitro, monocytes upregulated CD16 and mediated differentiation of resting B cells to plasmablasts as well as immunoglobulin G (IgG) and IgM secretion. These findings provide a detailed picture of innate responses to dengue and highlight a role for CD14+CD16+monocytes in promoting plasmablast differentiation and anti-DENV antibody responses. © 2014 Elsevier Inc.