Please use this identifier to cite or link to this item:
|Title:||Longitudinal study of cellular and systemic cytokine signatures to define the dynamics of a balanced immune environment during disease manifestation in Zika virus–infected patients||Authors:||Lum, Fok-Moon
Lye, David Chien Boon
Tan, Jeslin J. L.
Siti N. Amrun
Mok, Esther W. H.
Ng, Lisa F. P.
Lim, Vanessa W. X.
Pang, Vincent J. X.
|Issue Date:||2018||Source:||Lum, F.-M., Lye, D. C. B., Tan, J. J. L., Lee, B., Chia, P.-Y., Chua, T.-K., . . . Ng, L. F. P. (2018). Longitudinal study of cellular and systemic cytokine signatures to define the dynamics of a balanced immune environment during disease manifestation in Zika virus–infected patients. Journal of Infectious Diseases, 218(5), 814-824. doi:10.1093/infdis/jiy225||Series/Report no.:||Journal of Infectious Diseases||Abstract:||Background: Since its unexpected reemergence, Zika virus (ZIKV) has caused numerous outbreaks globally. This study characterized the host immune responses during ZIKV infection. Methods: Patient samples were collected longitudinally during the acute, convalescence and recovery phases of ZIKV infection over 6 months during the Singapore outbreak in late 2016. Plasma immune mediators were profiled via multiplex microbead assay, while changes in blood cell numbers were determined with immunophenotyping. Results: Data showed the involvement of various immune mediators during acute ZIKV infection accompanied by a general reduction in blood cell numbers for all immune subsets except CD14+ monocytes. Importantly, viremic patients experiencing moderate symptoms had significantly higher quantities of interferon γ–induced protein 10, monocyte chemotactic protein 1, interleukin 1 receptor antagonist, interleukin 8, and placental growth factor 1, accompanied by reduced numbers of peripheral CD8+ T cells, CD4+ T cells, and double-negative T cells. Levels of T-cell associated mediators, including interferon γ–induced protein 10, interferon γ, and interleukin 10, were high in recovery phases of ZIKV infection, suggesting a functional role for T cells. The identification of different markers at specific disease phases emphasizes the dynamics of a balanced cytokine environment in disease progression. Conclusions: This is the first comprehensive study that highlights specific cellular changes and immune signatures during ZIKV disease progression, and it provides valuable insights into ZIKV immunopathogenesis.||URI:||https://hdl.handle.net/10356/87188
|ISSN:||0022-1899||DOI:||10.1093/infdis/jiy225||Rights:||© 2018 The Author(s). Published by Oxford University Press for the Infectious Diseases Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.||Fulltext Permission:||open||Fulltext Availability:||With Fulltext|
|Appears in Collections:||LKCMedicine Journal Articles|
Updated on Sep 6, 2020
Updated on Mar 4, 2021
Updated on May 21, 2022
Updated on May 21, 2022
Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.