Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/44727
Title: Identification of changes in dendritic cell subsets that correlate with disease severity in dengue infection
Authors: Sakaorat Lertjuthaporn
Ladawan Khowawisetsut
Rassamon Keawvichit
Korakot Polsrila
Ampaiwan Chuansumrit
Kulkanya Chokephaibulkit
Premrutai Thitilertdecha
Nattawat Onlamoon
Aftab A. Ansari
Kovit Pattanapanyasat
Faculty of Medicine, Ramathibodi Hospital, Mahidol University
Faculty of Medicine, Siriraj Hospital, Mahidol University
Emory University School of Medicine
Keywords: Agricultural and Biological Sciences;Biochemistry, Genetics and Molecular Biology
Issue Date: 1-Jul-2018
Citation: PLoS ONE. Vol.13, No.7 (2018)
Abstract: © 2018 Lertjuthaporn et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Dengue virus (DENV) is the most prevalent arthropod-borne viral disease in humans. DENV causes a spectrum of illness ranging from mild to potentially severe complications. Dendritic cells (DCs) play a critical role in initiating and regulating highly effective antiviral immune response that include linking innate and adaptive immune responses. This study was conducted to comparatively characterize in detail the relative proportion, phenotypic changes, and maturation profile of subsets of both myeloid DCs (mDCs) and plasmacytoid DCs (pDCs) in children with dengue fever (DF), dengue hemorrhagic fever (DHF) and for purposes of control healthy individuals. The mDCs (Lin - CD11c + CD123 lo ), the pDCs (Lin - CD11c - CD123 + ) and the double negative (DN) subset (Lin - /HLA - DR + /CD11c - CD123 - ) were analyzed by polychromatic flow cytometry. The data were first analyzed on blood samples collected from DENV-infected patients at various times post-infection. Results showed that the relative proportion of mDCs were significantly decreased which was associated with an increase in disease severity in samples from DENV-infected patients. While there was no significant difference in the relative proportion of pDCs between healthy and DENV-infected patients, there was a marked increase in the DN subset. Analysis of the kinetics of changes of pDCs showed that there was an increase but only during the early febrile phase. Additionally, samples from patients during acute disease showed marked decreases in the relative proportion of CD141 + and CD16 + mDC subsets that were the major mDC subsets in healthy individuals. In addition, there was a significant decrease in the level of CD33-expressing mDCs in DENV patients. While the pDCs showed an up-regulation of maturation profile during acute DENV infection, the mDCs showed an alteration of maturation status. This study suggests that different relative proportion and phenotypic changes as well as alteration of maturation profile of DC subsets may play a critical role in the dengue pathogenesis and disease outcome.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85050854709&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/44727
ISSN: 19326203
Appears in Collections:Scopus 2018

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