Kinetic Changes of Peripheral Blood Monocyte Subsets and Expression of Co-Stimulatory Molecules during Acute Dengue Virus Infection

Monocytes, one of the main target cells for dengue virus (DENV) infection, contribute to the resolution of viremia and to pathogenesis. We performed a longitudinal study by a detailed phenotypic comparison of classical (CD14++CD16−, non-classical (CD14+CD16++) and intermediate (CD14++CD16+) monocyte...

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Autores principales: Sakaorat Lertjuthaporn, Rassamon Keawvichit, Korakot Polsrila, Kasama Sukapirom, Ampaiwan Chuansumrit, Kulkanya Chokephaibulkit, Aftab A. Ansari, Ladawan Khowawisetsut, Kovit Pattanapanyasat
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:497cad51658c43059e01617982a888202021-11-25T18:38:24ZKinetic Changes of Peripheral Blood Monocyte Subsets and Expression of Co-Stimulatory Molecules during Acute Dengue Virus Infection10.3390/pathogens101114582076-0817https://doaj.org/article/497cad51658c43059e01617982a888202021-11-01T00:00:00Zhttps://www.mdpi.com/2076-0817/10/11/1458https://doaj.org/toc/2076-0817Monocytes, one of the main target cells for dengue virus (DENV) infection, contribute to the resolution of viremia and to pathogenesis. We performed a longitudinal study by a detailed phenotypic comparison of classical (CD14++CD16−, non-classical (CD14+CD16++) and intermediate (CD14++CD16+) monocyte subsets in blood samples from dengue fever (DF) to the severe dengue hemorrhagic fever (DHF) and healthy individuals. Various costimulatory molecules of CD40, CD80, CD86 and inducible costimulatory ligand (ICOSL) expressed on these three monocyte subsets were also analyzed. DENV-infected patients showed an increase in the frequency of intermediate monocytes and a decrease in the classical monocytes when compared to healthy individuals. Although these differences did not correlate with disease severity, changes during the early phase of infection gradually returned to normal in the defervescence phase. Moreover, decreased frequency of classical monocytes was associated with a significant up-regulation of co-stimulatory molecules CD40, CD86 and ICOSL. Kinetics of these co-stimulatory molecule-expressing classical monocytes showed different patterns throughout the sampling times of acute DENV infection. Different distribution of monocyte subsets and their co-stimulatory molecules in the peripheral blood during acute infection might exacerbate immune responses like cytokine storms and ADE, and future studies on intracellular molecular pathways utilized by these monocyte linages are warranted.Sakaorat LertjuthapornRassamon KeawvichitKorakot PolsrilaKasama SukapiromAmpaiwan ChuansumritKulkanya ChokephaibulkitAftab A. AnsariLadawan KhowawisetsutKovit PattanapanyasatMDPI AGarticledengue infectionmonocyteflow cytometryco-stimulationMedicineRENPathogens, Vol 10, Iss 1458, p 1458 (2021)
institution DOAJ
collection DOAJ
language EN
topic dengue infection
monocyte
flow cytometry
co-stimulation
Medicine
R
spellingShingle dengue infection
monocyte
flow cytometry
co-stimulation
Medicine
R
Sakaorat Lertjuthaporn
Rassamon Keawvichit
Korakot Polsrila
Kasama Sukapirom
Ampaiwan Chuansumrit
Kulkanya Chokephaibulkit
Aftab A. Ansari
Ladawan Khowawisetsut
Kovit Pattanapanyasat
Kinetic Changes of Peripheral Blood Monocyte Subsets and Expression of Co-Stimulatory Molecules during Acute Dengue Virus Infection
description Monocytes, one of the main target cells for dengue virus (DENV) infection, contribute to the resolution of viremia and to pathogenesis. We performed a longitudinal study by a detailed phenotypic comparison of classical (CD14++CD16−, non-classical (CD14+CD16++) and intermediate (CD14++CD16+) monocyte subsets in blood samples from dengue fever (DF) to the severe dengue hemorrhagic fever (DHF) and healthy individuals. Various costimulatory molecules of CD40, CD80, CD86 and inducible costimulatory ligand (ICOSL) expressed on these three monocyte subsets were also analyzed. DENV-infected patients showed an increase in the frequency of intermediate monocytes and a decrease in the classical monocytes when compared to healthy individuals. Although these differences did not correlate with disease severity, changes during the early phase of infection gradually returned to normal in the defervescence phase. Moreover, decreased frequency of classical monocytes was associated with a significant up-regulation of co-stimulatory molecules CD40, CD86 and ICOSL. Kinetics of these co-stimulatory molecule-expressing classical monocytes showed different patterns throughout the sampling times of acute DENV infection. Different distribution of monocyte subsets and their co-stimulatory molecules in the peripheral blood during acute infection might exacerbate immune responses like cytokine storms and ADE, and future studies on intracellular molecular pathways utilized by these monocyte linages are warranted.
format article
author Sakaorat Lertjuthaporn
Rassamon Keawvichit
Korakot Polsrila
Kasama Sukapirom
Ampaiwan Chuansumrit
Kulkanya Chokephaibulkit
Aftab A. Ansari
Ladawan Khowawisetsut
Kovit Pattanapanyasat
author_facet Sakaorat Lertjuthaporn
Rassamon Keawvichit
Korakot Polsrila
Kasama Sukapirom
Ampaiwan Chuansumrit
Kulkanya Chokephaibulkit
Aftab A. Ansari
Ladawan Khowawisetsut
Kovit Pattanapanyasat
author_sort Sakaorat Lertjuthaporn
title Kinetic Changes of Peripheral Blood Monocyte Subsets and Expression of Co-Stimulatory Molecules during Acute Dengue Virus Infection
title_short Kinetic Changes of Peripheral Blood Monocyte Subsets and Expression of Co-Stimulatory Molecules during Acute Dengue Virus Infection
title_full Kinetic Changes of Peripheral Blood Monocyte Subsets and Expression of Co-Stimulatory Molecules during Acute Dengue Virus Infection
title_fullStr Kinetic Changes of Peripheral Blood Monocyte Subsets and Expression of Co-Stimulatory Molecules during Acute Dengue Virus Infection
title_full_unstemmed Kinetic Changes of Peripheral Blood Monocyte Subsets and Expression of Co-Stimulatory Molecules during Acute Dengue Virus Infection
title_sort kinetic changes of peripheral blood monocyte subsets and expression of co-stimulatory molecules during acute dengue virus infection
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/497cad51658c43059e01617982a88820
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