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The cellular immunophenotype expression of influenza A virus and influenza B virus infection in children.

Authors :
Shen CF
Ho TS
Wang SM
Liao YT
Hu YS
Tsai HP
Chen SH
Source :
Clinical immunology (Orlando, Fla.) [Clin Immunol] 2020 Oct; Vol. 219, pp. 108548. Date of Electronic Publication: 2020 Jul 29.
Publication Year :
2020

Abstract

Background: The innate immune response is the primary defense against influenza virus infection.<br />Methods: This is a prospective study carried out in children <18 years of age who were diagnosed with influenza A or influenza B infection. Demographic and clinical data, laboratory findings and cell immunophenotypes on first presentation were compared.<br />Results: With respect to immunophenotype, influenza A infection resulted in a higher fraction of CD14 <superscript>+</superscript> and CD4 <superscript>+</superscript> IL-17A <superscript>+</superscript> cells compared to children infected with influenza B. By contrast, influenza B infection resulted in a comparatively higher percentage of double-negative CD4 <superscript>-</superscript> CD8 <superscript>-</superscript> lymphocyte subsets. Influenza A infection was associated with comparatively higher percentages of CD4 <superscript>+</superscript> CD25 <superscript>high</superscript> Foxp3 <superscript>+</superscript> and CD4 <superscript>+</superscript> CD25 <superscript>low</superscript> Foxp3 <superscript>+</superscript> cells. By contrast, the percentage of CD8 <superscript>+</superscript> CD25 <superscript>high</superscript> and CD8 <superscript>+</superscript> CD25 <superscript>low</superscript> cells was similar among patients with influenza A infection and influenza B infection.<br />Conclusions: An improved understanding of the fraction of regulatory T cells with influenza virus infections may provide further understandings on immune responses.<br />Competing Interests: Declaration of Competing Interest No potential conflict of interest was reported by the author(s).<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1521-7035
Volume :
219
Database :
MEDLINE
Journal :
Clinical immunology (Orlando, Fla.)
Publication Type :
Academic Journal
Accession number :
32735869
Full Text :
https://doi.org/10.1016/j.clim.2020.108548