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  3. T-cell responses following Natural Influenza Infection or Vaccination in Solid Organ Transplant Recipients.
 

T-cell responses following Natural Influenza Infection or Vaccination in Solid Organ Transplant Recipients.

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BORIS DOI
10.7892/boris.144946
Date of Publication
June 22, 2020
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
L'Huillier, Arnaud G
Ferreira, Victor H
Hirzel, Cédricorcid-logo
Universitätsklinik für Infektiologie
Nellimarla, Srinivas
Ku, Terrance
Natori, Yoichiro
Humar, Atul
Kumar, Deepali
Subject(s)

600 - Technology::610...

Series
Scientific reports
ISSN or ISBN (if monograph)
2045-2322
Publisher
Springer Nature
Language
English
Publisher DOI
10.1038/s41598-020-67172-6
PubMed ID
32572168
Description
Little is known about cell-mediated immune responses to natural influenza infection in solid organ transplant (SOT) patients. The aim of our study was to evaluate the CD4+ and CD8+ responses to influenza A and B infection in a cohort of SOT patients. We collected peripheral blood mononuclear cells at influenza diagnosis and four weeks later from 31 SOT patients during the 2017-2018 influenza season. Infection-elicited influenza-specific CD4+ and CD8+ T-cell responses were measured using flow cytometry and intracellular cytokine staining and compared to responses following influenza vaccine in SOT patients. Natural infection was associated with a significant increase in CD4+ T-cell responses. For example, polyfunctional cells increased from 21 to 782 and from 193 to 1436 cells per 106 CD4+ T-cells among influenza A/H3N2 and B-infected patients (p = 0.006 and 0.004 respectively). Moreover, infection-elicited CD4+ responses were superior than vaccine-elicited responses for influenza A/H1N1 (931 vs 1; p = 0.026), A/H3N2 (647 vs 1; p = 0.041) and B (619 vs 1; p = 0.004). Natural influenza infection triggers a significant increase in CD4+ T-cell responses in SOT patients. Infection elicits significantly stronger CD4+ responses compared to the influenza vaccine and thereby likely elicits better protection against reinfection.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/36354
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41598_2020_Article_67172.pdfAdobe PDF1.39 MBpublishedOpen
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