AI Article Synopsis

  • The study investigates immune responses to influenza in solid organ transplant patients, focusing on CD4 and CD8 T-cells.
  • Significant increases in CD4 T-cell responses were observed after natural influenza infections, with polyfunctional cells increasing dramatically.
  • Natural infection leads to stronger immune responses compared to responses from the influenza vaccine, suggesting better protection against future infections for SOT patients.

Article Abstract

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 10 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308384PMC
http://dx.doi.org/10.1038/s41598-020-67172-6DOI Listing

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