AI Article Synopsis

  • Polyfunctional CD4 and CD8 T cells play a crucial role in controlling persistent viruses and enhancing vaccine efficacy.
  • The study utilized polychromatic flow cytometry to examine how an overnight resting period at 37 °C influences the activity of specific T-cell responses against viruses like HIV-1, EBV, CMV, HBV, and HCV.
  • Results showed that while the overall number of antigen-specific T cells did not change, their functionality increased significantly after resting, suggesting this method improves the detection of active T cell responses.

Article Abstract

Polyfunctional CD4 or CD8 T cells are proposed to represent a correlate of immune control for persistent viruses as well as for vaccine mediated protection against infection. A well-suited methodology to study complex functional phenotypes of antiviral T cells is the combined staining of intracellular cytokines and phenotypic marker expression using polychromatic flow cytometry. In this study we analyzed the effect of an overnight resting period at 37 °C on the quantity and functionality of HIV-1, EBV, CMV, HBV and HCV specific CD4 and CD8 T-cell responses in a cohort of 21 individuals. We quantified total antigen specific T cells by multimer staining and used 10-color intracellular cytokine staining (ICS) to determine IFNγ, TNFα, IL2 and MIP1β production. After an overnight resting significantly higher numbers of functionally active T cells were detectable by ICS for all tested antigen specificities, whereas the total number of antigen specific T cells determined by multimer staining remained unchanged. Overnight resting shifted the quality of T-cell responses towards polyfunctionality and increased antigen sensitivity of T cells. Our data suggest that the observed effect is mediated by T cells rather than by antigen presenting cells. We conclude that overnight resting of PBMC prior to ex vivo analysis of antiviral T-cell responses represents an efficient method to increase sensitivity of ICS-based methods and has a prominent impact on the functional phenotype of T cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3795753PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0076215PLOS

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