Measuring the effect of drug treatments on primary human CD8+ T cell activation and cytolytic potential

CD8+ T cells are key effector cells in adaptive immune responses against intracellular pathogens and cancer cells. Systemic drug treatments, like chemotherapy, may positively or negatively affect CD8+ T cell function. In this protocol, we describe robust and optimized ex vivo polyclonal activation a...

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Veröffentlicht in:STAR protocols 2021-06, Vol.2 (2), p.100549-100549, Article 100549
Hauptverfasser: Loo Yau, Helen, De Carvalho, Daniel D.
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Sprache:eng
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Zusammenfassung:CD8+ T cells are key effector cells in adaptive immune responses against intracellular pathogens and cancer cells. Systemic drug treatments, like chemotherapy, may positively or negatively affect CD8+ T cell function. In this protocol, we describe robust and optimized ex vivo polyclonal activation and cell culture conditions to measure drug treatments' effects on primary human CD8+ T cell activation and cytolytic potential. We provide streamlined methods for measuring effector cytokines and activation markers of CD8+ T cells via flow cytometry. For complete details on the use and execution of this protocol, please refer to Loo Yau et al. (2021). [Display omitted] •Protocol to measure effects of drug treatments on primary human CD8+ T cell•Method to measure effector and activation molecules of CD8+ T cells via flow cytometry•Detailed steps and resources to measure changes in CD8+ T cell cytolytic potential CD8+ T cells are key effector cells in adaptive immune responses against intracellular pathogens and cancer cells. Systemic drug treatments, like chemotherapy, may positively or negatively affect CD8+ T cell function. In this protocol, we describe robust and optimized ex vivo polyclonal activation and cell culture conditions to measure drug treatments' effects on primary human CD8+ T cell activation and cytolytic potential. We provide streamlined methods for measuring effector cytokines and activation markers of CD8+ T cells via flow cytometry.
ISSN:2666-1667
2666-1667
DOI:10.1016/j.xpro.2021.100549