T-cell activation-induced marker assays in health and disease
- PMID:36825901
- PMCID: PMC10952637
- DOI: 10.1111/imcb.12636
T-cell activation-induced marker assays in health and disease
Abstract
Activation-induced marker (AIM) assays have proven to be an accessible and rapid means of antigen-specific T-cell detection. The method typically involves short-term incubation of whole blood or peripheral blood mononuclear cells with antigens of interest, where autologous antigen-presenting cells process and present peptides in complex with major histocompatibility complex (MHC) molecules. Recognition of peptide-MHC complexes by T-cell receptors then induces upregulation of activation markers on the T cells that can be detected by flow cytometry. In this review, we highlight the most widely used activation markers for assays in the literature while identifying nuances and potential downfalls associated with the technique. We provide a summary of how AIM assays have been used in both discovery science and clinical studies, including studies of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) immunity. This review primarily focuses on AIM assays using human blood or peripheral blood mononuclear cell samples, with some considerations noted for tissue-derived T cells and nonhuman samples. AIM assays are a powerful tool that enables detailed analysis of antigen-specific T-cell frequency, phenotype and function without needing to know the precise antigenic peptides and their MHC restriction elements, enabling a wider analysis of immunity generated following infection and/or vaccination.
Keywords: AIM; CD4+ T cells; antigen-specific response; flow cytometry.
© 2023 The Authors. Immunology & Cell Biology published by John Wiley & Sons Australia, Ltd on behalf of the Australian and New Zealand Society for Immunology, Inc.
Conflict of interest statement
MKL received research funding from Bristol‐Myers Squibb and Takeda for work unrelated to this review. TSS received research funding from Merck, Sanofi Pasteur, Rebiotix, Seres, NuBiyota, Edesa, Summit and Pfizer for work unrelated to this review. The other authors have no commercial or financial interests to report.
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