The Quantification of Antigen-Specific T Cells by IFN-γ ELISpot

Methods Mol Biol. 2021:2183:525-536. doi: 10.1007/978-1-0716-0795-4_30.

Abstract

The enzyme-linked immune absorbent spot (ELISpot) assay allows for the quantification of the number of cells producing a particular secreted analyte. As T lymphocytes secrete cytokines such as interferon (IFN)-γ upon binding of the T cell receptor with its cognate antigen epitope, IFN-γ ELISpot allows for the measurement of antigen-specific T cells in an immune sample. Immune cells are isolated from the vaccinated subject and incubated with the epitope/antigen of interest on polyvinylidene difluoride (PVDF)-lined microplates precoated with a capture antibody to IFN-γ. Cytokine spots are then detected utilizing an IFN-γ-specific detection antibody and an enzyme-linked conjugate. Here, we describe the quantification of OVA-specific CD8 and CD4 T cells from mouse splenocytes to measure vaccine-induced cellular responses.

Keywords: ELISpot; Interferon-γ; Ovalbumin; T lymphocyte; Vaccines.

MeSH terms

  • Animals
  • Antigens / immunology*
  • Enzyme-Linked Immunospot Assay* / methods
  • Humans
  • Interferon-gamma*
  • Mice
  • Spleen / immunology
  • Spleen / metabolism
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism*

Substances

  • Antigens
  • Interferon-gamma