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. Author manuscript; available in PMC: 2013 Dec 1.
Published in final edited form as: Curr Opin Immunol. 2012 Aug 10;24(6):700–706. doi: 10.1016/j.coi.2012.07.009

Table 1.

Methods of characterization of allergen-specific CD4+ T cells.

Method Advantages Limitations Time T cell assay compatibility
MHCII-peptide tetramer Sensitive, epitope-specific, cells are viabl Availability of recombinant MHCII molecule, knowledge of epitopes Ex vivo: 5 h in vitro: 5–14 days ICS, CFSE, CCA, CD154
Intracellular cytokine staining (ICS) Allows functional detection of whole antigen-specific CD4+ T cell response. Cells are non-viable, dependent on specific T-cell function 4–12 h CFSE, CD154, MHCII tetramer
Cytokine capture assay (CCA) Allows functional detection of whole antigen-specific CD4+ T cell response, cells are viable. Limited to a few cytokines, carry-over of irrelevant cells 4–12 h MHCII tetramer, CD154, CFSE
CD154 assay Allows detection of whole antigen-specific CD4+ T cell response. Dependent on specific T-cell activation 3–8 h ICS, CFSE, CCA, MHCII tetramer
Elispot Sensitive, provides both qualitative and quantitative information. Limited to a few cytokines, dependent on specific T-cell function Ex vivo: 2–3 days in vitro: 5–14 days
CFSE-dilution assay Allows detection of whole antigen-specific CD4+ T cell response Limited to dividing cells, by-stander activation 3–10 days ICS, CCA, MHCII tetramer, CD154