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Rapid detection, enrichment and propagation of specific T cell subsets based on cytokine secretion
Author(s) -
Campbell J. D. M.,
Foerster A.,
Lasmanowicz V.,
Niemöller M.,
Scheffold A.,
Fahrendorff M.,
Rauser G.,
Assenmacher M.,
Richter A.
Publication year - 2011
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/j.1365-2249.2010.04261.x
Subject(s) - secretion , immunology , cytokine , biology , medicine , endocrinology
Summary T cell lines with defined cytokine profiles are an invaluable tool for assessing the control of immune responses both in vitro and in vivo . Production of such cell lines can be complex and time‐consuming. Here we present a powerful technique to assay the cytokines produced by T cells activated polyclonally or with specific antigens. This paper presents a detailed methodology for the identification and isolation of cytokine‐producing T cells activated with the artificial superantigen, CytoStim, or viral and fungal antigens. These cells can be analysed for different cytokines simultaneously, or cultured further to rapidly establish T cell lines making known cytokine types. We highlight the enumeration, isolation and phenotype of interleukin‐17‐producing T cells, and the rapid generation of virus‐specific Th1 T cell lines.

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