2008
DOI: 10.1002/cyto.a.20655
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Measuring Antigen‐Specific Immune Responses, 2008 update

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Cited by 11 publications
(9 citation statements)
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“…To determine the cytotoxicity of CD8 + T cells the human fluorescent antigen-transfected target cell (FATT)-CTL assay was adapted for use in sheep to identify the epitopes that induce CTL for inclusion in a multiepitope vaccine. The FATT-CTL assay combines non-radioactive quantification of target cell killing with an efficient plasmid transfection technology to achieve antigen expression in target cells [18]. It measures antigen-specific cell mediated cytotoxicity and is a convenient alternative to the classic radioactive Cr 51 -release assay.…”
Section: Introductionmentioning
confidence: 99%
“…To determine the cytotoxicity of CD8 + T cells the human fluorescent antigen-transfected target cell (FATT)-CTL assay was adapted for use in sheep to identify the epitopes that induce CTL for inclusion in a multiepitope vaccine. The FATT-CTL assay combines non-radioactive quantification of target cell killing with an efficient plasmid transfection technology to achieve antigen expression in target cells [18]. It measures antigen-specific cell mediated cytotoxicity and is a convenient alternative to the classic radioactive Cr 51 -release assay.…”
Section: Introductionmentioning
confidence: 99%
“…It is also needed in the course of immunotherapy studies, with the aim to establish immunological correlates of clinical efficacy. Various functional assays conducted following allergen stimulation are available to analyse specific CD4 + T cells, such as proliferation assessment, intracellular cytokine staining, cytokine secretion assay (CSA) and ELISPOT [4, 5]. However, immunodetection using major histocompatibility complex (MHC) class II/peptide tetramers (tetramers) is currently considered as the most specific approach in order to identify allergen‐reactive CD4 + T cells [6–8].…”
Section: Introductionmentioning
confidence: 99%
“…T cell response to a specific antigen is analyzed by several immune assays including direct multimer staining, ELISPOT, intracellular cytokine staining, and proliferation assays, based on detection following stimulation of the T cells in vitro with antigen [ 59 , 60 ]. However, many of these methods suffer from low sensitivity, and they show a significant variability in the quantitative readouts [ 61 , 62 , 63 ].…”
Section: Systems Vaccinology For Cancer Vaccines Applicationmentioning
confidence: 99%