The ELISPOT Assay: An Easily Transferable Method for Measuring Cellular Responses and Identifying T Cell Epitopes
Identifieur interne : 003374 ( Main/Exploration ); précédent : 003373; suivant : 003375The ELISPOT Assay: An Easily Transferable Method for Measuring Cellular Responses and Identifying T Cell Epitopes
Auteurs : Tumelo Mashishi ; Clive M. GraySource :
- Clinical Chemistry and Laboratory Medicine [ 1434-6621 ] ; 2002.
English descriptors
- Teeft :
- Amino, Amino acids, Assay, Cell immunity, Cell receptor, Cell responses, Clinical trials, Common peptide, Cytokine, Cytokine secretion, Cytotoxic, Different laboratories, Effector, Elispot, Elispot assay, Epitope, Human immunodeficiency virus type, Human leukocyte antigen, Immunodeficiency, Immunol, Immunol lett, Immunol methods, Lymphoblastoid cell lines, Lymphocyte, Mashishi, Matrix, Pbmc, Peptide, Peptide synthesis, Peripheral blood, Recombinant vaccinia virus, Representative example, Vaccine, Vaccinia, Viral.
Abstract
Characterization of human leukocyte antigen (HLA) class I restricted epitopes derived from viral pathogens is imperative for formulating therapeutic interventions, as well as for vaccine design and monitoring. Sensitive, easy and cost-effective assays that measure the frequency of antigen-specific T lymphocytes are crucial for evaluating and improving vaccines and therapies. This paper reviews the ELISPOT technique that allows for quantifying HIV-specific T lymphocytes at the single cell level from peripheral blood by detection of antigen-induced cytokine secretion. The assay can be used successfully to quantify T cell immune responses in humans infected with different pathogens and to assess T cell immunogenicity of vaccines in phase I/II and III clinical trials. This review focuses on the ELISPOT methodology and discusses how it can be standardized and potentially used by multiple international laboratories attached to clinical trial sites.
Url:
DOI: 10.1515/CCLM.2002.159
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Characterization of human leukocyte antigen (HLA) class I restricted epitopes derived from viral pathogens is imperative for formulating therapeutic interventions, as well as for vaccine design and monitoring. Sensitive, easy and cost-effective assays that measure the frequency of antigen-specific T lymphocytes are crucial for evaluating and improving vaccines and therapies. This paper reviews the ELISPOT technique that allows for quantifying HIV-specific T lymphocytes at the single cell level from peripheral blood by detection of antigen-induced cytokine secretion. The assay can be used successfully to quantify T cell immune responses in humans infected with different pathogens and to assess T cell immunogenicity of vaccines in phase I/II and III clinical trials. This review focuses on the ELISPOT methodology and discusses how it can be standardized and potentially used by multiple international laboratories attached to clinical trial sites.</div>
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