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Enumeration and Characterization of Human Memory T Cells by Enzyme-Linked Immunospot Assays

The enzyme-linked immunospot (ELISPOT) assay has advanced into a useful and widely applicable tool for the evaluation of T-cell responses in both humans and animal models of diseases and/or vaccine candidates. Using synthetic peptides (either individually or as overlapping peptide mixtures) or whole...

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Detalles Bibliográficos
Autores principales: Calarota, Sandra A., Baldanti, Fausto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844203/
https://www.ncbi.nlm.nih.gov/pubmed/24319467
http://dx.doi.org/10.1155/2013/637649
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author Calarota, Sandra A.
Baldanti, Fausto
author_facet Calarota, Sandra A.
Baldanti, Fausto
author_sort Calarota, Sandra A.
collection PubMed
description The enzyme-linked immunospot (ELISPOT) assay has advanced into a useful and widely applicable tool for the evaluation of T-cell responses in both humans and animal models of diseases and/or vaccine candidates. Using synthetic peptides (either individually or as overlapping peptide mixtures) or whole antigens, total lymphocyte or isolated T-cell subset responses can be assessed either after short-term stimulation (standard ELISPOT) or after their expansion during a 10-day culture (cultured ELISPOT). Both assays detect different antigen-specific immune responses allowing the analysis of effector memory T cells and central memory T cells. This paper describes the principle of ELISPOT assays and discusses their application in the evaluation of immune correlates of clinical interest with a focus on the vaccine field.
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spelling pubmed-38442032013-12-08 Enumeration and Characterization of Human Memory T Cells by Enzyme-Linked Immunospot Assays Calarota, Sandra A. Baldanti, Fausto Clin Dev Immunol Review Article The enzyme-linked immunospot (ELISPOT) assay has advanced into a useful and widely applicable tool for the evaluation of T-cell responses in both humans and animal models of diseases and/or vaccine candidates. Using synthetic peptides (either individually or as overlapping peptide mixtures) or whole antigens, total lymphocyte or isolated T-cell subset responses can be assessed either after short-term stimulation (standard ELISPOT) or after their expansion during a 10-day culture (cultured ELISPOT). Both assays detect different antigen-specific immune responses allowing the analysis of effector memory T cells and central memory T cells. This paper describes the principle of ELISPOT assays and discusses their application in the evaluation of immune correlates of clinical interest with a focus on the vaccine field. Hindawi Publishing Corporation 2013 2013-11-11 /pmc/articles/PMC3844203/ /pubmed/24319467 http://dx.doi.org/10.1155/2013/637649 Text en Copyright © 2013 S. A. Calarota and F. Baldanti. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Calarota, Sandra A.
Baldanti, Fausto
Enumeration and Characterization of Human Memory T Cells by Enzyme-Linked Immunospot Assays
title Enumeration and Characterization of Human Memory T Cells by Enzyme-Linked Immunospot Assays
title_full Enumeration and Characterization of Human Memory T Cells by Enzyme-Linked Immunospot Assays
title_fullStr Enumeration and Characterization of Human Memory T Cells by Enzyme-Linked Immunospot Assays
title_full_unstemmed Enumeration and Characterization of Human Memory T Cells by Enzyme-Linked Immunospot Assays
title_short Enumeration and Characterization of Human Memory T Cells by Enzyme-Linked Immunospot Assays
title_sort enumeration and characterization of human memory t cells by enzyme-linked immunospot assays
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844203/
https://www.ncbi.nlm.nih.gov/pubmed/24319467
http://dx.doi.org/10.1155/2013/637649
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