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Sensitive detection of human papillomavirus type 16 E7-specific T cells by ELISPOT after multiple in vitro stimulations of CD8(+ )T cells with peptide-pulsed autologous dendritic cells

BACKGROUND: Cervical cancer is the second most common gynecological cancer amongst women world-wide. Despite optimized protocols, standard treatments still face several disadvantages. Therefore, research aims at the development of immune-based strategies using tumor antigen-loaded dendritic cells fo...

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Autores principales: Cools, Nathalie, Ponsaerts, Peter, Lenjou, Marc, Nijs, Griet, Van Bockstaele, Dirk R, Van Tendeloo, Viggo FI, Berneman, Zwi N
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1634756/
https://www.ncbi.nlm.nih.gov/pubmed/17067378
http://dx.doi.org/10.1186/1476-4598-5-49
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author Cools, Nathalie
Ponsaerts, Peter
Lenjou, Marc
Nijs, Griet
Van Bockstaele, Dirk R
Van Tendeloo, Viggo FI
Berneman, Zwi N
author_facet Cools, Nathalie
Ponsaerts, Peter
Lenjou, Marc
Nijs, Griet
Van Bockstaele, Dirk R
Van Tendeloo, Viggo FI
Berneman, Zwi N
author_sort Cools, Nathalie
collection PubMed
description BACKGROUND: Cervical cancer is the second most common gynecological cancer amongst women world-wide. Despite optimized protocols, standard treatments still face several disadvantages. Therefore, research aims at the development of immune-based strategies using tumor antigen-loaded dendritic cells for the induction of cellular anti-tumor immunity. RESULTS: In this study, we used dendritic cells loaded with the HLA-A2-restricted HPV type 16 E7(11–20 )peptide in order to induce an in vitro CD8(+ )T cell response. For this purpose, peptide-pulsed dendritic cells were co-cultured with autologous CD8(+ )T cells. After 5 weekly stimulations with peptide-pulsed mature dendritic cells, cultured T cells were analyzed for antigen specificity by an IFN-γ ELISPOT assay. Using this ELISPOT assay, we were able to detect E7-specific IFN-γ-secreting CD8(+ )T cells in 5/5 healthy donors. CONCLUSION: We show that peptide-pulsed mature dendritic cells are able to stimulate a HPV type 16 E7 peptide-specific immune response in vitro. These experiments describe an efficient culture protocol for antigen-specific T cells for use in pre-clinical vaccination research and confirm the need for sensitive T cell assays for detection of tumor-specific immune responses in vitro.
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spelling pubmed-16347562006-11-04 Sensitive detection of human papillomavirus type 16 E7-specific T cells by ELISPOT after multiple in vitro stimulations of CD8(+ )T cells with peptide-pulsed autologous dendritic cells Cools, Nathalie Ponsaerts, Peter Lenjou, Marc Nijs, Griet Van Bockstaele, Dirk R Van Tendeloo, Viggo FI Berneman, Zwi N Mol Cancer Research BACKGROUND: Cervical cancer is the second most common gynecological cancer amongst women world-wide. Despite optimized protocols, standard treatments still face several disadvantages. Therefore, research aims at the development of immune-based strategies using tumor antigen-loaded dendritic cells for the induction of cellular anti-tumor immunity. RESULTS: In this study, we used dendritic cells loaded with the HLA-A2-restricted HPV type 16 E7(11–20 )peptide in order to induce an in vitro CD8(+ )T cell response. For this purpose, peptide-pulsed dendritic cells were co-cultured with autologous CD8(+ )T cells. After 5 weekly stimulations with peptide-pulsed mature dendritic cells, cultured T cells were analyzed for antigen specificity by an IFN-γ ELISPOT assay. Using this ELISPOT assay, we were able to detect E7-specific IFN-γ-secreting CD8(+ )T cells in 5/5 healthy donors. CONCLUSION: We show that peptide-pulsed mature dendritic cells are able to stimulate a HPV type 16 E7 peptide-specific immune response in vitro. These experiments describe an efficient culture protocol for antigen-specific T cells for use in pre-clinical vaccination research and confirm the need for sensitive T cell assays for detection of tumor-specific immune responses in vitro. BioMed Central 2006-10-26 /pmc/articles/PMC1634756/ /pubmed/17067378 http://dx.doi.org/10.1186/1476-4598-5-49 Text en Copyright © 2006 Cools et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Cools, Nathalie
Ponsaerts, Peter
Lenjou, Marc
Nijs, Griet
Van Bockstaele, Dirk R
Van Tendeloo, Viggo FI
Berneman, Zwi N
Sensitive detection of human papillomavirus type 16 E7-specific T cells by ELISPOT after multiple in vitro stimulations of CD8(+ )T cells with peptide-pulsed autologous dendritic cells
title Sensitive detection of human papillomavirus type 16 E7-specific T cells by ELISPOT after multiple in vitro stimulations of CD8(+ )T cells with peptide-pulsed autologous dendritic cells
title_full Sensitive detection of human papillomavirus type 16 E7-specific T cells by ELISPOT after multiple in vitro stimulations of CD8(+ )T cells with peptide-pulsed autologous dendritic cells
title_fullStr Sensitive detection of human papillomavirus type 16 E7-specific T cells by ELISPOT after multiple in vitro stimulations of CD8(+ )T cells with peptide-pulsed autologous dendritic cells
title_full_unstemmed Sensitive detection of human papillomavirus type 16 E7-specific T cells by ELISPOT after multiple in vitro stimulations of CD8(+ )T cells with peptide-pulsed autologous dendritic cells
title_short Sensitive detection of human papillomavirus type 16 E7-specific T cells by ELISPOT after multiple in vitro stimulations of CD8(+ )T cells with peptide-pulsed autologous dendritic cells
title_sort sensitive detection of human papillomavirus type 16 e7-specific t cells by elispot after multiple in vitro stimulations of cd8(+ )t cells with peptide-pulsed autologous dendritic cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1634756/
https://www.ncbi.nlm.nih.gov/pubmed/17067378
http://dx.doi.org/10.1186/1476-4598-5-49
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