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Immunization Route Dictates Cross-Priming Efficiency and Impacts the Optimal Timing of Adjuvant Delivery
Delivery of cell-associated antigen represents an important strategy for vaccination. While many experimental models have been developed in order to define the critical parameters for efficient cross-priming, few have utilized quantitative methods that permit the study of the endogenous repertoire....
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342317/ https://www.ncbi.nlm.nih.gov/pubmed/22566860 http://dx.doi.org/10.3389/fimmu.2011.00071 |
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author | Bouvier, Isabelle Jusforgues-Saklani, Hélène Lim, Annick Lemaître, Fabrice Lemercier, Brigitte Auriau, Charlotte Nicola, Marie-Anne Leroy, Sandrine Law, Helen K. Bandeira, Antonio Moon, James J. Bousso, Philippe Albert, Matthew L. |
author_facet | Bouvier, Isabelle Jusforgues-Saklani, Hélène Lim, Annick Lemaître, Fabrice Lemercier, Brigitte Auriau, Charlotte Nicola, Marie-Anne Leroy, Sandrine Law, Helen K. Bandeira, Antonio Moon, James J. Bousso, Philippe Albert, Matthew L. |
author_sort | Bouvier, Isabelle |
collection | PubMed |
description | Delivery of cell-associated antigen represents an important strategy for vaccination. While many experimental models have been developed in order to define the critical parameters for efficient cross-priming, few have utilized quantitative methods that permit the study of the endogenous repertoire. Comparing different strategies of immunization, we report that local delivery of cell-associated antigen results in delayed T cell cross-priming due to the increased time required for antigen capture and presentation. In comparison, delivery of disseminated antigen resulted in rapid T cell priming. Surprisingly, local injection of cell-associated antigen, while slower, resulted in the differentiation of a more robust, polyfunctional, effector response. We also evaluated the combination of cell-associated antigen with poly I:C delivery and observed an immunization route-specific effect regarding the optimal timing of innate immune stimulation. These studies highlight the importance of considering the timing and persistence of antigen presentation, and suggest that intradermal injection with delayed adjuvant delivery is the optimal strategy for achieving CD8(+) T cell cross-priming. |
format | Online Article Text |
id | pubmed-3342317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33423172012-05-07 Immunization Route Dictates Cross-Priming Efficiency and Impacts the Optimal Timing of Adjuvant Delivery Bouvier, Isabelle Jusforgues-Saklani, Hélène Lim, Annick Lemaître, Fabrice Lemercier, Brigitte Auriau, Charlotte Nicola, Marie-Anne Leroy, Sandrine Law, Helen K. Bandeira, Antonio Moon, James J. Bousso, Philippe Albert, Matthew L. Front Immunol Immunology Delivery of cell-associated antigen represents an important strategy for vaccination. While many experimental models have been developed in order to define the critical parameters for efficient cross-priming, few have utilized quantitative methods that permit the study of the endogenous repertoire. Comparing different strategies of immunization, we report that local delivery of cell-associated antigen results in delayed T cell cross-priming due to the increased time required for antigen capture and presentation. In comparison, delivery of disseminated antigen resulted in rapid T cell priming. Surprisingly, local injection of cell-associated antigen, while slower, resulted in the differentiation of a more robust, polyfunctional, effector response. We also evaluated the combination of cell-associated antigen with poly I:C delivery and observed an immunization route-specific effect regarding the optimal timing of innate immune stimulation. These studies highlight the importance of considering the timing and persistence of antigen presentation, and suggest that intradermal injection with delayed adjuvant delivery is the optimal strategy for achieving CD8(+) T cell cross-priming. Frontiers Research Foundation 2011-12-08 /pmc/articles/PMC3342317/ /pubmed/22566860 http://dx.doi.org/10.3389/fimmu.2011.00071 Text en Copyright © 2011 Bouvier, Jusforgues-Saklani, Lim, Lemaître, Lemercier, Auriau, Nicola, Leroy, Law, Bandeira, Moon, Bousso and Albert. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited. |
spellingShingle | Immunology Bouvier, Isabelle Jusforgues-Saklani, Hélène Lim, Annick Lemaître, Fabrice Lemercier, Brigitte Auriau, Charlotte Nicola, Marie-Anne Leroy, Sandrine Law, Helen K. Bandeira, Antonio Moon, James J. Bousso, Philippe Albert, Matthew L. Immunization Route Dictates Cross-Priming Efficiency and Impacts the Optimal Timing of Adjuvant Delivery |
title | Immunization Route Dictates Cross-Priming Efficiency and Impacts the Optimal Timing of Adjuvant Delivery |
title_full | Immunization Route Dictates Cross-Priming Efficiency and Impacts the Optimal Timing of Adjuvant Delivery |
title_fullStr | Immunization Route Dictates Cross-Priming Efficiency and Impacts the Optimal Timing of Adjuvant Delivery |
title_full_unstemmed | Immunization Route Dictates Cross-Priming Efficiency and Impacts the Optimal Timing of Adjuvant Delivery |
title_short | Immunization Route Dictates Cross-Priming Efficiency and Impacts the Optimal Timing of Adjuvant Delivery |
title_sort | immunization route dictates cross-priming efficiency and impacts the optimal timing of adjuvant delivery |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342317/ https://www.ncbi.nlm.nih.gov/pubmed/22566860 http://dx.doi.org/10.3389/fimmu.2011.00071 |
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