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Functional Specialty of CD40 and Dendritic Cell Surface Lectins for Exogenous Antigen Presentation to CD8(+) and CD4(+) T Cells
Dendritic cells (DCs) are major antigen-presenting cells that can efficiently prime and cross-prime antigen-specific T cells. Delivering antigen to DCs via surface receptors is thus an appealing strategy to evoke cellular immunity. Nonetheless, which DC surface receptor to target to yield the optima...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816850/ https://www.ncbi.nlm.nih.gov/pubmed/27077111 http://dx.doi.org/10.1016/j.ebiom.2016.01.029 |
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author | Yin, Wenjie Gorvel, Laurent Zurawski, Sandra Li, Dapeng Ni, Ling Duluc, Dorothée Upchurch, Katherine Kim, JongRok Gu, Chao Ouedraogo, Richard Wang, Zhiqing Xue, Yaming Joo, HyeMee Gorvel, Jean-Pierre Zurawski, Gerard Oh, SangKon |
author_facet | Yin, Wenjie Gorvel, Laurent Zurawski, Sandra Li, Dapeng Ni, Ling Duluc, Dorothée Upchurch, Katherine Kim, JongRok Gu, Chao Ouedraogo, Richard Wang, Zhiqing Xue, Yaming Joo, HyeMee Gorvel, Jean-Pierre Zurawski, Gerard Oh, SangKon |
author_sort | Yin, Wenjie |
collection | PubMed |
description | Dendritic cells (DCs) are major antigen-presenting cells that can efficiently prime and cross-prime antigen-specific T cells. Delivering antigen to DCs via surface receptors is thus an appealing strategy to evoke cellular immunity. Nonetheless, which DC surface receptor to target to yield the optimal CD8(+) and CD4(+) T cell responses remains elusive. Herein, we report the superiority of CD40 over 9 different lectins and scavenger receptors at evoking antigen-specific CD8(+) T cell responses. However, lectins (e.g., LOX-1 and Dectin-1) were more efficient than CD40 at eliciting CD4(+) T cell responses. Common and distinct patterns of subcellular and intracellular localization of receptor-bound αCD40, αLOX-1 and αDectin-1 further support their functional specialization at enhancing antigen presentation to either CD8(+) or CD4(+) T cells. Lastly, we demonstrate that antigen targeting to CD40 can evoke potent antigen-specific CD8(+) T cell responses in human CD40 transgenic mice. This study provides fundamental information for the rational design of vaccines against cancers and viral infections. |
format | Online Article Text |
id | pubmed-4816850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-48168502016-04-13 Functional Specialty of CD40 and Dendritic Cell Surface Lectins for Exogenous Antigen Presentation to CD8(+) and CD4(+) T Cells Yin, Wenjie Gorvel, Laurent Zurawski, Sandra Li, Dapeng Ni, Ling Duluc, Dorothée Upchurch, Katherine Kim, JongRok Gu, Chao Ouedraogo, Richard Wang, Zhiqing Xue, Yaming Joo, HyeMee Gorvel, Jean-Pierre Zurawski, Gerard Oh, SangKon EBioMedicine Research Paper Dendritic cells (DCs) are major antigen-presenting cells that can efficiently prime and cross-prime antigen-specific T cells. Delivering antigen to DCs via surface receptors is thus an appealing strategy to evoke cellular immunity. Nonetheless, which DC surface receptor to target to yield the optimal CD8(+) and CD4(+) T cell responses remains elusive. Herein, we report the superiority of CD40 over 9 different lectins and scavenger receptors at evoking antigen-specific CD8(+) T cell responses. However, lectins (e.g., LOX-1 and Dectin-1) were more efficient than CD40 at eliciting CD4(+) T cell responses. Common and distinct patterns of subcellular and intracellular localization of receptor-bound αCD40, αLOX-1 and αDectin-1 further support their functional specialization at enhancing antigen presentation to either CD8(+) or CD4(+) T cells. Lastly, we demonstrate that antigen targeting to CD40 can evoke potent antigen-specific CD8(+) T cell responses in human CD40 transgenic mice. This study provides fundamental information for the rational design of vaccines against cancers and viral infections. Elsevier 2016-01-28 /pmc/articles/PMC4816850/ /pubmed/27077111 http://dx.doi.org/10.1016/j.ebiom.2016.01.029 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Yin, Wenjie Gorvel, Laurent Zurawski, Sandra Li, Dapeng Ni, Ling Duluc, Dorothée Upchurch, Katherine Kim, JongRok Gu, Chao Ouedraogo, Richard Wang, Zhiqing Xue, Yaming Joo, HyeMee Gorvel, Jean-Pierre Zurawski, Gerard Oh, SangKon Functional Specialty of CD40 and Dendritic Cell Surface Lectins for Exogenous Antigen Presentation to CD8(+) and CD4(+) T Cells |
title | Functional Specialty of CD40 and Dendritic Cell Surface Lectins for Exogenous Antigen Presentation to CD8(+) and CD4(+) T Cells |
title_full | Functional Specialty of CD40 and Dendritic Cell Surface Lectins for Exogenous Antigen Presentation to CD8(+) and CD4(+) T Cells |
title_fullStr | Functional Specialty of CD40 and Dendritic Cell Surface Lectins for Exogenous Antigen Presentation to CD8(+) and CD4(+) T Cells |
title_full_unstemmed | Functional Specialty of CD40 and Dendritic Cell Surface Lectins for Exogenous Antigen Presentation to CD8(+) and CD4(+) T Cells |
title_short | Functional Specialty of CD40 and Dendritic Cell Surface Lectins for Exogenous Antigen Presentation to CD8(+) and CD4(+) T Cells |
title_sort | functional specialty of cd40 and dendritic cell surface lectins for exogenous antigen presentation to cd8(+) and cd4(+) t cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816850/ https://www.ncbi.nlm.nih.gov/pubmed/27077111 http://dx.doi.org/10.1016/j.ebiom.2016.01.029 |
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