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Screening and Identification of a Chicken Dendritic Cell Binding Peptide by Using a Phage Display Library
Dendritic cells (DCs), as antigen-presenting cells, can initiate adaptive immune responses efficiently. Although the DC-targeting strategy has attracted more attention, relevant studies on chicken are rare. Here, specific chicken bone marrow DC-binding peptides were selected using a phage display pe...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691127/ https://www.ncbi.nlm.nih.gov/pubmed/31447851 http://dx.doi.org/10.3389/fimmu.2019.01853 |
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author | Ma, Sunting Qiao, Xinyuan Xu, Yigang Wang, Li Zhou, Han Jiang, Yanping Cui, Wen Huang, Xuewei Wang, Xiaona Tang, Lijie Li, Yijing |
author_facet | Ma, Sunting Qiao, Xinyuan Xu, Yigang Wang, Li Zhou, Han Jiang, Yanping Cui, Wen Huang, Xuewei Wang, Xiaona Tang, Lijie Li, Yijing |
author_sort | Ma, Sunting |
collection | PubMed |
description | Dendritic cells (DCs), as antigen-presenting cells, can initiate adaptive immune responses efficiently. Although the DC-targeting strategy has attracted more attention, relevant studies on chicken are rare. Here, specific chicken bone marrow DC-binding peptides were selected using a phage display peptide library and confirmed through ELISA, flow cytometry, fluorescence microscopy, and laser confocal microscopy. The peptide candidate SPHLHTSSPWER, named SP, was fused to the infectious bursal disease virus (IBDV) structural protein and protective antigen VP2. In vitro, the expression of DC markers (CD80, CD83, CD86, DEC205, and MHCII) and some cytokines (IFN-γ, IL-12, TNF-α, IL-1β, IL-6, and CXCLi1) by VP2-SP-stimulated DCs was significantly higher than that by DCs treated with the VP2-control peptide at 4 h (p < 0.001). In addition, an oral vaccine targeting DCs was generated using chicken-borne Lactobacillus saerimneri M11 (L. sae M11) to deliver VP2 fused with SP. Anti-IBDV mucosal and humoral immune responses were induced efficiently via oral administration, resulting in higher protective efficacy in the VP2-SP group than the VP2 group. Therefore, chicken DC targeting of IBDV protective antigen VP2 delivered by L. sae provides effective immune protection in chicken. Our study may promote research on the DC-targeting strategy to enhance the effectiveness of chicken vaccines. |
format | Online Article Text |
id | pubmed-6691127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66911272019-08-23 Screening and Identification of a Chicken Dendritic Cell Binding Peptide by Using a Phage Display Library Ma, Sunting Qiao, Xinyuan Xu, Yigang Wang, Li Zhou, Han Jiang, Yanping Cui, Wen Huang, Xuewei Wang, Xiaona Tang, Lijie Li, Yijing Front Immunol Immunology Dendritic cells (DCs), as antigen-presenting cells, can initiate adaptive immune responses efficiently. Although the DC-targeting strategy has attracted more attention, relevant studies on chicken are rare. Here, specific chicken bone marrow DC-binding peptides were selected using a phage display peptide library and confirmed through ELISA, flow cytometry, fluorescence microscopy, and laser confocal microscopy. The peptide candidate SPHLHTSSPWER, named SP, was fused to the infectious bursal disease virus (IBDV) structural protein and protective antigen VP2. In vitro, the expression of DC markers (CD80, CD83, CD86, DEC205, and MHCII) and some cytokines (IFN-γ, IL-12, TNF-α, IL-1β, IL-6, and CXCLi1) by VP2-SP-stimulated DCs was significantly higher than that by DCs treated with the VP2-control peptide at 4 h (p < 0.001). In addition, an oral vaccine targeting DCs was generated using chicken-borne Lactobacillus saerimneri M11 (L. sae M11) to deliver VP2 fused with SP. Anti-IBDV mucosal and humoral immune responses were induced efficiently via oral administration, resulting in higher protective efficacy in the VP2-SP group than the VP2 group. Therefore, chicken DC targeting of IBDV protective antigen VP2 delivered by L. sae provides effective immune protection in chicken. Our study may promote research on the DC-targeting strategy to enhance the effectiveness of chicken vaccines. Frontiers Media S.A. 2019-08-06 /pmc/articles/PMC6691127/ /pubmed/31447851 http://dx.doi.org/10.3389/fimmu.2019.01853 Text en Copyright © 2019 Ma, Qiao, Xu, Wang, Zhou, Jiang, Cui, Huang, Wang, Tang and Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Ma, Sunting Qiao, Xinyuan Xu, Yigang Wang, Li Zhou, Han Jiang, Yanping Cui, Wen Huang, Xuewei Wang, Xiaona Tang, Lijie Li, Yijing Screening and Identification of a Chicken Dendritic Cell Binding Peptide by Using a Phage Display Library |
title | Screening and Identification of a Chicken Dendritic Cell Binding Peptide by Using a Phage Display Library |
title_full | Screening and Identification of a Chicken Dendritic Cell Binding Peptide by Using a Phage Display Library |
title_fullStr | Screening and Identification of a Chicken Dendritic Cell Binding Peptide by Using a Phage Display Library |
title_full_unstemmed | Screening and Identification of a Chicken Dendritic Cell Binding Peptide by Using a Phage Display Library |
title_short | Screening and Identification of a Chicken Dendritic Cell Binding Peptide by Using a Phage Display Library |
title_sort | screening and identification of a chicken dendritic cell binding peptide by using a phage display library |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691127/ https://www.ncbi.nlm.nih.gov/pubmed/31447851 http://dx.doi.org/10.3389/fimmu.2019.01853 |
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