Intranasal immunization with plasmid DNA encoding spike protein of SARS-coronavirus/polyethylenimine nanoparticles elicits antigen-specific humoral and cellular immune responses

<p>Abstract</p> <p>Background</p> <p>Immunization with the spike protein (S) of severe acute respiratory syndrome (SARS)-coronavirus (CoV) in mice is known to produce neutralizing antibodies and to prevent the infection caused by SARS-CoV. Polyethylenimine 25K (PEI) is...

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Main Authors: Yang Moon-Sik, Jang Yong-Suk, Kim Dong, Song Man, Chu Hyuk, Jere Dhananjay, Quan Ji-Shan, Park Sung-Moo, Shim Byoung-Shik, Han Seung, Park Yong-Ho, Cho Chong-Su, Yun Cheol-Heui
Format: Article
Language:English
Published: BMC 2010-12-01
Series:BMC Immunology
Online Access:http://www.biomedcentral.com/1471-2172/11/65
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spelling doaj-90d8b4d6405f4ea5b67c630e07722d112020-11-25T03:37:16ZengBMCBMC Immunology1471-21722010-12-011116510.1186/1471-2172-11-65Intranasal immunization with plasmid DNA encoding spike protein of SARS-coronavirus/polyethylenimine nanoparticles elicits antigen-specific humoral and cellular immune responsesYang Moon-SikJang Yong-SukKim DongSong ManChu HyukJere DhananjayQuan Ji-ShanPark Sung-MooShim Byoung-ShikHan SeungPark Yong-HoCho Chong-SuYun Cheol-Heui<p>Abstract</p> <p>Background</p> <p>Immunization with the spike protein (S) of severe acute respiratory syndrome (SARS)-coronavirus (CoV) in mice is known to produce neutralizing antibodies and to prevent the infection caused by SARS-CoV. Polyethylenimine 25K (PEI) is a cationic polymer which effectively delivers the plasmid DNA.</p> <p>Results</p> <p>In the present study, the immune responses of BALB/c mice immunized via intranasal (i.n.) route with SARS DNA vaccine (pci-S) in a PEI/pci-S complex form have been examined. The size of the PEI/pci-S nanoparticles appeared to be around 194.7 ± 99.3 nm, and the expression of the S mRNA and protein was confirmed <it>in vitro</it>. The mice immunized with i.n. PEI/pci-S nanoparticles produced significantly (<it>P </it>< 0.05) higher S-specific IgG1 in the sera and mucosal secretory IgA in the lung wash than those in mice treated with pci-S alone. Compared to those in mice challenged with pci-S alone, the number of B220<sup>+ </sup>cells found in PEI/pci-S vaccinated mice was elevated. Co-stimulatory molecules (CD80 and CD86) and class II major histocompatibility complex molecules (I-A<sup>d</sup>) were increased on CD11c<sup>+ </sup>dendritic cells in cervical lymph node from the mice after PEI/pci-S vaccination. The percentage of IFN-γ-, TNF-α- and IL-2-producing cells were higher in PEI/pci-S vaccinated mice than in control mice.</p> <p>Conclusion</p> <p>These results showed that intranasal immunization with PEI/pci-S nanoparticles induce antigen specific humoral and cellular immune responses.</p> http://www.biomedcentral.com/1471-2172/11/65
collection DOAJ
language English
format Article
sources DOAJ
author Yang Moon-Sik
Jang Yong-Suk
Kim Dong
Song Man
Chu Hyuk
Jere Dhananjay
Quan Ji-Shan
Park Sung-Moo
Shim Byoung-Shik
Han Seung
Park Yong-Ho
Cho Chong-Su
Yun Cheol-Heui
spellingShingle Yang Moon-Sik
Jang Yong-Suk
Kim Dong
Song Man
Chu Hyuk
Jere Dhananjay
Quan Ji-Shan
Park Sung-Moo
Shim Byoung-Shik
Han Seung
Park Yong-Ho
Cho Chong-Su
Yun Cheol-Heui
Intranasal immunization with plasmid DNA encoding spike protein of SARS-coronavirus/polyethylenimine nanoparticles elicits antigen-specific humoral and cellular immune responses
BMC Immunology
author_facet Yang Moon-Sik
Jang Yong-Suk
Kim Dong
Song Man
Chu Hyuk
Jere Dhananjay
Quan Ji-Shan
Park Sung-Moo
Shim Byoung-Shik
Han Seung
Park Yong-Ho
Cho Chong-Su
Yun Cheol-Heui
author_sort Yang Moon-Sik
title Intranasal immunization with plasmid DNA encoding spike protein of SARS-coronavirus/polyethylenimine nanoparticles elicits antigen-specific humoral and cellular immune responses
title_short Intranasal immunization with plasmid DNA encoding spike protein of SARS-coronavirus/polyethylenimine nanoparticles elicits antigen-specific humoral and cellular immune responses
title_full Intranasal immunization with plasmid DNA encoding spike protein of SARS-coronavirus/polyethylenimine nanoparticles elicits antigen-specific humoral and cellular immune responses
title_fullStr Intranasal immunization with plasmid DNA encoding spike protein of SARS-coronavirus/polyethylenimine nanoparticles elicits antigen-specific humoral and cellular immune responses
title_full_unstemmed Intranasal immunization with plasmid DNA encoding spike protein of SARS-coronavirus/polyethylenimine nanoparticles elicits antigen-specific humoral and cellular immune responses
title_sort intranasal immunization with plasmid dna encoding spike protein of sars-coronavirus/polyethylenimine nanoparticles elicits antigen-specific humoral and cellular immune responses
publisher BMC
series BMC Immunology
issn 1471-2172
publishDate 2010-12-01
description <p>Abstract</p> <p>Background</p> <p>Immunization with the spike protein (S) of severe acute respiratory syndrome (SARS)-coronavirus (CoV) in mice is known to produce neutralizing antibodies and to prevent the infection caused by SARS-CoV. Polyethylenimine 25K (PEI) is a cationic polymer which effectively delivers the plasmid DNA.</p> <p>Results</p> <p>In the present study, the immune responses of BALB/c mice immunized via intranasal (i.n.) route with SARS DNA vaccine (pci-S) in a PEI/pci-S complex form have been examined. The size of the PEI/pci-S nanoparticles appeared to be around 194.7 ± 99.3 nm, and the expression of the S mRNA and protein was confirmed <it>in vitro</it>. The mice immunized with i.n. PEI/pci-S nanoparticles produced significantly (<it>P </it>< 0.05) higher S-specific IgG1 in the sera and mucosal secretory IgA in the lung wash than those in mice treated with pci-S alone. Compared to those in mice challenged with pci-S alone, the number of B220<sup>+ </sup>cells found in PEI/pci-S vaccinated mice was elevated. Co-stimulatory molecules (CD80 and CD86) and class II major histocompatibility complex molecules (I-A<sup>d</sup>) were increased on CD11c<sup>+ </sup>dendritic cells in cervical lymph node from the mice after PEI/pci-S vaccination. The percentage of IFN-γ-, TNF-α- and IL-2-producing cells were higher in PEI/pci-S vaccinated mice than in control mice.</p> <p>Conclusion</p> <p>These results showed that intranasal immunization with PEI/pci-S nanoparticles induce antigen specific humoral and cellular immune responses.</p>
url http://www.biomedcentral.com/1471-2172/11/65
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