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Synthetic peptides coupled to the surface of liposomes effectively induce SARS coronavirus-specific cytotoxic T lymphocytes and viral clearance in HLA-A*0201 transgenic mice

We investigated whether the surface-linked liposomal peptide was applicable to a vaccine based on cytotoxic T lymphocytes (CTLs) against severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV). We first identified four HLA-A*0201-restricted CTL epitopes derived from SARS-CoV using HLA-A*0201...

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Autores principales: Ohno, Satoshi, Kohyama, Shunsuke, Taneichi, Maiko, Moriya, Osamu, Hayashi, Hidenori, Oda, Hiroshi, Mori, Masahito, Kobayashi, Akiharu, Akatsuka, Toshitaka, Uchida, Tetsuya, Matsui, Masanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115666/
https://www.ncbi.nlm.nih.gov/pubmed/19490987
http://dx.doi.org/10.1016/j.vaccine.2009.04.001
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author Ohno, Satoshi
Kohyama, Shunsuke
Taneichi, Maiko
Moriya, Osamu
Hayashi, Hidenori
Oda, Hiroshi
Mori, Masahito
Kobayashi, Akiharu
Akatsuka, Toshitaka
Uchida, Tetsuya
Matsui, Masanori
author_facet Ohno, Satoshi
Kohyama, Shunsuke
Taneichi, Maiko
Moriya, Osamu
Hayashi, Hidenori
Oda, Hiroshi
Mori, Masahito
Kobayashi, Akiharu
Akatsuka, Toshitaka
Uchida, Tetsuya
Matsui, Masanori
author_sort Ohno, Satoshi
collection PubMed
description We investigated whether the surface-linked liposomal peptide was applicable to a vaccine based on cytotoxic T lymphocytes (CTLs) against severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV). We first identified four HLA-A*0201-restricted CTL epitopes derived from SARS-CoV using HLA-A*0201 transgenic mice and recombinant adenovirus expressing predicted epitopes. These peptides were coupled to the surface of liposomes, and inoculated into mice. Two of the liposomal peptides were effective for peptide-specific CTL induction, and one of them was efficient for the clearance of vaccinia virus expressing epitopes of SARS-CoV, suggesting that the surface-linked liposomal peptide might offer an effective CTL-based vaccine against SARS.
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spelling pubmed-71156662020-04-02 Synthetic peptides coupled to the surface of liposomes effectively induce SARS coronavirus-specific cytotoxic T lymphocytes and viral clearance in HLA-A*0201 transgenic mice Ohno, Satoshi Kohyama, Shunsuke Taneichi, Maiko Moriya, Osamu Hayashi, Hidenori Oda, Hiroshi Mori, Masahito Kobayashi, Akiharu Akatsuka, Toshitaka Uchida, Tetsuya Matsui, Masanori Vaccine Article We investigated whether the surface-linked liposomal peptide was applicable to a vaccine based on cytotoxic T lymphocytes (CTLs) against severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV). We first identified four HLA-A*0201-restricted CTL epitopes derived from SARS-CoV using HLA-A*0201 transgenic mice and recombinant adenovirus expressing predicted epitopes. These peptides were coupled to the surface of liposomes, and inoculated into mice. Two of the liposomal peptides were effective for peptide-specific CTL induction, and one of them was efficient for the clearance of vaccinia virus expressing epitopes of SARS-CoV, suggesting that the surface-linked liposomal peptide might offer an effective CTL-based vaccine against SARS. Elsevier Ltd. 2009-06-12 2009-04-23 /pmc/articles/PMC7115666/ /pubmed/19490987 http://dx.doi.org/10.1016/j.vaccine.2009.04.001 Text en Copyright © 2009 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Ohno, Satoshi
Kohyama, Shunsuke
Taneichi, Maiko
Moriya, Osamu
Hayashi, Hidenori
Oda, Hiroshi
Mori, Masahito
Kobayashi, Akiharu
Akatsuka, Toshitaka
Uchida, Tetsuya
Matsui, Masanori
Synthetic peptides coupled to the surface of liposomes effectively induce SARS coronavirus-specific cytotoxic T lymphocytes and viral clearance in HLA-A*0201 transgenic mice
title Synthetic peptides coupled to the surface of liposomes effectively induce SARS coronavirus-specific cytotoxic T lymphocytes and viral clearance in HLA-A*0201 transgenic mice
title_full Synthetic peptides coupled to the surface of liposomes effectively induce SARS coronavirus-specific cytotoxic T lymphocytes and viral clearance in HLA-A*0201 transgenic mice
title_fullStr Synthetic peptides coupled to the surface of liposomes effectively induce SARS coronavirus-specific cytotoxic T lymphocytes and viral clearance in HLA-A*0201 transgenic mice
title_full_unstemmed Synthetic peptides coupled to the surface of liposomes effectively induce SARS coronavirus-specific cytotoxic T lymphocytes and viral clearance in HLA-A*0201 transgenic mice
title_short Synthetic peptides coupled to the surface of liposomes effectively induce SARS coronavirus-specific cytotoxic T lymphocytes and viral clearance in HLA-A*0201 transgenic mice
title_sort synthetic peptides coupled to the surface of liposomes effectively induce sars coronavirus-specific cytotoxic t lymphocytes and viral clearance in hla-a*0201 transgenic mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115666/
https://www.ncbi.nlm.nih.gov/pubmed/19490987
http://dx.doi.org/10.1016/j.vaccine.2009.04.001
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