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Induction of neutralising antibodies and cellular immune responses against SARS coronavirus by recombinant measles viruses
Live attenuated recombinant measles viruses (rMV) expressing a codon-optimised spike glycoprotein (S) or nucleocapsid protein (N) of severe acute respiratory syndrome-associated coronavirus (SARS-CoV) were generated (rMV-S and rMV-N). Both recombinant viruses stably expressed the corresponding SARS-...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115634/ https://www.ncbi.nlm.nih.gov/pubmed/18346823 http://dx.doi.org/10.1016/j.vaccine.2008.01.057 |
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author | Liniger, Matthias Zuniga, Armando Tamin, Azaibi Azzouz-Morin, Teldja N. Knuchel, Marlyse Marty, Rene R. Wiegand, Marian Weibel, Sara Kelvin, David Rota, Paul A. Naim, Hussein Y. |
author_facet | Liniger, Matthias Zuniga, Armando Tamin, Azaibi Azzouz-Morin, Teldja N. Knuchel, Marlyse Marty, Rene R. Wiegand, Marian Weibel, Sara Kelvin, David Rota, Paul A. Naim, Hussein Y. |
author_sort | Liniger, Matthias |
collection | PubMed |
description | Live attenuated recombinant measles viruses (rMV) expressing a codon-optimised spike glycoprotein (S) or nucleocapsid protein (N) of severe acute respiratory syndrome-associated coronavirus (SARS-CoV) were generated (rMV-S and rMV-N). Both recombinant viruses stably expressed the corresponding SARS-CoV proteins, grew to similar end titres as the parental strain and induced high antibody titres against MV and the vectored SARS-CoV antigens (S and N) in transgenic mice susceptible to measles infection. The antibodies induced by rMV-S had a high neutralising effect on SARS-CoV as well as on MV. Moreover, significant N-specific cellular immune responses were measured by IFN-γ ELISPOT assays. The pre-existence of anti-MV antibodies induced by the initial immunisation dose did not inhibit boost of anti-S and anti-N antibodies. Immunisations comprising a mixture of rMV-S and rMV-N induced immune responses similar in magnitude to that of vaccine components administered separately. These data support the suitability of MV as a bivalent candidate vaccine vector against MV and emerging viruses such as SARS-CoV. |
format | Online Article Text |
id | pubmed-7115634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71156342020-04-02 Induction of neutralising antibodies and cellular immune responses against SARS coronavirus by recombinant measles viruses Liniger, Matthias Zuniga, Armando Tamin, Azaibi Azzouz-Morin, Teldja N. Knuchel, Marlyse Marty, Rene R. Wiegand, Marian Weibel, Sara Kelvin, David Rota, Paul A. Naim, Hussein Y. Vaccine Article Live attenuated recombinant measles viruses (rMV) expressing a codon-optimised spike glycoprotein (S) or nucleocapsid protein (N) of severe acute respiratory syndrome-associated coronavirus (SARS-CoV) were generated (rMV-S and rMV-N). Both recombinant viruses stably expressed the corresponding SARS-CoV proteins, grew to similar end titres as the parental strain and induced high antibody titres against MV and the vectored SARS-CoV antigens (S and N) in transgenic mice susceptible to measles infection. The antibodies induced by rMV-S had a high neutralising effect on SARS-CoV as well as on MV. Moreover, significant N-specific cellular immune responses were measured by IFN-γ ELISPOT assays. The pre-existence of anti-MV antibodies induced by the initial immunisation dose did not inhibit boost of anti-S and anti-N antibodies. Immunisations comprising a mixture of rMV-S and rMV-N induced immune responses similar in magnitude to that of vaccine components administered separately. These data support the suitability of MV as a bivalent candidate vaccine vector against MV and emerging viruses such as SARS-CoV. Elsevier Ltd. 2008-04-16 2008-02-22 /pmc/articles/PMC7115634/ /pubmed/18346823 http://dx.doi.org/10.1016/j.vaccine.2008.01.057 Text en Copyright © 2008 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 Liniger, Matthias Zuniga, Armando Tamin, Azaibi Azzouz-Morin, Teldja N. Knuchel, Marlyse Marty, Rene R. Wiegand, Marian Weibel, Sara Kelvin, David Rota, Paul A. Naim, Hussein Y. Induction of neutralising antibodies and cellular immune responses against SARS coronavirus by recombinant measles viruses |
title | Induction of neutralising antibodies and cellular immune responses against SARS coronavirus by recombinant measles viruses |
title_full | Induction of neutralising antibodies and cellular immune responses against SARS coronavirus by recombinant measles viruses |
title_fullStr | Induction of neutralising antibodies and cellular immune responses against SARS coronavirus by recombinant measles viruses |
title_full_unstemmed | Induction of neutralising antibodies and cellular immune responses against SARS coronavirus by recombinant measles viruses |
title_short | Induction of neutralising antibodies and cellular immune responses against SARS coronavirus by recombinant measles viruses |
title_sort | induction of neutralising antibodies and cellular immune responses against sars coronavirus by recombinant measles viruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115634/ https://www.ncbi.nlm.nih.gov/pubmed/18346823 http://dx.doi.org/10.1016/j.vaccine.2008.01.057 |
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