Potential recombinant vaccine against influenza A virus based on M2e displayed on nodaviral capsid nanoparticles

Influenza A virus poses a major threat to human health, causing outbreaks from time to time. Currently available vaccines employ inactivated viruses of different strains to provide protection against influenza virus infection. However, high mutation rates of influenza virus hemagglutinin (H) and neu...

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Main Authors: Yong, Chean Yeah, Yeap, Swee Keong, Ho, Kok Lian, Omar, Abdul Rahman, Tan, Wen Siang
Format: Article
Language:English
Published: Dove Medical Press 2015
Online Access:http://psasir.upm.edu.my/id/eprint/36228/
http://psasir.upm.edu.my/id/eprint/36228/1/Potential%20recombinant%20vaccine%20against%20influenza%20A%20virus%20based%20on%20M2e%20displayed%20on%20nodaviral%20capsid%20nanoparticles.pdf
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author Yong, Chean Yeah
Yeap, Swee Keong
Ho, Kok Lian
Omar, Abdul Rahman
Tan, Wen Siang
author_facet Yong, Chean Yeah
Yeap, Swee Keong
Ho, Kok Lian
Omar, Abdul Rahman
Tan, Wen Siang
author_sort Yong, Chean Yeah
building UPM Institutional Repository
collection Online Access
description Influenza A virus poses a major threat to human health, causing outbreaks from time to time. Currently available vaccines employ inactivated viruses of different strains to provide protection against influenza virus infection. However, high mutation rates of influenza virus hemagglutinin (H) and neuraminidase (N) glycoproteins give rise to vaccine escape mutants. Thus, an effective vaccine providing protection against all strains of influenza virus would be a valuable asset. The ectodomain of matrix 2 protein (M2e) was found to be highly conserved despite mutations of the H and N glycoproteins. Hence, one to five copies of M2e were fused to the carboxyl-terminal end of the recombinant nodavirus capsid protein derived from Macrobrachium rosenbergii. The chimeric proteins harboring up to five copies of M2e formed nanosized virus-like particles approximately 30 nm in diameter, which could be purified easily by immobilized metal affinity chromatography. BALB/c mice immunized subcutaneously with these chimeric proteins developed antibodies specifically against M2e, and the titer was proportional to the copy numbers of M2e displayed on the nodavirus capsid nanoparticles. The fusion proteins also induced a type 1 T helper immune response. Collectively, M2e displayed on the nodavirus capsid nanoparticles could provide an alternative solution to a possible influenza pandemic in the future.
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spelling upm-362282015-10-22T03:15:58Z http://psasir.upm.edu.my/id/eprint/36228/ Potential recombinant vaccine against influenza A virus based on M2e displayed on nodaviral capsid nanoparticles Yong, Chean Yeah Yeap, Swee Keong Ho, Kok Lian Omar, Abdul Rahman Tan, Wen Siang Influenza A virus poses a major threat to human health, causing outbreaks from time to time. Currently available vaccines employ inactivated viruses of different strains to provide protection against influenza virus infection. However, high mutation rates of influenza virus hemagglutinin (H) and neuraminidase (N) glycoproteins give rise to vaccine escape mutants. Thus, an effective vaccine providing protection against all strains of influenza virus would be a valuable asset. The ectodomain of matrix 2 protein (M2e) was found to be highly conserved despite mutations of the H and N glycoproteins. Hence, one to five copies of M2e were fused to the carboxyl-terminal end of the recombinant nodavirus capsid protein derived from Macrobrachium rosenbergii. The chimeric proteins harboring up to five copies of M2e formed nanosized virus-like particles approximately 30 nm in diameter, which could be purified easily by immobilized metal affinity chromatography. BALB/c mice immunized subcutaneously with these chimeric proteins developed antibodies specifically against M2e, and the titer was proportional to the copy numbers of M2e displayed on the nodavirus capsid nanoparticles. The fusion proteins also induced a type 1 T helper immune response. Collectively, M2e displayed on the nodavirus capsid nanoparticles could provide an alternative solution to a possible influenza pandemic in the future. Dove Medical Press 2015 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/36228/1/Potential%20recombinant%20vaccine%20against%20influenza%20A%20virus%20based%20on%20M2e%20displayed%20on%20nodaviral%20capsid%20nanoparticles.pdf Yong, Chean Yeah and Yeap, Swee Keong and Ho, Kok Lian and Omar, Abdul Rahman and Tan, Wen Siang (2015) Potential recombinant vaccine against influenza A virus based on M2e displayed on nodaviral capsid nanoparticles. International Journal of Nanomedicine, 10. pp. 2751-2763. ISSN 1178-2013 http://www.dovepress.com/potential-recombinant-vaccine-against-influenza-a-virus-based-on-m2e-d-peer-reviewed-article-IJN 10.2147/IJN.S77405
spellingShingle Yong, Chean Yeah
Yeap, Swee Keong
Ho, Kok Lian
Omar, Abdul Rahman
Tan, Wen Siang
Potential recombinant vaccine against influenza A virus based on M2e displayed on nodaviral capsid nanoparticles
title Potential recombinant vaccine against influenza A virus based on M2e displayed on nodaviral capsid nanoparticles
title_full Potential recombinant vaccine against influenza A virus based on M2e displayed on nodaviral capsid nanoparticles
title_fullStr Potential recombinant vaccine against influenza A virus based on M2e displayed on nodaviral capsid nanoparticles
title_full_unstemmed Potential recombinant vaccine against influenza A virus based on M2e displayed on nodaviral capsid nanoparticles
title_short Potential recombinant vaccine against influenza A virus based on M2e displayed on nodaviral capsid nanoparticles
title_sort potential recombinant vaccine against influenza a virus based on m2e displayed on nodaviral capsid nanoparticles
url http://psasir.upm.edu.my/id/eprint/36228/
http://psasir.upm.edu.my/id/eprint/36228/
http://psasir.upm.edu.my/id/eprint/36228/
http://psasir.upm.edu.my/id/eprint/36228/1/Potential%20recombinant%20vaccine%20against%20influenza%20A%20virus%20based%20on%20M2e%20displayed%20on%20nodaviral%20capsid%20nanoparticles.pdf