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Mucosal Immunization and Adjuvants

The goal of the influenza vaccine is to prevent influenza virus infection and control the yearly seasonal epidemic and pandemic. However, the presently available parenteral influenza vaccine induces only systemic humoral immunity, which does not prevent influenza virus infection on the mucosal surfa...

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Autores principales: Hasegawa, Hideki, van Reit, Elly, Kida, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7120566/
https://www.ncbi.nlm.nih.gov/pubmed/25015787
http://dx.doi.org/10.1007/82_2014_402
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author Hasegawa, Hideki
van Reit, Elly
Kida, Hiroshi
author_facet Hasegawa, Hideki
van Reit, Elly
Kida, Hiroshi
author_sort Hasegawa, Hideki
collection PubMed
description The goal of the influenza vaccine is to prevent influenza virus infection and control the yearly seasonal epidemic and pandemic. However, the presently available parenteral influenza vaccine induces only systemic humoral immunity, which does not prevent influenza virus infection on the mucosal surface. Secretary IgA antibodies play an important role in preventing natural infection. Moreover, the IgA antibody response mediates cross-protection against variant viruses in animal models. Thus, a mucosal influenza vaccine that induces mucosal immunity would be a powerful tool to protect individuals from the influenza virus. Although the function of the mucosal immune system, especially in the respiratory tract, is not completely understood, there are several studies underway to develop mucosal influenza vaccines. Here, we will review current knowledge concerning the induction of IgA, the role of B-cell production of influenza virus specific IgA antibodies in anti-influenza immunity, and the role of humoral memory responses induced upon vaccination.
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spelling pubmed-71205662020-04-06 Mucosal Immunization and Adjuvants Hasegawa, Hideki van Reit, Elly Kida, Hiroshi Influenza Pathogenesis and Control - Volume II Article The goal of the influenza vaccine is to prevent influenza virus infection and control the yearly seasonal epidemic and pandemic. However, the presently available parenteral influenza vaccine induces only systemic humoral immunity, which does not prevent influenza virus infection on the mucosal surface. Secretary IgA antibodies play an important role in preventing natural infection. Moreover, the IgA antibody response mediates cross-protection against variant viruses in animal models. Thus, a mucosal influenza vaccine that induces mucosal immunity would be a powerful tool to protect individuals from the influenza virus. Although the function of the mucosal immune system, especially in the respiratory tract, is not completely understood, there are several studies underway to develop mucosal influenza vaccines. Here, we will review current knowledge concerning the induction of IgA, the role of B-cell production of influenza virus specific IgA antibodies in anti-influenza immunity, and the role of humoral memory responses induced upon vaccination. 2014-07-12 /pmc/articles/PMC7120566/ /pubmed/25015787 http://dx.doi.org/10.1007/82_2014_402 Text en © Springer International Publishing Switzerland 2014 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Hasegawa, Hideki
van Reit, Elly
Kida, Hiroshi
Mucosal Immunization and Adjuvants
title Mucosal Immunization and Adjuvants
title_full Mucosal Immunization and Adjuvants
title_fullStr Mucosal Immunization and Adjuvants
title_full_unstemmed Mucosal Immunization and Adjuvants
title_short Mucosal Immunization and Adjuvants
title_sort mucosal immunization and adjuvants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7120566/
https://www.ncbi.nlm.nih.gov/pubmed/25015787
http://dx.doi.org/10.1007/82_2014_402
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