Protection against influenza virus infection by intranasal vaccine with surf clam microparticles (SMP) as an adjuvant
Identifieur interne : 004198 ( Main/Exploration ); précédent : 004197; suivant : 004199Protection against influenza virus infection by intranasal vaccine with surf clam microparticles (SMP) as an adjuvant
Auteurs : Takeshi Ichinohe [Japon] ; Izumi Watanabe [Japon] ; Eriko Tao [Japon] ; Satoshi Ito [Japon] ; Akira Kawaguchi [Japon] ; Shin-Ichi Tamura [Japon] ; Hidehiro Takahashi [Japon] ; Hirofumi Sawa [Japon] ; Masami Moriyama [Japon] ; Joe Chiba [Japon] ; Katsuhiro Komase [Japon] ; Yujiro Suzuki [Japon] ; Takeshi Kurata [Japon] ; Tetsutaro Sata [Japon] ; Hideki Hasegawa [Japon]Source :
- Journal of Medical Virology [ 0146-6615 ] ; 2006-07.
English descriptors
- Teeft :
- Adjuvant, Aizawa, Assay, Body weight, Bronchoalveolar wash, Chitin microparticles, Cholera, Cholera toxin, Clam, Complete protection, Control mice, Effective mucosal adjuvant, Elisa, Escherichia coli enterotoxin, Hasegawa, Heterologous, Heterologous viruses, Holotoxin, Ichinohe, Immunization, Immunization protocol, Immunol, Immunol tamura, Infection, Infectious diseases, Initial body weight, Intracerebral, Intragastric, Intragastric administration, Intranasal, Intranasal administration, Intranasal immunization, Intranasal vaccination, Intranasal vaccine, Intranasally, Kurata, Lethal lung infection, Lethal pneumonia, Lethal virus challenge, Lung wash, Mdck, Mdck cells, Mice vaccinated, Microparticles, Mouse, Mucosal, Nasal, Nasal cavity, Nasal mucosa, Nasal vaccination, Nasal vaccine, Nasal wash, National institute, Neutralizing, Neutralizing activity, Other adjuvants, Plaque assay, Present study, Safe adjuvant, Subunit, Surf, Surf clam microparticles, Survival rates, Suzuki, Tamura, Time course, Titer, Toxin, Trace amount, Vaccinated, Vaccination, Vaccine, Vaccine tamura, Various adjuvants, Virol, Virus, Virus challenge, Virus infection, Virus titer, Virus titers, Watanabe.
Abstract
A safe and effective adjuvant is necessary to enhance mucosal immune responses for the development of an inactivated intranasal influenza vaccine. The present study demonstrated the effectiveness of surf clam microparticles (SMP) derived from natural surf clams as an adjuvant for an intranasal influenza vaccine. The adjuvant effect of SMP was examined when co‐administered intranasally with inactivated A/PR8 (H1N1) influenza virus hemagglutinin vaccine in BALB/c mice. Administration of the vaccine with SMP induced a high anti‐PR8 haemagglutinin (HA)‐specific immunoglobulin A (IgA) response in the nasal wash and immunoglobulin G (IgG) response in the serum, resulting in protection against both nasal‐restricted infection and lethal lung infection by A/PR8 virus. In addition, administration of SMP with A/Yamagata (H1N1), A/Beijing (H1N1), or A/Guizhou (H3N2) vaccine conferred complete protection against A/PR8 virus challenge in the nasal infection model, suggesting that SMP adjuvanted vaccine can confer cross‐protection against variant influenza viruses. The use of SMP is suggested as a new safe and effective mucosal adjuvant for nasal vaccination against influenza virus infection. J. Med. Virol. 78:954–963, 2006. © 2006 Wiley‐Liss, Inc.
Url:
DOI: 10.1002/jmv.20647
Affiliations:
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<term>Aizawa</term>
<term>Assay</term>
<term>Body weight</term>
<term>Bronchoalveolar wash</term>
<term>Chitin microparticles</term>
<term>Cholera</term>
<term>Cholera toxin</term>
<term>Clam</term>
<term>Complete protection</term>
<term>Control mice</term>
<term>Effective mucosal adjuvant</term>
<term>Elisa</term>
<term>Escherichia coli enterotoxin</term>
<term>Hasegawa</term>
<term>Heterologous</term>
<term>Heterologous viruses</term>
<term>Holotoxin</term>
<term>Ichinohe</term>
<term>Immunization</term>
<term>Immunization protocol</term>
<term>Immunol</term>
<term>Immunol tamura</term>
<term>Infection</term>
<term>Infectious diseases</term>
<term>Initial body weight</term>
<term>Intracerebral</term>
<term>Intragastric</term>
<term>Intragastric administration</term>
<term>Intranasal</term>
<term>Intranasal administration</term>
<term>Intranasal immunization</term>
<term>Intranasal vaccination</term>
<term>Intranasal vaccine</term>
<term>Intranasally</term>
<term>Kurata</term>
<term>Lethal lung infection</term>
<term>Lethal pneumonia</term>
<term>Lethal virus challenge</term>
<term>Lung wash</term>
<term>Mdck</term>
<term>Mdck cells</term>
<term>Mice vaccinated</term>
<term>Microparticles</term>
<term>Mouse</term>
<term>Mucosal</term>
<term>Nasal</term>
<term>Nasal cavity</term>
<term>Nasal mucosa</term>
<term>Nasal vaccination</term>
<term>Nasal vaccine</term>
<term>Nasal wash</term>
<term>National institute</term>
<term>Neutralizing</term>
<term>Neutralizing activity</term>
<term>Other adjuvants</term>
<term>Plaque assay</term>
<term>Present study</term>
<term>Safe adjuvant</term>
<term>Subunit</term>
<term>Surf</term>
<term>Surf clam microparticles</term>
<term>Survival rates</term>
<term>Suzuki</term>
<term>Tamura</term>
<term>Time course</term>
<term>Titer</term>
<term>Toxin</term>
<term>Trace amount</term>
<term>Vaccinated</term>
<term>Vaccination</term>
<term>Vaccine</term>
<term>Vaccine tamura</term>
<term>Various adjuvants</term>
<term>Virol</term>
<term>Virus</term>
<term>Virus challenge</term>
<term>Virus infection</term>
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<front><div type="abstract" xml:lang="en">A safe and effective adjuvant is necessary to enhance mucosal immune responses for the development of an inactivated intranasal influenza vaccine. The present study demonstrated the effectiveness of surf clam microparticles (SMP) derived from natural surf clams as an adjuvant for an intranasal influenza vaccine. The adjuvant effect of SMP was examined when co‐administered intranasally with inactivated A/PR8 (H1N1) influenza virus hemagglutinin vaccine in BALB/c mice. Administration of the vaccine with SMP induced a high anti‐PR8 haemagglutinin (HA)‐specific immunoglobulin A (IgA) response in the nasal wash and immunoglobulin G (IgG) response in the serum, resulting in protection against both nasal‐restricted infection and lethal lung infection by A/PR8 virus. In addition, administration of SMP with A/Yamagata (H1N1), A/Beijing (H1N1), or A/Guizhou (H3N2) vaccine conferred complete protection against A/PR8 virus challenge in the nasal infection model, suggesting that SMP adjuvanted vaccine can confer cross‐protection against variant influenza viruses. The use of SMP is suggested as a new safe and effective mucosal adjuvant for nasal vaccination against influenza virus infection. J. Med. Virol. 78:954–963, 2006. © 2006 Wiley‐Liss, Inc.</div>
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<name sortKey="Hasegawa, Hideki" sort="Hasegawa, Hideki" uniqKey="Hasegawa H" first="Hideki" last="Hasegawa">Hideki Hasegawa</name>
<name sortKey="Hasegawa, Hideki" sort="Hasegawa, Hideki" uniqKey="Hasegawa H" first="Hideki" last="Hasegawa">Hideki Hasegawa</name>
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