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Takeshi Kurata

Researcher at Centers for Disease Control and Prevention

Publications -  39
Citations -  2487

Takeshi Kurata is an academic researcher from Centers for Disease Control and Prevention. The author has contributed to research in topics: Vaccination & Virus. The author has an hindex of 27, co-authored 39 publications receiving 2444 citations. Previous affiliations of Takeshi Kurata include University of Tokyo.

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Protection against influenza virus infection by vaccine inoculated intranasally with cholera toxin B subunit.

TL;DR: The results suggest that either CT or CTB could be used as a potent adjuvant to induce protective secretory antibodies by nasal vaccination against pathogens impinging on respiratory mucosa.
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Isolation and characterization of mouse nasal-associated lymphoid tissue

TL;DR: The results suggest that this method for isolation of mouse nasal-associated lymphoid tissue (NALT) can be successfully used for investigating cellular dynamics of mucosal immunology in the upper respiratory tract.
Journal Article

Cross-protection against influenza virus infection afforded by trivalent inactivated vaccines inoculated intranasally with cholera toxin B subunit.

TL;DR: In mice immunized intranasally with a nasal site-restricted volume of inactivated vaccines together with cholera toxin B subunit (CTB) as an adjuvant, nasal inoculation of trivalent vaccines with CTB provides cross-protection against a broader range of viruses than does the current parenteral vaccination.
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Synergistic action of cholera toxin B subunit (and Escherichia coli heat-labile toxin B subunit) and a trace amount of cholera whole toxin as an adjuvant for nasal influenza vaccine.

TL;DR: Cholera toxin B subunit (CTB) and Escherichia coli heat-labile toxin (LTB) were examined for the adjuvant effect on antibody (Ab) response against influenza inactivated HA (haemagglutinin) vaccine in Balb/c mice as discussed by the authors.
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Cross-protection against influenza A virus infection by passively transferred respiratory tract IgA antibodies to different hemagglutinin molecules.

TL;DR: It is demonstrated that IgA antibodies to influenza A virus HA by themselves play a pivotal role in defence not only against homologous virus infection, but also against heterologous drift virus infection at the respiratory mucosa, the portal of entry for the viruses.