Immunogenicity of an inactivated adjuvanted whole‐virion influenza A (H5N1, NIBRG‐14) vaccine administered by intramuscular or subcutaneous injection
Identifieur interne : 000216 ( Istex/Checkpoint ); précédent : 000215; suivant : 000217Immunogenicity of an inactivated adjuvanted whole‐virion influenza A (H5N1, NIBRG‐14) vaccine administered by intramuscular or subcutaneous injection
Auteurs : Daisuke Ikeno ; Kazuhiko Kimachi ; Yoichiro Kino ; Seiichi Harada ; Kayo Yoshida ; Shinji Tochihara ; Shigeyuki Itamura ; Takato Odagiri ; Masato Tashiro ; Kenji Okada ; Chiaki Miyazaki ; Kohji Ueda [Japon]Source :
- Microbiology and Immunology [ 0385-5600 ] ; 2010-02.
English descriptors
- Teeft :
- Adjuvant, Administration route, Administration routes, Adverse events, Alum, Alum adjuvant, Aluminum hydroxide, Antibody titer, Antibody titers, Blackwell publishing asia, Cell culture, Chmp criteria, Clinical study, Clinical trial, Dos, Erythema, European union chmp criteria, Healthy adults, Healthy japanese, Horse erythrocytes, Immune, Immune response, Immune responses, Immunogenicity, Induration pruritus pyrexia headache malaise chill diarrhea, Infectious diseases, Injection, Kawabe kyokushi, Kikuchi research center, Microbiol immunol, More immunogenic, National institute, Pain erythema, Pandemic, Pruritus, Randomised trial, Research institute, Seasonal vaccines, Second dose, Second doses, Seroconversion, Seroconversion factor, Seroconversion factor seropositivity seroconversion, Serum samples, Statistical analysis, Subcutaneous injection, Titer, Vaccination, Vaccine, Whole virion vaccine.
Abstract
The immunogenicity and safety profile of an inactivated whole‐virion influenza A (H5N1, NIBRG‐14) vaccine with alum adjuvant that was administered by IM or SC injection in a phase I clinical study involving 120 healthy Japanese men aged 20–40 years is described. The serological response of the IM group was stronger than that of the SC group. Local adverse events were less severe with IM injection than with SC injection, while similar systemic adverse events were seen in both groups. These results indicate that, when administering an inactivated whole virion vaccine with alum adjuvant for pandemic influenza, IM injection may achieve better immunogenicity and safety than SC injection.
Url:
DOI: 10.1111/j.1348-0421.2009.00191.x
Affiliations:
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ISTEX:D8C94B5A650C9D8C073F65103101A6486AC3A45ELe document en format XML
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<front><div type="abstract" xml:lang="en">The immunogenicity and safety profile of an inactivated whole‐virion influenza A (H5N1, NIBRG‐14) vaccine with alum adjuvant that was administered by IM or SC injection in a phase I clinical study involving 120 healthy Japanese men aged 20–40 years is described. The serological response of the IM group was stronger than that of the SC group. Local adverse events were less severe with IM injection than with SC injection, while similar systemic adverse events were seen in both groups. These results indicate that, when administering an inactivated whole virion vaccine with alum adjuvant for pandemic influenza, IM injection may achieve better immunogenicity and safety than SC injection.</div>
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