Newborn mice vaccination with BCG.HIVA²²² + MVA.HIVA enhances HIV-1-specific immune responses: influence of age and immunization routes.
Newborn mice vaccination with BCG.HIVA²²² + MVA.HIVA enhances HIV-1-specific immune responses: influence of age and immunization routes.
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DOI:
10.1155/2011/516219
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发表时间:
2011
影响因子:
--
通讯作者:
Joseph J
中科院分区:
文献类型:
--
作者:
Saubi N;Im EJ;Fernández-Lloris R;Gil O;Cardona PJ;Gatell JM;Hanke T;Joseph J
We have evaluated the influence of age and immunization routes for induction of HIV-1- and M. tuberculosis-specific immune responses after neonatal (7 days old) and adult (7 weeks old) BALB/c mice immunization with BCG.HIVA222 prime and MVA.HIVA boost. The specific HIV-1 cellular immune responses were analyzed in spleen cells. The body weight of the newborn mice was weekly recorded. The frequencies of HIV-specific CD8+ T cells producing IFN-γ were higher in adult mice vaccinated intradermally and lower in adult and newborn mice vaccinated subcutaneously. In all cases the IFN-γ production was significantly higher when mice were primed with BCG.HIVA222 compared with BCGwt. When the HIV-specific CTL activity was assessed, the frequencies of specific killing were higher in newborn mice than in adults. The prime-boost vaccination regimen which includes BCG.HIVA222 and MVA.HIVA was safe when inoculated to newborn mice. The administration of BCG.HIVA222 to newborn mice is safe and immunogenic and increased the HIV-specific responses induced by MVA.HIVA vaccine. It might be a good model for infant HIV and Tuberculosis bivalent vaccine.
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DOI:
10.1099/00221287-142-4-915
发表时间:
1996-04-01
期刊:
MICROBIOLOGY-UK
影响因子:
--
作者:
Andersson, SGE;Sharp, PM
通讯作者:
Sharp, PM
影响因子:
1.5
作者:
Lagranderie, M;Winter, N;Gheorghiu, M
通讯作者:
Gheorghiu, M
影响因子:
5.4
作者:
Ami, Y;Izumi, Y;Honda, M
通讯作者:
Honda, M
DOI:
10.1073/pnas.92.23.10693
发表时间:
1995-11-07
影响因子:
11.1
作者:
HONDA, M;MATSUO, K;YAMAZAKI, S
通讯作者:
YAMAZAKI, S
影响因子:
--
作者:
Joseph, Joan;Fernandez-Lloris, Raquel;Maria Gatell, Josep
通讯作者:
Maria Gatell, Josep