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Human parainfluenza virus type I (HPIV1) vaccine candidates designed by reverse genetics are attenuated and efficacious in African green monkeys
被引:35
作者:

Bartlett, EJ
论文数: 0 引用数: 0
h-index: 0
机构:
NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA

Amaro-Carambot, E
论文数: 0 引用数: 0
h-index: 0
机构:
NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA

Surman, SR
论文数: 0 引用数: 0
h-index: 0
机构:
NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA

Newman, JT
论文数: 0 引用数: 0
h-index: 0
机构:
NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA

Collins, PL
论文数: 0 引用数: 0
h-index: 0
机构:
NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA

Murphy, BR
论文数: 0 引用数: 0
h-index: 0
机构:
NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA

Skiadopoulos, MH
论文数: 0 引用数: 0
h-index: 0
机构:
NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA
机构:
[1] NIAID, Infect Dis Lab, Resp Viruses Sect, NIH, Bethesda, MD 20892 USA
来源:
关键词:
human parainfluenza virus;
attenuating mutations;
vaccine candidates;
non-human primate study;
D O I:
10.1016/j.vaccine.2005.04.035
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
A set of recombinant, live attenuated human parainfluenza virus type I (rHPIV1) vaccine candidates was evaluated for attenuation, immunogenicity, and protective efficacy in African green monkeys (AGMs). Temperature sensitive (ts) and non-ts attenuating (att) mutations in the P/C and L genes were introduced individually or in various combinations into rHPIV1, including the C-R84G and HNT553A mutations identified in the present work and the C-F170S, L-Y942A, and L-L992C mutations identified previously. The rHPIV1 vaccine candidates exhibited a spectrum of attenuation in AGMs. One genetically and phenotypically stable vaccine candidate, rC(R84G/F170S)L(Y942A/L992C), was attenuated and efficacious in AGMs and is a promising live attenuated intranasal HPIV I vaccine candidate suitable for clinical evaluation. Published by Elsevier Ltd.
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页码:4631 / 4646
页数:16
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