PROTECTION AGAINST LETHAL SENDAI VIRUS-INFECTION BY INVIVO PRIMING OF VIRUS-SPECIFIC CYTOTOXIC LYMPHOCYTES-T WITH A FREE SYNTHETIC PEPTIDE

被引:345
作者
KAST, WM
ROUX, L
CURREN, J
BLOM, HJJ
VOORDOUW, AC
MELOEN, RH
KOLAKOFSKY, D
MELIEF, CJM
机构
[1] UNIV GENEVA, CH-1211 GENEVA 4, SWITZERLAND
[2] CENT VET INST, 8200 AB LELYSTAD, NETHERLANDS
关键词
IMMUNOLOGICAL MEMORY; VACCINATION;
D O I
10.1073/pnas.88.6.2283
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The only peptide of Sendai virus that is recognized by cytotoxic T lymphocytes (CTL) in B6 mice was found with (i) the use of recombinant vaccinia virus constructs containing separate genes of Sendai virus and (ii) a set of overlapping peptides completely spanning the identified nucleo-protein (NP) gene product. This immunodominant NP peptide is recognized by Sendai virus-specific CTL that are known to have therapeutic effects in vivo. By subcutaneous immunization, this peptide induced Sendai virus and NP peptide-specific CTL memory responses in vivo. Most importantly, mice that had been immunized with the peptide were protected against a lethal virus dose, indicating that viral peptides can be used as antiviral T-cell vaccines. The induction of T-cell memory by free peptide immunization potentially has wide applicability in biology and medicine, including protection against infectious disease.
引用
收藏
页码:2283 / 2287
页数:5
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