Dave V P, Allan J E, Slobod K S, Smith F S, Ryan K W, Takimoto T, Power U F, Portner A, Hurwitz J L
Department of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee 38101.
Virology. 1994 Mar;199(2):376-83. doi: 10.1006/viro.1994.1135.
To obtain information relevant to vaccination against human parainfluenza virus type 1 (hPIV-1), cytotoxic T-lymphocyte (CTL) responses to individual viral components were tested. The CD8-positive T-cell fraction was first enriched from human, adult PBL and grown for several passages in the presence of hPIV-1-infected stimulator cells. T-cell lines were then tested for CTL activity toward hPIV-1 and toward the related viruses hPIV-3 and Sendai virus (the murine parainfluenza type 1 virus). All tested cultures which responded to hPIV-1 also responded to hPIV-3 and Sendai virus, demonstrating sequence conservation between all three viruses among major antigenic determinants for CTL. Specificity for particular viral components was defined using recombinant vaccinia viruses expressing individual proteins from either mouse or human parainfluenza type 1 viruses. Strong CTL responses toward hemagglutinin-neuraminidase, phosphoprotein, and nucleoprotein (NP) were demonstrated. The testing of vaccinia constructs expressing truncated proteins then showed that there were multiple CTL determinants within NP. Several T-cell lines from one donor recognized an NP peptide (amino acids 321-336) conserved between the hPIV-1 and Sendai virus. In total, the results demonstrated that the human CTL response is directed to multiple determinants within several distinct hPIV-1 proteins.
为获取与1型人副流感病毒(hPIV-1)疫苗接种相关的信息,检测了细胞毒性T淋巴细胞(CTL)对单个病毒成分的反应。首先从成人外周血淋巴细胞(PBL)中富集CD8阳性T细胞组分,并在感染hPIV-1的刺激细胞存在下培养数代。然后检测T细胞系对hPIV-1、相关病毒hPIV-3和仙台病毒(鼠1型副流感病毒)的CTL活性。所有对hPIV-1有反应的测试培养物也对hPIV-3和仙台病毒有反应,表明这三种病毒在CTL主要抗原决定簇之间存在序列保守性。使用表达来自小鼠或人1型副流感病毒的单个蛋白质的重组痘苗病毒定义对特定病毒成分的特异性。结果表明对血凝素神经氨酸酶、磷蛋白和核蛋白(NP)有强烈的CTL反应。对表达截短蛋白的痘苗构建体的检测表明NP内有多个CTL决定簇。来自一名供体的几个T细胞系识别hPIV-1和仙台病毒之间保守的NP肽(氨基酸321-336)。总体而言,结果表明人类CTL反应针对几种不同hPIV-1蛋白内的多个决定簇。