Beauverger P, Buckland R, Wild F
Unité d'Immunologie et Stratégie Vaccinale, Institut Pasteur de Lyon, France.
J Virol Methods. 1993 Oct;44(2-3):199-210. doi: 10.1016/0166-0934(93)90055-v.
To advance our understanding of the immunobiology of measles virus (MV) infections, we have investigated the possibility of establishing cell lines constitutively expressing the individual MV antigens. In contrast to previously published studies, we show that it is possible to establish cell lines expressing high levels of fusion (F), nucleoprotein (NP) and matrix (M) MV proteins. Once cloned, the cell lines were stable with high levels of expression for more than six months. The size and cell distribution of the NP and F proteins were similar to those observed in MV- or vaccinia-MV recombinant-infected cells. In contrast, the distribution of the M protein, although being similar to that of MV-infected cells, differed from that of Vaccinia-M recombinant virus-infected cells. Preliminary results suggest that these cell lines will be useful tools for studying the contribution of individual MV antigens to the cell-mediated immune response to this virus.
为了增进我们对麻疹病毒(MV)感染免疫生物学的理解,我们研究了建立组成型表达单个MV抗原的细胞系的可能性。与先前发表的研究不同,我们发现有可能建立表达高水平融合(F)、核蛋白(NP)和基质(M)MV蛋白的细胞系。一旦克隆成功,这些细胞系在六个月以上的时间里表达稳定且水平较高。NP和F蛋白的大小及细胞分布与在MV或痘苗-MV重组病毒感染细胞中观察到的相似。相比之下,M蛋白的分布虽然与MV感染细胞的相似,但与痘苗-M重组病毒感染细胞的不同。初步结果表明,这些细胞系将成为研究单个MV抗原对该病毒细胞介导免疫反应作用的有用工具。