Terajima Masanori, Van Epps Heather L, Li Dexin, Leporati Anita M, Juhlin Sarah E, Mustonen Jukka, Vaheri Antti, Ennis Francis A
Center for Infectious Disease and Vaccine Research, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655, USA.
Virus Res. 2002 Mar 20;84(1-2):67-77. doi: 10.1016/s0168-1702(01)00416-6.
Puumala (PUU) virus causes a form of hemorrhagic fever with renal syndrome (HFRS), called nephropathia epidemica (NE), in Europe. HFRS is characterized by an increased capillary permeability, which we hypothesize is caused by hyperactivation of the host immune system, especially cellular immune responses. To identify cytotoxic T lymphocytes (CTLs) specific for the PUU virus from NE patients, we have made recombinant vaccinia viruses expressing PUU virus proteins, the nucleocapsid (N) and two surface glycoproteins, G1 and G2. Recombinant vaccinia viruses carrying the N or the first half of the G2 cDNA under the control of a strong synthetic promoter were made. To express G1 and the second half of the G2 proteins, however, we needed to use a T7 expression system, where the T7 RNA polymerase is produced from another recombinant vaccinia virus co-infecting the same cells. These recombinant vaccinia viruses were used to detect and clone PUU virus-specific CTLs from the peripheral blood mononuclear cells of NE patients. An HLA-A24-restricted CTL line recognizing the G2 protein was isolated and its 9-mer epitope was determined.
普马拉(PUU)病毒在欧洲引发一种肾综合征出血热(HFRS),称为流行性肾病(NE)。HFRS的特征是毛细血管通透性增加,我们推测这是由宿主免疫系统过度激活,尤其是细胞免疫反应引起的。为了从NE患者中鉴定出针对PUU病毒的细胞毒性T淋巴细胞(CTL),我们制备了表达PUU病毒蛋白、核衣壳(N)以及两种表面糖蛋白G1和G2的重组痘苗病毒。构建了在强合成启动子控制下携带N或G2 cDNA前半部分的重组痘苗病毒。然而,为了表达G1和G2蛋白的后半部分,我们需要使用T7表达系统,其中T7 RNA聚合酶由另一种共同感染同一细胞的重组痘苗病毒产生。这些重组痘苗病毒用于从NE患者的外周血单核细胞中检测和克隆PUU病毒特异性CTL。分离出了一条识别G2蛋白的HLA - A24限制性CTL系,并确定了其9肽表位。