Omar A R, Schat K A
Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.
Immunology. 1997 Apr;90(4):579-85. doi: 10.1046/j.1365-2567.1997.00211.x.
Previously we have reported that reticuloendotheliosis virus (REV)-transformed cell lines expressing Marek's disease virus (MDV) genes pp38, meq or gB were lysed by syngeneic MDV-specific splenocytes from major histocompatibility complex (MHC):B9B19 and MHC:B1B21 chickens. In contrast, REV-transformed cell lines expressing the MDV gene ICP4 were only lysed by syngeneic MDV-specific splenocytes from MHC:B21B21 chickens. In this study we report that this syngeneic cell-mediated immune response is induced by cytotoxic T lymphocytes (CTL). Splenocytes from MDV vaccine strain, SB-1 inoculated MHC:B19B19 and MHC:B21B21 chickens, depleted for CD4+, CD8+, TCR gamma delta +, TCR alpha beta 1+ and/or TCR alpha beta 2+ cells, were used as effector cells in chromium-release assays. Effector cells depleted of CD8+ or TCR alpha beta 1+, but not TCR gamma delta + or TCR alpha beta 2+, markedly reduced the MDV-specific release. Depletion of CD4+ effector cells did not influence the specific release significantly. This is the first report on identification of virus-specific CD8+ CTL in chickens inoculated with a non-oncogenic vaccine strain of MDV.
此前我们曾报道,表达马立克氏病病毒(MDV)基因pp38、meq或gB的网状内皮组织增殖病病毒(REV)转化细胞系,被来自主要组织相容性复合体(MHC):B9B19和MHC:B1B21鸡的同基因MDV特异性脾细胞裂解。相比之下,表达MDV基因ICP4的REV转化细胞系仅被来自MHC:B21B21鸡的同基因MDV特异性脾细胞裂解。在本研究中,我们报道这种同基因细胞介导的免疫反应是由细胞毒性T淋巴细胞(CTL)诱导的。来自接种MDV疫苗株SB-1的MHC:B19B19和MHC:B21B21鸡的脾细胞,经去除CD4 +、CD8 +、TCRγδ +、TCRαβ1 +和/或TCRαβ2 +细胞后,用作铬释放试验中的效应细胞。去除CD8 +或TCRαβ1 +而非TCRγδ +或TCRαβ2 +的效应细胞,显著降低了MDV特异性释放。去除CD4 +效应细胞对特异性释放没有显著影响。这是关于在接种非致瘤性MDV疫苗株的鸡中鉴定病毒特异性CD8 + CTL的首次报道。