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用病毒特异性细胞毒性T细胞对转染了马立克氏病病毒基因的网状内皮组织增殖病病毒转化细胞系进行同基因裂解。

Syngeneic lysis of reticuloendotheliosis virus-transformed cell lines transfected with Marek's disease virus genes by virus-specific cytotoxic T cells.

作者信息

Uni Z, Pratt W D, Miller M M, O'Connell P H, Schat K A

机构信息

Department of Avian and Aquatic Animal Medicine, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.

出版信息

Vet Immunol Immunopathol. 1994 Dec;44(1):57-69. doi: 10.1016/0165-2427(94)90169-4.

Abstract

Cell-mediated immune responses against Marek's disease virus (MDV) antigens were examined using reticuloendotheliosis virus (REV)-transformed cell lines of two haplotypes (B19B19 and B13B13). These cell lines were stably transfected with cloned fragments of MDV DNA resulting in the expression of the MDV-specific phosphoprotein pp38. Effector cells were obtained from P2a (B19B19) and S13 (B13B13) chickens at 7 days post inoculation with REV, oncogenic or attenuated serotype 1 MDV (JM-16/O and JM-16/A, respectively), serotype 2 MDV (SB-1), or herpesvirus of turkeys (HVT). Transfection of MDV genes did not influence the expression of Class I major histocompatibility complex antigens. The optimal effector to target cell ratio was determined to be 100:1. REV-sensitized effector cells lysed REV cell lines and REV cell lines transfected with MDV DNA in a syngeneic fashion. Effector cells from chickens inoculated with JM-16/O, JM-16/A, SB-1 or HVT lysed only the syngeneic, transfected cell lines, but not the parent REV cell lines. The percentage specific release caused by the MDV-sensitized effector cells was low, but statistically significant.

摘要

利用两种单倍型(B19B19和B13B13)的网状内皮组织增殖病病毒(REV)转化细胞系,检测了针对马立克氏病病毒(MDV)抗原的细胞介导免疫反应。这些细胞系用MDV DNA克隆片段进行稳定转染,导致MDV特异性磷蛋白pp38的表达。效应细胞在接种致癌或减毒1型MDV(分别为JM - 16/O和JM - 16/A)、2型MDV(SB - 1)或火鸡疱疹病毒(HVT)的REV后7天,从P2a(B19B19)和S13(B13B13)鸡中获得。MDV基因的转染不影响I类主要组织相容性复合体抗原的表达。确定最佳效应细胞与靶细胞比例为100:1。REV致敏的效应细胞以同基因方式裂解REV细胞系和用MDV DNA转染的REV细胞系。接种JM - 16/O、JM - 16/A、SB - 1或HVT的鸡的效应细胞仅裂解同基因的、转染的细胞系,而不裂解亲本REV细胞系。MDV致敏的效应细胞引起的特异性释放百分比很低,但具有统计学意义。

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