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In vivo immune selection of a Moloney murine leukemia virus-induced tumor results in the loss of viral- but not tumor-associated antigens.

作者信息

Jiang D, Flyer D C

机构信息

Department of Microbiology and Immunology, Pennsylvania State University College of Medicine, Hershey 17033.

出版信息

J Immunol. 1990 Nov 15;145(10):3502-6.

PMID:1700012
Abstract

A protocol of in vivo immune selection has been used to isolate a variant of the Moloney murine leukemia virus (MuLV)-induced tumor MBL-2. Characterization of the tumor variant indicated that selection resulted in the isolation of a cell which is incapable of producing infectious virus and no longer capable of synthesizing viral proteins. Although the failure to express viral Ag has rendered the variant tumor cells resistant to lysis by CTL specific for MuLV viral Ag, the variant tumor cells retained their susceptibility to lysis by CTL which appear to be directed against an MuLV-induced tumor-associated Ag. The data indicate that the expression of nonviral tumor-associated Ag by MBL-2 is not dependent upon continued viral gene expression.

摘要

相似文献

1
In vivo immune selection of a Moloney murine leukemia virus-induced tumor results in the loss of viral- but not tumor-associated antigens.
J Immunol. 1990 Nov 15;145(10):3502-6.
2
Immune response to Moloney murine leukemia virus nonviral, tumor-associated antigens fails to provide in vivo tumor protection.对莫洛尼鼠白血病病毒非病毒、肿瘤相关抗原的免疫反应无法在体内提供肿瘤保护。
J Immunol. 1992 Feb 1;148(3):974-80.
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The immune response to Moloney murine leukemia virus-induced tumors: induction of cytolytic T lymphocytes specific for both viral and tumor-associated antigens.对莫洛尼鼠白血病病毒诱导肿瘤的免疫反应:诱导针对病毒和肿瘤相关抗原的细胞毒性T淋巴细胞。
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Retrovirus-induced changes in major histocompatibility complex antigen expression influence susceptibility to lysis by cytotoxic T lymphocytes.逆转录病毒引起的主要组织相容性复合体抗原表达变化影响细胞毒性T淋巴细胞介导的裂解敏感性。
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In vitro studies of cell-mediated immunity to Moloney murine leukemia virus and Moloney leukemia-associated surface antigens.针对莫洛尼鼠白血病病毒和莫洛尼白血病相关表面抗原的细胞介导免疫的体外研究。
Cancer Res. 1979 Dec;39(12):4887-93.
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Virus-specific T cell response prevents lymphoma development in mice infected by intrathymic inoculation of Moloney leukaemia virus (M-MuLV).病毒特异性T细胞应答可预防经胸腺内接种莫洛尼白血病病毒(M-MuLV)感染的小鼠发生淋巴瘤。
Immunology. 1984 Jan;51(1):9-16.
7
Flow-microfluorometric monitoring of oligoclonal CD8+ T cell responses to an immunodominant Moloney leukemia virus-encoded epitope in vivo.体内寡克隆CD8 + T细胞对莫洛尼白血病病毒编码的免疫显性表位反应的流式微量荧光监测。
J Immunol. 1998 Feb 15;160(4):1659-65.
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Cell surface expression of cytotoxic T lymphocyte-defined, AKR/Gross leukemia virus-associated tumor antigens by normal AKR.H-2b splenic B cells.正常AKR.H-2b脾B细胞对细胞毒性T淋巴细胞定义的、AKR/格罗斯白血病病毒相关肿瘤抗原的细胞表面表达。
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Distinct proliferative T cell clonotypes are generated in response to a murine retrovirus-induced syngeneic T cell leukemia: viral gp70 antigen-specific MT4+ clones and Lyt-2+ cytolytic clones which recognize a tumor-specific cell surface antigen.针对小鼠逆转录病毒诱导的同基因T细胞白血病,会产生不同的增殖性T细胞克隆型:病毒gp70抗原特异性MT4 +克隆和识别肿瘤特异性细胞表面抗原的Lyt-2 +溶细胞克隆。
J Immunol. 1985 Jul;135(1):703-13.
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Cross-reacting antigens on L5178Y cells which serve as targets for cytotoxic T-lymphocyte lysis during establishment of the tumor dormant state.L5178Y细胞上的交叉反应抗原,在肿瘤休眠状态建立过程中作为细胞毒性T淋巴细胞裂解的靶标。
Cancer Res. 1982 Sep;42(9):3607-16.

引用本文的文献

1
An immunodominant Kb-restricted peptide from the p15E transmembrane protein of endogenous ecotropic murine leukemia virus (MuLV) AKR623 that restores susceptibility of a tumor line to anti-AKR/Gross MuLV cytotoxic T lymphocytes.一种来自内源性嗜亲性鼠白血病病毒(MuLV)AKR623的p15E跨膜蛋白的免疫显性Kb限制性肽,该肽可恢复肿瘤细胞系对抗AKR/格罗斯MuLV细胞毒性T淋巴细胞的敏感性。
J Virol. 1994 Feb;68(2):897-904. doi: 10.1128/JVI.68.2.897-904.1994.