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Murine cell-mediated immune response recognizes an enterovirus group-specific antigen(s).鼠细胞介导的免疫反应识别一种肠道病毒属特异性抗原。
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2
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Evidence for a group-specific enteroviral antigen(s) recognized by human T cells.人类T细胞识别的组特异性肠道病毒抗原的证据。
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Coxsackievirus B1 infections are associated with the initiation of insulin-driven autoimmunity that progresses to type 1 diabetes.柯萨奇病毒 B1 感染与胰岛素驱动的自身免疫的启动有关,而后者会进展为 1 型糖尿病。
Diabetologia. 2018 May;61(5):1193-1202. doi: 10.1007/s00125-018-4561-y. Epub 2018 Feb 5.
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5'-Terminal deletions occur in coxsackievirus B3 during replication in murine hearts and cardiac myocyte cultures and correlate with encapsidation of negative-strand viral RNA.在柯萨奇病毒B3于小鼠心脏和心肌细胞培养物中复制期间会发生5'端缺失,且这与负链病毒RNA的包装相关。
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8
Analysis of the human T-cell response to picornaviruses: identification of T-cell epitopes close to B-cell epitopes in poliovirus.人类对小核糖核酸病毒的T细胞反应分析:脊髓灰质炎病毒中靠近B细胞表位的T细胞表位的鉴定
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Characterization of poliovirus-specific T lymphocytes in the peripheral blood of Sabin-vaccinated humans.脊髓灰质炎疫苗接种者外周血中脊髓灰质炎病毒特异性T淋巴细胞的特征分析
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10
Picornavirus-specific CD4+ T lymphocytes possessing cytolytic activity confer protection in the absence of prophylactic antibodies.具有细胞溶解活性的微小核糖核酸病毒特异性CD4 + T淋巴细胞在缺乏预防性抗体的情况下可提供保护。
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本文引用的文献

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Coxsackievirus B-3 myocarditis in Balb/c mice. Evidence for autoimmunity to myocyte antigens.Balb/c小鼠的柯萨奇B-3型病毒心肌炎。针对心肌细胞抗原的自身免疫证据。
Am J Pathol. 1984 Jul;116(1):21-9.
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Enterovirus type 71 infections: a varied clinical pattern sometimes mimicking paralytic poliomyelitis.肠道病毒71型感染:一种有时会模仿麻痹性脊髓灰质炎的多样临床模式。
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Complete nucleotide sequences of all three poliovirus serotype genomes. Implication for genetic relationship, gene function and antigenic determinants.所有三种脊髓灰质炎病毒血清型基因组的完整核苷酸序列。对遗传关系、基因功能和抗原决定簇的意义。
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Migration and cell recruiting activity of specifically sensitized lymphocytes in sponge matrix allografts.海绵基质同种异体移植物中特异性致敏淋巴细胞的迁移和细胞募集活性。
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Cross-reactive cytotoxic T cells to serologically distinct vesicular stomatitis virus.对血清学上不同的水疱性口炎病毒具有交叉反应性的细胞毒性T细胞。
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鼠细胞介导的免疫反应识别一种肠道病毒属特异性抗原。

Murine cell-mediated immune response recognizes an enterovirus group-specific antigen(s).

作者信息

Beck M A, Tracy S M

机构信息

Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha 68105-1065.

出版信息

J Virol. 1989 Oct;63(10):4148-56. doi: 10.1128/JVI.63.10.4148-4156.1989.

DOI:10.1128/JVI.63.10.4148-4156.1989
PMID:2476566
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC251028/
Abstract

Splenocytes taken from mice inoculated with coxsackievirus B3 (CVB3) (Nancy) developed an in vitro proliferative response against CVB3 antigen. This response could not be detected earlier than 8 days postinoculation but could be detected up to 28 days after exposure to CB3. CVB3-sensitized splenocytes responded not only to the CVB3 antigen but to other enteroviruses as well. This response was found to be enterovirus specific in that no response was detected to a non-enteroviral picornavirus, encephalomyocarditis virus, or to an unrelated influenza virus. The generation of a splenocyte population capable of responding to an enterovirus group antigen(s) was not limited to inoculation of mice with CVB3, as similar responses were generated when mice were inoculated with CVB2. Cell subset depletions revealed that the major cell type responding to the enterovirus group antigen(s) was the CD4+ T cell. Current evidence suggests that the group antigen(s) resides in the structural proteins of the virus, since spleen cells from mice inoculated with a UV-inactivated, highly purified preparation of CVB3 virions also responded in vitro against enteroviral antigens.

摘要

从接种柯萨奇病毒B3(CVB3)(南希株)的小鼠中获取的脾细胞,对CVB3抗原产生了体外增殖反应。这种反应在接种后8天之前无法检测到,但在接触CVB3后28天内都能检测到。CVB3致敏的脾细胞不仅对CVB3抗原产生反应,对其他肠道病毒也有反应。这种反应被发现具有肠道病毒特异性,因为对非肠道病毒的微小核糖核酸病毒、脑心肌炎病毒或无关的流感病毒未检测到反应。能够对肠道病毒组抗原产生反应的脾细胞群体的产生并不局限于用CVB3接种小鼠,当用CVB2接种小鼠时也会产生类似反应。细胞亚群耗竭显示,对肠道病毒组抗原产生反应的主要细胞类型是CD4 + T细胞。目前的证据表明,组抗原存在于病毒的结构蛋白中,因为接种紫外线灭活的、高度纯化的CVB3病毒粒子制剂的小鼠的脾细胞在体外也对肠道病毒抗原产生反应。