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登革病毒血清型特异性人CD4+ CD8-细胞毒性T细胞克隆对包膜蛋白的识别。

Recognition of envelope protein by dengue virus serotype-specific human CD4+ CD8- cytotoxic T-cell clones.

作者信息

Livingston P G, Kurane I, Lai C J, Bray M, Ennis F A

机构信息

Department of Medicine, University of Massachusetts Medical Center, Worcester 01655.

出版信息

J Virol. 1994 May;68(5):3283-8. doi: 10.1128/JVI.68.5.3283-3288.1994.

Abstract

We analyzed dengue virus-specific CD4+ CD8- cytotoxic T lymphocytes (CTL) at the clonal level to further understand their role in dengue virus infections. Stimulation of peripheral blood mononuclear cells from two dengue virus type 4 (D4V)-immune donors with live D4V or noninfectious D4V antigen generated 17 HLA class II-restricted CD4+ CTL capable of specific lysis of dengue virus antigen-treated autologous lymphoblastoid cell lines. Thirteen clones were D4V specific, three clones were cross-reactive for D2V and D4V, and one clone was cross-reactive for D1V, D3V, and D4V. Antigen recognition by six D4V-specific clones and three D2V- and D4V-cross-reactive clones was restricted by HLA-DR7. Five D4V-specific CD4+ CTL clones lysed autologous lymphoblastoid cell lines infected with a dengue virus-vaccinia virus recombinant containing the E gene of D4V, whereas three serotype-cross-reactive CTL clones did not. These results indicate that E-specific clones are serotype specific and HLA-DR7 restricted in these two donors and suggest that a common epitope on E protein may be recognized. E protein-specific CD4+ CTL may be important mediators of virus clearance especially during reinfection with the same serotype as that in primary infection by providing help for virus-specific antibody production and lysis of virus-infected cells.

摘要

我们在克隆水平分析了登革病毒特异性CD4+ CD8-细胞毒性T淋巴细胞(CTL),以进一步了解它们在登革病毒感染中的作用。用活的D4V或无感染性的D4V抗原刺激两名对登革病毒4型(D4V)免疫的供体的外周血单个核细胞,产生了17个HLA II类限制性CD4+ CTL,它们能够特异性裂解经登革病毒抗原处理的自体淋巴母细胞系。13个克隆是D4V特异性的,3个克隆对D2V和D4V具有交叉反应性,1个克隆对D1V、D3V和D4V具有交叉反应性。6个D4V特异性克隆和3个D2V与D4V交叉反应性克隆的抗原识别受HLA-DR7限制。5个D4V特异性CD4+ CTL克隆裂解了感染了含有D4V E基因的登革病毒-痘苗病毒重组体的自体淋巴母细胞系,而3个血清型交叉反应性CTL克隆则没有。这些结果表明,在这两名供体中,E特异性克隆具有血清型特异性且受HLA-DR7限制,并提示可能识别E蛋白上的一个共同表位。E蛋白特异性CD4+ CTL可能是病毒清除的重要介质,特别是在再次感染与初次感染相同血清型的病毒时,通过为病毒特异性抗体产生和裂解病毒感染细胞提供帮助。

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本文引用的文献

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Research on dengue during World War II.第二次世界大战期间关于登革热的研究。
Am J Trop Med Hyg. 1952 Jan;1(1):30-50. doi: 10.4269/ajtmh.1952.1.30.

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