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1
Dengue virus-specific human CD4+ T-lymphocyte responses in a recipient of an experimental live-attenuated dengue virus type 1 vaccine: bulk culture proliferation, clonal analysis, and precursor frequency determination.一名实验性1型登革热病毒减毒活疫苗接种者体内的登革热病毒特异性人类CD4+ T淋巴细胞反应:大量培养增殖、克隆分析及前体频率测定
J Virol. 1993 Oct;67(10):5962-7. doi: 10.1128/JVI.67.10.5962-5967.1993.
2
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J Virol. 1996 Jan;70(1):141-7. doi: 10.1128/JVI.70.1.141-147.1996.
3
Dengue virus-specific, human CD4+ cytotoxic T lymphocytes generated in short-term culture.在短期培养中产生的登革病毒特异性人类CD4 + 细胞毒性T淋巴细胞。
Viral Immunol. 1993 Summer;6(2):143-51. doi: 10.1089/vim.1993.6.143.
4
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J Exp Med. 1989 Sep 1;170(3):763-75. doi: 10.1084/jem.170.3.763.
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Recognition of envelope protein by dengue virus serotype-specific human CD4+ CD8- cytotoxic T-cell clones.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。
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Identification of amino acids involved in recognition by dengue virus NS3-specific, HLA-DR15-restricted cytotoxic CD4+ T-cell clones.登革病毒NS3特异性、HLA-DR15限制性细胞毒性CD4+ T细胞克隆识别中涉及的氨基酸鉴定。
J Virol. 1996 May;70(5):3108-17. doi: 10.1128/JVI.70.5.3108-3117.1996.
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Dengue virus-specific, human CD4+ CD8- cytotoxic T-cell clones: multiple patterns of virus cross-reactivity recognized by NS3-specific T-cell clones.登革病毒特异性人类CD4+ CD8-细胞毒性T细胞克隆:NS3特异性T细胞克隆识别的多种病毒交叉反应模式
J Virol. 1991 Apr;65(4):1823-8. doi: 10.1128/JVI.65.4.1823-1828.1991.
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Definition of the region on NS3 which contains multiple epitopes recognized by dengue virus serotype-cross-reactive and flavivirus-cross-reactive, HLA-DPw2-restricted CD4+ T cell clones.NS3上包含多个表位的区域的定义,这些表位可被登革病毒血清型交叉反应性和黄病毒交叉反应性、HLA-DPw2限制性CD4+ T细胞克隆识别。
J Gen Virol. 1998 Apr;79 ( Pt 4):697-704. doi: 10.1099/0022-1317-79-4-697.
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Recognition of dengue virus NS1-NS2a proteins by human CD4+ cytotoxic T lymphocyte clones.人CD4+细胞毒性T淋巴细胞克隆对登革病毒NS1-NS2a蛋白的识别。
Virology. 1997 Aug 4;234(2):383-6. doi: 10.1006/viro.1997.8648.
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A single nine-amino acid peptide induces virus-specific, CD8+ human cytotoxic T lymphocyte clones of heterogeneous serotype specificities.一种单一的九氨基酸肽可诱导出具有不同血清型特异性的病毒特异性CD8⁺人细胞毒性T淋巴细胞克隆。
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Dendritic Cell Targeting Using a DNA Vaccine Induces Specific Antibodies and CD4 T Cells to the Dengue Virus Envelope Protein Domain III.树突状细胞靶向使用 DNA 疫苗诱导针对登革病毒包膜蛋白结构域 III 的特异性抗体和 CD4 T 细胞。
Front Immunol. 2019 Jan 29;10:59. doi: 10.3389/fimmu.2019.00059. eCollection 2019.
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Differential targeting of viral components by CD4+ versus CD8+ T lymphocytes in dengue virus infection.CD4+ 与 CD8+ T 淋巴细胞在登革病毒感染中对病毒成分的差异靶向作用。
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J Virol. 2012 Sep;86(17):9233-43. doi: 10.1128/JVI.06325-11. Epub 2012 Jun 20.
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T-cell responses to dengue virus in humans.人类对登革病毒的T细胞反应。
Trop Med Health. 2011 Dec;39(4 Suppl):45-51. doi: 10.2149/tmh.2011-S09. Epub 2011 Dec 1.
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The necessity and quandaries of dengue vaccine development.登革热疫苗研发的必要性与困境
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Memory CD8+ T cells from naturally acquired primary dengue virus infection are highly cross-reactive.从自然获得的初次登革热病毒感染中提取的记忆 CD8+ T 细胞具有高度的交叉反应性。
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Anamnestic immune response to dengue and decreased severity of yellow Fever.对登革热的回忆性免疫反应与黄热病严重程度降低
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Genome-wide screening of human T-cell epitopes in influenza A virus reveals a broad spectrum of CD4(+) T-cell responses to internal proteins, hemagglutinins, and neuraminidases.全基因组筛选甲型流感病毒的人类 T 细胞表位揭示了针对内部蛋白、血凝素和神经氨酸酶的广谱 CD4(+) T 细胞反应。
Hum Immunol. 2009 Sep;70(9):711-21. doi: 10.1016/j.humimm.2009.06.004. Epub 2009 Jun 11.
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West Nile virus-specific CD4 T cells exhibit direct antiviral cytokine secretion and cytotoxicity and are sufficient for antiviral protection.西尼罗河病毒特异性CD4 T细胞表现出直接的抗病毒细胞因子分泌和细胞毒性,并且足以提供抗病毒保护。
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本文引用的文献

1
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.
2
Dengue virus-specific, human CD4+ cytotoxic T lymphocytes generated in short-term culture.在短期培养中产生的登革病毒特异性人类CD4 + 细胞毒性T淋巴细胞。
Viral Immunol. 1993 Summer;6(2):143-51. doi: 10.1089/vim.1993.6.143.
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Limiting dilution assays for the determination of immunocompetent cell frequencies. I. Data analysis.用于确定免疫活性细胞频率的有限稀释分析。I. 数据分析。
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4
Lysis of dengue virus-infected cells by natural cell-mediated cytotoxicity and antibody-dependent cell-mediated cytotoxicity.通过自然细胞介导的细胞毒性和抗体依赖性细胞介导的细胞毒性对登革病毒感染细胞进行裂解。
J Virol. 1984 Oct;52(1):223-30. doi: 10.1128/JVI.52.1.223-230.1984.
5
Isolation of mononuclear cells and granulocytes from human blood. Isolation of monuclear cells by one centrifugation, and of granulocytes by combining centrifugation and sedimentation at 1 g.从人血中分离单核细胞和粒细胞。通过一次离心分离单核细胞,通过离心和1g沉降相结合的方法分离粒细胞。
Scand J Clin Lab Invest Suppl. 1968;97:77-89.
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Lack of attenuation of a candidate dengue 1 vaccine (45AZ5) in human volunteers.
Am J Trop Med Hyg. 1987 Mar;36(2):435-42. doi: 10.4269/ajtmh.1987.36.435.
7
Limiting dilution analysis of the human T cell response to mycobacterial antigens from BCG vaccinated individuals and leprosy patients.对卡介苗接种个体和麻风病患者的分枝杆菌抗原的人T细胞反应的有限稀释分析。
Clin Exp Immunol. 1987 Jun;68(3):510-20.
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Pathogenesis of dengue: challenges to molecular biology.登革热的发病机制:对分子生物学的挑战
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9
Human cytomegalovirus-specific cytotoxic T cells: their precursor frequency and stage specificity.人巨细胞病毒特异性细胞毒性T细胞:其前体频率和阶段特异性。
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Human T cell responses to dengue virus antigens. Proliferative responses and interferon gamma production.人类T细胞对登革病毒抗原的反应。增殖反应和γ干扰素产生。
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一名实验性1型登革热病毒减毒活疫苗接种者体内的登革热病毒特异性人类CD4+ T淋巴细胞反应:大量培养增殖、克隆分析及前体频率测定

Dengue virus-specific human CD4+ T-lymphocyte responses in a recipient of an experimental live-attenuated dengue virus type 1 vaccine: bulk culture proliferation, clonal analysis, and precursor frequency determination.

作者信息

Green S, Kurane I, Edelman R, Tacket C O, Eckels K H, Vaughn D W, Hoke C H, Ennis F A

机构信息

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

出版信息

J Virol. 1993 Oct;67(10):5962-7. doi: 10.1128/JVI.67.10.5962-5967.1993.

DOI:10.1128/JVI.67.10.5962-5967.1993
PMID:8371350
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC238017/
Abstract

We analyzed the CD4+ T-lymphocyte responses to dengue, West Nile, and yellow fever viruses 4 months after immunization of a volunteer with an experimental live-attenuated dengue virus type 1 vaccine (DEN-1 45AZ5). We examined bulk culture proliferation to noninfectious antigens, determined the precursor frequency of specific CD4+ T cells by limiting dilution, and established and analyzed CD4+ T-cell clones. Bulk culture proliferation was predominantly dengue virus type 1 specific with a lesser degree of cross-reactive responses to other dengue virus serotypes, West Nile virus, and yellow fever virus. Precursor frequency determination by limiting dilution in the presence of noninfectious dengue virus antigens revealed a frequency of antigen-reactive cells of 1 in 1,686 peripheral blood mononuclear cells (PBMC) for dengue virus type 1, 1 in 9,870 PBMC for dengue virus type 3, 1 in 14,053 PBMC for dengue virus type 2, and 1 in 17,690 PBMC for dengue virus type 4. Seventeen CD4+ T-cell clones were then established by using infectious dengue virus type 1 as antigen. Two patterns of dengue virus specificity were found in these clones. Thirteen clones were dengue virus type 1 specific, and four clones recognized both dengue virus types 1 and 3. Analysis of human leukocyte antigen (HLA) restriction revealed that five clones are HLA-DRw52 restricted, one clone is HLA-DP3 restricted, and one clone is HLA-DP4 restricted. These results indicate that in this individual, the CD4+ T-lymphocyte responses to immunization with live-attenuated dengue virus type 1 vaccine are predominantly serotype specific and suggest that a multivalent vaccine may be necessary to elicit strong serotype-cross-reactive CD4+ T-lymphocyte responses in such individuals.

摘要

我们在一名志愿者接种实验性1型减毒活登革病毒疫苗(DEN-1 45AZ5)4个月后,分析了其对登革病毒、西尼罗河病毒和黄热病毒的CD4+ T淋巴细胞反应。我们检测了对非感染性抗原的大量培养增殖情况,通过有限稀释法确定特异性CD4+ T细胞的前体频率,并建立和分析了CD4+ T细胞克隆。大量培养增殖主要是1型登革病毒特异性的,对其他登革病毒血清型、西尼罗河病毒和黄热病毒的交叉反应程度较低。在存在非感染性登革病毒抗原的情况下通过有限稀释法测定前体频率,结果显示1型登革病毒抗原反应性细胞在外周血单个核细胞(PBMC)中的频率为1/1686,3型登革病毒为1/9870 PBMC,2型登革病毒为1/14053 PBMC,4型登革病毒为1/17690 PBMC。然后以感染性1型登革病毒为抗原建立了17个CD4+ T细胞克隆。在这些克隆中发现了两种登革病毒特异性模式。13个克隆是1型登革病毒特异性的,4个克隆同时识别1型和3型登革病毒。对人类白细胞抗原(HLA)限制的分析表明,5个克隆受HLA-DRw52限制,1个克隆受HLA-DP3限制,1个克隆受HLA-DP4限制。这些结果表明,在该个体中,接种1型减毒活登革病毒疫苗后的CD4+ T淋巴细胞反应主要是血清型特异性的,并提示在此类个体中可能需要一种多价疫苗来引发强烈的血清型交叉反应性CD4+ T淋巴细胞反应。