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本文引用的文献

1
Critical role of CD4 T cells and IFNγ signaling in antibody-mediated resistance to Zika virus infection.CD4 T 细胞和 IFNγ 信号通路在抗体介导的抗寨卡病毒感染中的关键作用。
Nat Commun. 2018 Aug 7;9(1):3136. doi: 10.1038/s41467-018-05519-4.
2
Zika Virus Vaccine: Progress and Challenges.寨卡病毒疫苗:进展与挑战。
Cell Host Microbe. 2018 Jul 11;24(1):12-17. doi: 10.1016/j.chom.2018.05.021. Epub 2018 Jun 28.
3
serocomplex cross-reactive immunity is protective by activating heterologous memory CD4 T cells.血清复合物交叉反应性免疫通过激活异源记忆 CD4 T 细胞起到保护作用。
Sci Adv. 2018 Jul 4;4(7):eaar4297. doi: 10.1126/sciadv.aar4297. eCollection 2018 Jul.
4
Structural Influence on the Dominance of Virus-Specific CD4 T Cell Epitopes in Zika Virus Infection.寨卡病毒感染中病毒特异性CD4 T细胞表位优势的结构影响
Front Immunol. 2018 May 30;9:1196. doi: 10.3389/fimmu.2018.01196. eCollection 2018.
5
Correlates of adjuvanticity: A review on adjuvants in licensed vaccines.佐剂的相关性:已上市疫苗中的佐剂概述。
Semin Immunol. 2018 Oct;39:14-21. doi: 10.1016/j.smim.2018.05.001. Epub 2018 May 23.
6
T cell immunity to Zika virus targets immunodominant epitopes that show cross-reactivity with other Flaviviruses.T 细胞对寨卡病毒的免疫反应针对免疫显性表位,这些表位与其他黄病毒显示交叉反应。
Sci Rep. 2018 Jan 12;8(1):672. doi: 10.1038/s41598-017-18781-1.
7
Prior Dengue Virus Exposure Shapes T Cell Immunity to Zika Virus in Humans.先前登革热病毒感染会影响人体对寨卡病毒的 T 细胞免疫反应。
J Virol. 2017 Nov 30;91(24). doi: 10.1128/JVI.01469-17. Print 2017 Dec 15.
8
Protein structure shapes immunodominance in the CD4 T cell response to yellow fever vaccination.蛋白结构决定黄热病疫苗接种后 CD4 T 细胞免疫优势。
Sci Rep. 2017 Aug 21;7(1):8907. doi: 10.1038/s41598-017-09331-w.
9
Structural Basis for CD4+ T Cell Epitope Dominance in Arbo-Flavivirus Envelope Proteins: A Meta-Analysis.虫媒黄病毒包膜蛋白中CD4 + T细胞表位优势的结构基础:一项荟萃分析
Viral Immunol. 2017 Sep;30(7):479-489. doi: 10.1089/vim.2017.0008. Epub 2017 Jun 14.
10
Recent advances in human flavivirus vaccines.人类黄病毒疫苗的最新进展。
Curr Opin Virol. 2017 Apr;23:95-101. doi: 10.1016/j.coviro.2017.04.002. Epub 2017 May 6.

CD4 T 细胞对黄病毒的反应。

CD4 T cell responses to flaviviruses.

机构信息

Center for Virology, Medical University of Vienna, Vienna, Austria.

Center for Virology, Medical University of Vienna, Vienna, Austria.

出版信息

J Clin Virol. 2018 Nov;108:126-131. doi: 10.1016/j.jcv.2018.09.020. Epub 2018 Oct 3.

DOI:10.1016/j.jcv.2018.09.020
PMID:30312909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7611868/
Abstract

Flaviviruses pose an increasing threat to global health with their potential to cause severe disease in millions of people. Protective and long-lived immunity is closely linked to the generation of CD4 T cells, which provide B cell help and support high affinity neutralizing antibody responses. Research performed during the last years revealed important new insights into the antigen specificities and diverse effector functions of CD4 T cell responses to flaviviruses. Moreover, the identification of mechanisms involved in the regulation of T cell specificity and function provides significant advances in our understanding of how durable protective immunity is established. Here, we summarize what is known about human CD4 T cell responses to flaviviruses, with a special emphasis on CD4 T cells that provide direct help to B cells producing neutralizing and protective antibodies. We review recent progress in the identification of epitope sites in the context of the atomic structures of flavivirus proteins and highlight specific influences that shape the human CD4 T cell response in the context of infection or vaccination. Finally, we discuss challenges facing vaccine efforts to generate appropriate CD4 T cell responses, as well as recent strategies to enhance T cell-mediated antibody responses.

摘要

黄病毒对全球健康构成的威胁日益增加,它们有可能导致数百万人患上严重疾病。保护性和持久的免疫与 CD4 T 细胞的产生密切相关,CD4 T 细胞为 B 细胞提供帮助,并支持高亲和力中和抗体反应。在过去几年中进行的研究揭示了有关 CD4 T 细胞对黄病毒反应的抗原特异性和多种效应功能的重要新见解。此外,鉴定参与 T 细胞特异性和功能调节的机制为我们理解如何建立持久的保护性免疫提供了重要进展。在这里,我们总结了已知的人类 CD4 T 细胞对黄病毒的反应,特别强调了为产生中和和保护性抗体的 B 细胞提供直接帮助的 CD4 T 细胞。我们回顾了在黄病毒蛋白的原子结构背景下鉴定表位位点的最新进展,并强调了在感染或接种疫苗的背景下塑造人类 CD4 T 细胞反应的具体影响。最后,我们讨论了疫苗接种努力面临的挑战,以产生适当的 CD4 T 细胞反应,以及最近增强 T 细胞介导的抗体反应的策略。