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本文引用的文献

1
New direct-acting antiviral agents for the treatment of hepatitis C virus infection and perspectives.新型直接作用抗病毒药物治疗丙型肝炎病毒感染及展望。
Gut. 2012 May;61 Suppl 1:i36-46. doi: 10.1136/gutjnl-2012-302144.
2
Biosafety aspects of modified vaccinia virus Ankara (MVA)-based vectors used for gene therapy or vaccination.基于改良安卡拉痘苗病毒(MVA)载体的基因治疗或疫苗接种的生物安全方面。
Vaccine. 2012 Mar 30;30(16):2623-32. doi: 10.1016/j.vaccine.2012.02.016. Epub 2012 Feb 17.
3
Cytosolic DNA triggers mitochondrial apoptosis via DNA damage signaling proteins independently of AIM2 and RNA polymerase III.细胞质 DNA 通过 DNA 损伤信号蛋白触发线粒体凋亡,而不依赖于 AIM2 和 RNA 聚合酶 III。
J Immunol. 2012 Jan 1;188(1):394-403. doi: 10.4049/jimmunol.1100523. Epub 2011 Dec 2.
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Tuberculosis vaccines: beyond bacille Calmette-Guerin.结核病疫苗:超越卡介苗。
Philos Trans R Soc Lond B Biol Sci. 2011 Oct 12;366(1579):2782-9. doi: 10.1098/rstb.2011.0097.
5
A poxvirus vaccine is safe, induces T-cell responses, and decreases viral load in patients with chronic hepatitis C.一种痘病毒疫苗是安全的,可诱导 T 细胞应答,并降低慢性丙型肝炎患者的病毒载量。
Gastroenterology. 2011 Sep;141(3):890-899.e1-4. doi: 10.1053/j.gastro.2011.06.009. Epub 2011 Jun 13.
6
Immunogenicity of the tuberculosis vaccine MVA85A is reduced by coadministration with EPI vaccines in a randomized controlled trial in Gambian infants.在冈比亚婴儿中进行的一项随机对照试验表明,与 EPI 疫苗同时接种结核疫苗 MVA85A 会降低其免疫原性。
Sci Transl Med. 2011 Jun 22;3(88):88ra56. doi: 10.1126/scitranslmed.3002461.
7
Telaprevir for previously untreated chronic hepatitis C virus infection.替拉瑞韦治疗初治慢性丙型肝炎病毒感染。
N Engl J Med. 2011 Jun 23;364(25):2405-16. doi: 10.1056/NEJMoa1012912.
8
Dendritic cells exposed to MVA-based HIV-1 vaccine induce highly functional HIV-1-specific CD8(+) T cell responses in HIV-1-infected individuals.树突状细胞暴露于基于 MVA 的 HIV-1 疫苗可诱导 HIV-1 感染个体中具有高度功能性的 HIV-1 特异性 CD8(+) T 细胞应答。
PLoS One. 2011;6(5):e19644. doi: 10.1371/journal.pone.0019644. Epub 2011 May 18.
9
Boceprevir for untreated chronic HCV genotype 1 infection.博赛泼维用于治疗未经治疗的慢性 HCV 基因 1 型感染。
N Engl J Med. 2011 Mar 31;364(13):1195-206. doi: 10.1056/NEJMoa1010494.
10
Interplay between modified vaccinia virus Ankara and dendritic cells: phenotypic and functional maturation of bystander dendritic cells.安卡拉改良痘苗病毒与树突状细胞的相互作用:旁观者树突状细胞的表型和功能成熟。
J Virol. 2011 Jun;85(11):5532-45. doi: 10.1128/JVI.02267-10. Epub 2011 Mar 16.

基于 MVA 的疫苗治疗慢性传染病的治疗性疫苗接种:当前的临床进展。

Therapeutic vaccination to treat chronic infectious diseases: current clinical developments using MVA-based vaccines.

机构信息

Transgene, Department of Infectious Diseases, Centre d'Infectiologie, Lyon, France.

出版信息

Hum Vaccin Immunother. 2012 Dec 1;8(12):1746-57. doi: 10.4161/hv.21689. Epub 2012 Aug 16.

DOI:10.4161/hv.21689
PMID:22894957
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3656061/
Abstract

A famous milestone in the vaccine field has been the first successful vaccination against smallpox, in 1798, by Edward Jenner. Using the vaccinia cowpox virus, Jenner was able to protect vaccinees from variola or smallpox. The Modified Virus Ankara (MVA) poxvirus strain has been one of the vaccines subsequently developed to prevent smallpox infection and was selected by the US government in their Biodefense strategy. Progress in molecular biology and immunology associated with MVA infection has led to the development of MVA as vaccine platform, both in the field of preventive and therapeutic vaccines. This later class of therapeutics has witnessed growing interest that has translated into an increasing number of vaccine candidates reaching the clinics. Among those, MVA-based therapeutic vaccines have addressed four major chronic infections including viral hepatitis, AIDS, human papillomavirus-linked pathologies and tuberculosis. Clinical trials encompass phase 1 and 2 and have started to show significant results and promises.

摘要

疫苗领域的一个重要里程碑是 1798 年爱德华·詹纳(Edward Jenner)首次成功接种牛痘疫苗以预防天花。詹纳使用牛痘病毒(vaccinia cowpox virus)成功地使疫苗接种者免受天花或天花的侵害。随后开发的预防天花感染的疫苗之一是改良安卡拉病毒(Modified Virus Ankara,MVA)痘苗病毒株,美国政府在其生物防御策略中选择了该疫苗。与 MVA 感染相关的分子生物学和免疫学的进展导致了 MVA 作为疫苗平台的发展,无论是在预防性疫苗还是治疗性疫苗领域。这类治疗方法的兴趣日益浓厚,越来越多的疫苗候选者进入临床阶段。其中,基于 MVA 的治疗性疫苗针对包括病毒性肝炎、艾滋病、人乳头瘤病毒相关疾病和结核病在内的四大慢性感染。临床试验包括 1 期和 2 期,已经开始显示出显著的结果和前景。