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本文引用的文献

1
Murine immune responses to virus-like particle-associated pre- and postfusion forms of the respiratory syncytial virus F protein.小鼠对呼吸道合胞病毒F蛋白的病毒样颗粒相关融合前和融合后形式的免疫反应。
J Virol. 2015 Jul;89(13):6835-47. doi: 10.1128/JVI.00384-15. Epub 2015 Apr 22.
2
Zinc binding activity of human metapneumovirus M2-1 protein is indispensable for viral replication and pathogenesis in vivo.人偏肺病毒M2-1蛋白的锌结合活性对于病毒在体内的复制和致病机制必不可少。
J Virol. 2015 Jun;89(12):6391-405. doi: 10.1128/JVI.03488-14. Epub 2015 Apr 8.
3
HRA2pl peptide: a fusion inhibitor for human metapneumovirus produced in tobacco plants by transient transformation.HRA2pl肽:一种通过瞬时转化在烟草植株中产生的人偏肺病毒融合抑制剂。
Planta. 2015 Jul;242(1):69-76. doi: 10.1007/s00425-015-2277-5. Epub 2015 Apr 1.
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Adjuvant effect of the human metapneumovirus (HMPV) matrix protein in HMPV subunit vaccines.人偏肺病毒(HMPV)基质蛋白在HMPV亚单位疫苗中的佐剂作用。
J Gen Virol. 2015 Apr;96(Pt 4):767-774. doi: 10.1099/vir.0.000031. Epub 2014 Dec 17.
5
Ribavirin induced hemolysis: a novel mechanism of action against chronic hepatitis C virus infection.利巴韦林诱导的溶血:一种针对慢性丙型肝炎病毒感染的新作用机制。
World J Gastroenterol. 2014 Nov 21;20(43):16184-90. doi: 10.3748/wjg.v20.i43.16184.
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Programmed death-1 impairs secondary effector lung CD8⁺ T cells during respiratory virus reinfection.程序性死亡-1在呼吸道病毒再次感染期间损害继发性效应肺CD8⁺ T细胞。
J Immunol. 2014 Nov 15;193(10):5108-17. doi: 10.4049/jimmunol.1302208. Epub 2014 Oct 22.
7
Rational design of human metapneumovirus live attenuated vaccine candidates by inhibiting viral mRNA cap methyltransferase.通过抑制病毒 mRNA 帽甲基转移酶来合理设计人偏肺病毒活减毒疫苗候选物。
J Virol. 2014 Oct;88(19):11411-29. doi: 10.1128/JVI.00876-14. Epub 2014 Jul 23.
8
A broadly neutralizing human monoclonal antibody exhibits in vivo efficacy against both human metapneumovirus and respiratory syncytial virus.一种广泛中和性人源单克隆抗体在体内对人偏肺病毒和呼吸道合胞病毒均显示出疗效。
J Infect Dis. 2015 Jan 15;211(2):216-25. doi: 10.1093/infdis/jiu307. Epub 2014 May 26.
9
Human metapneumovirus SH and G glycoproteins inhibit macropinocytosis-mediated entry into human dendritic cells and reduce CD4+ T cell activation.人类偏肺病毒 SH 和 G 糖蛋白抑制巨胞饮介导的人树突状细胞进入,并减少 CD4+T 细胞激活。
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10
Human metapneumovirus virus-like particles induce protective B and T cell responses in a mouse model.人偏肺病毒样颗粒在小鼠模型中诱导保护性 B 和 T 细胞应答。
J Virol. 2014 Jun;88(11):6368-79. doi: 10.1128/JVI.00332-14. Epub 2014 Mar 26.

针对人偏肺病毒的免疫和治疗新方法。

New Approaches for Immunization and Therapy against Human Metapneumovirus.

作者信息

Wen Sherry C, Williams John V

机构信息

Department of Pathology, Microbiology & Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

Department of Pediatrics, University of Pittsburgh School of Medicine, Children's Hospital of Pittsburgh and University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA

出版信息

Clin Vaccine Immunol. 2015 Aug;22(8):858-66. doi: 10.1128/CVI.00230-15. Epub 2015 Jun 10.

DOI:10.1128/CVI.00230-15
PMID:26063237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4519717/
Abstract

Human metapneumovirus (HMPV) is a paramyxovirus discovered in 2001 in the Netherlands. Studies have identified HMPV as an important causative agent of acute respiratory disease in infants, the elderly, and immunocompromised individuals. Clinical signs of infection range from mild upper respiratory illness to more serious lower respiratory illness, including bronchiolitis and pneumonia. There are currently no licensed therapeutics or vaccines against HMPV. However, several research groups have tested vaccine candidates and monoclonal antibodies in various animal models. Several of these approaches have shown promise in animal models. This minireview summarizes the current therapies used to treat HMPV infection as well as different approaches for immunization.

摘要

人偏肺病毒(HMPV)是2001年在荷兰发现的一种副粘病毒。研究已确定HMPV是婴儿、老年人和免疫功能低下个体急性呼吸道疾病的重要病原体。感染的临床症状从轻度上呼吸道疾病到更严重的下呼吸道疾病,包括细支气管炎和肺炎。目前尚无针对HMPV的许可治疗方法或疫苗。然而,几个研究小组已在各种动物模型中测试了候选疫苗和单克隆抗体。其中一些方法在动物模型中已显示出前景。本综述总结了目前用于治疗HMPV感染的疗法以及不同的免疫方法。