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一种对流感病毒复制具有强效抑制作用且具有强大佐剂活性的Toll样受体3(TLR3)配体,在流感大流行中具有双重应用潜力。

A TLR3 ligand that exhibits potent inhibition of influenza virus replication and has strong adjuvant activity has the potential for dual applications in an influenza pandemic.

作者信息

Lau Yuk-Fai, Tang Lay-Hoon, Ooi Eng-Eong

机构信息

Medical Countermeasures (Biological) Laboratory, Defense Medical and Environmental Research Institute, DSO National Laboratories, 27 Medical Drive #13-00, The Republic of Singapore, 117510, Singapore.

出版信息

Vaccine. 2009 Feb 25;27(9):1354-64. doi: 10.1016/j.vaccine.2008.12.048. Epub 2009 Jan 15.

DOI:10.1016/j.vaccine.2008.12.048
PMID:19150474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7115584/
Abstract

The appearance and spread of the H5N1 highly pathogenic avian influenza (HPAI) raise concern of a possible pandemic. Current preventive measures include the development of a pre-pandemic influenza vaccine and stockpiling of neuraminidase inhibitors. However, their benefits can be significantly reduced by mutations in the hemagglutinin or neuraminidase resulting in antigenic changes and the appearance of drug-resistance, respectively. Drugs that target the innate immune system to achieve a 'heightened antiviral' state represent another class of antiviral agents that could contribute to the control and treatment of influenza infection. In this study, PIKA (a stabilized dsRNA) provides broad-spectrum prophylaxis against a number of influenza A viruses. In addition, when PIKA was admixed with influenza vaccine preparations, including a formalin-inactivated whole-virion H5 vaccine, significant adjuvanting effect leading to accelerated viral clearance was observed in a murine model. These biological effects appear to be mediated by the ability of PIKA to promote the maturation of dendritic cells, including up-regulation of co-stimulatory molecules, such as CD80 and CD86, and the induction of various cytokines and chemokines. Toll-like receptor 3 (TLR3) was shown to recognize PIKA in a concentration-dependent manner. The potency and versatility in its activities make PIKA an attractive candidate for use in an influenza pandemic.

摘要

H5N1高致病性禽流感(HPAI)的出现和传播引发了对可能大流行的担忧。当前的预防措施包括研发大流行前流感疫苗和储备神经氨酸酶抑制剂。然而,血凝素或神经氨酸酶的突变分别导致抗原性变化和耐药性的出现,可能会显著降低它们的益处。靶向先天免疫系统以达到“增强抗病毒”状态的药物代表了另一类抗病毒剂,可能有助于控制和治疗流感感染。在本研究中,PIKA(一种稳定的双链RNA)对多种甲型流感病毒具有广谱预防作用。此外,当PIKA与流感疫苗制剂(包括福尔马林灭活全病毒H5疫苗)混合时,在小鼠模型中观察到显著的佐剂效应,导致病毒清除加速。这些生物学效应似乎是由PIKA促进树突状细胞成熟的能力介导的,包括共刺激分子如CD80和CD86的上调以及各种细胞因子和趋化因子的诱导。Toll样受体3(TLR3)被证明以浓度依赖的方式识别PIKA。其活性的效力和多功能性使PIKA成为流感大流行中一个有吸引力的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/ccc2f8939551/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/7b33ea8fc630/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/53d8d1a98cb7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/125879b19fe6/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/8eba702f39b2/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/4d34a6631a50/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/f6dd4de7a40e/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/ccc2f8939551/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/7b33ea8fc630/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/53d8d1a98cb7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/125879b19fe6/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/8eba702f39b2/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/4d34a6631a50/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/f6dd4de7a40e/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd90/7115584/ccc2f8939551/gr7.jpg

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