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一种阳离子脂质体-DNA复合物佐剂(JVRS-100)可增强雪貂体内大流行前甲型流感病毒(H5N1)疫苗的免疫原性和交叉保护效力。

A cationic liposome-DNA complexes adjuvant (JVRS-100) enhances the immunogenicity and cross-protective efficacy of pre-pandemic influenza A (H5N1) vaccine in ferrets.

作者信息

Liu Feng, Sun Xiangjie, Fairman Jeffery, Lewis David B, Katz Jacqueline M, Levine Min, Tumpey Terrence M, Lu Xiuhua

机构信息

Influenza Division, Centers for Disease Control and Prevention, Atlanta, GA, USA.

Juvaris BioTherapeutics, Pleasanton, CA 94566, USA.

出版信息

Virology. 2016 May;492:197-203. doi: 10.1016/j.virol.2016.02.024. Epub 2016 Mar 21.

DOI:10.1016/j.virol.2016.02.024
PMID:26967975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5796654/
Abstract

Influenza A (H5N1) viruses continue to pose a public health threat. As inactivated H5N1 vaccines are poorly immunogenic, adjuvants are needed to improve the immunogenicity of H5N1 vaccine in humans. Here, we investigated the immunogenicity and cross-protective efficacy in ferrets of a clade 2.2-derived vaccine with addition of JVRS-100, an adjuvant consisting of cationic liposome-DNA complexes (CLDC). After the first vaccination, significantly higher levels of hemagglutination-inhibition (HAI) and neutralizing antibody titers were detected in ferrets immunized with adjuvanted vaccine compared to unadjuvanted vaccine. Following a second dose of adjuvanted vaccine, HAI antibody titers of ≥ 40 were detected against viruses from multiple H5N1 clades. HAI antibodies against newly isolated H5N2 and H5N8 viruses were also augmented by JVRS-100. Ferrets were challenged with a heterologous H5N1 virus. All ferrets that received two doses of adjuvanted vaccine exhibited mild illness, significantly reduced nasal wash virus titers and protection from lethal challenge. In contrast, ferrets that received unadjuvanted vaccine showed greater weight loss, high viral titers and 3 of 6 animals succumbed to the lethal challenge. Our results indicate that the addition of JVRS-100 to H5N1 vaccine enhanced immunogenicity and cross-protection against lethal H5N1 virus disease in ferrets. JVRS-100 warrants further investigation as a potential adjuvant for influenza vaccines.

摘要

甲型流感病毒(H5N1)持续构成公共卫生威胁。由于灭活H5N1疫苗的免疫原性较差,因此需要佐剂来提高H5N1疫苗在人体内的免疫原性。在此,我们研究了添加了JVRS-100(一种由阳离子脂质体-DNA复合物(CLDC)组成的佐剂)的2.2分支来源疫苗在雪貂中的免疫原性和交叉保护效力。首次接种疫苗后,与未添加佐剂的疫苗相比,接种添加佐剂疫苗的雪貂体内检测到的血凝抑制(HAI)和中和抗体滴度显著更高。在接种第二剂添加佐剂的疫苗后,检测到针对多种H5N1分支病毒的HAI抗体滴度≥40。JVRS-100还增强了针对新分离的H5N2和H5N8病毒的HAI抗体。用异源H5N1病毒对雪貂进行攻毒。所有接种两剂添加佐剂疫苗的雪貂均表现出轻度疾病,鼻腔冲洗液中的病毒滴度显著降低,并对致死性攻毒具有保护作用。相比之下,接种未添加佐剂疫苗的雪貂体重减轻更明显,病毒滴度高,6只动物中有3只死于致死性攻毒。我们的结果表明,在H5N1疫苗中添加JVRS-100可增强免疫原性,并对雪貂致死性H5N1病毒病产生交叉保护作用。JVRS-100作为流感疫苗的潜在佐剂值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e77/5796654/c2ad81b460b8/nihms936838f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e77/5796654/fd4ce612c5cb/nihms936838f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e77/5796654/c2ad81b460b8/nihms936838f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e77/5796654/fd4ce612c5cb/nihms936838f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e77/5796654/c2ad81b460b8/nihms936838f2.jpg

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