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首页> 外文期刊>Virology >A cationic liposome-DNA complexes adjuvant (JVRS-100) enhances the immunogenicity and cross-protective efficacy of pre-pandemic influenza A (H5N1) vaccine in ferrets
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A cationic liposome-DNA complexes adjuvant (JVRS-100) enhances the immunogenicity and cross-protective efficacy of pre-pandemic influenza A (H5N1) vaccine in ferrets

机译:阳离子脂质体-DNA复合物佐剂(JVRS-100)增强了雪貂中大流行性流感A(H5N1)疫苗的免疫原性和交叉保护效果

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摘要

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 Glade 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. Published by Elsevier Inc.
机译:流感A(H5N1)病毒继续提出公共卫生威胁。作为灭活的H5N1疫苗是免疫原性差的,需要佐剂来改善人体H5N1疫苗的免疫原性。在这里,我们研究了Glade 2.2-衍生疫苗的雪铁中的免疫原性和交叉保护功效,所述疫苗的添加JVRS-100,一种由阳离子脂质体-DNA复合物(CLDC)组成的佐剂。在第一次疫苗接种后,与辅助疫苗免疫的雪卷中,在用辅助疫苗免疫的雪卷中检测到血晶抑制(Hai)和中和抗体滴度的显着较高水平。在第二剂量辅助疫苗之后,检测HAI抗体滴度> = 40的滴度,从多个H5N1蛹中检测到病毒。对新分离的H5N2和H5N8病毒的HAI抗体也通过JVRS-100增强。雪貂用异源H5N1病毒挑战。所有接受两剂辅助疫苗的所有雪貂都表现出轻微的疾病,显着降低鼻腔洗涤病毒滴度和免受致命攻击的保护。相比之下,接受未驱逐的疫苗的雪貂显示出更大的体重减轻,高病毒滴度,3只动物的3只持续到致命挑战。我们的结果表明,添加JVRS-100至H5N1疫苗增强了雪貂中致死H5N1病毒病的免疫原性和交叉保护。 JVRS-100作为流感疫苗的潜在佐剂进行进一步调查。 elsevier公司出版

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