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欧亚H7禽流感病毒免疫反应及交叉保护效力评估

Evaluation of the Immune Responses to and Cross-Protective Efficacy of Eurasian H7 Avian Influenza Viruses.

作者信息

Kwon Hyeok-Il, Kim Young-Il, Park Su-Jin, Song Min-Suk, Kim Eun-Ha, Kim Se Mi, Si Young-Jae, Lee In-Won, Song Byung-Min, Lee Youn-Jeong, Yun Seok Joong, Kim Wun-Jae, Choi Young Ki

机构信息

College of Medicine and Medical Research Institute, Chungbuk National University, Cheongju, Republic of Korea.

Zoonotic Infectious Diseases Research Center, Chungbuk National University, Cheongju, Republic of Korea.

出版信息

J Virol. 2017 May 12;91(11). doi: 10.1128/JVI.02259-16. Print 2017 Jun 1.

Abstract

Due to increasing concerns about human infection by various H7 influenza viruses, including recent H7N9 viruses, we evaluated the genetic relationships and cross-protective efficacies of three different Eurasian H7 avian influenza viruses. Phylogenic and molecular analyses revealed that recent Eurasian H7 viruses can be separated into two different lineages, with relatively high amino acid identities within groups (94.8 to 98.8%) and low amino acid identities between groups (90.3 to 92.6%). immunization with representatives of each group revealed that while group-specific cross-reactivity was induced, cross-reactive hemagglutination inhibition (HI) titers were approximately 4-fold lower against heterologous group viruses than against homologous group viruses. Moreover, the group I (RgW109/06) vaccine protected 100% of immunized mice from various group I viruses, while only 20 to 40% of immunized mice survived lethal challenge with heterologous group II viruses and exhibited high viral titers in the lung. Moreover, while the group II (RgW478/14) vaccine also protected mice from lethal challenge with group II viruses, it failed to elicit cross-protection against group I viruses. However, it is noteworthy that vaccination with RgAnhui1/13, a virus of a sublineage of group I, cross-protected immunized mice against lethal challenge with both group I and II viruses and significantly attenuated lung viral titers. Interestingly, immune sera from RgAnhui1/13-vaccinated mice showed a broad neutralizing spectrum rather than the group-specific pattern observed with the other viruses. These results suggest that the recent human-infective H7N9 strain may be a candidate broad cross-protective vaccine for Eurasian H7 viruses. Genetic and phylogenic analyses have demonstrated that the Eurasian H7 viruses can be separated into at least two different lineages, both of which contain human-infective fatal H7 viruses, including the recent novel H7N9 viruses isolated in China since 2013. Due to the increasing concerns regarding the global public health risk posed by H7 viruses, we evaluated the genetic relationships between Eurasian H7 avian influenza viruses and the cross-protective efficacies of three different H7 viruses: W109/06 (group I), W478/14 (group II), and Anhui1/13 (a sublineage of group I). While each vaccine induced group-specific antibody responses and cross-protective efficacy, only Anhui1/13 was able to cross-protect immunized hosts against lethal challenge across groups. In fact, the Anhui1/13 virus induced not only cross-protection but also broad serum neutralizing antibody responses against both groups of viruses. This suggests that Anhui1/13-like H7N9 viruses may be viable vaccine candidates for broad protection against Eurasian H7 viruses.

摘要

由于对包括近期H7N9病毒在内的各种H7流感病毒感染人类的担忧日益增加,我们评估了三种不同的欧亚H7禽流感病毒的遗传关系和交叉保护效力。系统发育和分子分析表明,近期的欧亚H7病毒可分为两个不同的谱系,组内氨基酸同一性相对较高(94.8%至98.8%),组间氨基酸同一性较低(90.3%至92.6%)。用每组的代表进行免疫显示,虽然诱导了组特异性交叉反应,但异源组病毒的交叉反应性血凝抑制(HI)效价比同源组病毒低约4倍。此外,I组(RgW109/06)疫苗保护100%的免疫小鼠免受各种I组病毒的侵害,而只有20%至40%的免疫小鼠在接受异源II组病毒的致死性攻击后存活下来,并在肺部表现出高病毒滴度。此外,虽然II组(RgW478/14)疫苗也保护小鼠免受II组病毒的致死性攻击,但它未能引发针对I组病毒的交叉保护。然而,值得注意的是,用I组一个亚谱系的病毒RgAnhui1/13进行疫苗接种,可交叉保护免疫小鼠免受I组和II组病毒的致死性攻击,并显著降低肺部病毒滴度。有趣的是,来自接种RgAnhui1/13疫苗小鼠的免疫血清显示出广泛的中和谱,而不是其他病毒所观察到的组特异性模式。这些结果表明,近期感染人类的H7N9毒株可能是一种针对欧亚H7病毒的广泛交叉保护疫苗的候选毒株。遗传和系统发育分析表明,欧亚H7病毒可分为至少两个不同的谱系,两个谱系都包含感染人类的致命H7病毒,包括2013年以来在中国分离出的近期新型H7N9病毒。由于对H7病毒对全球公共卫生风险的担忧日益增加,我们评估了欧亚H7禽流感病毒之间的遗传关系以及三种不同H7病毒:W109/06(I组)、W478/14(II组)和Anhui1/13(I组的一个亚谱系)的交叉保护效力。虽然每种疫苗都诱导了组特异性抗体反应和交叉保护效力,但只有Anhui1/13能够交叉保护免疫宿主免受不同组的致死性攻击。事实上,Anhui1/13病毒不仅诱导了交叉保护,还诱导了针对两组病毒的广泛血清中和抗体反应。这表明,类似Anhui1/13的H7N9病毒可能是针对欧亚H7病毒进行广泛保护的可行疫苗候选毒株。

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