添加 Toll 样受体配体佐剂的流感灭活疫苗对 H9N2 禽流感病毒在鸡体内传播的效力

IF 1.4 3区 农林科学 Q4 IMMUNOLOGY
Sugandha Raj , Mohammadali Alizadeh , Ayumi Matsuyama-Kato , Nitish Boodhoo , Myles St Denis , Éva Nagy , Samira Mubareka , Khalil Karimi , Shahriar Behboudi , Shayan Sharif
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引用次数: 0

摘要

禽流感病毒(AIV),包括 H9N2 亚型,对家禽业和人类健康构成重大威胁。虽然疫苗接种是一种保护性控制措施,但其对鸡的传播效果仍不确定。本研究的目的是探讨 beta-丙内酯(BPL)H9N2 病毒全灭活疫苗(WIV)单独或与 CpG ODN 2007(CpG)、poly(I:C) 或 AddaVaxTM(ADD)联合使用对预防 H9N2 AIV 在鸡中传播的功效。播种鸡(试验 1)和受种鸡(试验 2)分别接种两次不同配方的疫苗。二次接种疫苗 10 天后,种鸡感染 H9N2 AIV(试验 1),并与健康的受种鸡同舍饲养。在试验 2 中,受体鸡接种疫苗后接触感染 H9N2 AIV 的种鸡。结果表明,在两次试验中,经 BPL+ CpG 和 BPL+ poly(I:C) 处理的鸡在暴露后(PE)的口腔和泄殖腔脱落均有所减少。BPL+ CpG 组(试验 1)的 H9N2 AIV+ 受体鸡数量低于其他接种组,而在试验 2 中,BPL+ CpG 受体鸡的 H9N2 AIV+ 受体鸡数量减少得更多。接种 BPL+ CpG 疫苗的鸡表现出更强的全身抗体反应,IgM 和 IgY 滴度较高,初次接种后第 21 天的血清保护率更高(ppv)。此外,BPL+ CpG 处理鸡的 IFN-γ 表达和生成诱导率更高。在刺激后 12 小时和 24 小时,BPL+ CpG 组和 BPL+ poly(I:C) 组的白细胞介素 (IL)-2 表达均上调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of an inactivated influenza vaccine adjuvanted with Toll-like receptor ligands against transmission of H9N2 avian influenza virus in chickens

Avian influenza viruses (AIV), including the H9N2 subtype, pose a major threat to the poultry industry as well as to human health. Although vaccination provides a protective control measure, its effect on transmission remains uncertain in chickens. The objective of the present study was to investigate the efficacy of beta-propiolactone (BPL) whole inactivated H9N2 virus (WIV) vaccine either alone or in combination with CpG ODN 2007 (CpG), poly(I:C) or AddaVax™ (ADD) to prevent H9N2 AIV transmission in chickens. The seeder chickens (trial 1) and recipient chickens (trial 2) were vaccinated twice with different vaccine formulations. Ten days after secondary vaccination, seeder chickens were infected with H9N2 AIV (trial 1) and co-housed with healthy recipient chickens. In trial 2, the recipient chickens were vaccinated and then exposed to H9N2 AIV-infected seeder chickens. Our results demonstrated that BPL+ CpG and BPL+ poly(I:C) treated chickens exhibited reduced oral and cloacal shedding in both trials post-exposure (PE). The number of H9N2 AIV+ recipient chickens in the BPL+ CpG group (trial 1) was lower than in other vaccinated groups, and the reduction was higher in BPL+ CpG recipient chickens in trial 2. BPL+ CpG vaccinated chickens demonstrated enhanced systemic antibody responses with high IgM and IgY titers with higher rates of seroprotection by day 21 post-primary vaccination (ppv). Additionally, the induction of IFN-γ expression and production was higher in the BPL+ CpG treated chickens. Interleukin (IL)− 2 expression was upregulated in both BPL+ CpG and BPL+ poly(I:C) groups at 12 and 24 hr post-stimulation.

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来源期刊
CiteScore
3.40
自引率
5.60%
发文量
79
审稿时长
70 days
期刊介绍: The journal reports basic, comparative and clinical immunology as they pertain to the animal species designated here: livestock, poultry, and fish species that are major food animals and companion animals such as cats, dogs, horses and camels, and wildlife species that act as reservoirs for food, companion or human infectious diseases, or as models for human disease. Rodent models of infectious diseases that are of importance in the animal species indicated above,when the disease requires a level of containment that is not readily available for larger animal experimentation (ABSL3), will be considered. Papers on rabbits, lizards, guinea pigs, badgers, armadillos, elephants, antelope, and buffalo will be reviewed if the research advances our fundamental understanding of immunology, or if they act as a reservoir of infectious disease for the primary animal species designated above, or for humans. Manuscripts employing other species will be reviewed if justified as fitting into the categories above. The following topics are appropriate: biology of cells and mechanisms of the immune system, immunochemistry, immunodeficiencies, immunodiagnosis, immunogenetics, immunopathology, immunology of infectious disease and tumors, immunoprophylaxis including vaccine development and delivery, immunological aspects of pregnancy including passive immunity, autoimmuity, neuroimmunology, and transplanatation immunology. Manuscripts that describe new genes and development of tools such as monoclonal antibodies are also of interest when part of a larger biological study. Studies employing extracts or constituents (plant extracts, feed additives or microbiome) must be sufficiently defined to be reproduced in other laboratories and also provide evidence for possible mechanisms and not simply show an effect on the immune system.
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