首页> 外文期刊>Veterinary Microbiology >Different counteracting host immune responses to Glade 2.2.1.1 and 2.2.1.2 Egyptian H5N1 highly pathogenic avian influenza viruses in naive and vaccinated chickens
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Different counteracting host immune responses to Glade 2.2.1.1 and 2.2.1.2 Egyptian H5N1 highly pathogenic avian influenza viruses in naive and vaccinated chickens

机译:天真和接种疫苗的鸡对Glade 2.2.1.1和2.2.1.2埃及H5N1高致病性禽流感病毒的不同抵抗宿主免疫反应

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In Egypt, two distinct lineages of H5N1 highly pathogenic avian influenza (HPAI) viruses, "classic 2.2.1.2" and "variant 2.2.1.1" strains, have evolved. The underlying host immune responses counteracting these viruses in chickens remain not well understood. In the present study, the cytokine responses to a classic strain (C121) and those to a variant strain (V1063) were compared in naive and vaccinated chickens. In naive chickens, the C121 replicated more efficiently than the V1063. Both the C121 and the V1063 increased interferon (IFN)-gamma and interleukin (IL)-10 gene expression at 48 h post inoculation (hpi) in the lung and spleen but the levels of these cytokines were lower in chickens infected with the C121 than those infected with the V1063. In contrast, in chickens vaccinated with inactivated C121-based vaccine, the C121 replicated less than the V1063. Both challenge with the C121 and that with the V1063 did not increase IFN-gamma gene expression at 48 hpi; rather, the C121 increased IL-4 gene expression in the lung accompanied with lower viral titer and higher HI titers. These results suggested that the pathogenicity of HPAI viruses correlated with IFN-gamma-producing helper and/or cytotoxic T cell responses in naive chickens, whereas vaccine efficacy to HPAI viruses correlated with IL-4 producing helper T cell responses in the lung in vaccinated chickens. It implies that IL-4 in the lung, in addition to the traditional serum HI titers, could be used to screen novel vaccine strategies, such as strains, adjuvant, prime/boost protocols, against HPAI in chickens. (C) 2015 Elsevier B.V. All rights reserved.
机译:在埃及,已经进化出H5N1高致病性禽流感(HPAI)病毒的两个不同谱系,即“经典2.2.1.2”和“变异2.2.1.1”毒株。抵抗鸡中这些病毒的潜在宿主免疫反应仍不清楚。在本研究中,比较了未处理和接种疫苗的鸡对经典品系(C121)和变异株(V1063)的细胞因子反应。在幼稚的鸡中,C121的复制效率要高于V1063。在肺和脾中接种后(hpi)48小时,C121和V1063均增加了干扰素(IFN)-γ和白介素(IL)-10基因的表达,但这些细胞因子的水平在感染C121的鸡中低于那些感染了V1063的人。相反,在接种了灭活的基于C121的疫苗的鸡中,C121的复制少于V1063。用C121和用V1063挑战都没有增加48 hpi的IFN-γ基因表达。相反,C121增加了肺中IL-4基因的表达,并伴有病毒滴度降低和HI滴度升高。这些结果表明,HPAI病毒的致病性与幼稚鸡中产生IFN-γ的辅助细胞和/或细胞毒性T细胞反应相关,而对HPAI病毒的疫苗效力与接种鸡的肺中IL-4产生辅助性T细胞反应相关。 。这意味着除传统的血清HI滴度外,肺中的IL-4还可用于筛选针对鸡HPAI的新型疫苗策略,例如菌株,佐剂,初免/加强方案。 (C)2015 Elsevier B.V.保留所有权利。

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