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Pivotal role of ChIFNgamma in the pathogenesis and immunosuppression of infectious bursal disease

机译:ChIFNgamma在传染性法氏囊病的发病机理和免疫抑制中的关键作用

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摘要

This study investigates the pivotal role of chicken interferon-gamma (ChIFNgamma) in the pathogenesis and immunosuppression of infectious bursal disease virus (IBDV) infection and is divided into in vivo, ex vivo and in vitro experiments. Two-week-old specific pathogen free chickens were inoculated with the 849VB very virulent strain of IBDV. The levels of systemic ChIFNgamma and chicken interleukin-6 in the serum were followed for 2 weeks during in vivo experiments. Then, splenocytes and bursal cells from infected chickens were analysed for their immunocompetence after mitogenic activation in ex vivo experiments. Finally, in vitro experiments were conducted to assess the direct immunosuppressive effect of ChIFNgamma on splenocytes and peripheral blood lymphocytes from non-inoculated specific pathogen free chickens. Our results reveal that the acute phase of infectious bursal disease coincides, on one hand, with high levels of systemic ChIFNgamma and chicken interleukin-6 and, on the other hand, with a strong inhibition of proliferation and activation of mitogen-stimulated splenocytes from infected chickens, as measured by ChIFNgamma production. Two weeks after viral inoculation, T lymphocytes infiltrating the bursa of Fabricius had recovered their activation capability. Finally, an in vitro study showed that the proliferation of naive splenocytes and peripheral blood lymphocytes was directly and specifically inhibited by ChIFNgamma. In conclusion, a ChIFNgamma dysregulation occurs in chickens infected with IBDV and the overproduction of ChIFNgamma by T lymphocytes plays a key role in the pathogenesis and immunosuppression induced by this virus.
机译:这项研究调查鸡干扰素-γ(ChIFNgamma)在传染性法氏囊病病毒(IBDV)感染的发病机理和免疫抑制中的关键作用,并分为体内,离体和体外实验。给两周大的无特定病原体的鸡接种IBDV 849VB强毒株。在体内实验期间,追踪血清中全身性ChIFNγ和鸡白介素-6的水平2周。然后,在离体实验中分析有丝分裂活化后,来自感染鸡的脾细胞和囊细胞的免疫能力。最后,进行了体外实验,以评估ChIFNγ对未接种无特定病原体的鸡的脾细胞和外周血淋巴细胞的直接免疫抑制作用。我们的结果表明,传染性法氏囊病的急性期一方面与高水平的全身性ChIFNgamma和鸡白细胞介素6相吻合,另一方面与被感染的促分裂原刺激性脾细胞的增殖和活化强烈抑制相吻合。鸡,通过ChIFNgamma产量来衡量。病毒接种后两周,浸入Fabricius滑囊的T淋巴细胞恢复了其活化能力。最后,一项体外研究表明,ChIFNgamma可直接和特异性地抑制幼稚脾细胞和外周血淋巴细胞的增殖。总之,在感染IBDV的鸡中发生ChIFNgamma失调,T淋巴细胞过量产生ChIFNgamma在这种病毒引起的发病机理和免疫抑制中起关键作用。

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