Laboratory of Virology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Vet J. 2011 Jan;187(1):48-53. doi: 10.1016/j.tvjl.2009.12.012. Epub 2010 Jan 22.
This study set out to investigate the cytokines and acute phase proteins (APPs) associated with the acute stages of experimentally-induced swine influenza virus (SIV) infection in 3-week-old, colostrum-deprived, caesarean-derived piglets. The piglets were inoculated intratracheally with 10(7.5) 50% egg infective dose [EID(50)] Swine/Belgium/1/98 (H1N1) SIV and were euthanased at time-points between 0 and 120h post-inoculation (PI). Broncho-alveolar lavage fluid (BALF), lung homogenates and sera were examined for inflammatory mediators by bioassay or ELISA. Interferon (IFN)-α, interleukin (IL)-6, IL-1 and tumour necrosis factor (TNF)-α peaked in BALF 24-30h PI, when virus titres and the severity of clinical signs were maximal. Whereas IFN-γ and IL-12, but not IL-18, increased in tandem in BALF, serum cytokine concentrations were either undetectable or were up to 100-fold lower. The APP C-reactive protein (CRP) and haptoglobin peaked 24h later than the cytokines and reached higher levels in serum than in BALF. In contrast, lipopolysaccharide (LPS)-binding protein (LBP) only increased in BALF. Lung virus titres tightly correlated with BALF IFN-α, IL-6, IL-1, TNF-α, IFN-γ and IL-12, as well as with serum IL-6, IFN-α and IFN-γ. Signs of disease correlated with the same cytokines in BALF and serum, as well as with BALF LBP and serum CRP. The findings suggest that IFN-γ and IL-12 play a role in the pathogenesis of SIV and that APPs are induced by cytokines. This influenza infection model may have value in assessing the therapeutic potential of cytokine antagonists.
本研究旨在探讨与实验诱导的猪流感病毒(SIV)感染急性阶段相关的细胞因子和急性时相蛋白(APPs)。3 周龄、初乳剥夺的剖腹产仔猪通过气管内接种 10(7.5)50%鸡蛋感染剂量 [EID(50)] Swine/Belgium/1/98(H1N1)SIV,并在接种后 0 至 120 小时(PI)的时间点安乐死。通过生物测定或 ELISA 检查支气管肺泡灌洗液(BALF)、肺匀浆和血清中的炎症介质。IFN-α、IL-6、IL-1 和 TNF-α在 BALF 中 24-30 小时 PI 时达到峰值,此时病毒滴度和临床症状的严重程度达到最大值。而 IFN-γ 和 IL-12 虽然与 IL-18 一起增加,但在 BALF 中的浓度要么无法检测到,要么低 100 倍。APP C-反应蛋白(CRP)和触珠蛋白在细胞因子后 24 小时达到峰值,在血清中的水平高于 BALF。相比之下,脂多糖(LPS)结合蛋白(LBP)仅在 BALF 中增加。肺病毒滴度与 BALF IFN-α、IL-6、IL-1、TNF-α、IFN-γ 和 IL-12 以及血清 IL-6、IFN-α 和 IFN-γ 密切相关。疾病的迹象与 BALF 和血清中的相同细胞因子以及 BALF LBP 和血清 CRP 相关。研究结果表明,IFN-γ 和 IL-12 在 SIV 的发病机制中起作用,而 APPs 是由细胞因子诱导的。这种流感感染模型可能对评估细胞因子拮抗剂的治疗潜力具有价值。