Hughes H D, Carroll J A, Burdick Sanchez N C, Roberts S L, Broadway P R, May N D, Ballou M A, Richeson J T
J Anim Sci. 2017 Apr;95(4):1502-1511. doi: 10.2527/jas.2017.1374.
The objective of this research was to examine the effects of dexamethasone (DEX) treatment on various aspects of immunity following administration of a multivalent respiratory vaccine, using a model intended to mimic acute versus chronic stress. Angus × Hereford steers ( = 32; 209 ± 8 kg) were stratified by BW and randomly assigned to 1 of 3 treatments: 1) acute stress (ACU), in which 0.5 mg/kg BW DEX was intravenously administered at 1000 h only on d 0; 2) chronic stress (CHR), in which 0.5 mg/kg BW DEX was intravenously administered at 1000 h on d -3 to 0; or 3) control (CON), in which no DEX was administered. Steers were fitted with indwelling jugular catheters and rectal temperature (RT) recording devices on d -4 relative to vaccination and placed in individual stanchions in an environmentally controlled facility. Blood samples were collected and serum was isolated at -74, -50, and -26 h; at 0.5-h intervals from -4 to 6 h; and at 12, 24, 36, 48, and 72 h relative to multivalent respiratory vaccination at 1200 h on d 0. Additional blood samples were used to analyze complete blood cell count (CBC) and functional capacities of neutrophils. There was a treatment × time interaction ( < 0.01) for RT such that DEX treatment in CHR and ACU steers decreased RT on d -3 and 0, respectively. A treatment × time interaction ( < 0.01) was observed for total white blood cells (WBC), neutrophils, lymphocytes, and monocytes. Specifically, DEX increased WBC and neutrophils in CHR and ACU steers ( < 0.001) yet decreased lymphocytes in CHR steers ( = 0.02) compared with CON steers. Neutrophil concentration increased rapidly, within 2 h of the DEX infusion, in ACU steers. Monocytes transiently increased ( < 0.001) in response to DEX treatment in CHR and ACU steers. In contrast, eosinophils were greater ( < 0.01) in CON steers than in ACU and CHR steers. A treatment × time interaction ( = 0.004) was observed for interferon-γ, with CON cattle exhibiting greater concentrations than the ACU and CHR cattle at 5 h after vaccination, through d 3. Treatment also influenced ( ≤ 0.001) the expression of L-selectin on the surface of neutrophils. The percentage of neutrophils engaging in phagocytosis and the oxidative burst were suppressed ( ≤ 0.001) among only the CHR steers, whereas the intensity of the oxidative burst was suppressed ( ≤ 0.001) for both ACU and CHR steers. These data suggest that our model induced acute and chronic immunosuppression and defined the acute response to a multivalent vaccine in CON steers.
本研究的目的是使用一个旨在模拟急性应激与慢性应激的模型,研究地塞米松(DEX)治疗对多价呼吸道疫苗接种后免疫各方面的影响。安格斯×赫里福德阉牛(n = 32;体重209±8千克)按体重分层,随机分配至3种处理中的1种:1)急性应激(ACU),仅在第0天1000时静脉注射0.5毫克/千克体重的DEX;2)慢性应激(CHR),在第-3天至第0天的1000时静脉注射0.5毫克/千克体重的DEX;或3)对照(CON),不注射DEX。在相对于疫苗接种的第-4天,给阉牛安装颈静脉留置导管和直肠温度(RT)记录装置,并将其放置在环境控制设施中的个体牛栏内。在相对于第0天1200时多价呼吸道疫苗接种的-74、-50和-26小时;从-4至6小时每隔0.5小时;以及在12、24、36、48和72小时采集血样并分离血清。另外采集血样用于分析全血细胞计数(CBC)和中性粒细胞的功能能力。RT存在处理×时间交互作用(P<0.01),使得CHR和ACU阉牛中的DEX处理分别在第-3天和第0天降低了RT。总白细胞(WBC)、中性粒细胞、淋巴细胞和单核细胞存在处理×时间交互作用(P<0.01)。具体而言,与CON阉牛相比,DEX增加了CHR和ACU阉牛中的WBC和中性粒细胞(P<0.001),但降低了CHR阉牛中的淋巴细胞(P = 0.02)。在ACU阉牛中,DEX输注后2小时内中性粒细胞浓度迅速增加。CHR和ACU阉牛中,单核细胞对DEX处理有短暂增加(P<0.001)。相比之下,CON阉牛中的嗜酸性粒细胞比ACU和CHR阉牛中的多(P<0.01)。干扰素-γ存在处理×时间交互作用(P = 0.004),在接种疫苗后5小时至第3天,CON牛的浓度高于ACU和CHR牛。处理也影响(P≤0.001)中性粒细胞表面L-选择素的表达。仅在CHR阉牛中,参与吞噬作用的中性粒细胞百分比和氧化爆发受到抑制(P≤0.001),而ACU和CHR阉牛的氧化爆发强度均受到抑制(P≤0.001)。这些数据表明,我们的模型诱导了急性和慢性免疫抑制,并确定了CON阉牛对多价疫苗的急性反应。