Escola Superior de Agricultura Luiz de Queiroz-ESALQ/USP, Departamento de Zootecnia, Laboratório de Biotecnologia Animal, Piracicaba, SP, Brazil.
Vet Parasitol. 2010 Jul 15;171(1-2):68-73. doi: 10.1016/j.vetpar.2010.03.020. Epub 2010 Mar 19.
This study aimed to evaluate the expression of a subset of cytokine genes in response to Haemonchus placei infections in Nelore cattle presenting different degrees of resistance to natural infections. One hundred weaned bulls, initially 11-12 months old, were evaluated and kept on the same pasture. Faecal and blood samples were collected for parasitological and immunological assays. The seven most resistant and the eight most susceptible animals were selected based on nematode faecal egg counts (FEC) and worm burden. Serum was collected to measure antibody titres, and abomasum and abomasal lymph node tissue samples were collected to analyse the expression of a subset of cytokine genes (IL-2, IL-4, IL-8, IL-12p35, IL-13, TNF-alpha, IFN-gamma, MCP-1, MCP-2, MUC-1) using real-time RT-PCR. Mast cells, eosinophils and globule leukocytes in the abomasal mucosa were enumerated, and IgA levels in the mucus were assessed. Gene expression analysis in the abomasal tissue indicated that IL-4 and IL-13 (TH2 cytokines) were up-regulated in the resistant group, whereas TNF-alpha (TH1/TH2 cytokine) was up-regulated in the susceptible group. In abomasal lymph nodes, IL-4 and IFN-gamma were up-regulated in the resistant and susceptible groups, respectively. In the resistant group, serum IgG1 levels were higher against antigens of H. placei infective larvae on days 14, 42, 70 and 84 and against antigens of H. placei adults on day 84 (P<0.05). The resistant group had higher mast cell counts in the abomasal mucosa than the susceptible group (P<0.05). These results indicate a protective TH2-mediated immune response against H. placei in the resistant group and a less protective TH1 response in the susceptible group.
本研究旨在评估一组细胞因子基因在感染不同程度天然抗性的Nelore 牛的 Haemonchus placei 感染中的表达。100 头断奶公牛,最初 11-12 个月大,进行了评估,并饲养在同一牧场上。收集粪便和血液样本进行寄生虫学和免疫学检测。根据线虫粪便卵计数(FEC)和蠕虫负担,选择 7 头最具抗性和 8 头最敏感的动物。采集血清以测量抗体滴度,并采集皱胃和皱胃淋巴结组织样本,使用实时 RT-PCR 分析一组细胞因子基因(IL-2、IL-4、IL-8、IL-12p35、IL-13、TNF-α、IFN-γ、MCP-1、MCP-2、MUC-1)的表达。计数皱胃黏膜中的肥大细胞、嗜酸性粒细胞和颗粒白细胞,并评估黏液中的 IgA 水平。皱胃组织中的基因表达分析表明,抗性组中 IL-4 和 IL-13(TH2 细胞因子)上调,而敏感组中 TNF-α(TH1/TH2 细胞因子)上调。在皱胃淋巴结中,抗性和敏感组中分别上调了 IL-4 和 IFN-γ。在抗性组中,针对 H. placei 感染性幼虫的抗原在第 14、42、70 和 84 天以及针对 H. placei 成虫的抗原在第 84 天的血清 IgG1 水平较高(P<0.05)。抗性组的肥大细胞计数高于敏感组(P<0.05)。这些结果表明,抗性组对 H. placei 存在保护性的 TH2 介导的免疫反应,而敏感组的 TH1 反应则不太具有保护性。