细胞因子在牛分枝杆菌感染不同阶段牛外周血单核细胞中的表达

Díaz-Otero, Fernando, Manzo-Sandoval, Anabelle, J. Laura, Lugo-Arriaga, María Teresa
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引用次数: 0

摘要

在牛结核病(bTB)中,观察到细胞、体液或两种类型的免疫反应。本研究的目的是基于与Th1 (IFN-γ, IL-2)或Th2 (IL-4, IL-10)应答相关的细胞因子基因表达差异来检测结核病奶牛的免疫状态。研究人员选择了23头奶牛,这些奶牛属于位于msamuxico伊达尔戈州农村地区的一个奶牛群。采用单次皮内比较宫颈结核素(SICCT)试验、干扰素γ (IFN-γ)释放试验(BOVIGAM)和酶联免疫吸附试验(ELISA)检测牛支原体感染。13头奶牛各项试验均呈阳性(1组);10头奶牛ELISA阳性(第2组),其余奶牛均阴性(第3组,对照组)。用牛纯化蛋白衍生物(PPD)、禽类PPD和豆豆蛋白A (Con A)丝裂原体外刺激动物外周血单核细胞(PBMC) 72h。以β-肌动蛋白基因为内对照,采用逆转录聚合酶链式反应(RT-PCR)检测各组细胞因子mRNA表达水平的变化。在第1组中,PPD牛和Con a刺激的细胞大量产生IFN-γ、IL-2和IL-4,但不产生IL-10。相比之下,PPD刺激的细胞显示出较低的细胞因子转录产物。在第2组中,细胞对牛PPD反应显著产生IL-10 (P< 0.001)。在对照组中,仅在Con a刺激的细胞中观察到IFN-γ和IL-2的高产量。1组动物死后检查发现淋巴结有轻微和中度病变,而2组动物的病变范围更广。结果表明,在评估组中,决定Th1/Th2反应平衡的细胞因子的基因表达水平存在差异。此外,当结核性失能牛的结核菌素试验和IFN-γ试验均为阴性时,PBMC中抗牛分枝杆菌抗体水平高和IL-10表达高是进展性bTB的指标。在诊断清单中纳入血清学和IL-10细胞因子表达可提高对感染牛的检测,从而帮助控制牛结核病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytokine Expression in Peripheral Blood Mononuclear Cell Cultures Obtained from Cattle with Different Stages of Natural Mycobacterium bovis Infection
In bovine tuberculosis (bTB), cellular, humoral, or both types of immune responses have been observed. The purpose of this study was to examine the immune status of tuberculous cows based on the differential cytokine gene expression associated with Th1 (IFN-γ, IL-2), or Th2 (IL-4, IL-10) responses. Twenty-three (23) cows belonging to a dairy herd located in a rural region of the State of Hidalgo, México, were selected for the study. Single Intradermal Comparative Cervical Tuberculin (SICCT) Test, Interferon-Gamma (IFN-γ) Release Assay (BOVIGAM), and Enzyme-Linked Immunosorbent Assay (ELISA) were used for detection of cattle infected by M. bovis. Thirteen cows were positive to all the tests (Group 1); ten cows were positive only to ELISA (Group 2), and the remaining Group (Group 3, control) included cows negative to all the tests. Peripheral blood mononuclear cells (PBMC) from animals were in vitro stimulated by bovin purified protein derivative (PPD), avian PPD, and Concanavalin A (Con A) mitogen for 72h. Changes in the levels of expression of mRNA of the respective cytokines was measured by Reverse Transcription-Polymerase Chain Reaction (RT-PCR) using β-actin gene as internal control. In group 1, PPD bovis and Con A-stimulated cells exhibited high production of IFN-γ, IL-2 and IL-4, but not IL-10. In contrast, PPD avium-stimulated cells displayed a low production of cytokine transcripts. In group 2, cells showed a significant production of IL-10 in response to bovine PPD (P< 0.001). In the control group, a high production of IFN-γ and IL-2 was observed only in Con A-stimulated cells. Post-mortem examinations in animals of group 1 showed slight and medium lesions in lymph nodes, whereas in group 2, the lesions were more extensive. Results indicate differences on gene expression levels of cytokines considered to determine balance in Th1/Th2 response among the evaluated groups. In addition, high levels of antibodies against M. bovis and high IL-10 expression in PBMC together are indicators of progressive bTB when both tuberculin test and IFN-γ assay are negative in tuberculous anergic cattle. Inclusion of serology and IL-10 cytokine expression in in the diagnosis checklist improves detection of infected cattle to help control bovine tuberculosis.
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