首页> 外文期刊>Infection and immunity >Cytokine Gene Expression in Innately Susceptible BALB/c Mice and Relatively Resistant C57BL/6 Mice during Infection with Virulent Burkholderia pseudomallei
【24h】

Cytokine Gene Expression in Innately Susceptible BALB/c Mice and Relatively Resistant C57BL/6 Mice during Infection with Virulent Burkholderia pseudomallei

机译:先天性易感BALB / c小鼠和相对抗性的C57BL / 6小鼠感染强毒性伯克霍尔德氏菌时的细胞因子基因表达

获取原文
获取外文期刊封面目录资料

摘要

Production of cytokines including gamma interferon (IFN-γ) and tumor necrosis factor alpha (TNF-α) is an important early-stage host response following infection with intracellular pathogens. Development of immunity to these pathogens is determined to a large extent by the timing and relative level of expression of the cytokines. Numerous studies have shown that early cytokine responses involving interleukin-12 (IL-12) and IFN-γ are important for resistance to intracellular pathogens, whereas responses involving IL-4 and IL-10 increase host susceptibility. These often-indistinct early cytokine responses influence the differentiation of na??ve CD4+ T helper cells, which later develop into what have commonly been termed Th1- and Th2-type cells. The characterization of CD4+ T-helper-cell responses as Th1 or Th2 type is based largely on the cytokine profiles during the specific phase and has been used in recent years to account for the innate resistance and susceptibility of different inbred strains of mice to several intracellular pathogens. Studies investigating cytokine production in terms of CD4+ T-helper-cell polarization inBurkholderia pseudomallei infection have not been undertaken. In this study, we used semiquantitative reverse transcription-PCR to assess induction of cytokine mRNA in liver and spleen of B. pseudomallei-susceptible BALB/c and relatively resistant C57BL/6 mice following infection with virulent B. pseudomallei. The levels of mRNA for IFN-γ, TNF-α, IL-1β, IL-6, IL-10, and IL-12 increased in both BALB/c and C57BL/6 mice 24 to 36 h after infection. A comparison of BALB/c and C57BL/6 responses revealed the relative levels of expression of mRNA for several of these cytokines, including IFN-γ, were greater in BALB/c mice, suggesting a role for endotoxic shock and cytokine-mediated immunopathology in the development of acute melioidosis. Early induction of mRNA for the cytokines classically associated with development of Th1- and Th2-type responses was absent or minimal, and induction levels in both strains of mice were similar. During the specific phase, cytokine mRNA profiles occurred as a combination of Th1- and Th2-type patterns. Collectively, these results demonstrate that cytokine mRNA responses in BALB/c and C57BL/6 mice following infection with virulent B. pseudomallei do not develop as polarized Th1- or Th2-type profiles. Considering the role of TNF-α and IFN-γ in the processes of endotoxic shock, these results also indicate that selected cytokines, while important for resistance to B. pseudomallei infection, are also potential contributors to immunopathology and the development of acute fulminating disease.
机译:感染细胞内病原体后,包括γ干扰素(IFN-γ)和肿瘤坏死因子α(TNF-α)在内的细胞因子的产生是重要的早期宿主反应。对这些病原体的免疫力的发展在很大程度上取决于细胞因子表达的时间和相对水平。大量研究表明,涉及白细胞介素12(IL-12)和IFN-γ的早期细胞因子应答对于抵抗细胞内病原体很重要,而涉及IL-4和IL-10的应答会增加宿主易感性。这些通常不清楚的早期细胞因子反应影响幼稚的CD4 + T辅助细胞的分化,后来又发展成通常被称为Th1和Th2型细胞。将CD4 + T辅助细胞反应表征为Th1或Th2类型主要是基于特定阶段的细胞因子谱,近年来已用于解释不同近交系小鼠对几种细胞内膜的先天性耐药性和易感性病原体。尚未进行关于假伯克霍尔德氏菌感染中CD4 + T辅助细胞极化的细胞因子产生的研究。在这项研究中,我们使用半定量逆转录-PCR评估了感染假性双歧杆菌后,假性双歧杆菌易感性BALB / c和相对耐药的C57BL / 6小鼠肝脏和脾脏中细胞因子mRNA的诱导。感染后24至36小时,BALB / c和C57BL / 6小鼠的IFN-γ,TNF-α,IL-1β,IL-6,IL-10和IL-12的mRNA水平均升高。对BALB / c和C57BL / 6反应的比较显示,BALB / c小鼠中某些细胞因子(包括IFN-γ)的相对mRNA表达水平更高,表明其对内毒素休克和细胞因子介导的免疫病理学具有重要作用。急性类li虫病的发展。传统上与Th1和Th2型反应的发展相关的经典细胞因子的早期诱导缺失或极少,并且两种小鼠品系中的诱导水平相似。在特定阶段,细胞因子mRNA谱以Th1和Th2型模式的组合出现。总的来说,这些结果表明在BALB / c和C57BL / 6小鼠中,用强毒假单胞菌感染后,细胞因子mRNA应答未发展为极化的Th1-或Th2型谱。考虑到TNF-α和IFN-γ在内毒素性休克过程中的作用,这些结果还表明,所选的细胞因子尽管对抵抗假性马来芽孢杆菌感染很重要,但也可能是免疫病理学和急性暴发性疾病发展的潜在原因。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号