首页> 美国卫生研究院文献>The Journal of Veterinary Medical Science >Cytokine elevation in the mouse small intestine at the early stage ofinfection with the gastrointestinal parasite Heligmosomoidespolygyrus
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Cytokine elevation in the mouse small intestine at the early stage ofinfection with the gastrointestinal parasite Heligmosomoidespolygyrus

机译:在早期阶段的小鼠小肠中的细胞因子升降用胃肠寄生虫寄生虫感染多曲

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摘要

To eliminate pathogens, the initiation of an appropriate immune response is critical.When the gastrointestinal nematode, Heligmosomoides polygyrus (Hp),invades the small intestine, a type-2 cytokine response is initiated; however, thisresponse is not sufficient to clear the infection, and chronic infection can ensue. Inthis study, the host defense against Hp was investigated in mice with a focus on the roleof CD4+ T cells. To this end, tissues from the small intestine and mesenteric lymph node(MLN) were collected every day from just after infection until Day 5 because many previousstudies have described the later stages of infection from Day 8 to Day 12, during which Hpreturns to the lumen and Th2 cytokine expression reaches its peak. In this study, wefocused on investigating the initiation of the type-2 immune response. Our resultsindicated that the larvae encysted by Day 3. Increased type-2 cytokine gene expressionstarted in the small intestine before Day 2 and increased again on Day 5. Interferon (IFN)γ increased significantly on the second day. Flow cytometry and gene expression analysisof MLN cells revealed that CD4+ T cells were not activated until Day 4. These resultssuggested that innate immune cells in submucosa are activated immediately after infection,but CD4+ T cells accumulate in the cyst zone later. In addition, IFNγ may have animportant role in converting type-2 cytokine-producing cells from innate cells to CD4+ Tcells.
机译:为了消除病原体,对适当的免疫反应的起始至关重要。当胃肠线虫线虫,Heligmosomoides Polygyrus(HP),侵入小肠,启动了2型细胞因子响应;但是,这是这样的响应不足以清除感染,慢性感染可以随之而来。在本研究,对惠普的主持人防御在小鼠中进行了调查,重点是作用CD4 + T细胞。为此,来自小肠和肠系膜淋巴结的组织(MLN)每天从感染后每天收集,直到第5天,因为许多以前研究已经描述了在第8天至第12天感染的后期感染阶段,在此期间HP返回腔和Th2细胞因子表达达到其峰值。在这项研究中,我们专注于调查2型免疫应答的启动。我们的结果表明幼虫在第3天患者。增加2型细胞因子基因表达在第2天之前开始在小肠中,并在第5天再次增加。干扰素(IFN)γ在第二天显着增加。流式细胞术和基因表达分析MLN细胞显示,在第4天之前未激活CD4 + T细胞。这些结果建议在感染后立即激活粘膜下的先天免疫细胞,但CD4 + T细胞以后在囊肿区积聚。此外,IFNγ可能有一个将2型细胞因子产生细胞从先天细胞转化为CD4 + T的重要作用细胞。

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