首页> 美国卫生研究院文献>Infection and Immunity >Differential stimulation of interleukin-12 (IL-12) and IL-10 by live and killed Helicobacter pylori in vitro and association of IL-12 production with gamma interferon-producing T cells in the human gastric mucosa.
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Differential stimulation of interleukin-12 (IL-12) and IL-10 by live and killed Helicobacter pylori in vitro and association of IL-12 production with gamma interferon-producing T cells in the human gastric mucosa.

机译:活的和杀死的幽门螺杆菌在体外对白介素12(IL-12)和IL-10的差异刺激以及IL-12产生与人胃粘膜中产生γ干扰素的T细胞的相关性。

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摘要

The objective of these experiments was to examine the ability of Helicobacter pylori to stimulate interleukin-10 (IL-10) or IL-12 and select for either Th1 or Th2 cells. Gastric biopsy specimens were collected from patients who were categorized with respect to the presence of H. pylori and gastric disease as well as their age, gender, medications, and other factors. As Th1 and Th2 cells are selected by IL-12 and IL-10, respectively, biopsy specimens were screened for mRNA and protein for these cytokines. Although mRNA for IL-12 and IL-10 was detected in biopsy specimens obtained from both infected and uninfected patients, IL-12 protein predominated. Levels of IL-10 and IL-12 in gastric tissue did not change in response to infection. Moreover, gamma interferon (IFN-gamma)-producing T cells were found in both the infected and the uninfected gastric mucosa. Stimulation of peripheral blood leukocytes from either infected or uninfected donors with various concentrations of live or killed H. pylori induced immunoreactive IL-12 and IL-10. After stimulation with live H. pylori, IL-12 levels increased more than 30-fold, whereas IL-10 levels increased only 2- to 5-fold, compared to cells stimulated with medium alone. Interestingly, killed H. pylori induced significantly more IL-10 (P < 0.05) than live H. pylori, while recombinant urease only induced IL-10. These results demonstrate that live H. pylori selectively stimulates the induction of IL-12 and Th1 cells that produce IFN-gamma, whereas preparations used in oral vaccines induce more IL-10 and may favor Th2 cell responses.
机译:这些实验的目的是检查幽门螺杆菌刺激白介素10(IL-10)或IL-12的能力,并选择Th1或Th2细胞。从幽门螺杆菌和胃病的存在,年龄,性别,用药和其他因素进行分类的患者中收集胃活检标本。由于分别通过IL-12和IL-10选择Th1和Th2细胞,因此针对这些细胞因子筛选了活检标本的mRNA和蛋白质。尽管在感染和未感染患者的活检标本中均检测到IL-12和IL-10的mRNA,但IL-12蛋白占主导。胃组织中IL-10和IL-12的水平并未因感染而改变。此外,在感染的和未感染的胃粘膜中均发现了产生γ干扰素(IFN-γ)的T细胞。用各种浓度的活的或杀死的幽门螺杆菌从感染或未感染的供体中刺激外周血白细胞诱导免疫反应性IL-12和IL-10。与单独用培养基刺激的细胞相比,用活幽门螺杆菌刺激后,IL-12水平增加超过30倍,而IL-10水平仅增加2至5倍。有趣的是,杀死的幽门螺杆菌比活的幽门螺杆菌诱导的IL-10明显更多(P <0.05),而重组脲酶仅诱导IL-10。这些结果表明,活幽门螺杆菌选择性刺激诱导产生IFN-γ的IL-12和Th1细胞的诱导,而用于口服疫苗的制剂则诱导更多的IL-10,并可能促进Th2细胞应答。

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