首页> 美国卫生研究院文献>Immunology >Contribution of CD4+ and CD8+ T lymphocyte subsets to the cytokine secretion patterns induced in mice during sensitization to contact and respiratory chemical allergens.
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Contribution of CD4+ and CD8+ T lymphocyte subsets to the cytokine secretion patterns induced in mice during sensitization to contact and respiratory chemical allergens.

机译:CD4 +和CD8 + T淋巴细胞亚群对接触和呼吸化学过敏原致敏的小鼠诱导的细胞因子分泌模式的贡献。

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摘要

Chemical allergens of different types, those that cause in humans allergic contact dermatitis or occupational asthma induce in mice divergent immune responses characteristic, respectively, of T-helper 1 (Th1)- and Th2-type cell activation. Such responses are associated with the development of different cytokine secretion patterns by draining lymph node cells (LNC), such that contact allergens stimulate vigorous interferon-gamma (IFN-gamma) production, but little secretion of the Th2 cytokines interleukin-4 and interleukin-10 (IL-4 and IL-10), whereas the converse pattern is provoked by respiratory allergens. Using selective depletion with antibody and complement we have here examined the relative contribution of CD4+ and CD8+ T lymphocytes to the cytokine secretion patterns of draining LNC isolated from mice sensitized to chemical allergens. Mice received repeated topical applications of respiratory allergens, trimellitic anhydride (TMA) or diphenylmethane diisocyanate (MDI), or of contact allergens 2,4-dinitrochlorobenzene (DNCB) or formaldehyde. Thirteen days following the initiation of exposure the production by draining LNC of IL-10, IFN-gamma and mitogen (concanavalin A)-inducible IL-4 was measured by enzyme-linked immunosorbent assay (ELISA) after various periods of culture. It was found that the high levels of IL-4 and IL-10 secretion stimulated by TMA or MDI, and the lower levels of these cytokines induced by DNCB or formaldehyde, were in all cases dependent upon the presence of CD4- cells. In contrast, the comparatively high concentrations of IFN-gamma observed following exposure to contact allergens were found to be derived from CD4+ cells, and in the case of DNCB from CD8+ cells also. The low levels of IFN-gamma induced by treatment with TMA or MDI were associated largely or wholly with CD8+ cells. These data indicate that the type 2 cytokine responses induced to different extents by both contact and respiratory chemical allergens are almost exclusively a function of CD4+ cells, but that IFN-gamma is produced by either CD4+ cells in the case of contact allergens or largely by CD8+ cells in the case of chemical respiratory allergens.
机译:不同类型的化学过敏原,分别在人类中引起的过敏性接触性皮炎或职业性哮喘,在小鼠中分别诱导出不同的T辅助1(Th1)和Th2型细胞活化特征的免疫应答。此类反应与通过排空淋巴结细胞(LNC)引起的不同细胞因子分泌模式的发展有关,从而使接触性变应原刺激剧烈的干扰素-γ(IFN-γ)产生,但Th2细胞因子白介素4和白介素-的分泌很少。 10(IL-4和IL-10),相反的模式是由呼吸道过敏原引起的。使用抗体和补体的选择性耗竭,我们在这里检查了CD4 +和CD8 + T淋巴细胞对从对化学过敏原敏感的小鼠中分离的引流LNC的细胞因子分泌模式的相对贡献。小鼠反复接受呼吸道过敏原,偏苯三酸酐(TMA)或二苯基甲烷二异氰酸酯(MDI)或接触性过敏原2,4-二硝基氯苯(DNCB)或甲醛的局部应用。在暴露开始后的第十三天,通过在各个培养阶段后通过酶联免疫吸附测定(ELISA)来测量通过排泄L-10的LNC产生的IL-10,IFN-γ和促分裂原(伴刀豆球蛋白A)诱导的IL-4的产量。已经发现,在所有情况下,由TMA或MDI刺激的高水平的IL-4和IL-10分泌,以及由DNCB或甲醛诱导的这些细胞因子的较低水平,都取决于CD4-细胞的存在。相反,发现接触接触变应原后观察到的较高浓度的IFN-γ来源于CD4 +细胞,对于DNCB而言,也来源于CD8 +细胞。通过TMA或MDI处理诱导的低水平的IFN-γ很大程度上或完全与CD8 +细胞相关。这些数据表明,接触和呼吸化学过敏原在不同程度上诱导的2型细胞因子应答几乎完全是CD4 +细胞的功能,但是在接触过敏原的情况下,CD4 +细胞或大部分由CD8 +产生IFN-γ。在化学呼吸道过敏原的情况下出现细胞。

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