首页> 美国卫生研究院文献>Immunology >Type-1 and type-2 CD8+ T-cell subsets isolated from chronic adult periodontitis tissue differ in surface phenotype and biological functions.
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Type-1 and type-2 CD8+ T-cell subsets isolated from chronic adult periodontitis tissue differ in surface phenotype and biological functions.

机译:从慢性成人牙周炎组织中分离出的1型和2型CD8 + T细胞亚群在表面表型和生物学功能上有所不同。

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摘要

Cloning of CD8+ T cells expressing the alpha beta T-cell receptor from inflamed human gingiva revealed that at least two different subsets were found within the tissue and that these subsets were able to interact with each other. One subset produced high levels of interferon-gamma (IFN-gamma) and no interleukin-4 (IL-4) or IL-5, exhibited phytohaemagglutinin (PHA)- or anti-CD3-mediated cytolytic activity, and were CD28+. The other subset produced high levels of IL-4 in combination with IL-5, displayed no cytotoxicity and were CD28-. From the latter subset CD8+ T-cell clones were able to suppress the proliferative response of cytotoxic CD8+ T-cell clones. This suppression could be abolished by anti-IL-4 monoclonal antibodies. However, IL-4 alone was not able to induce the suppression. Our results indicate that CD8+ T cells might participate in local immune responses by the suppression of IFN-gamma-producing cells and by favouring humoral responses via the production of IL-4 and IL-5.
机译:从发炎的人牙龈中克隆表达α-βT-细胞受体的CD8 + T细胞表明,在组织中至少发现了两个不同的亚群,这些亚群之间能够相互作用。一个子集产生高水平的干扰素-γ(IFN-γ),而没有白介素4(IL-4)或IL-5,没有显示植物血凝素(PHA)或抗CD3介导的溶细胞活性,并且是CD28 +。其他亚群与IL-5联合产生高水平的IL-4,无细胞毒性,为CD28-。从后面的子集中,CD8 + T细胞克隆能够抑制细胞毒性CD8 + T细胞克隆的增殖反应。抗IL-4单克隆抗体可以消除这种抑制作用。然而,单独的IL-4不能诱导抑制。我们的结果表明,CD8 + T细胞可能通过抑制产生IFN-γ的细胞和通过产生IL-4和IL-5促进体液应答而参与局部免疫应答。

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