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人类肠道上皮细胞上Ia分子功能的证据。

Evidence for function of Ia molecules on gut epithelial cells in man.

作者信息

Mayer L, Shlien R

机构信息

Division of Clinical Immunology, Mount Sinai Medical Center, New York, NY 10029.

出版信息

J Exp Med. 1987 Nov 1;166(5):1471-83. doi: 10.1084/jem.166.5.1471.

Abstract

Using freshly isolated Ia+ gut epithelial cells we have been able to demonstrate that these cells can function as accessory cells in an immune response. The cells can act as stimulators in both autologous and allogeneic MLRs. More importantly, these cells are capable of taking up the soluble antigen, tetanus toxoid, processing it, and presenting it to tetanus-primed T cells. These functions appear to relate to the presence of surface Ia in that a hetero-anti-Ia antibody can block these effects. Noteworthy is the finding that the subpopulation of T cells stimulated when epithelial cells are used as accessory cells is the T8+, 9.3-T cell. These cells function as potent antigen-nonspecific suppressor cells in both MLR, T cell antigen responses, and induction of B cell differentiation by PWM. These findings have significant implications in local gut immune responses and may help explain several poorly characterized phenomena of mucosal immunity.

摘要

利用新鲜分离的Ia⁺肠道上皮细胞,我们已经能够证明这些细胞在免疫反应中可作为辅助细胞发挥作用。这些细胞在自体和异体混合淋巴细胞反应(MLR)中均可充当刺激细胞。更重要的是,这些细胞能够摄取可溶性抗原破伤风类毒素,对其进行加工处理,并将其呈递给经破伤风免疫的T细胞。这些功能似乎与表面Ia的存在有关,因为一种异源性抗Ia抗体可阻断这些效应。值得注意的是,当上皮细胞用作辅助细胞时所刺激的T细胞亚群是T8⁺、9.3⁻T细胞。这些细胞在MLR、T细胞抗原反应以及PWM诱导B细胞分化过程中均作为有效的抗原非特异性抑制细胞发挥作用。这些发现对局部肠道免疫反应具有重要意义,并且可能有助于解释黏膜免疫中一些特征尚不明确的现象。

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