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小鼠树突状细胞产生高水平白细胞介素-12:通过主要组织相容性复合体II类分子和CD40分子上调,以及被白细胞介素-4和白细胞介素-10下调。

High level IL-12 production by murine dendritic cells: upregulation via MHC class II and CD40 molecules and downregulation by IL-4 and IL-10.

作者信息

Koch F, Stanzl U, Jennewein P, Janke K, Heufler C, Kämpgen E, Romani N, Schuler G

机构信息

Department of Dermatology, University of Innsbruck, Austria.

出版信息

J Exp Med. 1996 Aug 1;184(2):741-6. doi: 10.1084/jem.184.2.741.

Abstract

We have shown previously that dendritic cells (DC) produce IL-12 upon interaction with CD4+ T cells. Here we ask how this IL-12 production is induced and regulated. Quantitative PCR and in situ hybridization for IL-12 p40 and an ELISA specific for the p70 heterodimer were used to determine IL-12 production. We demonstrate that ligation of either CD40 or MHC class II molecules independently trigger IL-12 production in DC, and that IL-12 production is downregulated by IL-4 and IL-10. The levels of bioactive IL-12 that can be released by triggering with an anti-CD40 mAb or with a T cell hybridoma are high (range 260-4700 pg/ml from 1 X 10(6) DC in 72 h). The CD40-mediated pathway indicates that IL-12 production is induced in DC upon interaction with activated, CD40 ligand-expressing helper T cells, even in the absence of cognate antigen recognition. Side-by-side comparison of IL-12 production, and blocking experiments employing an anti-CD40 ligand mAb, suggest that the CD40-mediated pathway is quantitatively more significant than induction via the MHC class II molecule. The importance of the CD40/CD40 ligand interaction for IL-12 induction in DC likely contributes to the recent finding that mice lacking the CD40 ligand are impaired in mounting Th1 type cell-mediated immune responses.

摘要

我们之前已经表明,树突状细胞(DC)在与CD4+T细胞相互作用时会产生白细胞介素-12(IL-12)。在此我们探究这种IL-12的产生是如何被诱导和调控的。使用针对IL-12 p40的定量PCR和原位杂交以及针对p70异二聚体的特异性酶联免疫吸附测定(ELISA)来确定IL-12的产生。我们证明,CD40或MHC II类分子的连接可独立触发DC中IL-12的产生,并且IL-12的产生会被IL-4和IL-10下调。通过用抗CD40单克隆抗体或T细胞杂交瘤触发释放的生物活性IL-12水平很高(在72小时内,来自1×10(6)个DC的范围为260 - 4700 pg/ml)。CD40介导的途径表明,即使在没有同源抗原识别的情况下,DC在与表达CD40配体的活化辅助性T细胞相互作用时也会诱导产生IL-12。对IL-12产生的并排比较以及使用抗CD40配体单克隆抗体的阻断实验表明,CD40介导的途径在数量上比通过MHC II类分子的诱导更重要。CD40/CD40配体相互作用对DC中IL-12诱导的重要性可能有助于最近的一项发现,即缺乏CD40配体的小鼠在引发Th1型细胞介导的免疫反应方面存在缺陷。

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