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将抗原靶向树突状细胞上的Dec-205可在小鼠实验性结肠炎中诱导免疫保护。

Targeting Antigens to Dec-205 on Dendritic Cells Induces Immune Protection in Experimental Colitis in Mice.

作者信息

Wadwa Munisch, Klopfleisch Robert, Buer Jan, Westendorf Astrid M

机构信息

Institute of Medical Microbiology, University Hospital Essen, University Duisburg Essen , Essen, Germany.

Institute of Veterinary Pathology, Freie Universität Berlin , Berlin, Germany.

出版信息

Eur J Microbiol Immunol (Bp). 2016 Jan 27;6(1):1-8. doi: 10.1556/1886.2015.00048. eCollection 2016 Mar.

Abstract

The endocytotic c-type lectin receptor DEC-205 is highly expressed on immature dendritic cells. In previous studies, it was shown that antigen-targeting to DEC-205 is a useful tool for the induction of antigen-specific Foxp3(+) regulatory T cells and thereby can prevent inflammatory processes. However, whether this approach is sufficient to mediate tolerance in mucosal tissues like the gut is unknown. In this study, we established a new mouse model in which the adoptive transfer of naive hemagglutinin (HA)-specific CD4(+)Foxp3(-) T cells into VILLIN-HA transgenic mice leads to severe colitis. To analyze if antigen-targeting to DEC-205 could protect against inflammation of the gut, VILLIN-HA transgenic mice were injected with an antibody-antigen complex consisting of the immunogenic HA110-120 peptide coupled to an α-DEC-205 antibody (DEC-HA) before adoptive T cell transfer. DEC-HA-treated mice showed significantly less signs of intestinal inflammation as was demonstrated by reduced loss of body weight and histopathology in the gut. Strikingly, abrogated intestinal inflammation was mediated via the conversion of naive HA-specific CD4(+)Foxp3(-) T cells into HA-specific CD4(+)Foxp3(+) regulatory T cells. In this study, we provide evidence that antigen-targeting to DEC-205 can be utilized for the induction of tolerance in mucosal organs that are confronted with large numbers of exogenous antigens.

摘要

内吞型C型凝集素受体DEC-205在未成熟树突状细胞上高度表达。在先前的研究中,已表明将抗原靶向DEC-205是诱导抗原特异性Foxp3(+)调节性T细胞的有用工具,从而可以预防炎症过程。然而,这种方法是否足以介导像肠道这样的黏膜组织中的耐受性尚不清楚。在本研究中,我们建立了一种新的小鼠模型,将天然血凝素(HA)特异性CD4(+)Foxp3(-) T细胞过继转移到VILLIN-HA转基因小鼠中会导致严重的结肠炎。为了分析将抗原靶向DEC-205是否可以预防肠道炎症,在过继T细胞转移之前,给VILLIN-HA转基因小鼠注射由与α-DEC-205抗体(DEC-HA)偶联的免疫原性HA110-120肽组成的抗体-抗原复合物。DEC-HA处理的小鼠表现出明显较少的肠道炎症迹象,体重减轻和肠道组织病理学检查结果均表明了这一点。令人惊讶的是,肠道炎症的消除是通过将天然HA特异性CD4(+)Foxp3(-) T细胞转化为HA特异性CD4(+)Foxp3(+)调节性T细胞来介导的。在本研究中,我们提供了证据表明将抗原靶向DEC-205可用于在面临大量外源性抗原的黏膜器官中诱导耐受性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8bc/4838981/7975522aff73/eujmi-06-01-g001.jpg

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