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白细胞介素-10 条件化树突状细胞可预防 NOD 及 HLA-DQ8/RIP-B7.1 人源化小鼠的自身免疫性糖尿病。

IL-10-conditioned dendritic cells prevent autoimmune diabetes in NOD and humanized HLA-DQ8/RIP-B7.1 mice.

机构信息

Yale University School of Medicine, Department of Internal Medicine, Section of Endocrinology, USA.

出版信息

Clin Immunol. 2011 Jun;139(3):336-49. doi: 10.1016/j.clim.2011.03.003. Epub 2011 Mar 9.

Abstract

This study was to determine whether BMDCs cultured in the presence of IL-10 (G/10-DCs) could promote T cell tolerance and prevent autoimmune diabetes in two different animal models of T1D. Our results showed that G/10-DCs suppressed both insulitis and spontaneous diabetes in NOD and HLA-DQ8/RIP-B7.1 mice. The suppression was likely to be mediated by T cells, as we found that regulatory CD4(+)CD25(+)Foxp3(+) cells were significantly increased in G/10-DC treated animals. In vivo, the G/10-DCs inhibited diabetogenic T cell proliferation; in vitro, they had reduced expression of costimulatory molecules and produced little IL-12/23 p40 or IL-6 but a large amount of IL-10 when compared with DCs matured in the presence of IL-4 (G/4-DC). We conclude that IL-10-treated DCs are tolerogenic and induce islet-directed immune tolerance, which was likely to be mediated by T regulatory cells. This non-antigen-specific DC-based approach offers potential for a new therapeutic intervention in T1D.

摘要

本研究旨在确定在 IL-10 存在下培养的 BMDC 是否可以在两种不同的 T1D 动物模型中促进 T 细胞耐受并预防自身免疫性糖尿病。我们的结果表明,G/10-DC 可抑制 NOD 和 HLA-DQ8/RIP-B7.1 小鼠的胰岛炎和自发性糖尿病。这种抑制可能是通过 T 细胞介导的,因为我们发现,在 G/10-DC 处理的动物中,调节性 CD4(+)CD25(+)Foxp3(+)细胞明显增加。在体内,G/10-DC 抑制了致糖尿病 T 细胞的增殖;在体外,与在 IL-4 存在下成熟的 DC(G/4-DC)相比,它们表达的共刺激分子减少,产生的 IL-12/23 p40 或 IL-6 很少,但产生大量的 IL-10。我们得出结论,IL-10 处理的 DC 具有耐受性,并诱导胰岛定向免疫耐受,这可能是由 T 调节细胞介导的。这种基于非抗原特异性 DC 的方法为 T1D 的新治疗干预提供了潜力。

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