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产生白细胞介素-10的调节性树突状细胞对小鼠自身免疫性胃炎的保护作用。

Protective role of interleukin-10-producing regulatory dendritic cells against murine autoimmune gastritis.

作者信息

Torisu Masamoto, Murakami Hidehiro, Akbar Fazle, Matsui Hidetaka, Hiasa Yoichi, Matsuura Bunzo, Onji Morikazu

机构信息

Department of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, 454 Shitsukawa, Toon, 791-0295, Japan.

出版信息

J Gastroenterol. 2008;43(2):100-7. doi: 10.1007/s00535-007-2133-x. Epub 2008 Feb 29.

Abstract

BACKGROUND

Regulatory dendritic cells (Reg-DCs), which induce regulatory T cells and interleukin (IL)-10 in vitro, are capable of inducing immunogenic tolerance in vivo. In this study, we assessed whether Reg-DCs modulate the course of autoimmune processes in a murine model of autoimmune gastritis (AIG).

METHODS

AIG mice were produced by neonatal thymectomy of 3-day old BALB/c mice followed by administration of polyinosinic:polycytidylic acid (poly I:C). Reg-DCs were produced by culturing bone marrow DCs with IL-10, lipopolysaccharide, and parietal cell (PC) antigen for 2 days. In the course of development of AIG, BALB/c mice were administered either Reg-DCs, mature DCs, or phosphate-buffered saline, intraperitoneally, four times. The levels of gastritis and autoantibody to PC antigen were assessed serially in these mice.

RESULTS

The stages of gastritis and the titers of autoantibody to PC antigen were significantly lower in Reg-DC-treated mice than in mature DC-treated mice (P<0.05). Spleen cells from Reg-DC-treated mice produced increased levels of IL-10 and decreased levels of IL-12p70 and interferon-gamma (P<0.05). Also, frequencies of IL-10-producing CD4(+)CD25(+) T cells in the spleen and Foxp3(+)CD4(+)CD25(+) T cells in the peripheral blood were significantly higher in Reg-DC-treated mice than in mature DC-treated mice (P<0.05).

CONCLUSIONS

Taken together, these results suggest that increased induction of CD4(+)CD25(+) regulatory T cells by Reg-DCs might contribute to downregulation of inflammatory processes and autoantibody production during AIG development in mice.

摘要

背景

调节性树突状细胞(Reg-DCs)在体外可诱导调节性T细胞和白细胞介素(IL)-10,能够在体内诱导免疫原性耐受。在本研究中,我们评估了Reg-DCs是否能调节自身免疫性胃炎(AIG)小鼠模型中自身免疫过程的进程。

方法

通过对3日龄BALB/c小鼠进行新生期胸腺切除,随后给予聚肌苷酸:聚胞苷酸(poly I:C)来制备AIG小鼠。通过用IL-10、脂多糖和壁细胞(PC)抗原培养骨髓树突状细胞2天来制备Reg-DCs。在AIG发展过程中,给BALB/c小鼠腹腔内注射Reg-DCs、成熟树突状细胞或磷酸盐缓冲盐水,共4次。连续评估这些小鼠的胃炎水平和针对PC抗原的自身抗体水平。

结果

Reg-DC处理的小鼠的胃炎阶段和针对PC抗原的自身抗体滴度显著低于成熟树突状细胞处理的小鼠(P<0.05)。Reg-DC处理的小鼠的脾细胞产生的IL-10水平升高,IL-12p70和干扰素-γ水平降低(P<0.05)。此外,Reg-DC处理的小鼠脾脏中产生IL-10的CD4(+)CD25(+) T细胞频率和外周血中Foxp3(+)CD4(+)CD25(+) T细胞频率显著高于成熟树突状细胞处理的小鼠(P<0.05)。

结论

综上所述,这些结果表明Reg-DCs对CD4(+)CD25(+)调节性T细胞的诱导增加可能有助于在小鼠AIG发展过程中下调炎症过程和自身抗体产生。

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