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脐带间充质干细胞在胶原诱导性关节炎中的治疗潜力与TNF抑制剂或抗CD20治疗相当。

Comparable therapeutic potential of umbilical cord mesenchymal stem cells in collagen-induced arthritis to TNF inhibitor or anti-CD20 treatment.

作者信息

Sun Yue, Kong Wei, Huang Saisai, Shi Bingyu, Zhang Hanyu, Chen Weiwei, Zhang Huayong, Zhao Cheng, Tang Xiaojun, Yao Genhong, Feng Xuebing, Sun Lingyun

机构信息

Department of Rheumatology and Immunology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.

出版信息

Clin Exp Rheumatol. 2017 Mar-Apr;35(2):288-295. Epub 2017 Jan 15.

Abstract

OBJECTIVES

The effects of mesenchymal stem cell (MSC) transplantation on established collagen-induced arthritis (CIA) were evaluated and compared to biologic therapies.

METHODS

CIA was induced with the immunisation of type II collagen (CII) in DBA/1 mice. Human umbilical cord MSC, anti-TNF antibody, rhTNFR:Fc fusion protein and anti-CD20 antibody were respectively injected intraperitoneally into CIA mice. Arthritis severity was assessed by clinical and histological scoring. The frequencies of lymphocytes in spleen were analysed, and serum concentrations of cytokines and autoantibody to CII were also measured. The ability of MSC to regulate the balance of T helper cell subsets in CII stimulated CIA CD4+ T cells was assessed in vitro.

RESULTS

MSC treatment significantly decreased the severity of arthritis, which was comparable to biologic treatments. All the treatments down-regulated Th1 subset. Except anti-CD20 all the treatments decreased Th17 subset. MSC treatment enhanced the proportion of regulatory T (Treg) cells and inhibited the generation of T follicular helper (Tfh) cells. The decrease in autoantibody level was detectable in all the treated groups. In vitro MSC induced Foxp3+ T cells, and down-regulated IL-17+, IFNγ+ T cells and pathogenic IL-17+IFNγ+ or IL-17+Foxp3+ T cells. MSC also reduced the secretion of IL-1β, IL-6, IL-17 and TNF-α among collagen-specific T cells.

CONCLUSIONS

MSC show comparable effects to the known biologic treatments and correct immune imbalance in CIA. MSC might provide a promising approach for the treatment of rheumatoid arthritis.

摘要

目的

评估间充质干细胞(MSC)移植对已建立的胶原诱导性关节炎(CIA)的影响,并与生物疗法进行比较。

方法

通过在DBA/1小鼠中免疫II型胶原(CII)诱导CIA。将人脐带MSC、抗TNF抗体、重组人TNFR:Fc融合蛋白和抗CD20抗体分别腹腔注射到CIA小鼠体内。通过临床和组织学评分评估关节炎严重程度。分析脾脏中淋巴细胞的频率,并测量细胞因子血清浓度和针对CII的自身抗体。在体外评估MSC调节CII刺激的CIA CD4+ T细胞中辅助性T细胞亚群平衡的能力。

结果

MSC治疗显著降低了关节炎的严重程度,这与生物治疗相当。所有治疗均下调了Th1亚群。除抗CD20外,所有治疗均降低了Th17亚群。MSC治疗增加了调节性T(Treg)细胞的比例,并抑制了滤泡辅助性T(Tfh)细胞的产生。在所有治疗组中均可检测到自身抗体水平的降低。在体外,MSC诱导Foxp3+ T细胞,并下调IL-17+、IFNγ+ T细胞以及致病性IL-17+IFNγ+或IL-17+Foxp3+ T细胞。MSC还减少了胶原特异性T细胞中IL-1β、IL-6、IL-17和TNF-α的分泌。

结论

MSC显示出与已知生物治疗相当的效果,并纠正了CIA中的免疫失衡。MSC可能为类风湿性关节炎的治疗提供一种有前景的方法。

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