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白细胞介素 9 中和可减轻小鼠胶原诱导性关节炎的严重程度。

Interleukin 9 neutralisation reduces collagen-induced arthritis severity in mouse models.

机构信息

Department ProMISE, Section of Rheumatology, University of Palermo, Italy.

Department of Biopathology and Medical Biotechnology, University of Palermo, Italy.

出版信息

Clin Exp Rheumatol. 2023 Jan;41(1):94-102. doi: 10.55563/clinexprheumatol/chima7. Epub 2022 May 23.

Abstract

OBJECTIVES

Interleukin 9 (IL-9) is a mediator of tissue damage in several inflammatory diseases. In this study we aimed to evaluate the effects of in vivo IL-9 neutralisation in mice developing collagen induced arthritis (CIA).

METHODS

DBA/1 were immunised with collagen in Freund's complete adjuvant (CFA) to induce arthritis. Anti-IL-9 mAb was injected in mice after the onset of arthritis (Group A) or on the same day as sensitisation and again on the day of the challenge (Group B). Histological analysis was performed in joints of mice and spleen cells were also analysed by flow cytometry. A geneset analysis was carried out on whole tarsal joint tissue transcriptomes.

RESULTS

IL-9 was over-expressed in swollen joints of mice developing arthritis. Treatment with anti-IL-9 mAb after arthritis onset efficiently down-modulated the severity of joint inflammation. Similarly, anti-IL-9 mAb administered on the same day as sensitisation and on the day of challenge also delayed the onset of arthritis. Anti-IL-9 mAb injection after the onset of arthritis was associated with a decrease of CD4+ TNF-α+ cells and an increase of CD4+ FoxP3+ IL-10+ cells. Geneset analysis in CIA showed an up-regulation of GATA3 with no significant direct interactions between IL-9 and GATA3, which instead was mediated by IL-5 through STAT6.

CONCLUSIONS

Our results suggest that IL-9 is involved in the immunopathogenesis of CIA. Further implications for the clinical translation of our findings are discussed.

摘要

目的

白细胞介素 9(IL-9)是几种炎症性疾病中组织损伤的介质。在这项研究中,我们旨在评估在发生胶原诱导关节炎(CIA)的小鼠中体内中和 IL-9 的效果。

方法

用弗氏完全佐剂(CFA)中的胶原免疫 DBA/1 以诱导关节炎。关节炎发作后(A 组)或致敏当日以及再次在挑战日(B 组)向小鼠注射抗 IL-9 mAb。对小鼠关节进行组织学分析,并通过流式细胞术分析脾细胞。对整个跗关节组织转录组进行基因集分析。

结果

在发生关节炎的小鼠肿胀关节中过度表达了 IL-9。关节炎发作后用抗 IL-9 mAb 治疗可有效下调关节炎症的严重程度。同样,在致敏当日和挑战日给予抗 IL-9 mAb 也可延迟关节炎的发作。关节炎发作后给予抗 IL-9 mAb 与 CD4+TNF-α+细胞减少和 CD4+FoxP3+IL-10+细胞增加有关。CIA 中的基因集分析显示 GATA3 上调,但 IL-9 和 GATA3 之间没有明显的直接相互作用,而是通过 STAT6 介导的 IL-5 实现的。

结论

我们的结果表明 IL-9 参与了 CIA 的免疫发病机制。讨论了我们的发现对临床转化的进一步影响。

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