Anti-arthritis Effect of Anti-chitinase-3-like 1 Antibody Through Inhibition of MMP3.

IF 4.3 4区 医学 Q2 IMMUNOLOGY
Immune Network Pub Date : 2025-02-07 eCollection Date: 2025-04-01 DOI:10.4110/in.2025.25.e5
Dae Hwan Kim, Ji Eun Yu, Dong Hun Lee, Min Ji Kim, Seong Hee Jeon, Jaesuk Yun, Dong Ju Son, Bongcheol Kim, Yoon Ji Yong, Young-Soo Lim, Tae Hun Kim, Azizi Mohammad Khalid, Sang-Bae Han, Yong Sun Lee, Jin Tae Hong
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引用次数: 0

Abstract

Chitinase-3-like 1 (CHI3L1) is a key factor in regulating inflammatory processes and development of rheumatoid arthritis (RA) since is highly produced by synoviocytes and macrophages in the development RA. Collagen-induced arthritis (CIA) model is the most widely used because its pathogenesis is similar to human RA. Thus, we aimed to investigate if anti-CHI3L1 antibody could reduce RA development in the CIA model. To induce CIA, DBA1/J mice were immunized with a type II bovine collagen emulsion in complete Freund's adjuvant, and boosted type II bovine collagen. THP-1 and MH7A cells were used for pro-inflammation responses. Anti-CHI3L1 Ab treatment reduced the RA clinical score and paw thickness of mice. Inflammation-induced matrix metalloproteinase 3 (MMP3) expression was reduced by inhibiting CHI3L1, and MMP3 knockdown suppressed the expression of RA-related inflammatory cytokines in LPS-treated THP-1 and MH7A cells. Our findings suggest that anti-CHI3L1 Ab showed significant anti-arthritic effects by inhibiting MMP3 expression.

抗几丁质酶-3样1抗体通过抑制MMP3抗关节炎的作用。
几甲壳素酶-3样1 (CHI3L1)在类风湿关节炎(RA)的发展过程中由滑膜细胞和巨噬细胞大量产生,是调节炎症过程和发展的关键因子。胶原诱导关节炎(CIA)模型因其发病机制与人类类风湿关节炎相似而被广泛应用。因此,我们的目的是研究抗chi3l1抗体是否可以减少CIA模型中RA的发展。为了诱导CIA, DBA1/J小鼠用含完全弗氏佐剂的II型牛胶原乳剂免疫,并增强II型牛胶原。THP-1和MH7A细胞用于促炎症反应。抗chi3l1抗体治疗可降低RA临床评分和小鼠脚掌厚度。通过抑制CHI3L1,炎症诱导的基质金属蛋白酶3 (MMP3)表达降低,MMP3敲低抑制lps处理的THP-1和MH7A细胞中ra相关炎症因子的表达。我们的研究结果表明,抗chi3l1抗体通过抑制MMP3的表达而具有明显的抗关节炎作用。
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来源期刊
Immune Network
Immune Network Immunology and Microbiology-Immunology
CiteScore
2.90
自引率
3.30%
发文量
36
期刊介绍: Immune Network publishes novel findings in basic and clinical immunology and aims to provide a medium through which researchers in various fields of immunology can share and connect. The journal focuses on advances and insights into the regulation of the immune system and the immunological mechanisms of various diseases. Research that provides integrated insights into translational immunology is given preference for publication. All submissions are evaluated based on originality, quality, clarity, and brevity
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