• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

分析补体系统经典途径、替代途径和甘露糖结合凝集素途径在寡关节型幼年特发性关节炎发病机制中的作用。

Analysis of the classical, alternative, and mannose binding lectin pathway of the complement system in the pathogenesis of oligoarticular juvenile idiopathic arthritis.

机构信息

Medical University Innsbruck, Innsbruck, Austria.

出版信息

Rheumatol Int. 2012 Jun;32(6):1815-8. doi: 10.1007/s00296-011-1973-0. Epub 2011 Jun 7.

DOI:10.1007/s00296-011-1973-0
PMID:21647665
Abstract

The complement system plays a role in the pathogenesis of some autoimmunopathies. This longitudinal study evaluates the contribution of the complement system in the pathogenesis of oligoarticular juvenile idiopathic arthritis (JIA). Serum of the peripheral blood and the synovial fluid were investigated for the activity of the classical (CP), the mannose binding lectin (MBL), and the alternative pathway (AP). A total of 12 samples from peripheral blood (PB) and two samples from synovial fluid (SF) of girls with oligoarticular JIA were investigated in a longitudinal observation from the time point of the diagnosis of JIA. The differences between the complement activity in the PB and in the SF were extremely statistically significant (CP and MBL: P < 0.0001; AP: < 0.0087). The activity of the CP and the MBL pathway was reduced. The AP is the main contributor in the pathogenesis of oligoarticular JIA. Anti-C5 therapy may be an option to avoid the creation of the membrane attack complex.

摘要

补体系统在某些自身免疫性疾病的发病机制中起作用。这项纵向研究评估了补体系统在寡关节型幼年特发性关节炎(JIA)发病机制中的作用。研究了外周血血清和滑液中经典途径(CP)、甘露糖结合凝集素(MBL)和替代途径(AP)的活性。对 12 名寡关节型 JIA 女孩的外周血(PB)和 2 份滑液(SF)样本进行了纵向观察,从 JIA 诊断时间点开始。PB 和 SF 中的补体活性差异具有统计学意义(CP 和 MBL:P < 0.0001;AP:< 0.0087)。CP 和 MBL 途径的活性降低。AP 是寡关节型 JIA 发病机制的主要贡献者。抗 C5 治疗可能是避免形成膜攻击复合物的一种选择。

相似文献

1
Analysis of the classical, alternative, and mannose binding lectin pathway of the complement system in the pathogenesis of oligoarticular juvenile idiopathic arthritis.分析补体系统经典途径、替代途径和甘露糖结合凝集素途径在寡关节型幼年特发性关节炎发病机制中的作用。
Rheumatol Int. 2012 Jun;32(6):1815-8. doi: 10.1007/s00296-011-1973-0. Epub 2011 Jun 7.
2
Investigation of Complement-activating Pattern Recognition Molecules and Associated Enzymes as Possible Inflammatory Markers in Oligoarticular and Systemic Juvenile Idiopathic Arthritis.寡关节型和全身型幼年特发性关节炎中补体激活模式识别分子及相关酶作为潜在炎症标志物的研究
J Rheumatol. 2015 Jul;42(7):1252-8. doi: 10.3899/jrheum.141449. Epub 2015 Jun 1.
3
Lectin pathway factors in patients suffering from juvenile idiopathic arthritis.患有幼年特发性关节炎患者的凝集素途径相关因子。
Immunol Cell Biol. 2017 Sep;95(8):666-675. doi: 10.1038/icb.2017.31. Epub 2017 Apr 13.
4
Children with oligoarticular juvenile idiopathic arthritis have skewed synovial monocyte polarization pattern with functional impairment-a distinct inflammatory pattern for oligoarticular juvenile arthritis.少关节型幼年特发性关节炎患儿滑膜单核细胞极化模式异常且伴有功能障碍——这是少关节型幼年关节炎独特的炎症模式。
Arthritis Res Ther. 2020 Aug 12;22(1):186. doi: 10.1186/s13075-020-02279-9.
5
Significance of complement components C1q and C4 bound to circulating immune complexes in juvenile idiopathic arthritis: support for classical complement pathway activation.补体成分 C1q 和 C4 与循环免疫复合物结合在幼年特发性关节炎中的意义:支持经典补体途径的激活。
Clin Exp Rheumatol. 2011 Nov-Dec;29(6):1049-56. Epub 2011 Dec 22.
6
Depressed activation of the lectin pathway of complement in hereditary angioedema.遗传性血管性水肿中补体凝集素途径的激活受抑。
Clin Exp Immunol. 2008 Jul;153(1):68-74. doi: 10.1111/j.1365-2249.2008.03671.x. Epub 2008 May 5.
7
Differential Accumulation and Activation of Monocyte and Dendritic Cell Subsets in Inflamed Synovial Fluid Discriminates Between Juvenile Idiopathic Arthritis and Septic Arthritis.在炎症性滑液中,单核细胞和树突状细胞亚群的差异积累和激活可区分幼年特发性关节炎和化脓性关节炎。
Front Immunol. 2020 Jul 31;11:1716. doi: 10.3389/fimmu.2020.01716. eCollection 2020.
8
Complement activation pathways in murine immune complex-induced arthritis and in C3a and C5a generation in vitro.补体激活途径在鼠免疫复合物诱导性关节炎和体外 C3a 和 C5a 生成中的作用。
Clin Exp Immunol. 2010 Jan;159(1):100-8. doi: 10.1111/j.1365-2249.2009.04035.x. Epub 2009 Oct 19.
9
Interleukin-18 as a mediator of systemic juvenile idiopathic arthritis.白细胞介素-18作为全身型幼年特发性关节炎的介质
Clin Rheumatol. 2007 Aug;26(8):1332-4. doi: 10.1007/s10067-006-0474-0. Epub 2006 Nov 25.
10
Phenotypic and functional characterization of switch memory B cells from patients with oligoarticular juvenile idiopathic arthritis.寡关节型幼年特发性关节炎患者转换记忆 B 细胞的表型和功能特征。
Arthritis Res Ther. 2009;11(5):R150. doi: 10.1186/ar2824. Epub 2009 Oct 5.

引用本文的文献

1
Population-level single-cell genomics reveals conserved gene programs in systemic juvenile idiopathic arthritis.人群水平单细胞基因组学揭示了系统性幼年特发性关节炎中的保守基因程序。
J Clin Invest. 2023 Nov 15;133(22):e166741. doi: 10.1172/JCI166741.
2
Single-cell RNA sequencing reveals the fragility of male spermatogenic cells to Zika virus-induced complement activation.单细胞 RNA 测序揭示了 Zika 病毒诱导的补体激活对雄性生殖细胞的脆弱性。
Nat Commun. 2023 Apr 29;14(1):2476. doi: 10.1038/s41467-023-38223-z.
3
Complement lectin pathway protein levels reflect disease activity in juvenile idiopathic arthritis: a longitudinal study of the Nordic JIA cohort.

本文引用的文献

1
Partial C4 deficiency in juvenile idiopathic arthritis patients.青少年特发性关节炎患者的部分C4缺乏症
J Clin Rheumatol. 2007 Oct;13(5):256-60. doi: 10.1097/RHU.0b013e318156b9e3.
2
Rheumatoid arthritis and the complement system.类风湿关节炎与补体系统。
Ann Med. 2007;39(7):517-30. doi: 10.1080/07853890701477546.
3
Alternative complement pathway activation is essential for inflammation and joint destruction in the passive transfer model of collagen-induced arthritis.在胶原诱导性关节炎的被动转移模型中,替代补体途径的激活对于炎症和关节破坏至关重要。
补体凝集素途径蛋白水平反映幼年特发性关节炎的疾病活动度:北欧 JIA 队列的纵向研究。
Pediatr Rheumatol Online J. 2019 Sep 9;17(1):63. doi: 10.1186/s12969-019-0367-9.
4
Lectin pathway factors in patients suffering from juvenile idiopathic arthritis.患有幼年特发性关节炎患者的凝集素途径相关因子。
Immunol Cell Biol. 2017 Sep;95(8):666-675. doi: 10.1038/icb.2017.31. Epub 2017 Apr 13.
5
Complement activation by merozoite antigens of Plasmodium falciparum.恶性疟原虫裂殖子抗原激活补体。
PLoS One. 2014 Aug 21;9(8):e105093. doi: 10.1371/journal.pone.0105093. eCollection 2014.
J Immunol. 2006 Aug 1;177(3):1904-12. doi: 10.4049/jimmunol.177.3.1904.
4
Role of complement in innate and autoimmunity.补体在固有免疫和自身免疫中的作用。
J Nephrol. 2005 Nov-Dec;18(6):642-53.
5
Extra corporeal membrane oxygenation and plasmapheresis for pulmonary hemorrhage in microscopic polyangiitis.
Pediatr Nephrol. 2005 Apr;20(4):526-8. doi: 10.1007/s00467-004-1724-5. Epub 2005 Feb 16.
6
Proinflammatory S100 proteins in arthritis and autoimmune disease.关节炎和自身免疫性疾病中的促炎S100蛋白。
Arthritis Rheum. 2004 Dec;50(12):3762-71. doi: 10.1002/art.20631.
7
International League of Associations for Rheumatology classification of juvenile idiopathic arthritis: second revision, Edmonton, 2001.国际风湿病协会联盟青少年特发性关节炎分类:第二次修订版,埃德蒙顿,2001年
J Rheumatol. 2004 Feb;31(2):390-2.
8
Local production of complement proteins in rheumatoid arthritis synovium.类风湿性关节炎滑膜中补体蛋白的局部产生。
Arthritis Rheum. 2002 Apr;46(4):934-45. doi: 10.1002/art.10183.
9
Arthritis critically dependent on innate immune system players.关节炎严重依赖先天性免疫系统参与者。
Immunity. 2002 Feb;16(2):157-68. doi: 10.1016/s1074-7613(02)00275-3.
10
Revision of the proposed classification criteria for juvenile idiopathic arthritis: Durban, 1997.青少年特发性关节炎拟议分类标准的修订:德班,1997年。
J Rheumatol. 1998 Oct;25(10):1991-4.