• 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

血清 RGC-32 在儿童系统性红斑狼疮中的表达。

Serum RGC-32 in children with systemic lupus erythematosus.

机构信息

Department of Nephrology, Rheumatology and Immunology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200062, China.

出版信息

Sci Rep. 2023 Jul 8;13(1):11047. doi: 10.1038/s41598-023-38092-y.

DOI:10.1038/s41598-023-38092-y
PMID:37422503
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10329644/
Abstract

Childhood-onset systemic lupus erythematosus (SLE) can be more severe than adult patients. Early diagnosis and accurate evaluation of the disease are very important for the patients. Response gene to complement-32 (RGC-32) protein is the downstream regulator of C5b-9 complex which is the terminal pathway of complement activation. Complement system plays a very important role in the pathogenesis of SLE. RGC-32 in patients with SLE has not been reported yet. We aimed to examine the clinical value of RGC-32 in children with SLE. A total of 40 children with SLE and another 40 healthy children were enrolled for this study. Clinical data were obtained prospectively. Serum RGC-32 was determined by ELISA. We found that serum RGC-32 was significantly elevated in children with SLE than that in the healthy group. Serum RGC-32 was significantly higher in the children with moderately/severely active SLE than that in the children with no/mildly active SLE. Furthermore, serum RGC-32 level correlated positively with C-reactive protein, erythrocyte sedimentation rate and ferritin and correlated negatively with white blood cell counts and C3. RGC-32 may be involved in the pathogenesis of SLE. RGC-32 might become a good biomarker in the diagnosis and evaluation of SLE.

摘要

儿童起病系统性红斑狼疮(SLE)可能比成人患者更为严重。早期诊断和准确评估疾病对患者非常重要。补体 3 反应基因(RGC-32)蛋白是补体激活终末途径 C5b-9 复合物的下游调节因子。补体系统在 SLE 的发病机制中起着非常重要的作用。SLE 患者的 RGC-32 尚未见报道。我们旨在研究 RGC-32 在儿童 SLE 中的临床价值。本研究共纳入 40 例 SLE 患儿和 40 例健康儿童。前瞻性收集临床资料。采用 ELISA 法检测血清 RGC-32。结果显示,SLE 患儿血清 RGC-32 水平明显高于健康对照组。中重度活动组患儿血清 RGC-32 水平明显高于无/轻度活动组。此外,血清 RGC-32 水平与 C 反应蛋白、红细胞沉降率和铁蛋白呈正相关,与白细胞计数和 C3 呈负相关。RGC-32 可能参与了 SLE 的发病机制。RGC-32 可能成为 SLE 诊断和评估的一个良好生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/041b/10329644/c600930eef9f/41598_2023_38092_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/041b/10329644/c600930eef9f/41598_2023_38092_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/041b/10329644/c600930eef9f/41598_2023_38092_Fig1_HTML.jpg

相似文献

1
Serum RGC-32 in children with systemic lupus erythematosus.血清 RGC-32 在儿童系统性红斑狼疮中的表达。
Sci Rep. 2023 Jul 8;13(1):11047. doi: 10.1038/s41598-023-38092-y.
2
Association of Blood Concentrations of Complement Split Product iC3b and Serum C3 With Systemic Lupus Erythematosus Disease Activity.补体片段 iC3b 血浓度与血清 C3 与系统性红斑狼疮疾病活动的相关性。
Arthritis Rheumatol. 2019 Mar;71(3):420-430. doi: 10.1002/art.40747. Epub 2019 Jan 24.
3
C-reactive protein and complement components but not other acute-phase reactants discriminate between clinical subsets and organ damage in systemic lupus erythematosus.C反应蛋白和补体成分而非其他急性期反应物可区分系统性红斑狼疮的临床亚组和器官损伤。
Clin Lab. 2011;57(7-8):607-13.
4
Complement as a Biomarker for Systemic Lupus Erythematosus.补体作为系统性红斑狼疮的生物标志物。
Biomolecules. 2023 Feb 15;13(2):367. doi: 10.3390/biom13020367.
5
Elevated semaphorin5A in systemic lupus erythematosus is in association with disease activity and lupus nephritis.系统性红斑狼疮中信号素5A升高与疾病活动及狼疮性肾炎相关。
Clin Exp Immunol. 2017 May;188(2):234-242. doi: 10.1111/cei.12924. Epub 2017 Feb 17.
6
Anti-GAPDH Autoantibody Is Associated with Increased Disease Activity and Intracranial Pressure in Systemic Lupus Erythematosus.抗 GAPDH 自身抗体与系统性红斑狼疮的疾病活动度和颅内压升高相关。
J Immunol Res. 2019 Mar 31;2019:7430780. doi: 10.1155/2019/7430780. eCollection 2019.
7
Cross-sectional study of plasma Axl, ferritin, IGFBP4 and sTNFR2 as biomarkers of disease activity in childhood-onset SLE: A study of the Pediatric Nephrology Research Consortium.儿童起病系统性红斑狼疮患者血浆 Axl、铁蛋白、IGFBP4 和 sTNFR2 作为疾病活动标志物的横断面研究:儿科肾脏病研究联盟的研究。
Lupus. 2021 Aug;30(9):1394-1404. doi: 10.1177/09612033211016100. Epub 2021 May 14.
8
Decreased serum levels of TGF-β1 are associated with renal damage in female patients with systemic lupus erythematosus.血清转化生长因子-β1 水平降低与女性红斑狼疮患者的肾损伤有关。
Lupus. 2012 Mar;21(3):310-8. doi: 10.1177/0961203311425528. Epub 2011 Nov 9.
9
Urine neopterin as a parameter of disease activity in patients with systemic lupus erythematosus: comparisons with serum sIL-2R and antibodies to dsDNA, erythrocyte sedimentation rate, and plasma C3, C4, and C3 degradation products.尿新蝶呤作为系统性红斑狼疮患者疾病活动的一个参数:与血清可溶性白细胞介素-2受体、抗双链DNA抗体、红细胞沉降率以及血浆C3、C4和C3降解产物的比较
Ann Rheum Dis. 1993 Jun;52(6):429-35. doi: 10.1136/ard.52.6.429.
10
Serum Interleukin-34 Levels Are Elevated in Patients with Systemic Lupus Erythematosus.系统性红斑狼疮患者血清白细胞介素-34水平升高。
Molecules. 2016 Dec 28;22(1):35. doi: 10.3390/molecules22010035.

引用本文的文献

1
Biomarkers for systemic lupus erythematosus: A scoping review.系统性红斑狼疮的生物标志物:系统评价。
Immun Inflamm Dis. 2024 Oct;12(10):e70022. doi: 10.1002/iid3.70022.

本文引用的文献

1
Biomarkers in Childhood-Onset Systemic Lupus Erythematosus.儿童发病系统性红斑狼疮的生物标志物。
Rheum Dis Clin North Am. 2022 Feb;48(1):271-285. doi: 10.1016/j.rdc.2021.09.003.
2
An Update on the Management of Childhood-Onset Systemic Lupus Erythematosus.儿童发病系统性红斑狼疮的治疗进展。
Paediatr Drugs. 2021 Jul;23(4):331-347. doi: 10.1007/s40272-021-00457-z. Epub 2021 Jul 10.
3
RGC-32 and diseases: the first 20 years.RGC-32 与疾病:前 20 年。
Immunol Res. 2019 Jun;67(2-3):267-279. doi: 10.1007/s12026-019-09080-0.
4
Decreased expression of response gene to complement 32 in psoriasis and its association with reduced M2 macrophage polarization.银屑病中补体反应基因32表达降低及其与M2巨噬细胞极化减弱的关联。
J Dermatol. 2019 Feb;46(2):166-168. doi: 10.1111/1346-8138.14733. Epub 2019 Jan 2.
5
Systematic Analysis of Differential Expression Profile in Rheumatoid Arthritis Chondrocytes Using Next-Generation Sequencing and Bioinformatics Approaches.采用下一代测序和生物信息学方法分析类风湿关节炎软骨细胞差异表达谱的系统分析。
Int J Med Sci. 2018 Jul 13;15(11):1129-1142. doi: 10.7150/ijms.27056. eCollection 2018.
6
Plasma C4d as marker for lupus nephritis in systemic lupus erythematosus.血浆 C4d 作为系统性红斑狼疮狼疮肾炎的标志物。
Arthritis Res Ther. 2017 Dec 6;19(1):266. doi: 10.1186/s13075-017-1470-2.
7
Response gene to complement 32 regulates the G2/M phase checkpoint during renal tubular epithelial cell repair.补体32反应基因在肾小管上皮细胞修复过程中调节G2/M期检查点。
Cell Mol Biol Lett. 2016 Sep 20;21:19. doi: 10.1186/s11658-016-0021-1. eCollection 2016.
8
RGC-32 is a novel regulator of the T-lymphocyte cell cycle.RGC-32是T淋巴细胞细胞周期的一种新型调节因子。
Exp Mol Pathol. 2015 Jun;98(3):328-37. doi: 10.1016/j.yexmp.2015.03.011. Epub 2015 Mar 11.
9
Childhood onset systemic lupus erythematosus: how is it different from adult SLE?儿童期起病的系统性红斑狼疮:它与成人系统性红斑狼疮有何不同?
Int J Rheum Dis. 2015 Feb;18(2):182-91. doi: 10.1111/1756-185X.12419. Epub 2014 Jun 26.
10
An update on childhood-onset systemic lupus erythematosus.儿童发病系统性红斑狼疮的研究进展。
Curr Opin Rheumatol. 2013 Sep;25(5):616-22. doi: 10.1097/BOR.0b013e328363e868.