• 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

炎症性肠病的生物治疗:争议与未来选择。

Biological therapies for inflammatory bowel disease: controversies and future options.

机构信息

Istituto di Medicina Interna e Geriatria, Policlinico A. Gemelli, Università Cattolica del S. Cuore, L.go A. Gemelli, 8 00168 Roma, Italy.

出版信息

Expert Rev Clin Pharmacol. 2009 Jul;2(4):391-403. doi: 10.1586/ecp.09.12.

DOI:10.1586/ecp.09.12
PMID:22112183
Abstract

Over the last few years, advances in understanding the pathogenesis of inflammatory bowel disease, together with progress in biotechnology, have led to the availability of several biological drugs that have dramatically changed the therapeutic approach to these disorders. Indeed, several molecules targeting crucial inflammatory cytokines, blocking T-cell activation/proliferation or the recruitment of inflammatory cells into the inflamed bowel, have been discovered and commercialized. However, the increasing use of biological agents has raised some concerns regarding their short- and long-term safety. This review offers a critical evaluation of the efficacy and safety of biological agents in the management of both Crohn's disease and ulcerative colitis. In addition, promising therapeutic options are discussed.

摘要

在过去的几年中,对炎症性肠病发病机制的认识的进步,以及生物技术的进步,导致了几种生物药物的出现,这些药物极大地改变了对这些疾病的治疗方法。事实上,已经发现并商业化了几种针对关键炎症细胞因子的分子,这些分子可以阻断 T 细胞的激活/增殖或炎症细胞招募到炎症肠道中。然而,生物制剂的使用越来越多,引起了人们对其短期和长期安全性的一些关注。这篇综述对生物制剂在克罗恩病和溃疡性结肠炎治疗中的疗效和安全性进行了批判性评估。此外,还讨论了有前途的治疗选择。

相似文献

1
Biological therapies for inflammatory bowel disease: controversies and future options.炎症性肠病的生物治疗:争议与未来选择。
Expert Rev Clin Pharmacol. 2009 Jul;2(4):391-403. doi: 10.1586/ecp.09.12.
2
Physiological basis for novel drug therapies used to treat the inflammatory bowel diseases. I. Immunology and therapeutic potential of antiadhesion molecule therapy in inflammatory bowel disease.用于治疗炎症性肠病的新型药物疗法的生理基础。I. 炎症性肠病中抗粘附分子疗法的免疫学及治疗潜力。
Am J Physiol Gastrointest Liver Physiol. 2005 Feb;288(2):G169-74. doi: 10.1152/ajpgi.00423.2004.
3
Appropriateness of immunosuppressive drugs in inflammatory bowel diseases assessed by RAND method: Italian Group for IBD (IG-IBD) position statement.通过RAND方法评估炎症性肠病中免疫抑制药物的适用性:意大利炎症性肠病研究小组(IG-IBD)立场声明
Dig Liver Dis. 2005 Jun;37(6):407-17. doi: 10.1016/j.dld.2004.12.013.
4
Inflammatory bowel disease. Current concepts of pathogenesis and implications for therapy.炎症性肠病。发病机制的当前概念及其对治疗的影响。
Minerva Gastroenterol Dietol. 2002 Sep;48(3):215-26.
5
Diagnostic problems and advances in inflammatory bowel disease.炎症性肠病的诊断问题与进展
Mod Pathol. 2003 Apr;16(4):347-58. doi: 10.1097/01.MP.0000064746.82024.D1.
6
[Advances in biologic therapy for inflammatory bowel disease].[炎症性肠病生物治疗的进展]
Recenti Prog Med. 2008 Jan;99(1):10-8.
7
Analysis of direct tissue isoelectric focused protein profiles of resected intestinal mucosa and endoscopic biopsies from patients with inflammatory bowel disease.炎症性肠病患者切除的肠黏膜和内镜活检组织的直接组织等电聚焦蛋白质谱分析。
Clin Invest Med. 1992 Feb;15(1):49-59.
8
Beyond tumor necrosis factor: next-generation biologic therapy for inflammatory bowel disease.超越肿瘤坏死因子:炎症性肠病的新一代生物疗法。
Dig Dis. 2009;27(3):366-9. doi: 10.1159/000228575. Epub 2009 Sep 24.
9
Mechanisms and efficacy of immunobiologic therapies for inflammatory bowel diseases.炎症性肠病免疫生物治疗的机制和疗效。
Int Rev Immunol. 2010;29(1):4-37. doi: 10.3109/08830180903437212.
10
New therapies for inflammatory bowel disease: from the bench to the bedside.炎症性肠病的新疗法:从实验室到临床。
Gut. 2012 Jun;61(6):918-32. doi: 10.1136/gutjnl-2011-300904. Epub 2011 Nov 23.

引用本文的文献

1
Multifunctional nanoparticle-mediated combining therapy for human diseases.多功能纳米颗粒介导的人类疾病联合治疗。
Signal Transduct Target Ther. 2024 Jan 1;9(1):1. doi: 10.1038/s41392-023-01668-1.
2
Nucleic acid strategies for infectious disease treatments: The nanoparticle-based oral delivery route.传染病治疗的核酸策略:基于纳米颗粒的口服给药途径。
Front Pharmacol. 2022 Aug 29;13:984981. doi: 10.3389/fphar.2022.984981. eCollection 2022.
3
TNFα gene silencing mediated by orally targeted nanoparticles combined with interleukin-22 for synergistic combination therapy of ulcerative colitis.
通过口服靶向纳米颗粒介导的 TNFα 基因沉默联合白细胞介素-22 进行协同组合治疗溃疡性结肠炎。
J Control Release. 2018 Oct 10;287:235-246. doi: 10.1016/j.jconrel.2018.08.021. Epub 2018 Aug 11.
4
Oral nucleic acid therapy using multicompartmental delivery systems.口服核酸治疗的多腔室递药系统。
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2018 Mar;10(2). doi: 10.1002/wnan.1478. Epub 2017 May 24.
5
Nanomedicine and drug delivery strategies for treatment of inflammatory bowel disease.用于治疗炎症性肠病的纳米医学与药物递送策略
World J Gastroenterol. 2015 Oct 28;21(40):11343-52. doi: 10.3748/wjg.v21.i40.11343.
6
Lactic acid bacteria: reviewing the potential of a promising delivery live vector for biomedical purposes.乳酸菌:审视一种有前景的用于生物医学目的的活体递送载体的潜力。
Microb Cell Fact. 2015 Sep 16;14:137. doi: 10.1186/s12934-015-0313-6.
7
Glycoprotein CD98 as a receptor for colitis-targeted delivery of nanoparticle.糖蛋白CD98作为纳米颗粒靶向递送治疗结肠炎的受体。
J Mater Chem B. 2014 Mar 21;2(11):1499-1508. doi: 10.1039/C3TB21564D.
8
Mannosylated bioreducible nanoparticle-mediated macrophage-specific TNF-α RNA interference for IBD therapy.甘露糖化生物还原性纳米颗粒介导的巨噬细胞特异性 TNF-α RNA 干扰治疗 IBD。
Biomaterials. 2013 Oct;34(30):7471-82. doi: 10.1016/j.biomaterials.2013.06.008. Epub 2013 Jun 29.
9
Dual TNF-α/Cyclin D1 Gene Silencing With an Oral Polymeric Microparticle System as a Novel Strategy for the Treatment of Inflammatory Bowel Disease.口服聚合微粒系统双重靶向 TNF-α/细胞周期蛋白 D1 基因沉默:治疗炎症性肠病的新策略。
Clin Transl Gastroenterol. 2011 Mar 24;2(3):e2. doi: 10.1038/ctg.2011.1.
10
Oral TNF-α gene silencing using a polymeric microsphere-based delivery system for the treatment of inflammatory bowel disease.利用基于聚合微球的递药系统进行口腔 TNF-α 基因沉默治疗炎症性肠病。
J Control Release. 2011 Feb 28;150(1):77-86. doi: 10.1016/j.jconrel.2010.10.002. Epub 2010 Oct 17.