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炎症性肠病治疗的最新进展:靶点、机制及相关疗法。

Recent advances in the treatment of IBD: Targets, mechanisms and related therapies.

作者信息

Liu Juan, Di Bin, Xu Li-Li

机构信息

Jiangsu Key Laboratory of Drug Design and Optimization, China Pharmaceutical University, Nanjing 210009, China; Key Laboratory of Drug Quality Control and Pharmacovigilance, Ministry of Education, China Pharmaceutical University, Nanjing 210009, China.

Jiangsu Key Laboratory of Drug Design and Optimization, China Pharmaceutical University, Nanjing 210009, China; Key Laboratory of Drug Quality Control and Pharmacovigilance, Ministry of Education, China Pharmaceutical University, Nanjing 210009, China.

出版信息

Cytokine Growth Factor Rev. 2023 Jun-Aug;71-72:1-12. doi: 10.1016/j.cytogfr.2023.07.001. Epub 2023 Jul 13.

Abstract

Inflammatory bowel disease (IBD), as a representative inflammatory disease, currently has multiple effective treatment options available and new therapeutic strategies are being actively explored to further increase the treatment options for patients with IBD. Furthermore, biologic agents and small molecule drugs developed for ulcerative colitis (UC) and Crohn's disease (CD) have evolved toward fewer side effects and more accurate targeting. Novel inhibitors that target cytokines (such as IL-12/23 inhibitors, PDE4 inhibitors), integrins (such as integrin inhibitors), cytokine signaling pathways (such as JAK inhibitors, SMAD7 blocker) and cell signaling receptors (such as S1P receptor modulator) have become the preferred treatment choice for many IBD patients. Conventional therapies such as 5-aminosalicylic acid, corticosteroids, immunomodulators and anti-tumor necrosis factor agents continue to demonstrate therapeutic efficacy, particularly in combination with drug therapy. This review integrates research from chemical, biological and adjuvant therapies to evaluate current and future IBD therapies, highlighting the mechanism of action of each therapy and emphasizing the potential of development prospects.

摘要

炎症性肠病(IBD)作为一种典型的炎症性疾病,目前有多种有效的治疗选择,并且正在积极探索新的治疗策略,以进一步增加IBD患者的治疗选择。此外,为溃疡性结肠炎(UC)和克罗恩病(CD)开发的生物制剂和小分子药物已朝着副作用更少、靶向更精确的方向发展。靶向细胞因子(如IL-12/23抑制剂、PDE4抑制剂)、整合素(如整合素抑制剂)、细胞因子信号通路(如JAK抑制剂、SMAD7阻断剂)和细胞信号受体(如S1P受体调节剂)的新型抑制剂已成为许多IBD患者的首选治疗选择。传统疗法如5-氨基水杨酸、皮质类固醇、免疫调节剂和抗肿瘤坏死因子药物继续显示出治疗效果,特别是在联合药物治疗时。本综述整合了化学、生物和辅助治疗的研究,以评估当前和未来的IBD治疗方法,突出每种治疗方法的作用机制,并强调发展前景的潜力。

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