• 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

血友病的非因子治疗:成就与展望

Non-factor Therapies for Hemophilia: Achievements and Perspectives.

作者信息

Jiménez-Yuste Victor

机构信息

Department of Haematology, Hospital Universitario La Paz-IdiPaz, Autónoma University, Madrid, Spain.

出版信息

Semin Thromb Hemost. 2025 Feb;51(1):23-27. doi: 10.1055/s-0044-1796651. Epub 2024 Nov 29.

DOI:10.1055/s-0044-1796651
PMID:39613145
Abstract

Non-factor replacement therapies (NFTs) have been developed to address the limitations of conventional replacement therapies, aiming to improve hemostasis and provide enhanced protection against bleeding episodes and long-term joint damage for patients both with and without inhibitors. Factor VIII (FVIII)-mimetic agents, such as emicizumab, have transformed the management of hemophilia A with inhibitors, offering a lower treatment burden and an effective alternative for those without inhibitors as well. Rebalancing agents, including anti-tissular factor pathway inhibitor agents (concizumab and marstacimab) and serpin inhibitors like fitusiran, have shown promising efficacy for patients with hemophilia B with inhibitors and other hemophilia subtypes. Administered subcutaneously, NFTs generate stable thrombin levels and feature a long half-life, which can shift severe hemophilia toward a milder phenotype. These therapies are effective regardless of inhibitor status and hold potential for application in other bleeding disorders. Evaluating the potential thrombotic risk after implementing mitigation measures, along with the development of anti-drug antibodies (ADAs), remain critical areas for further analysis. NFTs pose additional challenges due to their complex mechanism of action and the absence of a standardized laboratory assessment method. Unresolved issues include optimal management strategies for major surgeries and tailored approaches for safe use in older populations. This review highlights the progress and future potential of NFTs in treating persons with hemophilia.

摘要

非因子替代疗法(NFTs)已被开发出来以解决传统替代疗法的局限性,旨在改善止血功能,并为有和没有抑制剂的患者提供增强的保护,防止出血发作和长期关节损伤。因子VIII(FVIII)模拟剂,如艾美赛珠单抗,已经改变了伴有抑制剂的A型血友病的治疗方式,对于没有抑制剂的患者来说,也提供了更低的治疗负担和有效的替代方案。再平衡剂,包括抗组织因子途径抑制剂(康西珠单抗和玛斯塔西单抗)以及丝氨酸蛋白酶抑制剂(如fitusiran),已显示出对伴有抑制剂的B型血友病患者和其他血友病亚型有良好疗效。通过皮下给药,NFTs可产生稳定的凝血酶水平,且半衰期长,这可使重度血友病转变为较轻的表型。这些疗法无论抑制剂状态如何均有效,并且在其他出血性疾病中具有应用潜力。在实施缓解措施后评估潜在的血栓形成风险以及抗药物抗体(ADA)的产生,仍然是需要进一步分析的关键领域。由于其复杂的作用机制和缺乏标准化的实验室评估方法,NFTs带来了额外的挑战。未解决的问题包括重大手术的最佳管理策略以及针对老年人群安全使用的定制方法。本综述强调了NFTs在治疗血友病患者方面的进展和未来潜力。

相似文献

1
Non-factor Therapies for Hemophilia: Achievements and Perspectives.血友病的非因子治疗:成就与展望
Semin Thromb Hemost. 2025 Feb;51(1):23-27. doi: 10.1055/s-0044-1796651. Epub 2024 Nov 29.
2
Non-clotting factor therapies for preventing bleeds in people with congenital hemophilia A or B.用于预防先天性 A 型或 B 型血友病患者出血的非凝血因子治疗方法。
Cochrane Database Syst Rev. 2024 Feb 27;2(2):CD014544. doi: 10.1002/14651858.CD014544.pub2.
3
New therapies using nonfactor products for patients with hemophilia and inhibitors.新型疗法使用非因子产品治疗血友病合并抑制物患者。
Blood. 2019 Jan 31;133(5):399-406. doi: 10.1182/blood-2018-07-820712. Epub 2018 Dec 17.
4
Factor VIII replacement is still the standard of care in haemophilia A.VIII 因子替代疗法仍然是 A 型血友病的标准治疗方法。
Blood Transfus. 2019 Nov;17(6):479-486. doi: 10.2450/2019.0211-19. Epub 2019 Dec 11.
5
Current and future therapies for haemophilia-Beyond factor replacement therapies.血友病的当前和未来治疗方法——超越因子替代疗法。
Br J Haematol. 2023 Jan;200(1):23-34. doi: 10.1111/bjh.18379. Epub 2022 Jul 23.
6
Emicizumab for routine prophylaxis to prevent bleeding episodes in patients with hemophilia A.艾美赛珠单抗用于常规预防以防止甲型血友病患者出血发作。
Drugs Today (Barc). 2018 Oct;54(10):591-600. doi: 10.1358/dot.2018.54.10.2869771.
7
Emicizumab Prophylaxis in Patients Who Have Hemophilia A without Inhibitors.艾美赛珠单抗预防无抑制剂的血友病 A 患者出血。
N Engl J Med. 2018 Aug 30;379(9):811-822. doi: 10.1056/NEJMoa1803550.
8
[Emicizumab: a paradigm shift in hemophilia treatment].[依米珠单抗:血友病治疗的范式转变]
Rinsho Ketsueki. 2020;61(5):536-541. doi: 10.11406/rinketsu.61.536.
9
New therapies for hemophilia.血友病的新疗法。
Blood. 2019 Jan 31;133(5):389-398. doi: 10.1182/blood-2018-08-872291. Epub 2018 Dec 17.
10
Intrinsic differences between FVIIIa mimetic bispecific antibodies and FVIII prevent assignment of FVIII-equivalence.FVIIIa 模拟双特异性抗体和 FVIII 之间的固有差异使得 FVIII 等价性无法确定。
J Thromb Haemost. 2019 Jul;17(7):1044-1052. doi: 10.1111/jth.14430. Epub 2019 Apr 26.

引用本文的文献

1
Haemophilia Prophylaxis in the Age of Innovation: Exploring Opportunities for Personalized Treatment.创新时代的血友病预防:探索个性化治疗的机遇
Haemophilia. 2025 Jul;31(4):607-616. doi: 10.1111/hae.70015. Epub 2025 Apr 17.