Suppr超能文献

阵发性睡眠性血红蛋白尿症的抗补体治疗:我们的现状与未来走向

Anti-Complement Treatment in Paroxysmal Nocturnal Hemoglobinuria: Where we Stand and Where we are Going.

作者信息

Risitano Antonio M

机构信息

Hematology, Department of Clinical Medicine and Surgery; Federico II University , Naples (Italy).

出版信息

Transl Med UniSa. 2014 Feb 4;8:43-52. eCollection 2014 Jan.

Abstract

Paroxysmal nocturnal hemoglobinuria (PNH) is a clonal, non-malignant, hematological disorder characterized by the expansion of hematopoietic stem cells and progeny mature blood cells which are deficient in some surface proteins, including the two complement regulators CD55 and CD59. PNH is the paradigm of diseases implying complement dysregulation as main pathogenic mechanism; in fact, PNH erythrocytes are uncapable to modulate on their surface physiologic complement activation, which eventually leads to the typical clinical hallmark of PNH - the chronic complement-mediated intravascular anemia. Indeed, due to the lack of CD55 complement is continuously activated on erythrocyte surface, which subsequently enables the terminal lytic complement because of the lack of CD59, finally resulting in erythrocyte lysis. The availability of eculizumab as the first complement inhibitor for clinical use renewed the interest for this rare hematological disease. Indeed, in the last decad the anti-C5 monoclonal antibody has proven effective for the treatment of PNH, resulting in a sustained control of complement-mediated intravascular hemolysis, with a remarkable clinical benefit. Anti-complement treatment allowed transfusion independence in at least half of PNH patients receiving eculizumab, with adequate control of all hemolysis-associated symptoms even in almost all remaining patients. In addition, the risk of thromboembolic events - an other clinical hallmark of PNH, which significantly affects prognosis and survival - seems substantially reduced on eculizumab treatment, apparently resulting in improved survival. Even with all these remarkable effects, eculizumab treatment does not result in hemoglobin normalization, and most patients remain anemic. It has been demonstrated that this is due to persistent activation of the early phases of complement activation (upstream the C5), leading to complement-mediated extravascular hemolysis. Ongoing researches are focusing on possible strategies to improve current anti-complement therapies, aiming to develop second-generation complement therapeutics. Here we review PNH and its complement-mediated pathophysiology, summarizing available data on anti-complement treatment; we'll also discuss recent pathogenic insights which drive the development of novel strategies of complement inhibition.

摘要

阵发性睡眠性血红蛋白尿(PNH)是一种克隆性、非恶性血液系统疾病,其特征是造血干细胞及其子代成熟血细胞扩增,这些细胞缺乏某些表面蛋白,包括两种补体调节蛋白CD55和CD59。PNH是以补体失调为主要致病机制的疾病范例;事实上,PNH红细胞无法调节其表面的生理性补体激活,最终导致PNH的典型临床特征——慢性补体介导的血管内溶血。的确,由于缺乏CD55,补体在红细胞表面持续激活,随后由于缺乏CD59而激活末端溶细胞补体,最终导致红细胞溶解。依库珠单抗作为首个临床可用的补体抑制剂,重新引发了人们对这种罕见血液疾病的关注。的确,在过去十年中,抗C5单克隆抗体已被证明对PNH治疗有效,可持续控制补体介导的血管内溶血,具有显著的临床益处。抗补体治疗使至少一半接受依库珠单抗治疗的PNH患者不再需要输血,即使在几乎所有其余患者中,与溶血相关的所有症状也得到了充分控制。此外,血栓栓塞事件的风险——PNH的另一个临床特征,显著影响预后和生存——在依库珠单抗治疗后似乎大幅降低,显然提高了生存率。即使有所有这些显著效果,依库珠单抗治疗也不会使血红蛋白恢复正常,大多数患者仍贫血。已经证明,这是由于补体激活早期阶段(C5上游)的持续激活,导致补体介导的血管外溶血。正在进行的研究集中在改善当前抗补体疗法的可能策略上,旨在开发第二代补体疗法。在这里,我们回顾PNH及其补体介导的病理生理学,总结抗补体治疗的现有数据;我们还将讨论推动新型补体抑制策略发展的最新致病机制见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa0d/4000462/9f638c59d49a/tm-08-43-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验