BMPR2型
肺动脉高压
激活素受体
内皮素受体
一氧化氮
受体
医学
肺
骨形态发生蛋白
内科学
药理学
内皮素1
祖细胞
胚胎血管重塑
内分泌学
前列环素
癌症研究
生物
细胞生物学
生物化学
干细胞
基因
作者
Rosalinda Madonna,Sandra Ghelardoni
摘要
Abstract Sotatercept binds free activins by mimicking the extracellular domain of the activin receptor type IIA (ACTRIIA). Additional ligands are BMP/TGF‐beta, GDF8, GDF11 and BMP10. The binding with activins leads to the inhibition of the signalling pathway and the deactivation of the bone morphogenic protein (BMP) receptor type 2. In this way, sotatercept activates an antiproliferative signalling to the cells of the pulmonary arteries and arterioles with the aim of rebalancing the proliferative and antiproliferative pathway that characterizes the pulmonary arterial hypertension (PAH). Sotatercept is indicated for the treatment of group 1 PAH in combination with drugs that act through the endothelin receptor, nitric oxide or prostacyclin. Its effects, demonstrated in the STELLAR study, are the improvement of exercise capacity and the FC‐WHO functional class, together with the reduction of the risk of clinical worsening events. In addition to its antiremodeling effects on the pulmonary circulation, sotatercept has several haematological effects that could suggest its use in the treatment of some blood disorders other than PAH. In this review, we will discuss the effects of the drug on PAH and in parallel provide an in‐depth overview of its application in haematological disorders, focusing on clinical and preclinical studies.
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