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马方综合征血管疾病的药物治疗:从小鼠模型到人类患者

Drug-based therapies for vascular disease in Marfan syndrome: from mouse models to human patients.

作者信息

Cook Jason R, Nistala Harikiran, Ramirez Francesco

机构信息

Mount Sinai School of Medicine, New York, NY, USA.

出版信息

Mt Sinai J Med. 2010 Jul-Aug;77(4):366-73. doi: 10.1002/msj.20200.

Abstract

Marfan syndrome is a congenital disorder of the connective tissue with a long history of clinical and basic science breakthroughs that have forged our understanding of vascular-disease pathogenesis. The biomedical importance of Marfan syndrome was recently underscored by the discovery that the underlying genetic lesion impairs both tissue integrity and transforming growth factor-beta regulation of cell behavior. This discovery has led to the successful implementation of the first pharmacological intervention in a connective-tissue disorder otherwise incurable by either gene-based or stem cell-based therapeutic strategies. More generally, information gathered from the study of Marfan syndrome pathogenesis has the potential to improve the clinical management of common acquired disorders of connective-tissue degeneration.

摘要

马凡综合征是一种先天性结缔组织疾病,在临床和基础科学方面有着悠久的突破历史,这些突破塑造了我们对血管疾病发病机制的理解。最近,马凡综合征的生物医学重要性因一项发现而得到凸显,即潜在的基因病变会损害组织完整性以及细胞行为的转化生长因子-β调节。这一发现促使在一种结缔组织疾病中成功实施了首例药物干预,而这种疾病此前无论是基于基因的治疗策略还是基于干细胞的治疗策略都无法治愈。更广泛地说,从马凡综合征发病机制研究中收集到的信息有可能改善常见后天性结缔组织退行性疾病的临床管理。

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