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心包生物人工心脏瓣膜的长期稳定性和生物相容性

Long-Term Stability and Biocompatibility of Pericardial Bioprosthetic Heart Valves.

作者信息

Williams David F, Bezuidenhout Deon, de Villiers Jandre, Human Paul, Zilla Peter

机构信息

Strait Access Technologies Ltd. Pty., Cape Town, South Africa.

Wake Forest Institute of Regenerative Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States.

出版信息

Front Cardiovasc Med. 2021 Sep 13;8:728577. doi: 10.3389/fcvm.2021.728577. eCollection 2021.

Abstract

The use of bioprostheses for heart valve therapy has gradually evolved over several decades and both surgical and transcatheter devices are now highly successful. The rapid expansion of the transcatheter concept has clearly placed a significant onus on the need for improved production methods, particularly the pre-treatment of bovine pericardium. Two of the difficulties associated with the biocompatibility of bioprosthetic valves are the possibilities of immune responses and calcification, which have led to either catastrophic failure or slow dystrophic changes. These have been addressed by evolutionary trends in cross-linking and decellularization techniques and, over the last two decades, the improvements have resulted in somewhat greater durability. However, as the need to consider the use of bioprosthetic valves in younger patients has become an important clinical and sociological issue, the requirement for even greater longevity and safety is now paramount. This is especially true with respect to potential therapies for young people who are afflicted by rheumatic heart disease, mostly in low- to middle-income countries, for whom no clinically acceptable and cost-effective treatments currently exist. To extend longevity to this new level, it has been necessary to evaluate the mechanisms of pericardium biocompatibility, with special emphasis on the interplay between cross-linking, decellularization and anti-immunogenicity processes. These mechanisms are reviewed in this paper. On the basis of a better understanding of these mechanisms, a few alternative treatment protocols have been developed in the last few years. The most promising protocol here is based on a carefully designed combination of phases of tissue-protective decellularization with a finely-titrated cross-linking sequence. Such refined protocols offer considerable potential in the progress toward superior longevity of pericardial heart valves and introduce a scientific dimension beyond the largely disappointing 'anti-calcification' treatments of past decades.

摘要

生物假体用于心脏瓣膜治疗已有数十年的逐步发展历程,如今外科和经导管装置都非常成功。经导管概念的迅速扩展显然给改进生产方法带来了重大责任,尤其是牛心包的预处理。与生物假体瓣膜生物相容性相关的两个难题是免疫反应和钙化的可能性,这会导致灾难性失败或缓慢的营养不良性变化。交联和脱细胞技术的发展趋势已解决了这些问题,在过去二十年中,改进措施已使耐久性有所提高。然而,由于考虑在年轻患者中使用生物假体瓣膜已成为一个重要的临床和社会学问题,现在对更高的寿命和安全性的要求至关重要。对于主要在低收入和中等收入国家中患风湿性心脏病的年轻人来说尤其如此,目前尚无临床上可接受且具有成本效益的治疗方法。为了将寿命延长到这个新水平,有必要评估心包生物相容性的机制,特别强调交联、脱细胞和抗免疫原性过程之间的相互作用。本文对这些机制进行了综述。基于对这些机制的更好理解,在过去几年中已开发出一些替代治疗方案。这里最有前景的方案是基于精心设计的组织保护性脱细胞阶段与精确调整的交联序列的组合。这种精细的方案在实现心包心脏瓣膜更长寿命方面具有巨大潜力,并引入了一个超越过去几十年令人失望的“抗钙化”治疗的科学维度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90cc/8473620/b3c85a0ddebf/fcvm-08-728577-g0001.jpg

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