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在重新设计巨核细胞分化概念的基础上,探索体外血小板生成。

On the Quest for In Vitro Platelet Production by Re-Tailoring the Concepts of Megakaryocyte Differentiation.

机构信息

Platelet Research Lab, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), 33011 Oviedo, Spain.

Department of Medicine, University of Oviedo, 33003 Oviedo, Spain.

出版信息

Medicina (Kaunas). 2020 Dec 3;56(12):671. doi: 10.3390/medicina56120671.

Abstract

The demand of platelet transfusions is steadily growing worldwide, inter-donor variation, donor dependency, or storability/viability being the main contributing factors to the current global, donor-dependent platelet concentrate shortage concern. In vitro platelet production has been proposed as a plausible alternative to cover, at least partially, the increasing demand. However, in practice, such a logical production strategy does not lack complexity, and hence, efforts are focused internationally on developing large scale industrial methods and technologies to provide efficient, viable, and functional platelet production. This would allow obtaining not only sufficient numbers of platelets but also functional ones fit for all clinical purposes and civil scenarios. In this review, we cover the evolution around the in vitro culture and differentiation of megakaryocytes into platelets, the progress made thus far to bring the culture concept from basic research towards good manufacturing practices certified production, and subsequent clinical trial studies. However, little is known about how these in vitro products should be stored or whether any safety measure should be implemented (e.g., pathogen reduction technology), as well as their quality assessment (how to isolate platelets from the rest of the culture cells, debris, microvesicles, or what their molecular and functional profile is). Importantly, we highlight how the scientific community has overcome the old dogmas and how the new perspectives influence the future of platelet-based therapy for transfusion purposes.

摘要

血小板输注的需求在全球范围内稳步增长,供体间的变异性、对供体的依赖性以及储存/存活能力是导致当前全球、供体依赖性血小板浓缩物短缺问题的主要因素。体外血小板生成已被提议作为一种可行的替代方案,至少部分满足不断增长的需求。然而,实际上,这种合理的生产策略并非没有复杂性,因此,国际上的努力集中在开发大规模的工业方法和技术上,以提供高效、有活力和功能正常的血小板生成。这不仅可以获得足够数量的血小板,还可以获得适合所有临床用途和民用场景的功能正常的血小板。在这篇综述中,我们涵盖了体外培养和巨核细胞分化为血小板的演变过程,以及迄今为止为将培养概念从基础研究推进到经过良好生产规范认证的生产,以及随后的临床试验研究所取得的进展。然而,人们对这些体外产品应该如何储存,或者是否应该采取任何安全措施(例如,病原体减少技术),以及它们的质量评估(如何从培养细胞、碎片、微泡或其他物质中分离血小板,以及它们的分子和功能特征是什么)知之甚少。重要的是,我们强调了科学界是如何克服旧观念的,以及新观点如何影响未来用于输血的基于血小板的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5433/7761839/a45325e42ded/medicina-56-00671-g001.jpg

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