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2019 年 11/12 月异种移植文献更新。

Xenotransplantation literature update, November/December 2019.

机构信息

The Centre for Transplant & Renal Research, The Westmead Institute for Medical Research, Westmead, NSW, Australia.

The Department of Surgery, University of Sydney, Westmead Hospital, Westmead, NSW, Australia.

出版信息

Xenotransplantation. 2020 Jan;27(1):e12582. doi: 10.1111/xen.12582. Epub 2020 Jan 26.

Abstract

The ever-increasing disparity between the lack of organ donors and patients on the transplant waiting list is increasing worldwide. For the past several decades xenotransplantation has led the way to correct this deficit and remains clearly the only feasible option to provide a means to meet the demand for patients in need of an organ transplant. Xenotransplantation's ability to provide a specifically designed unlimited supply of organs, suited to treat the various needs for transplant organs and cells, has recently been championed by successful pre-clinical trials that have run long-term in non-human primate studies. In this review we show how these improvements have come about due to long-term dedicated research and recent advances in biomedical engineering technology, such as genome editing tools including zinc finger nucleases, TALEN, and CRISPER/Cas9 which have paved the way for significant breakthroughs in improving xenograft outcomes through genetic modifications to the donor source pig. Other novel approaches include the development of decellularized porcine tissue, such as corneas which can now be transplanted into patients with the minimal need for immunosuppression or other side effects. Further genetic variants of the porcine genome are also now being optimized to abrogate rejection. The emergence of new modalities such as; mesenchymal stem cells, donor thymic vascularization, in vivo bioreactors, chemokine and cytokine therapies have come to show improvements in xenograft outcomes. Furthermore, new studies confirm the safety status of using porcine xenografts, verifying that with current technologies and approaches, the issue of PERV transmission is a moot point. These breakthroughs and technological advancements push the reality of xenotransplantation one step closer to the clinic.

摘要

全世界范围内,可供移植的器官与等待移植名单上的患者数量之间的差距越来越大。在过去的几十年里,异种移植一直引领着弥补这一缺陷的道路,并且显然仍然是提供满足需要器官移植的患者的唯一可行选择。异种移植能够提供专门设计的、无限供应的器官,以满足各种移植器官和细胞的需求,这一能力最近在非人类灵长类动物研究中进行的长期成功的临床前试验中得到了支持。在这篇综述中,我们展示了由于长期的专门研究和生物医学工程技术的最新进展,这些改进是如何实现的,例如基因组编辑工具,包括锌指核酸酶、TALEN 和 CRISPR/Cas9,这些工具为通过对供体猪源进行基因修饰来提高异种移植物的结果铺平了道路。其他新颖的方法包括脱细胞猪组织的开发,例如角膜,现在可以移植到患者体内,而无需最低限度的免疫抑制或其他副作用。猪基因组的其他新型变体也在不断优化以消除排斥反应。新方法的出现,如间充质干细胞、供体胸腺血管化、体内生物反应器、趋化因子和细胞因子治疗,都表明异种移植物的结果有所改善。此外,新的研究证实了使用猪异种移植物的安全性,证实了在当前技术和方法下,PERV 传播的问题是一个没有实际意义的问题。这些突破和技术进步使异种移植更接近临床现实。

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