Suppr超能文献

用于人类异种移植的基因工程猪器官

Genetically Engineered Porcine Organs for Human Xenotransplantation.

作者信息

Shahab Maryam, Din Nihal Ud, Shahab Nimra

机构信息

Internal Medicine, Queens Internal Medicine and Geriatrics, New York, USA.

Internal Medicine, Nowshera Medical College, Nowshera, PAK.

出版信息

Cureus. 2022 Sep 12;14(9):e29089. doi: 10.7759/cureus.29089. eCollection 2022 Sep.

Abstract

Xenotransplantation holds a promising future for many patients, especially those with end-stage renal disease or uncontrollable serum glucose levels. Porcine organs are viewed as the perfect candidate for a source of xenografts. However, the recipient's immunity, incompatibility of biologic systems, and transfer of new pathogenic organisms are all obstacles to clinical xenotransplantation, in addition to the risk of zoonosis and xenoantigens. Genetic modification of pigs using clustered regularly interspaced short palindromic repeat (CRISPR)-CRISPR-associated protein 9 (Cas9) resulted in the production of porcine endogenous retrovirus (PERV)-free offsprings with the consequent removal of many clinical complications post-transplantation. Such as minimizing both acute and chronic inflammation, in addition to suppressing rejection reactions, which may prolong graft survival. To build on these recent successes, it is important to look at the limits of genetic engineering and develop ways to advance the field of xenotransplantation and reverse xenotransplantation clinical applications forward. Still, significant problems remain with clinical human xenotransplantation; future work should focus on developing an ideal genetically engineered swine donor source that can improve long-term graft survival and suppress the immune system in a clinically useful way.

摘要

异种移植对许多患者,尤其是终末期肾病患者或血糖水平无法控制的患者来说,前景广阔。猪器官被视为异种移植物来源的理想选择。然而,除了人畜共患病和异种抗原的风险外,受者的免疫反应、生物系统的不相容性以及新病原体的传播都是临床异种移植的障碍。使用成簇规律间隔短回文重复序列(CRISPR)-CRISPR相关蛋白9(Cas9)对猪进行基因改造,产生了无猪内源性逆转录病毒(PERV)的后代,从而消除了移植后的许多临床并发症。例如,除了抑制排斥反应以延长移植物存活时间外,还能将急性和慢性炎症降至最低。为了在这些近期成功的基础上更进一步,审视基因工程的局限性并开发推进异种移植领域和推动异种移植临床应用向前发展的方法很重要。尽管如此,临床人体异种移植仍存在重大问题;未来的工作应集中在开发一种理想的基因工程猪供体来源,以提高移植物的长期存活并以临床上有用的方式抑制免疫系统。

相似文献

1
Genetically Engineered Porcine Organs for Human Xenotransplantation.用于人类异种移植的基因工程猪器官
Cureus. 2022 Sep 12;14(9):e29089. doi: 10.7759/cureus.29089. eCollection 2022 Sep.
2
Porcine genome engineering for xenotransplantation.猪的异种器官移植基因工程。
Adv Drug Deliv Rev. 2021 Jan;168:229-245. doi: 10.1016/j.addr.2020.04.001. Epub 2020 Apr 7.
4
Corneal xenotransplantation: Where are we standing?角膜异种移植:我们处于什么位置?
Prog Retin Eye Res. 2021 Jan;80:100876. doi: 10.1016/j.preteyeres.2020.100876. Epub 2020 Aug 2.
5
The Resurgence of Xenotransplantation.异种器官移植的复兴。
Am J Transplant. 2017 Oct;17(10):2531-2536. doi: 10.1111/ajt.14311. Epub 2017 May 8.
7
Xenotransplantation literature update, November/December 2019.2019 年 11/12 月异种移植文献更新。
Xenotransplantation. 2020 Jan;27(1):e12582. doi: 10.1111/xen.12582. Epub 2020 Jan 26.

本文引用的文献

2
IL-6 Directed Therapy in Transplantation.移植中的白细胞介素-6定向治疗。
Curr Transplant Rep. 2021;8(3):191-204. doi: 10.1007/s40472-021-00331-4. Epub 2021 Jun 3.
3
Current status of porcine islet xenotransplantation.猪胰岛异种移植的现状。
Curr Opin Organ Transplant. 2020 Oct;25(5):449-456. doi: 10.1097/MOT.0000000000000794.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验