胎儿游离DNA
移植
生物标志物
器官移植
计算生物学
DNA测序
生物标志物发现
医学
疾病监测
DNA
生物信息学
生物
疾病
病理
内科学
基因
遗传学
蛋白质组学
胎儿
产前诊断
怀孕
作者
Annette M. Jackson,Carly J. Amato-Menker,Maria P. Bettinotti
标识
DOI:10.1016/j.humimm.2021.07.006
摘要
The use of Next Generation Sequencing (NGS) to interrogate cell-free DNA (cfDNA) as a transplant diagnostic provides a crucial step in improving the accuracy of post-transplant monitoring of allograft health. cfDNA interrogation provides a powerful, yet minimally invasive, biomarker for disease and tissue injury. cfDNA can be isolated from a variety of body fluids and analyzed using bioinformatics to unlock its origins. Furthermore, cfDNA characteristics can reveal the mechanisms and conditions under which it was generated and released. In transplantation, donor-derived cfDNA monitoring provides a tool for identifying active allograft injury at the time of transplant, infection, and rejection. Multiple detection and interrogation methods for cfDNA detection are now being evaluated for clinical validity and hold the promise to provide minimally invasive, quantitative, and reproducible measures of allograft injury across organ types.
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