Two‐field resolution on‐call HLA typing for deceased donors using nanopore sequencing

基因分型 打字 人类白细胞抗原 仆从 计算机科学 协议(科学) 计算生物学 纳米孔测序 免疫学 医学 基因型 生物 DNA测序 遗传学 抗原 DNA 病理 基因 替代医学
作者
Magali Devriese,Sephora Da Silva,Melchior Le Mene,Julien Rouquie,Vincent Allain,Libor Kolesár,Krisztina Rigó,Lisa E. Creary,Nina Lauterbach,Cédric Usureau,Mathieu Dewez,Sophie Caillat‐Zucman,G. Werner,Jean‐Luc Taupin
出处
期刊:HLA: Immune Response Genetics [Wiley]
卷期号:103 (3): e15441-e15441 被引量:11
标识
DOI:10.1111/tan.15441
摘要

The current practice of HLA genotyping in deceased donors poses challenges due to limited resolution within time constraints. Nevertheless, the assessment of compatibility between anti-HLA sensitized recipients and mismatched donors remains a critical medical need, particularly when dealing with allele-specific (second field genotyping level) donor-specific antibodies. In this study, we present a customized protocol based on the NanoTYPE® HLA typing kit, employing the MinION® sequencer, which enables rapid HLA typing of deceased donors within a short timeframe of 3.75 h on average at a three-field resolution with almost no residual ambiguities. Through a prospective real-time analysis of HLA typing in 18 donors, we demonstrated the efficacy and precision of our nanopore-based method in comparison to the conventional approach and without delaying organ allocation. Indeed, this duration was consistent with the deceased donor organ donation procedure leading to organ allocation via the French Biomedicine Agency. The improved resolution achieved with our protocol enhances the security of organ allocation, particularly benefiting highly sensitized recipients who often present intricate HLA antibody profiles. By overcoming technical challenges and providing comprehensive genotyping data, this approach holds the potential to significantly impact deceased donor HLA genotyping, thereby facilitating optimal organ allocation strategies.
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