RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Avoidance of related donors in CAEBV with germline immune variants: long-termoutcome of matched unrelated donor HSCT - a case report.
Avoidance of related donors in CAEBV with germline immune variants: long-termoutcome of matched unrelated donor HSCT - a case report.
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本文报告一例成人起病、以NK细胞为主的慢性活动性EB病毒感染(CAEBV),患者携带多个影响抗病毒免疫的杂合胚系变异。对患者及家属进行NK细胞细胞毒作用和脱颗粒功能评估后,发现数名亲属存在亚临床免疫缺陷,因此排除相关供者。患者最终接受HLA全相合无关供者造血干细胞移植(MUD-HSCT),早期实现病毒学缓解和完全供者嵌合。
然而,移植后出现严重免疫相关不良事件,包括急性和慢性移植物抗宿主病(GVHD)、血栓性微血管病、病毒再激活及继发性噬血细胞性淋巴组织细胞增多症,最终因严重肺部感染和多器官衰竭死亡。本病例凸显免疫遗传风险分层在移植决策中的关键作用。结合全面功能和遗传筛查的相合无关供者移植可避免使用免疫功能受损供者,同时仍具有治愈潜力。
不过,CAEBV长期结局不仅取决于病毒学缓解,也依赖持续免疫重建。此外,本文回顾整合宿主遗传背景、免疫功能和病毒动态的精准移植策略,为未来CAEBV管理提供路线图。
This study reports an adult-onset case of NK cell-predominant chronic active Epstein-Barr virus infection (CAEBV) harboring multiple heterozygous germline variants affecting antiviral immunity.
Functional assessments of NK cell cytotoxicity and degranulation in the patient and her family members revealed subclinical immune defects in several relatives, leading to the exclusion of related donors. The patient ultimately underwent a fully HLA-matched unrelated donor hematopoietic stem cell transplantation (MUD-HSCT), achieving early virologic remission and complete donor chimerism.
However, the post-transplant course was complicated by severe immune-related adverse events, including acute and chronic graft-versus-host disease (GVHD), thrombotic microangiopathy, viral reactivations, and secondary hemophagocytic lymphohistiocytosis, ultimately resulting in death due to severe pulmonary infection and multi-organ failure.
This case underscores the critical role of immunogenetic risk stratification in guiding transplant decisions. Matched unrelated donor transplantation, supported by comprehensive functional and genetic screening, offers curative potential while avoiding the use of immunologically compromised donors. Nevertheless, long-term outcomes in CAEBV depend not only on virologic remission but also on sustained immune reconstitution.
In addition, this report reviews precision transplantation strategies that integrate host genetic background, immune function, and viral dynamics, providing a roadmap for the future management of CAEBV.
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