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外周血用于监测骨髓增生异常综合征基因组学和肿瘤免疫微环境的准确性

Fidelity of peripheral blood for monitoring genomics and tumor immune-microenvironment in myelodysplastic syndromes.

作者信息

Lee Sung-Eun, Wang Feng, Trujillo-Ocampo Abel, Ruiz-Vasquez Wilfredo, Cho Hyun-Woo, Takahashi Koichi, Molldrem Jeffrey J, Futreal Andrew, Garcia-Manero Guillermo, Im Jin S

机构信息

Department of Stem Cell Transplantation and Cellular Therapy, Division of Cancer Medicine The University of Texas M.D. Anderson Cancer Center Houston Texas USA.

Department of Hematology, Seoul St. Mary's Hospital, College of Medicine The Catholic University of Korea Seoul South Korea.

出版信息

EJHaem. 2020 Oct 5;1(2):552-557. doi: 10.1002/jha2.112. eCollection 2020 Nov.

DOI:10.1002/jha2.112
PMID:35844984
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9175915/
Abstract

The aim of this study is to investigate whether the peripheral blood (PB) can serve as a surrogate immune-microenvironment to bone marrow for genetic and immune monitoring in myelodysplastic syndrome (MDS). We compared the composition of T cell subsets and somatic mutation burden in 36 pairs of PB and matching bone marrow aspirate (BMA) using multi-parameter flow cytometry and NGS-based targeted sequencing analysis, respectively. Our immune-subset and NGS-based mutation analysis of BMA showed significant concordance with those of PB in MDS. Therefore, PB can provide easily accessible tumor immune-microenvironment for monitoring in the immune and genetic landscapes for MDS patients.

摘要

本研究的目的是调查外周血(PB)是否可作为骨髓的替代免疫微环境,用于骨髓增生异常综合征(MDS)的基因和免疫监测。我们分别使用多参数流式细胞术和基于NGS的靶向测序分析,比较了36对PB和匹配的骨髓穿刺液(BMA)中T细胞亚群的组成和体细胞突变负担。我们对BMA进行的免疫亚群和基于NGS的突变分析显示,与MDS患者PB的分析结果具有显著一致性。因此,PB可为MDS患者的免疫和基因图谱监测提供易于获取的肿瘤免疫微环境。

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本文引用的文献

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Mutation-Driven Therapy in MDS.MDS 中的驱动突变治疗。
Curr Hematol Malig Rep. 2019 Dec;14(6):550-560. doi: 10.1007/s11899-019-00554-4.
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TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups.TP53 基因突变状态将复杂核型骨髓增生异常综合征分为不同的预后亚组。
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Molecular Determinants of Response to Anti-Programmed Cell Death (PD)-1 and Anti-Programmed Death-Ligand 1 (PD-L1) Blockade in Patients With Non-Small-Cell Lung Cancer Profiled With Targeted Next-Generation Sequencing.采用靶向下一代测序技术对非小细胞肺癌患者进行分析,明确了对抗程序性细胞死亡蛋白 1(PD-1)和抗程序性死亡配体 1(PD-L1)阻断治疗的反应的分子决定因素。
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Integrating liquid biopsies into the management of cancer.将液体活检纳入癌症管理中。
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Preleukaemic clonal haemopoiesis and risk of therapy-related myeloid neoplasms: a case-control study.白血病前期克隆性造血与治疗相关髓系肿瘤的风险:一项病例对照研究。
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