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T 细胞受体库的独特演变可对治疗抵抗性胃肠道急性移植物抗宿主病进行分类。

A distinct evolution of the T-cell repertoire categorizes treatment refractory gastrointestinal acute graft-versus-host disease.

机构信息

Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.

出版信息

Blood. 2013 Jun 13;121(24):4955-62. doi: 10.1182/blood-2013-03-489757. Epub 2013 May 7.

DOI:10.1182/blood-2013-03-489757
PMID:23652802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3682344/
Abstract

Steroid refractory gastrointestinal (GI) acute graft-versus-host disease (aGVHD) is a major cause of mortality in hematopoietic stem cell transplantation (HCT) without immune markers to establish a diagnosis or guide therapy. We found that T-cell receptor β (TCRβ) complementarity-determining region 3 repertoire sequencing reveals patterns that could eventually serve as a disease biomarker of T-cell alloreactivity in aGVHD. We identified T-cell clones in GI biopsies in a heterogeneous group of 15 allogeneic HCT patients with GI aGVHD symptoms. Seven steroid-refractory aGVHD patients showed a more conserved TCRβ clonal structure between different biopsy sites in the GI tract than 8 primary therapy-responsive patients. Tracking GI clones identified longitudinally at endoscopy in the blood also revealed an increased clonal expansion in patients with steroid-refractory disease. Immune repertoire sequencing-based methods could enable a novel personalized way to guide diagnosis and therapy in diseases where T-cell activity is a major determinant.

摘要

类固醇难治性胃肠道 (GI) 急性移植物抗宿主病 (aGVHD) 是造血干细胞移植 (HCT) 患者死亡的主要原因,目前尚无免疫标志物可用于诊断或指导治疗。我们发现,T 细胞受体 β (TCRβ) 互补决定区 3 序列分析揭示了可能最终成为 aGVHD 中 T 细胞同种反应性疾病生物标志物的模式。我们在 15 名具有 GI aGVHD 症状的异基因 HCT 患者的 GI 活检中鉴定出了 T 细胞克隆。7 名类固醇难治性 aGVHD 患者的 GI 肠道不同活检部位之间的 TCRβ 克隆结构比 8 名原发性治疗反应患者更为保守。在结肠镜检查中纵向追踪血液中的 GI 克隆也表明,类固醇难治性疾病患者的克隆扩增增加。基于免疫受体库测序的方法可以为 T 细胞活性是主要决定因素的疾病提供一种新的个性化诊断和治疗方法。

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