Identification of gene microarray expression profiles in patients with chronic graft-versus-host disease following allogeneic hematopoietic cell transplantation

被引:11
作者
Kohrt, Holbrook E. [1 ]
Tian, Lu [2 ]
Li, Li [3 ]
Alizadeh, Ash A. [1 ]
Hsieh, Sue [3 ]
Tibshirani, Robert J. [2 ]
Strober, Samuel [1 ]
Sarwal, Minnie [3 ]
Lowsky, Robert [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Hlth Res & Policy, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Pediat, Stanford, CA 94305 USA
关键词
Graft-versus-host-disease; Bone marrow transplantation; Genomic markers; Gene expression; ANTIGEN-PRESENTING CELLS; II IL-1 RECEPTOR; CLINICAL-TRIALS; DIAGNOSIS; BIOMARKERS; LEUKEMIA; DERMATOSPARAXIS; MANIFESTATIONS; MULTICENTER; MARROW;
D O I
10.1016/j.clim.2013.04.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chronic graft-versus-host disease (GVHD) results in significant morbidity and mortality, limiting the benefit of allogeneic hematopoietic cell transplantation (HCT). Peripheral blood gene expression profiling of the donor immune repertoire following HCT may provide associated genes and pathways thereby improving the pathophysiologic understanding of chronic GVHD. We profiled 70 patients and identified candidate genes that provided mechanistic insight in the biologic pathways that underlie chronic GVHD. Our data revealed that the dominant gene signature in patients with chronic GVHD represented compensatory responses that control inflammation and included the interleukin-1 decoy receptor, IL-1 receptor type II, and genes that were profibrotic and associated with the IL-4, IL-6 and IL-10 signaling pathways. In addition, we identified three genes that were important regulators of extracellular matrix. Validation of this discovery phase study will determine if the identified genes have diagnostic, prognostic or therapeutic implications. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:124 / 135
页数:12
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