Regulation of acute graft-versus-host disease by microRNA-155

Author:

Ranganathan Parvathi1,Heaphy Catherine E. A.1,Costinean Stefan2,Stauffer Nicole1,Na Caroline1,Hamadani Mehdi3,Santhanam Ramasamy2,Mao Charlene1,Taylor Patricia A.4,Sandhu Sukhinder2,He Gang5,Shana'ah Arwa6,Nuovo Gerard J.6,Lagana Alessandro2,Cascione Luciano27,Obad Susanna8,Broom Oliver8,Kauppinen Sakari89,Byrd John C.1,Caligiuri Michael1,Perrotti Danilo2,Hadley Gregg A.10,Marcucci Guido12,Devine Steven M.1,Blazar Bruce R.4,Croce Carlo M.2,Garzon Ramiro1

Affiliation:

1. Division of Hematology, Department of Internal Medicine and Comprehensive Cancer Center, and

2. Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH;

3. Divison of Hematology and Oncology, Department of Medicine, West Virginia University, Morgantown, WV;

4. Masonic Cancer Center and Department of Pediatrics, Division of Blood and Marrow Transplantation, University of Minnesota, Minneapolis, MN;

5. Department of Pathology, University of Manitoba, Winnipeg, MB;

6. Department of Pathology, The Ohio State University, Columbus, OH;

7. Department of Molecular and Clinical Biomedicine, University of Catania, Catania, Italy;

8. Santaris Pharma, Hørsholm, Denmark;

9. Copenhagen Institute of Technology, Aalborg University, Ballerup, Denmark; and

10. Division of Transplantation, Department of Surgery, The Ohio State University, Columbus, OH

Abstract

Abstract Acute graft-versus-host disease (aGVHD) remains a major complication of allogeneic hematopoietic stem cell transplant (alloHSCT), underscoring the need to further elucidate its mechanisms and develop novel treatments. Based on recent observations that microRNA-155 (miR-155) is up-regulated during T-cell activation, we hypothesized that miR-155 is involved in the modulation of aGVHD. Here we show that miR-155 expression was up-regulated in T cells from mice developing aGVHD after alloHSCT. Mice receiving miR-155–deficient donor lymphocytes had markedly reduced lethal aGVHD, whereas lethal aGVHD developed rapidly in mice recipients of miR-155 overexpressing T cells. Blocking miR-155 expression using a synthetic anti–miR-155 after alloHSCT decreased aGVHD severity and prolonged survival in mice. Finally, miR-155 up-regulation was shown in specimens from patients with pathologic evidence of intestinal aGVHD. Altogether, our data indicate a role for miR-155 in the regulation of GVHD and point to miR-155 as a novel target for therapeutic intervention in this disease.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3