Systems analysis uncovers inflammatory Th/Tc17-driven modules during acute GVHD in monkey and human T cells

Author:

Furlan Scott N.123ORCID,Watkins Benjamin123,Tkachev Victor123,Cooley Sarah4ORCID,Panoskaltsis-Mortari Angela4,Betz Kayla123,Brown Melanie123,Hunt Daniel J.123,Schell John B.123,Zeleski Katie123,Yu Alison123,Giver Cynthia R.5,Waller Edmund K.5,Miller Jeffrey S.4,Blazar Bruce R.4,Kean Leslie S.123

Affiliation:

1. Ben Towne Center for Childhood Cancer Research, Seattle Children’s Research Institute, Seattle, WA;

2. Department of Pediatrics, University of Washington, Seattle, WA;

3. Fred Hutchinson Cancer Research Center, Seattle, WA;

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

5. Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA

Abstract

Key PointsThe transcriptional networks controlling breakthrough acute GVHD can be mapped, and correlate closely with clinical disease. Breakthrough acute GVHD is transcriptionally controlled by T-cell persistence, inflammation, and Th/Tc17 skewing.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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