Lung parenchyma-derived IL-6 promotes IL-17A–dependent acute lung injury after allogeneic stem cell transplantation

Author:

Varelias Antiopi1,Gartlan Kate H.1,Kreijveld Ellen1,Olver Stuart D.1,Lor Mary1,Kuns Rachel D.1,Lineburg Katie E.1,Teal Bianca E.1,Raffelt Neil C.1,Cheong Melody1,Alexander Kylie A.1,Koyama Motoko1,Markey Kate A.1,Sturgeon Elise12,Leach Justine12,Reddy Pavan3,Kennedy Glen A.12,Yanik Gregory A.3,Blazar Bruce R.4,Tey Siok-Keen12,Clouston Andrew D.5,MacDonald Kelli P. A.1,Cooke Kenneth R.6,Hill Geoffrey R.12

Affiliation:

1. QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia;

2. Department of Bone Marrow Transplantation, The Royal Brisbane and Women’s Hospital, Brisbane, QLD, Australia;

3. Division of Hematology and Oncology, Blood and Marrow Transplantation Program, University of Michigan, Ann Arbor, MI;

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

5. Envoi Specialist Pathologists, Brisbane, QLD, Australia; and

6. Department of Oncology, Blood and Marrow Stem Cell Transplantation Program, Sidney Kimmel Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD

Abstract

Key Points IL-6 is dysregulated after experimental allogeneic SCT and promotes alloantigen-dependent Th17 expansion within the lung. IL-6 is dysregulated in patients with IPS after clinical allogeneic SCT.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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