ROCK1/2 signaling contributes to corticosteroid-refractory acute graft-versus-host disease

  • Nat Commun. 2024 Jan 10;15(1):446. doi: 10.1038/s41467-024-44703-7.
Kristina Maas-Bauer  #  1 Anna-Verena Stell  #  1 Kai-Li Yan  #  1 Enrique de Vega  #  1  2 Janaki Manoja Vinnakota  #  1 Susanne Unger  3 Nicolas Núñez  3 Johana Norona  1 Nana Talvard-Balland  1 Stefanie Koßmann  1 Carsten Schwan  4 Cornelius Miething  1 Uta S Martens  1  4 Khalid Shoumariyeh  1  5 Rosa P Nestor  1 Sandra Duquesne  1 Kathrin Hanke  1 Michal Rackiewicz  6  7 Zehan Hu  6  7 Nadia El Khawanky  1 Sanaz Taromi  1 Hana Andrlova  1 Hemin Faraidun  2 Stefanie Walter  1 Dietmar Pfeifer  1 Marie Follo  1 Johannes Waldschmidt  1 Wolfgang Melchinger  1 Michael Rassner  1 Claudia Wehr  1 Annette Schmitt-Graeff  8 Sebastian Halbach  5  9 James Liao  10 Georg Häcker  11 Tilman Brummer  5  9  12 Joern Dengjel  6  7 Geoffroy Andrieux  13 Robert Grosse  4  14 Sonia Tugues  3 Bruce R Blazar  15 Burkhard Becher  3 Melanie Boerries  5  13 Robert Zeiser  16  17  18
Affiliations
  • 1. Department of Medicine I, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • 2. Faculty of Biology, University of Freiburg, Freiburg, Germany.
  • 3. Institute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
  • 4. Institute of Experimental and Clinical Pharmacology and Toxicology, Medical Faculty, University of Freiburg, Freiburg, Germany.
  • 5. German Cancer Consortium (DKTK), Partner Site Freiburg, a partnership between German Cancer Research Center (DKFZ) and Medical Center - University of Freiburg, Freiburg, Germany.
  • 6. Department of Biology, University of Fribourg, Fribourg, Switzerland.
  • 7. Department of Dermatology, Medical Center, University of Freiburg, Freiburg, Germany.
  • 8. Institute of Pathology, University Hospital Freiburg, Freiburg, Germany.
  • 9. IMMZ, University of Freiburg, Faculty of Medicine, Freiburg, Germany.
  • 10. Department of Medicine, University of Arizona, Tucson, USA.
  • 11. IMMH, University Hospital Freiburg, Faculty of Medicine, Freiburg, Germany.
  • 12. Signaling Research Centres BIOSS and CIBSS - Centre for Integrative Biological Signaling Studies, University of Freiburg, Freiburg, Germany.
  • 13. Institute of Medical Bioinformatics and Systems Medicine, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • 14. CIBSS-Centre for Integrative Biological Signalling Studies, University of Freiburg, Freiburg, Germany.
  • 15. Department of Pediatrics, Division of Blood & Marrow Transplant & Cellular Therapy, University of Minnesota, Minneapolis, MN, USA.
  • 16. Department of Medicine I, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany. [email protected].
  • 17. German Cancer Consortium (DKTK), Partner Site Freiburg, a partnership between German Cancer Research Center (DKFZ) and Medical Center - University of Freiburg, Freiburg, Germany. [email protected].
  • 18. Signaling Research Centres BIOSS and CIBSS - Centre for Integrative Biological Signaling Studies, University of Freiburg, Freiburg, Germany. [email protected].
  • # Contributed equally.
Abstract

Patients with corticosteroid-refractory acute graft-versus-host disease (aGVHD) have a low one-year survival rate. Identification and validation of novel targetable kinases in patients who experience corticosteroid-refractory-aGVHD may help improve outcomes. Kinase-specific proteomics of leukocytes from patients with corticosteroid-refractory-GVHD identified rho kinase type 1 (ROCK1) as the most significantly upregulated kinase. ROCK1/2 inhibition improved survival and histological GVHD severity in mice and was synergistic with JAK1/2 inhibition, without compromising graft-versus-leukemia-effects. ROCK1/2-inhibition in macrophages or dendritic cells prior to transfer reduced GVHD severity. Mechanistically, ROCK1/2 inhibition or ROCK1 knockdown interfered with CD80, CD86, MHC-II expression and IL-6, IL-1β, iNOS and TNF production in myeloid cells. This was accompanied by impaired T cell activation by dendritic cells and inhibition of cytoskeletal rearrangements, thereby reducing macrophage and DC migration. NF-κB signaling was reduced in myeloid cells following ROCK1/2 inhibition. In conclusion, ROCK1/2 inhibition interferes with immune activation at multiple levels and reduces acute GVHD while maintaining GVL-effects, including in corticosteroid-refractory settings.

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