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IMMUNOLOGY2026™ Conference Recordings For Attendee ...
Inflammatory hematopoiesis drives intestinal infla ...
Inflammatory hematopoiesis drives intestinal inflammation and is modulated by anti-TNF therapy
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Video Summary
The speaker presented research on how inflammatory hematopoiesis may worsen Crohn’s disease. Using enriched CD34+ cells from blood and 10x multiome profiling in healthy donors and Crohn’s patients, the team found that early hematopoietic progenitors in Crohn’s are reprogrammed toward inflammatory, metabolic, and antigen-presentation programs, driven by TF networks such as NF-kB, AP-1, and CEBPβ. These progenitor programs were also reflected in monocytes, suggesting inflammatory memory is passed from bone marrow precursors to mature immune cells. In a DSS colitis mouse model, gut inflammation altered bone marrow progenitors, increased inflammatory motifs, and produced myeloid cells with enhanced cytokine production and migration. Bone marrow from DSS-experienced mice worsened colitis when transferred into recipients. Importantly, anti-TNF therapy partially reset these progenitor programs, showing the changes are reversible. Overall, HSPCs act as a treatment-responsive inflammatory reservoir in IBD.
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Date
April 16, 2026 5:00 PM - 5:15 PM
Room
104AB
Session
Bone Marrow Hematopoiesis
Speaker
Jin-Gyu Cheong
Track
Hematopoiesis and Immune System Development (HEM)
Year
2026
Keywords
Crohn’s disease
inflammatory hematopoiesis
CD34+ progenitor cells
NF-kB AP-1 CEBPβ
anti-TNF therapy
April 16, 2026 5:00 PM - 5:15 PM
104AB
Bone Marrow Hematopoiesis
Jin-Gyu Cheong
Hematopoiesis and Immune System Development (HEM)
2026
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