A 17-year quest to understand Langerhans-cell histiocytosis (LCH)—an inflammatory blood disease that mostly affects children and can result in dementia and death—has led researchers at the Icahn School of Medicine at Mount Sinai and their colleagues in Texas to a transformational discovery and a potential new treatment. Their findings were published in May in Nature Medicine. The team, led by Miriam Merad, MD, PhD, Director of the Precision Immunology Institute at Icahn Mount Sinai, and Carl E. Allen, MD, PhD, Professor of Pediatrics, Hematology-Oncology, at Baylor College of Medicine, found that individuals with LCH have a mutation that puts a subset of white blood cells into a state called senescence.
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