Hematopoietic origin of Langerhans cell histiocytosis and Erdheim-Chester disease in adults Journal Article


Authors: Milne, P.; Bigley, V.; Bacon, C. M.; Néel, A.; McGovern, N.; Bomken, S.; Haniffa, M.; Diamond, E. L.; Durham, B. H.; Visser, J.; Hunt, D.; Gunawardena, H.; Macheta, M.; McClain, K. L.; Allen, C.; Abdel-Wahab, O.; Collin, M.
Article Title: Hematopoietic origin of Langerhans cell histiocytosis and Erdheim-Chester disease in adults
Abstract: Langerhans cell histiocytosis (LCH) and Erdheim-Chester disease (ECD) are rare histiocytic disorders induced by somatic mutation of MAPK pathway genes. BRAFV600E mutation is the most common mutation in both conditions and also occurs in the hematopoietic neoplasm hairy cell leukemia (HCL). It is not known if adult LCH or ECD arises from hematopoietic stem cells (HSCs), nor which potential blood borne precursors lead to the formation of histiocytic lesions. In this study, BRAFV600E allele–specific polymerase chain reaction was used to map the neoplastic clone in 20 adults with LCH, ECD, and HCL. BRAFV600E was tracked to classical monocytes, nonclassical monocytes, and CD1c1 myeloid dendritic cells (DCs) in the blood, and mutations were observed in HSCs and myeloid progenitors in the bone marrow of 4 patients. The pattern of involvement of peripheral blood myeloid cells was indistinguishable between LCH and ECD, although the histiocytic disorders were distinct to HCL. As reported in children, detection of BRAFV600E in peripheral blood of adults was a marker of active multisystem LCH. The healthy counterparts of myeloid cells affected by BRAF mutation had a range of differentiation potentials depending on exogenous signals. CD1c1 DCs acquired high langerin and CD1a with granulocyte-macrophage colony-stimulating factor and transforming growth factor b alone, whereas CD141 classical monocytes required additional notch ligation. Both classical and nonclassical monocytes, but not CD1c1 DCs, made foamy macrophages easily in vitro with macrophage colony-stimulating factor and human serum. These studies are consistent with a hematopoietic origin and >1 immediate cellular precursor in both LCH and ECD. © 2017 by The American Society of Hematology
Journal Title: Blood
Volume: 130
Issue: 2
ISSN: 0006-4971
Publisher: American Society of Hematology  
Date Published: 2017-07-13
Start Page: 167
End Page: 175
Language: English
DOI: 10.1182/blood-2016-12-757823
PROVIDER: scopus
PUBMED: 28512190
PMCID: PMC5524529
DOI/URL:
Notes: Article -- Export Date: 2 August 2017 -- Source: Scopus
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  1. Eli Louis Diamond
    125 Diamond
  2. Benjamin Heath Durham
    85 Durham