BRAFV600E mutant protein is expressed in cells of variable maturation in Langerhans cell histiocytosis

Author:

Sahm Felix12,Capper David12,Preusser Matthias3,Meyer Jochen2,Stenzinger Albrecht4,Lasitschka Felix4,Berghoff Anna-Sophie5,Habel Antje1,Schneider Marion6,Kulozik Andreas7,Anagnostopoulos Ioannis8,Müllauer Leonhard9,Mechtersheimer Gunhild4,von Deimling Andreas12

Affiliation:

1. Department of Neuropathology, Institute of Pathology, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Germany;

2. Clinical Cooperation Unit Neuropathology, German Cancer Research Center (DKFZ), Heidelberg, Germany;

3. Department of Medicine I and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria;

4. Department of General Pathology, Institute of Pathology, Ruprecht-Karls-Universität Heidelberg, Heidelberg, Germany;

5. Institute of Neurology and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria;

6. Experimental Anaesthesiology, University Hospital Ulm, Ulm, Germany;

7. Department of Pediatric Oncology, Hematology and Immunology, University Children's Hospital of Heidelberg, Heidelberg, Germany;

8. Institute of Pathology, Charité-University Medicine Berlin, Berlin, Germany; and

9. Institute of Pathology, Medical University Vienna, Vienna, Austria

Abstract

AbstractLangerhans cell histiocytosis (LCH) is a clinically and histologically heterogeneous disorder. Its classification as either reactive inflammatory or neoplastic has been a matter of debate. However, the recent finding of frequent BRAFV600E mutations in LCH argues for the latter. The exact cell type that harbors the mutation and is responsible for proliferation remains to be identified. We here apply a BRAFV600E mutation-specific antibody to detect the BRAF mutant cells in lesions from 89 patients with LCH. We found BRAFV600E mutations in 34 of 89 (38%) lesions. In lesions with the BRAFV600E mutation, the majority of cells coexpressing S-100 and CD1a harbored mutant BRAFV600E protein. These cells also expressed CD14 and CD36, whereas various fractions exhibited CD207. On the other hand, CD80 and CD86 expression was also present on BRAFV600E-positive cells. Thus, cells of variable maturation, exhibiting an immunohistochemical profile compatible either with myeloid cell or with dedifferentiated Langerhans cell antigens, carry the BRAFV600E mutation. In conclusion, we identify and characterize the neoplastic cells in LCH with BRAFV600E mutations by applying a mutation-specific marker and demonstrate feasibility for routine screening.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference37 articles.

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