Langerhans cell histiocytosis: current advances in molecular pathogenesis.

BRAFV600E MAP2K1 dendritic cells langerhans cell histiocytosis monocytes oncogene senescence

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2023
Historique:
received: 09 08 2023
accepted: 16 10 2023
medline: 15 11 2023
pubmed: 15 11 2023
entrez: 15 11 2023
Statut: epublish

Résumé

Langerhans cell histiocytosis (LCH) is a rare and clinically heterogeneous hematological disease characterized by the accumulation of mononuclear phagocytes in various tissues and organs. LCH is often characterized by activating mutations of the mitogen-activated protein kinase (MAPK) pathway with

Identifiants

pubmed: 37965340
doi: 10.3389/fimmu.2023.1275085
pmc: PMC10642229
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1275085

Informations de copyright

Copyright © 2023 Sconocchia, Foßelteder, Sconocchia and Reinisch.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Tommaso Sconocchia (T)

Division of Hematology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Johannes Foßelteder (J)

Division of Hematology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Giuseppe Sconocchia (G)

Institute of Translational Pharmacology, National Research Council (CNR), Rome, Italy.

Andreas Reinisch (A)

Division of Hematology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Department of Blood Group Serology and Transfusion Medicine, Medical University of Graz, Graz, Austria.

Classifications MeSH