| Literature DB >> 33075129 |
Begüm Alankus1,2, Veronika Ecker1,2, Nathalie Vahl1, Martina Braun1,2, Wilko Weichert3,4, Stephan Macher-Göppinger5, Torben Gehring1, Tanja Neumayer1,2, Thorsten Zenz6, Maike Buchner1,2,4, Jürgen Ruland1,2,4,7.
Abstract
Clinical evidence suggests alterations in receptor activator of NF-κB (RANK) signaling are key contributors to B cell autoimmunity and malignancy, but the pathophysiological consequences of aberrant B cell-intrinsic RANK signaling remain unknown. We generated mice that express a human lymphoma-derived, hyperactive RANKK240E variant in B lymphocytes in vivo. Forced RANK signaling disrupted B cell tolerance and induced a fully penetrant systemic lupus erythematosus-like disease in addition to the development of chronic lymphocytic leukemia (CLL). Importantly, RANKK240E transgenic CLL cells as well as CLL cells of independent murine and of human origin depend on microenvironmental RANK ligand (RANKL) for tumor cell survival. Consequently, inhibition of the RANKL-RANK axis with anti-RANKL antibodies killed murine and human CLL cells in vitro and in vivo. These results establish pathological B cell-intrinsic RANK signaling as a potential driver of autoimmunity and B cell malignancy, and they suggest the exploitation of clinically available anti-RANKL compounds for CLL treatment.Entities:
Year: 2021 PMID: 33075129 PMCID: PMC7868734 DOI: 10.1084/jem.20200517
Source DB: PubMed Journal: J Exp Med ISSN: 0022-1007 Impact factor: 14.307