| Literature DB >> 29955130 |
Lorenz Thurner1, Sylvia Hartmann2, Natalie Fadle3, Maria Kemele3, Theresa Bock3, Moritz Bewarder3, Evi Regitz3, Frank Neumann3, Anna Nimmesgern4, Lutz von Müller4, Christiane Pott5, Yoo-Jin Kim6, Rainer Maria Bohle6, Mariusz Wasik7, Stephen J Schuster7, Martin-Leo Hansmann2, Klaus-Dieter Preuss3, Michael Pfreundschuh3.
Abstract
The predominant usage of VH4-34 and V3-21 and reports of stereotyped CDR3s suggest a shared antigenic target of B-cell receptors (BCR) from mantle cell lymphomas (MCL). To identify the target antigens of MCL-BCRs, BCRs from 21 patients and seven MCL cell lines were recombinantly expressed and used for antigen screening. The BCRs from 8/21 patients and 2/7 MCL cell lines reacted specifically with the autoantigen low-density lipoprotein receptor-related protein-associated protein 1 (LRPAP1). High-titered and light chain-restricted anti-LRPAP1 serum antibodies were found in MCL patients, but not in controls. LRPAP1 induced proliferation by BCR pathway activation, while an LRPAP1-ETA' toxin-conjugate specifically killed MCL cells with LRPAP1-specific BCRs. Our results suggest a role of LRPAP1 in lymphomagenesis and maintenance of a considerable proportion of MCL cases by chronic autoantigenic stimulation, likely evolving from a chronic autoreactive B-cell response. Importantly, LRPAP1 can be used for a novel therapeutic approach that targets MCL with LRPAP1-reactive BCRs with high specificity.Entities:
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Year: 2018 PMID: 29955130 DOI: 10.1038/s41375-018-0182-1
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528