LRPAP1 is a frequent proliferation-inducing antigen of BCRs of mantle cell lymphomas and can be used for specific therapeutic targeting.
Lorenz ThurnerSylvia HartmannNatalie FadleMaria KemeleTheresa BockMoritz BewarderEvi RegitzFrank NeumannAnna NimmesgernLutz von MüllerChristiane PottYoo-Jin KimRainer Maria BohleMariusz WasikStephen J SchusterMartin-Leo HansmannKlaus-Dieter PreussMichael PfreundschuhPublished in: Leukemia (2018)
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.
Keyphrases
- end stage renal disease
- chronic kidney disease
- newly diagnosed
- ejection fraction
- prognostic factors
- acute lymphoblastic leukemia
- escherichia coli
- single cell
- signaling pathway
- emergency department
- cell therapy
- tyrosine kinase
- bone marrow
- immune response
- drug delivery
- mesenchymal stem cells
- oxidative stress
- cancer therapy
- endothelial cells
- dendritic cells
- cell death
- high glucose
- electronic health record
- structural basis