The origin, diagnosis, and prognosis of oligomannose-type diffuse large B-cell lymphoma
The acquisition of N-glycosylation sites that are occupied by oligomannose-type glycans in the immunoglobulin complementarity-determining region (CDR) is an early, clonal, tumor-specific identifier of follicular lymphoma (FL). CDR-located N-glycosylation sites are also acquired in germinal center B-cell-like diffuse large B-cell lymphomas (GCB-DLBCLs), but their significance is less defined. We used RNA sequencing immunoglobulin assembly to determine frequency and CDR location of the acquired N-glycosylation sites (AGSs) in 2 independent DLBCL cohorts. Composition of the glycans occupying the AGSs was determined using liquid chromatography-mass spectrometry and correlated with cell of origin, FL signature (defined by EZB phenotype or BCL2 translocation), transcript profile, and clinical outcome. CDR-located AGSs were observed in 41% to 46% of GCB-DLBCLs but were rare in other DLBCLs. Only CDR-located AGSs of DLBCL with an FL signature were occupied by oligomannose-type glycans. These DLBCLs were termed Mann-type DLBCL. Conversely, the AGSs of the other DLBCLs were either nonglycosylated or occupied by complex-type glycans. Mann-type status was an independent marker of short progression-free survival and overall survival. In contrast, the other GCB-DLBCLs, including those with an FL signature but without AGSs, had the best outcomes. Mann-type DLBCLs overexpressed gene sets of cell growth, survival, and cycling, and underexpressed proinflammatory and apoptotic pathways, irrespective of the presence of concomitant MYC translocations. The acquisition of Mann-type glycans is a highly selective environmental pressure enabling the identification of an aggressive GCB-DLBCL type with origin related to FL. The detection of AGSs in the CDR of GCB-DLBCLs with an FL signature defines Mann-type DLBCLs, refines prognosis, and marks a precise tumor interaction to block early therapeutically.
Authors
- Benjamin Sale (ORCID: https://orcid.org/0000-0003-3292-1886)
- Giorgia Chiodin (ORCID: https://orcid.org/0000-0002-1456-8997)
- David W. Scott (ORCID: https://orcid.org/0000-0002-0435-5947)
- Dylan Tatterton (ORCID: https://orcid.org/0000-0002-1453-7496)
- Dean Bryant (ORCID: https://orcid.org/0000-0003-3163-608X)
- Maddy L. Newby (ORCID: https://orcid.org/0000-0003-0624-245X)
- Max Crispin (ORCID: https://orcid.org/0000-0002-1072-2694)
- Andrew John Davies (ORCID: https://orcid.org/0000-0002-7517-6938)
- Joel D. Allen (ORCID: https://orcid.org/0000-0003-2547-968X)
- Francesco Forconi (ORCID: https://orcid.org/0000-0002-2211-1831)
- Ryan D. Morin (ORCID: https://orcid.org/0000-0003-2932-7800)
- Katy J. McCann (ORCID: https://orcid.org/0000-0003-4388-7265)
- Patrick J. Duriez (ORCID: https://orcid.org/0000-0003-1814-2552)
- Kostiantyn Dreval (ORCID: https://orcid.org/0000-0002-6214-2843)
- John Butler (ORCID: https://orcid.org/0000-0001-8086-0964)
Institutions
- University of British Columbia (CA)
- Simon Fraser University (CA)
- Spinal Cord Injury BC (CA)
- University Hospital Southampton NHS Foundation Trust (GB)
- Canada's Michael Smith Genome Sciences Centre (CA)
- University of Southampton (GB)
Publication Details
- Journal
- Blood
- Published
- 2025-09-02
- DOI
- https://doi.org/10.1182/blood.2025029163
- Citations
- 1
- Primary Topic
- Glycosylation and Glycoproteins Research
- Type
- article
- Field-Weighted Citation Impact
- 0.81