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Insertion of atypical glycans into the tumor antigen-binding site identifies DLBCLs with distinct origin and behavior

Insertion of atypical glycans into the tumor antigen-binding site identifies DLBCLs with distinct origin and behavior
Insertion of atypical glycans into the tumor antigen-binding site identifies DLBCLs with distinct origin and behavior

Glycosylation of the surface immunoglobulin (Ig) variable region is a remarkable follicular lymphoma–associated feature rarely seen in normal B cells. Here, we define a subset of diffuse large B-cell lymphomas (DLBCLs) that acquire N-glycosylation sites selectively in the Ig complementarity-determining regions (CDRs) of the antigen-binding sites. Mass spectrometry and X-ray crystallography demonstrate how the inserted glycans are stalled at oligomannose-type structures because they are buried in the CDR loops. Acquisition of sites occurs in ∼50% of germinal-center B-cell–like DLBCL (GCB-DLBCL), mainly of the genetic EZB subtype, irrespective of IGHV-D-J use. This markedly contrasts with the activated B-cell–like DLBCL Ig, which rarely has sites in the CDR and does not seem to acquire oligomannose-type structures. Acquisition of CDR-located acceptor sites associates with mutations of epigenetic regulators and BCL2 translocations, indicating an origin shared with follicular lymphoma. Within the EZB subtype, these sites are associated with more rapid disease progression and with significant gene set enrichment of the B-cell receptor, PI3K/AKT/MTORC1 pathway, glucose metabolism, and MYC signaling pathways, particularly in the fraction devoid of MYC translocations. The oligomannose-type glycans on the lymphoma cells interact with the candidate lectin dendritic cell–specific intercellular adhesion molecule 3 grabbing non-integrin (DC-SIGN), mediating low-level signals, and lectin-expressing cells form clusters with lymphoma cells. Both clustering and signaling are inhibited by antibodies specifically targeting the DC-SIGN carbohydrate recognition domain. Oligomannosylation of the tumor Ig is a posttranslational modification that readily identifies a distinct GCB-DLBCL category with more aggressive clinical behavior, and it could be a potential precise therapeutic target via antibody-mediated inhibition of the tumor Ig interaction with DC-SIGN–expressing M2-polarized macrophages.

0006-4971
1570-1582
Chiodin, Giorgia
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Allen, Joel D
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Bryant, Dean
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Rock, Philip
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Martino, Enrica Antonia
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Valle-Argos, Beatriz
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Duriez, Patrick J
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Watanabe, Yasunori
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Henderson, Isla
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Blachly, James S
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McCann, Katy J
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Strefford, Jonathan C
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Packham, Graham
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Geijtenbeek, Teunis Bh
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Figdor, Carl
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Wright, George
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Staudt, Louis Michael
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Burack, Richard
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Bowden, Thomas
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Crispin, Max
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Stevenson, Freda Kathryn
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Forconi, Francesco
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Chiodin, Giorgia
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Allen, Joel D
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Bryant, Dean
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Rock, Philip
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Martino, Enrica Antonia
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Valle-Argos, Beatriz
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Duriez, Patrick J
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Watanabe, Yasunori
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Henderson, Isla
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Blachly, James S
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McCann, Katy J
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Strefford, Jonathan C
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Packham, Graham
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Geijtenbeek, Teunis Bh
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Figdor, Carl
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Wright, George
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Staudt, Louis Michael
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Burack, Richard
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Bowden, Thomas
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Crispin, Max
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Stevenson, Freda Kathryn
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Forconi, Francesco
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Chiodin, Giorgia, Allen, Joel D, Bryant, Dean, Rock, Philip, Martino, Enrica Antonia, Valle-Argos, Beatriz, Duriez, Patrick J, Watanabe, Yasunori, Henderson, Isla, Blachly, James S, McCann, Katy J, Strefford, Jonathan C, Packham, Graham, Geijtenbeek, Teunis Bh, Figdor, Carl, Wright, George, Staudt, Louis Michael, Burack, Richard, Bowden, Thomas, Crispin, Max, Stevenson, Freda Kathryn and Forconi, Francesco (2021) Insertion of atypical glycans into the tumor antigen-binding site identifies DLBCLs with distinct origin and behavior. Blood, 138 (17), 1570-1582. (doi:10.1182/blood.2021012052).

Record type: Article

Abstract

Glycosylation of the surface immunoglobulin (Ig) variable region is a remarkable follicular lymphoma–associated feature rarely seen in normal B cells. Here, we define a subset of diffuse large B-cell lymphomas (DLBCLs) that acquire N-glycosylation sites selectively in the Ig complementarity-determining regions (CDRs) of the antigen-binding sites. Mass spectrometry and X-ray crystallography demonstrate how the inserted glycans are stalled at oligomannose-type structures because they are buried in the CDR loops. Acquisition of sites occurs in ∼50% of germinal-center B-cell–like DLBCL (GCB-DLBCL), mainly of the genetic EZB subtype, irrespective of IGHV-D-J use. This markedly contrasts with the activated B-cell–like DLBCL Ig, which rarely has sites in the CDR and does not seem to acquire oligomannose-type structures. Acquisition of CDR-located acceptor sites associates with mutations of epigenetic regulators and BCL2 translocations, indicating an origin shared with follicular lymphoma. Within the EZB subtype, these sites are associated with more rapid disease progression and with significant gene set enrichment of the B-cell receptor, PI3K/AKT/MTORC1 pathway, glucose metabolism, and MYC signaling pathways, particularly in the fraction devoid of MYC translocations. The oligomannose-type glycans on the lymphoma cells interact with the candidate lectin dendritic cell–specific intercellular adhesion molecule 3 grabbing non-integrin (DC-SIGN), mediating low-level signals, and lectin-expressing cells form clusters with lymphoma cells. Both clustering and signaling are inhibited by antibodies specifically targeting the DC-SIGN carbohydrate recognition domain. Oligomannosylation of the tumor Ig is a posttranslational modification that readily identifies a distinct GCB-DLBCL category with more aggressive clinical behavior, and it could be a potential precise therapeutic target via antibody-mediated inhibition of the tumor Ig interaction with DC-SIGN–expressing M2-polarized macrophages.

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1-s2.0-S0006497121015111-main - Accepted Manuscript
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Accepted/In Press date: 3 August 2021
Published date: 28 October 2021

Identifiers

Local EPrints ID: 451100
URI: http://eprints.soton.ac.uk/id/eprint/451100
ISSN: 0006-4971
PURE UUID: 8b78093f-b27f-47e0-a38f-76f186f52386
ORCID for Joel D Allen: ORCID iD orcid.org/0000-0003-2547-968X
ORCID for Dean Bryant: ORCID iD orcid.org/0000-0003-3163-608X
ORCID for Patrick J Duriez: ORCID iD orcid.org/0000-0003-1814-2552
ORCID for Jonathan C Strefford: ORCID iD orcid.org/0000-0002-0972-2881
ORCID for Graham Packham: ORCID iD orcid.org/0000-0002-9232-5691
ORCID for Max Crispin: ORCID iD orcid.org/0000-0002-1072-2694
ORCID for Freda Kathryn Stevenson: ORCID iD orcid.org/0000-0002-0933-5021
ORCID for Francesco Forconi: ORCID iD orcid.org/0000-0002-2211-1831

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Date deposited: 07 Sep 2021 16:35
Last modified: 17 Mar 2024 06:48

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Contributors

Author: Giorgia Chiodin
Author: Joel D Allen ORCID iD
Author: Dean Bryant ORCID iD
Author: Philip Rock
Author: Enrica Antonia Martino
Author: Beatriz Valle-Argos
Author: Patrick J Duriez ORCID iD
Author: Yasunori Watanabe
Author: Isla Henderson
Author: James S Blachly
Author: Katy J McCann
Author: Graham Packham ORCID iD
Author: Teunis Bh Geijtenbeek
Author: Carl Figdor
Author: George Wright
Author: Louis Michael Staudt
Author: Richard Burack
Author: Thomas Bowden
Author: Max Crispin ORCID iD

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