Pathogen-specific B-cell receptors drive chronic lymphocytic leukemia by light-chain-dependent cross-reaction with autoantigens

N Jiménez de Oya, M De Giovanni, J Fioravanti, R Übelhart, P Di Lucia, A Fiocchi, S Iacovelli, DG Efremov, F Caligaris-Cappio, H Jumaa, P Ghia, LG Guidotti, M Iannacone

Research output: Contribution to journalArticle

Abstract

Several lines of evidence indirectly suggest that antigenic stimulation through the B-cell receptor (BCR) supports chronic lymphocytic leukemia (CLL) development. In addition to self-antigens, a number of microbial antigens have been proposed to contribute to the selection of the immunoglobulins expressed in CLL. How pathogen-specific BCRs drive CLL development remains, however, largely unexplored. Here, we utilized mouse models of CLL pathogenesis to equip B cells with virus-specific BCRs and study the effect of antigen recognition on leukemia growth. Our results show that BCR engagement is absolutely required for CLL development. Unexpectedly, however, neither acute nor chronic exposure to virus-derived antigens influenced leukemia progression. Rather, CLL clones preferentially selected light chains that, when paired with virus-specific heavy chains, conferred B cells the ability to recognize a broad range of autoantigens. Taken together, our results suggest that pathogens may drive CLL pathogenesis by selecting and expanding pathogen-specific B cells that cross-react with one or more self-antigens. © 2017 EMBO.
Original languageEnglish
Pages (from-to)1482-1490
Number of pages9
JournalEMBO Molecular Medicine
Volume9
Issue number11
Publication statusPublished - 2017

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Cross Reactions
Autoantigens
B-Cell Chronic Lymphocytic Leukemia
B-Lymphocytes
Light
Viruses
Antigens
Leukemia
Immunoglobulins
Clone Cells
Growth

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Pathogen-specific B-cell receptors drive chronic lymphocytic leukemia by light-chain-dependent cross-reaction with autoantigens. / Jiménez de Oya, N; De Giovanni, M; Fioravanti, J; Übelhart, R; Di Lucia, P; Fiocchi, A; Iacovelli, S; Efremov, DG; Caligaris-Cappio, F; Jumaa, H; Ghia, P; Guidotti, LG; Iannacone, M.

In: EMBO Molecular Medicine, Vol. 9, No. 11, 2017, p. 1482-1490.

Research output: Contribution to journalArticle

Jiménez de Oya, N, De Giovanni, M, Fioravanti, J, Übelhart, R, Di Lucia, P, Fiocchi, A, Iacovelli, S, Efremov, DG, Caligaris-Cappio, F, Jumaa, H, Ghia, P, Guidotti, LG & Iannacone, M 2017, 'Pathogen-specific B-cell receptors drive chronic lymphocytic leukemia by light-chain-dependent cross-reaction with autoantigens', EMBO Molecular Medicine, vol. 9, no. 11, pp. 1482-1490.
Jiménez de Oya, N ; De Giovanni, M ; Fioravanti, J ; Übelhart, R ; Di Lucia, P ; Fiocchi, A ; Iacovelli, S ; Efremov, DG ; Caligaris-Cappio, F ; Jumaa, H ; Ghia, P ; Guidotti, LG ; Iannacone, M. / Pathogen-specific B-cell receptors drive chronic lymphocytic leukemia by light-chain-dependent cross-reaction with autoantigens. In: EMBO Molecular Medicine. 2017 ; Vol. 9, No. 11. pp. 1482-1490.
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AB - Several lines of evidence indirectly suggest that antigenic stimulation through the B-cell receptor (BCR) supports chronic lymphocytic leukemia (CLL) development. In addition to self-antigens, a number of microbial antigens have been proposed to contribute to the selection of the immunoglobulins expressed in CLL. How pathogen-specific BCRs drive CLL development remains, however, largely unexplored. Here, we utilized mouse models of CLL pathogenesis to equip B cells with virus-specific BCRs and study the effect of antigen recognition on leukemia growth. Our results show that BCR engagement is absolutely required for CLL development. Unexpectedly, however, neither acute nor chronic exposure to virus-derived antigens influenced leukemia progression. Rather, CLL clones preferentially selected light chains that, when paired with virus-specific heavy chains, conferred B cells the ability to recognize a broad range of autoantigens. Taken together, our results suggest that pathogens may drive CLL pathogenesis by selecting and expanding pathogen-specific B cells that cross-react with one or more self-antigens. © 2017 EMBO.

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