Frontiers in Oncology (Oct 2022)

Mass cytometry analysis reveals attrition of naïve and anergized self-reactive non-malignant B cells in chronic lymphocytic leukemia patients

  • Thibault Andrieu,
  • Paul Mondière,
  • Pierre-Emmanuel Jouve,
  • Sébastien Dussurgey,
  • Victor Malassigné,
  • Hugo Servanton,
  • Lucille Baseggio,
  • Frédéric Davi,
  • Anne-Sophie Michallet,
  • Thierry Defrance

DOI
https://doi.org/10.3389/fonc.2022.1020740
Journal volume & issue
Vol. 12

Abstract

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Chronic Lymphocytic Leukemia (CLL) is characterized by the progressive accumulation of monoclonal mature B lymphocytes. Autoimmune complications are common in CLL occurring in up to a quarter of all patients during the course of the illness. Etiology of autoimmunity in CLL is unknown but it is widely admitted that the pathogenic auto-Abs do not originate from the tumoral clone but from the non-malignant B cell pool. This indicates that the developmental scheme of non-malignant B cells could also be perturbed in CLL patients. To address this question, we have designed a B cell-centered antibody panel and used time-of-flight mass cytometry to compare the residual non-malignant B cell pool of CLL patients with the peripheral B cell pool of age-matched healthy donors. We show that the non-malignant B cell compartment of the patients is characterized by profound attrition of naïve B cells and of a population of anergized autoreactive B cells, suggesting impaired B cell lymphopoeisis as well as perturbations of the B cell tolerance checkpoints.

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