Persistence of monoclonal B‐cell expansion and intraclonal diversification despite virus eradication in patients affected by hepatitis C virus‐associated lymphoproliferative disorders

Author:

Mazzaro Cesare1,Visentini Marcella2ORCID,Gragnani Laura3,Vit Filippo1,Tissino Erika1,Pozzo Federico1,Papotti Robel1,Casato Milvia2,Zignego Anna Linda4,Bittolo Tamara1,Zucchetto Antonella1,Degan Massimo1,Bomben Riccardo1ORCID,Gattei Valter1

Affiliation:

1. Clinical and Experimental Onco‐Haematology Unit Centro di Riferimento Oncologico di Aviano (CRO), IRCCS Aviano Italy

2. Division of Clinical Immunology, Department of Internal Medicine Sapienza Unversity of Rome Rome Italy

3. Department of Translational Research and New Technologies in Medicine and Surgery Medical School, University of Pisa Pisa Italy

4. Centro Manifestazioni Sistemiche da Virus Epatitici University of Florence Florence Italy

Abstract

SummaryWe investigated 23 hepatitis C virus (HCV)‐infected patients with overt lymphoproliferative diseases (15 cases) or monoclonal B lymphocytosis (8 cases) treated with direct agent antiviral (DAAs) per clinical practice. DAA therapy yielded undetectable HCV‐RNA, the complete response of cryoglobulinemia vasculitis and related signs, whilst the presence of B‐cell clones (evaluated by flow cytometry, IGHV, and BCL2‐IGH rearrangements), detected in 19/23 cases at baseline, was maintained (17/19). Similarly, IGHV intraclonal diversification, supporting an antigen‐driven selection mechanism, was identified in B‐cell clones at baseline and end of follow‐up. DAA therapy alone, despite HCV eradication and good immunological responses, was less effective on the pathological B‐cell clones.

Funder

Associazione Italiana per la Ricerca sul Cancro

Ministero della Salute

Publisher

Wiley

Subject

Hematology

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