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
Cited by
4 articles.
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