Abstract
B cells play diverse and fundamental roles in the pathogenesis of autoimmune diseases. Consequently, therapeutic targeting of B cells is gaining prominence in our clinical armamentarium for an ever expanding array of autoimmune and neoplastic disorders. Therefore, it is of great importance to understand the mechanism of action of B cell depletion. Given that the ideal consequence of B cell depletion would be the subsequent re-establishment of immunologic tolerance, a detailed analysis of the properties of the emerging repertoire will be required. The results presented by Rouzière and coworkers in their study of rheumatoid arthritis patients shed some light on this question and are discussed in this commentary.
MeSH Terms
Adult
Antibodies, Monoclonal/pharmacology,therapeutic use
Antibodies, Monoclonal, Murine-Derived
Antigens, CD19/analysis
Arthritis, Rheumatoid/drug therapy,immunology
Autoimmune Diseases/drug therapy,immunology
B-Lymphocyte Subsets/immunology,pathology
Gene Rearrangement, B-Lymphocyte, Heavy Chain
Hematopoiesis
Humans
Immunoglobulin G/genetics
Immunoglobulin M/genetics
Immunophenotyping
Lymphocyte Depletion
Polymerase Chain Reaction
Rituximab
Somatic Hypermutation, Immunoglobulin
Tumor Necrosis Factor Receptor Superfamily, Member 7/analysis
Chemicals
Antibodies, Monoclonal
Antibodies, Monoclonal, Murine-Derived
Antigens, CD19
Immunoglobulin G
Immunoglobulin M
Tumor Necrosis Factor Receptor Superfamily, Member 7
Rituximab
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Sanz Iñaki
Division of Clinical Immunology & Rheumatology, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA. Ignacio_Sanz@urmc.rochester.edu
Anolik Jennifer
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