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Erschienen in: Journal of Clinical Immunology 1/2010

01.01.2010

B-Cell Reconstitution and BAFF After Alemtuzumab (Campath-1H) Treatment of Multiple Sclerosis

verfasst von: Sara A. J. Thompson, Joanne L. Jones, Amanda L. Cox, D. Alastair S. Compston, Alasdair J. Coles

Erschienen in: Journal of Clinical Immunology | Ausgabe 1/2010

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Abstract

Introduction

Treatment with alemtuzumab is highly effective in relapsing–remitting multiple sclerosis; however, 30% of patients develop autoimmunity. Alemtuzumab (previously called Campath 1-H) induces a prolonged T-cell lymphopenia with memory cells dominating the reconstituting T-cell pool for at least 3 months.

Results

Here we show that B-cell recovery is rapid, returning to baseline by 3 months and rising to 165% of baseline by 12 months after treatment. Immature transitional 1 B cells are the predominant cell type 1 month after treatment. This coincides with a surge in serum B-cell activating factor (BAFF), which remains elevated by 33% for at least 12 months after alemtuzumab. BAFF is critical for transition to the mature naive B-cell phenotype, which dominates from 3 months after alemtuzumab. Differentiation to memory B cells is slow so there are radical and prolonged alterations to the B-cell pool after alemtuzumab.
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Metadaten
Titel
B-Cell Reconstitution and BAFF After Alemtuzumab (Campath-1H) Treatment of Multiple Sclerosis
verfasst von
Sara A. J. Thompson
Joanne L. Jones
Amanda L. Cox
D. Alastair S. Compston
Alasdair J. Coles
Publikationsdatum
01.01.2010
Verlag
Springer US
Erschienen in
Journal of Clinical Immunology / Ausgabe 1/2010
Print ISSN: 0271-9142
Elektronische ISSN: 1573-2592
DOI
https://doi.org/10.1007/s10875-009-9327-3

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