Natalizumab treatment decreases serum IgM and IgG levels in multiple sclerosis patients

Rebecca C. Selter, Viola Biberacher, Verena Grummel, Dorothea Buck, Christian Eienbröker, Wolfgang H. Oertel, Achim Berthele, Björn Tackenberg, Bernhard Hemmer

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

Abstract

Background: Treatment with natalizumab, a humanized monoclonal antibody against alpha4beta1 integrin, is associated with an increase in lymphoid progenitor cells and B cells in peripheral blood. Objective: The objective of this study was to examine the impact of natalizumab therapy on serum levels of total IgG, IgA and IgM in patients with multiple sclerosis (MS). Methods: In two independent cross-sectional patient cohorts, serum levels of IgG, IgA and IgM were compared between patients treated with natalizumab and those not receiving natalizumab. Further, serum levels of IgG, IgA and IgM before and during natalizumab treatment were compared in two longitudinal patient cohorts. Results: In patients treated with natalizumab, serum IgM and IgG levels were significantly lower compared with therapy nave patients (p<0.0001). IgM levels significantly decreased after initiation of natalizumab treatment in both longitudinal patient cohorts (p<0.01). Moreover, patients treated with natalizumab showed a time-dependent decrease in IgM levels during the first 2 years of treatment. Conclusion: Natalizumab treatment leads to a significant decrease in serum IgM and IgG levels in patients with MS. IgM levels decrease with treatment duration during the first 2 years of treatment. These findings might support the hypothesis that natalizumab interferes with homing of B cells, possibly leading to impaired differentiation into plasma cells and subsequently disturbed immunoglobulin synthesis.

Original languageEnglish
Pages (from-to)1454-1461
Number of pages8
JournalMultiple Sclerosis Journal
Volume19
Issue number11
DOIs
StatePublished - Oct 2013

Keywords

  • B cell homing
  • Multiple sclerosis
  • alpha4beta1 integrin
  • immunoglobulin G
  • immunoglobulin M
  • natalizumab

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