Association between soluble L-selectin and anti-JCV antibodies in natalizumab-treated relapsing-remitting MS patients

Pabitra Basnyat1, Sanna Hagman1, Marcin Kolasa1

  • 1Neuroimmunology Unit, Medical School, University of Tampere, Tampere, Finland.

Abstract

Insights

Soluble L-selectin (sL-selectin) levels correlate with the anti-JC Virus (JCV) antibody index in relapsing-remitting MS patients treated with natalizumab. This finding suggests sL-selectin may serve as a biomarker for predicting progressive multifocal leukoencephalopathy (PML) risk.

Area of Science:

  • Neuroimmunology
  • Virology
  • Biomarker Discovery

Background:

  • Progressive multifocal leukoencephalopathy (PML) is a risk in relapsing-remitting MS (RRMS) patients on natalizumab.
  • Low levels of L-selectin-expressing CD4+ T cells are associated with PML risk.

Purpose of the Study:

  • To investigate the correlation between serum soluble L-selectin (sL-selectin) levels and the anti-JC Virus (JCV) antibody index in RRMS patients undergoing natalizumab treatment.

Main Methods:

  • Serum sL-selectin levels were measured using ELISA.
  • The anti-JCV antibody index was determined via a second-generation ELISA assay.
  • Study included 44 RRMS patients on natalizumab, 30 on interferon beta, and 25 healthy controls.

Main Results:

  • A significant positive correlation (r=0.402, p=0.007) was observed between sL-selectin levels and anti-JCV antibody indices in natalizumab-treated RRMS patients.
  • No significant correlation was found in patients treated with interferon beta.
  • The correlation strengthened in JCV seropositive patients on natalizumab for over 18 months (r=0.529, p=0.043).

Conclusions:

  • Serum sL-selectin levels are linked to anti-JCV antibody index values in natalizumab-treated RRMS patients.
  • sL-selectin may be associated with cellular L-selectin expression.
  • Further research is warranted to evaluate serum sL-selectin as a potential biomarker for predicting PML risk.

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