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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.
Objective:
In relapsing-remitting MS (RRMS) patients treated with natalizumab, the low level of L-selectin-expressing CD4+ T cells has been associated with the risk of progressive multifocal leukoencephalopathy (PML). In this study, our aim was to correlate the levels of soluble L-selectin and the anti-JCV antibody index in the sera of RRMS patients treated with natalizumab.
Methods:
This study included 99 subjects, including 44 RRMS patients treated with natalizumab, 30 with interferon beta (IFN-β) and 25 healthy controls. The levels of soluble L-selectin (sL-selectin) in sera were measured by ELISA, and the anti-JC Virus (JCV) antibody index was determined by the second-generation ELISA (STRATIFY JCV™ DxSelect™) assay.
Results:
A significant correlation was found between the levels of sL-selectin and anti-JCV antibody indices in sera in the natalizumab-treated patients (r=0.402; p=0.007; n=44), but not in those treated with IFN-β. This correlation became even stronger in JCV seropositive patients treated with natalizumab for longer than 18 months (r=0.529; p=0.043; n=15).
Conclusion:
The results support the hypothesis of sL-selectin being connected to the anti-JCV antibody index values and possibly cellular L-selectin. Measurement of serum sL-selectin should be evaluated further as a potential biomarker for predicting the risk of developing PML.
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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