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Updated: May 24, 2026

A Murine Ommaya Xenograft Model to Study Direct-Targeted Therapy of Leptomeningeal Disease
Published on: January 29, 2021
Ofatumumab therapy modulates the meningeal lymphatic draining function in patients with multiple sclerosis: a pilot
Shu Yang1, Xiu-Wei Fu2, Zhi-Xuan Liu2
1Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Tianjin, China.
Background And Objectives:
Meningeal lymphatic vessels (mLVs) are critical for central nervous system waste clearance and immunomodulation, implicated in multiple sclerosis pathogenesis. Although ofatumumab is effective in treating relapsing-remitting MS (RRMS), its effects on mLVs function remain unclear. This study aimed to investigate its impact on mLVs drainage in RRMS patients.
Methods:
Fifteen RRMS patients were enrolled in this prospective cohort study with ofatumumab, and nine healthy controls were recruited. Drainage function of mLVs was quantified via dynamic contrast-enhanced magnetic resonance imaging at baseline, month 6 and month 12. Correlations between changes in drainage function and immune cell subsets were analyzed.
Results:
Following ofatumumab treatment, significant reductions were observed in mean time-to-peak (0.75 to 0.52, p = 0.007) and area under the curve (AUC, 30.70 to 12.67, p = 0.001) within mLVs. Baseline mLVs parameters did not differ between RRMS patients and healthy controls. Change of AUC (ΔAUC) was positively associated with regulatory T cell frequency (ΔTreg, r = 0.539, p = 0.038) and negatively associated with central memory CD4+ T cells (ΔTCM, r = -0.535, p = 0.040). Symbol Digit Modalities Test scores were negatively associated with TTP at baseline (r = -0.535, p = 0.040), whereas no correlations were observed between changes in mLVs parameters and clinical outcomes (all p > 0.05).
Conclusion:
Ofatumumab improved mLVs drainage in RRMS and was associated with a shift toward regulatory T cell phenotype. These findings suggest that modulation of meningeal lymphatics may contribute to the immunomodulatory effects of anti-CD20 therapy.
