TY - JOUR
T1 - Quantifying the Impact of Ocrelizumab on Paramagnetic Rim Lesions in Multiple Sclerosis
AU - Markowitz, Kimberly H.
AU - Safi, Neha V.
AU - Pliska-Bloch, Iliana
AU - Kaunzner, Ulrike W.
AU - Luu, Ha
AU - Wang, Yi
AU - Nguyen, Thanh D.
AU - Hurtado Rua, Sandra M.
AU - Gauthier, Susan A.
PY - 2026/1/1
Y1 - 2026/1/1
N2 - Paramagnetic rim lesions (PRLs) are a subset of chronic active multiple sclerosis (MS) lesions marked by iron-laden microglia and macrophages. Ocrelizumab, a monoclonal antibody targeting CD20+ B cells, suppresses acute MS activity, but its effect on PRLs remains unclear. In a longitudinal study of 29 ocrelizumab-treated patients with at least one PRL on quantitative susceptibility mapping (QSM), 97 PRLs were identified. Before treatment, PRLs showed higher QSM values than non-PRLs (p = 0.001), indicating iron enrichment. After treatment, PRLs demonstrated a greater QSM reduction (p < 0.001), with an accelerated decline in susceptibility. These findings suggest ocrelizumab may attenuate iron-related inflammation in PRLs.
AB - Paramagnetic rim lesions (PRLs) are a subset of chronic active multiple sclerosis (MS) lesions marked by iron-laden microglia and macrophages. Ocrelizumab, a monoclonal antibody targeting CD20+ B cells, suppresses acute MS activity, but its effect on PRLs remains unclear. In a longitudinal study of 29 ocrelizumab-treated patients with at least one PRL on quantitative susceptibility mapping (QSM), 97 PRLs were identified. Before treatment, PRLs showed higher QSM values than non-PRLs (p = 0.001), indicating iron enrichment. After treatment, PRLs demonstrated a greater QSM reduction (p < 0.001), with an accelerated decline in susceptibility. These findings suggest ocrelizumab may attenuate iron-related inflammation in PRLs.
KW - multiple sclerosis
KW - ocrelizumab
KW - quantitative susceptibility mapping
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U2 - 10.1002/acn3.70357
DO - 10.1002/acn3.70357
M3 - Article
SN - 2328-9503
VL - n/a
JO - Annals of Clinical and Translational Neurology
JF - Annals of Clinical and Translational Neurology
IS - n/a
ER -