Purpose: To assess the efficacy and safety of
rituximab treatment as second-line
immunotherapy in pediatric cases of anti-
NMDA receptor (NMDAR)
encephalitis. Methods: We retrospectively recruited 8 patients with
anti-NMDAR encephalitis who were treated with
rituximab as second-line
immunotherapy. We evaluated the clinical features, laboratory examination results and treatment protocols of the Chinese children and defined good outcomes based on the modified Rankin scale (mRS) score (0-2) at the last follow-up. Results: A total of eight pediatric patients (median age 6.7 years; four female) with refractory
anti-NMDAR encephalitis were recruited to the study.
Rituximab was given after a median duration of disease of 57 days (range 50.5-113.75 days). The use of
rituximab led to a significant reduction in the mRS and CD19+ B-cells compared to before
rituximab infusion (P < 0.05). Five patients (62.5%) had a good outcome (mRS ≤ 2) including four patients (50%) who showed complete recovery (mRS = 0) at the last follow-up. Transient infusion adverse events were recorded in 2 patients (25%). Two patients (25%) had severe infectious adverse events (AEs) and two patients with grade 5 (death). None of the patients developed
progressive multifocal leukoencephalopathy (PML). Conclusion: Our study provides evidence that
rituximab can efficiently improve the clinical symptoms of
anti-NMDAR encephalitis in children. However, due to the risk of adverse
infections,
rituximab should be restricted in pediatric patients with high rates of mortality and disability.