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Updated: May 7, 2026

The bm12 Inducible Model of Systemic Lupus Erythematosus SLE in C57BL/6 Mice
Published on: November 1, 2015
[Rituximab in pediatric patients with systemic lupus erythematosus]
José Manuel Pavón-Sánchez1, Luz María Sánchez-Sánchez
1Servicio de Pediatría de la Unidad Médica de Alta Especialidad (UMAE) N.o 25, Centro Médico Nacional del Noreste, Monterrey, N.L. luzsanchez68@hotmail.com.
Insights
Rituximab treatment in pediatric patients with systemic lupus erythematosus (SLE) showed reduced disease activity and improved complement levels. However, outcomes varied, with a 50% mortality rate observed in this small cohort.
Area of Science:
- Pediatric Rheumatology
- Autoimmune Diseases
- Immunotherapy
Context:
- Systemic lupus erythematosus (SLE) presents more severely in children than adults.
- Conventional therapies are often insufficient for pediatric SLE.
- Biological therapy, specifically anti-CD20 (rituximab), is a newer option for refractory pediatric SLE.
Purpose:
- To evaluate the clinical response of pediatric patients with SLE treated with rituximab.
- To assess the efficacy of rituximab in a cohort of children with severe SLE unresponsive to standard treatments.
Summary:
- Eight pediatric patients with SLE received rituximab treatment.
- Significant reductions in the MEX-SLEDAI activity index were observed post-treatment (p=0.038).
- Complement levels (C3 and C4) showed significant increases after rituximab therapy (p=0.048 and p=0.032).
Impact:
- Rituximab demonstrates potential in reducing disease activity and improving immunological markers in pediatric SLE.
- The study highlights a significant difference in pre-treatment disease activity between patients who survived and those who did not (p=0.002).
- Further research is warranted to optimize rituximab use and improve outcomes in this vulnerable population.
Unlabelled:
Systemic lupus erythematosus (SLE) is an autoimmune disease that is more severe in pediatric population than in adults. Biological therapy with anti-CD20 (rituximab) in children with SLE was begun to use only a few years ago, in patients that do not respond to conventional therapy. The aim of this study is to determine the clinical response in pediatric patients with SLE that received treatment with rituximab in a third level hospital.
Results:
Eight pediatric patients with SLE treated with rituximab were included. Female gender predominated with six (75%). The age at diagnosis of SLE was a mean of 11.3 ± 1.03 years. The mean time between the onset of symptoms and diagnosis was 4.12 ± 1.01 months, and the application of rituximab was 20.7 ± 6.2 months after diagnosis. The most common diagnostic criteria were: malar erythema, hematologic disease, arthritis and kidney disease. Positive ANA title was found in 62.5% of the patients. The clinical activity index MEX-SLEDAI before rituximab was 11.63 ± 6.8 points. Four patients (50%) died, they had activity index before rituximab of 23 ± 1.7 and the survivors of 12.2 ± 3.2 (p = 0.002). After treatment with rituximab the patients that died had 17.6 ± 8.5 points and the survivors 8 ± 2.1 (p = 0.038). In laboratory findings, only C3 and C4 had a significant change after treatment (p = 0.048 and 0.032).
Conclusions:
Rituximab reduces lupus activity index and increases complement levels in children with LES that don't respond to conventional therapy.
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