Publication | Open Access
Successful treatment of secondary macrophage activation syndrome with emapalumab in a patient with newly diagnosed adult-onset Still’s disease: case report and review of the literature
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Citations
16
References
2020
Year
ImmunohematologySuccessful TreatmentImmunodeficienciesImmunologyImmune RegulationPathologyImmunotherapyImmune SystemImmune DysregulationInflammationTranslational MedicineHematologyInflammatory Marker’ S DiseaseAutoimmune DiseaseSerum Interferon GammaImmune SurveillanceAutoimmunityHumoral ImmunityImmunologic DiseaseImmune FunctionImmune-mediated Inflammatory DiseasesSecondary MasSclerodermaInborn Error Of ImmunityCase ReportImmunosuppression22-Year-old Female PatientMedicineSystemic Juvenile Idiopathic Arthritis
Here, we present a 22-year-old female patient with adult-onset Still's disease (AOSD) who was newly diagnosed in the setting of secondary macrophage activation syndrome (MAS), a rare, life-threatening inflammatory disease with 50% mortality due to multi-organ failure. She met the diagnostic criteria of AOSD and MAS, while genetic testing excluded primary causes of MAS. She had high fevers, anemia, thrombocytopenia, splenomegaly, hematophagocytosis, and elevated serum ferritin (37,950 ng/mL) and CD25 levels (11,870 pg/mL), which remained unresponsive to corticosteroids and anakinra. Her serum interferon gamma (IFN-γ) levels were elevated (7 pg/mL). She was markedly responsive to IFN-γ blockade with emapalumab that eliminated her fevers and all MAS-associated laboratory abnormalities. This report provides initial evidence for therapeutic efficacy for IFN-γ blockade in AOSD and secondary MAS.
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