by Dana T. Lounder, Qiong Bin, Cristina de Min, and Michael B. Jordan

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by Dana T. Lounder, Qiong Bin, Cristina de Min, and Michael B. Jordan Treatment of refractory hemophagocytic lymphohistiocytosis with emapalumab despite severe concurrent infections by Dana T. Lounder, Qiong Bin, Cristina de Min, and Michael B. Jordan BloodAdv Volume 3(1):47-50 January 8, 2019 © 2019 by The American Society of Hematology

Dana T. Lounder et al. Blood Adv 2019;3:47-50 © 2019 by The American Society of Hematology

HLH disease features and viremias after treatment with emapalumab. HLH disease features and viremias after treatment with emapalumab. (A-B) Absolute neutrophil and platelet counts, both heavily supported by transfusion until about day 21. (C-D) Fibrinogen (supported by fresh-frozen plasma transfusion until day 21) and D-dimer levels. (E-F) Alanine aminotransferase (ALT) and direct bilirubin levels. (G-H) The inflammatory markers ferritin and soluble interleukin-2 receptor (sIL2r [sCD25]). Reported ferritin values are limited to 40 000 μg/L by the clinical laboratory. Ferritin values decreased to <500 μg/L by day 180. (I-J) Blood levels of EBV and CMV. Arrows on the x-axis of each graph indicate the start of emapalumab treatment, and initial and final values for each marker are shown. Dana T. Lounder et al. Blood Adv 2019;3:47-50 © 2019 by The American Society of Hematology

IFN-γ–associated chemokines after treatment with emapalumab. IFN-γ–associated chemokines after treatment with emapalumab. The levels of CXCL9 (A) and CXCL10 (B), 2 chemokines induced by IFN-γ, after initiation of therapy with emapalumab. Baseline and final levels for each biomarker are indicated. Dana T. Lounder et al. Blood Adv 2019;3:47-50 © 2019 by The American Society of Hematology