Volume 156, Issue 4, Pages e1 (March 2019)

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Volume 156, Issue 4, Pages 1206-1210.e1 (March 2019) Efficacy of Ruxolitinib Therapy in a Patient With Severe Enterocolitis Associated With a STAT3 Gain-of-Function Mutation  Marianna Parlato, Fabienne Charbit-Henrion, Abi Nader Elie, Bernadette Begue, Nicolas Guegan, Julie Bruneau, Shérine Khater, Elizabeth Macintyre, Capucine Picard, Rieux-Laucat Frédéric, Lionel Le Bourhis, Matthieu Allez, Olivier Goulet, Christophe Cellier, Olivier Hermine, Nadine Cerf-Bensussan, Georgia Malamut  Gastroenterology  Volume 156, Issue 4, Pages 1206-1210.e1 (March 2019) DOI: 10.1053/j.gastro.2018.11.065 Copyright © 2019 AGA Institute Terms and Conditions

Figure 1 Novel STAT3 GoF mutation. (A) WES analysis. (B, C) Sanger sequencing confirming de novo mutation. (D) Schematic representation of STAT3 domains. (E) Conservation of N401 among orthologs. (F) STAT3 transcriptional activity following 48-hour activation with IL6 (10 ng/mL) of HEK293T cells containing STAT3-responsive luciferase and stably transduced with empty vector (EV), wild-type (WT), and mutant STAT3. Results represent the mean of 5 independent experiments (**P < .01, ***P < .001, 1-way analysis of variance). (G) Reverse transcriptase PCR of STAT3-target SOCS3 in IL21 or IL6 activated EBV cell lines treated or not with ruxolitinib (RX). Results are shown as relative expression normalized to RPLPO housekeeping gene and represent the mean of 4 independent experiments. IL6 vs IL6 + RX (*P < .01, Mann-Whitney), control vs STAT3 mutants (**P < .01, ****P < .0001, 1-way analysis of variance). Gastroenterology 2019 156, 1206-1210.e1DOI: (10.1053/j.gastro.2018.11.065) Copyright © 2019 AGA Institute Terms and Conditions

Figure 2 Induction of mucosal healing by ruxolitinib. (A, B) HES staining (×100) and immunohistochemistry staining (×200) of CD3+, CD8+, GzmB+ lymphocytes before and after 6 months of ruxolitinib (RX). (C and D) Reverse transcriptase PCR quantification of indicated cytokines in patient’s duodenum (C) and colon (D) before (BRu) and after ruxolitinib (ARu). Results are compared with histologically normal duodenal (n = 4) or colonic biopsies (n = 4) (CT), and with duodenal biopsies from 5 active celiac disease (ACeD) (C) and colonic biopsies from 5 active Crohn disease (CrD) (D). Gastroenterology 2019 156, 1206-1210.e1DOI: (10.1053/j.gastro.2018.11.065) Copyright © 2019 AGA Institute Terms and Conditions