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SYK inhibitor entospletinib prevents ocular and skin GVHD in mice
Jonathan C. Poe, Wei Jia, Julie A. Di Paolo, Nancy J. Reyes, Ji Yun Kim, Hsuan Su, John S. Sundy, Adela R. Cardones, Victor L. Perez, Benny J. Chen, Nelson J. Chao, Diana M. Cardona, Daniel R. Saban, Stefanie Sarantopoulos
Jonathan C. Poe, Wei Jia, Julie A. Di Paolo, Nancy J. Reyes, Ji Yun Kim, Hsuan Su, John S. Sundy, Adela R. Cardones, Victor L. Perez, Benny J. Chen, Nelson J. Chao, Diana M. Cardona, Daniel R. Saban, Stefanie Sarantopoulos
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Research Article Immunology Transplantation

SYK inhibitor entospletinib prevents ocular and skin GVHD in mice

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Abstract

Graft-versus-host disease (GVHD) is a major complication of hematopoietic stem cell transplantation (HCT). The tyrosine kinase SYK contributes to both acute and chronic GVHD development, making it an attractive target for GVHD prevention. Entospletinib (ENTO) is a second-generation highly selective SYK inhibitor with a high safety profile. Potential utility of ENTO as GVHD prophylaxis in patients was examined using a preclinical mouse model of eye and skin GVHD and ENTO-compounded chow. We found that early SYK inhibition improved blood immune cell reconstitution in GVHD mice and prolonged survival, with 60% of mice surviving to day +120 compared with 10% of mice treated with placebo. Compared with mice receiving placebo, mice receiving ENTO had dramatic improvements in clinical eye scores, alopecia scores, and skin scores. Infiltrating SYK+ cells expressing B220 or F4/80, resembling SYK+ cells found in lichenoid skin lesions of chronic GVHD patients, were abundant in the skin of placebo mice but were rare in ENTO-treated mice. Thus, ENTO given early after HCT safely prevented GVHD.

Authors

Jonathan C. Poe, Wei Jia, Julie A. Di Paolo, Nancy J. Reyes, Ji Yun Kim, Hsuan Su, John S. Sundy, Adela R. Cardones, Victor L. Perez, Benny J. Chen, Nelson J. Chao, Diana M. Cardona, Daniel R. Saban, Stefanie Sarantopoulos

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Figure 6

ENTO enhanced Tregs in +Spl GVHD mice.

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ENTO enhanced Tregs in +Spl GVHD mice.
(A) Representative flow cytometry...
(A) Representative flow cytometry plots showing gating strategies for Foxp3 expression, cytokine production, and CXCR5 expression for the Treg, Th1, Th17, and Tfh subsets. To detect Tregs, splenocytes were surface stained for CD4, followed by intracellular staining for Foxp3. To detect Th1 and Th17 cells, splenocytes were cultured in the presence of PMA and ionomycin for 5 hours and then stained for surface CD4 and stained intracellularly for IFN-γ or IL-17 (utilizing a Mouse BD Biosciences Th1/Th2/Th17 Phenotyping Kit). To detect Tfh cells, splenocytes were surface stained for CD4 and CXCR5. (B) Splenocytes from mice in all treatment groups (n = 5 each) analyzed for the subsets described in A. Bars indicate the median ± range. Statistical analysis was performed by 1-way ANOVA with Tukey’s multiple comparisons test (GraphPad Prism). *P < 0.05; **P < 0.01; ***P < 0.001.

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