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SYK inhibitor entospletinib prevents ocular and skin GVHD in mice
Jonathan C. Poe, … , Daniel R. Saban, Stefanie Sarantopoulos
Jonathan C. Poe, … , Daniel R. Saban, Stefanie Sarantopoulos
Published October 4, 2018
Citation Information: JCI Insight. 2018;3(19):e122430. https://doi.org/10.1172/jci.insight.122430.
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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 7

ENTO prolongs the survival of +Spl mice.

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ENTO prolongs the survival of +Spl mice.
(A) Data represent Kaplan-Meier...
(A) Data represent Kaplan-Meier plots comparing the survival of mice in all HCT groups (n = 9–10/group) through day +120. Statistical analysis was performed between the groups shown using the log-rank test (GraphPad Prism). P values reaching statistical significance are as indicated. (B) Top: Day +120 images of the single surviving +Spl/placebo group mouse, along with images of representative mice from all other groups. Bottom: Masson’s trichrome staining of eyelid tissue, showing marked hyperplasia in the surviving +Spl/placebo mouse compared with representative mice from all other groups. Scale bar: 115 μm.

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