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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 5

ENTO reduces activated B cells and Th2 cells in +Spl GVHD mice.

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ENTO reduces activated B cells and Th2 cells in +Spl GVHD mice.
(A) Repr...
(A) Representative flow cytometry plots showing gating strategies for GL7 expression by activated B cells and IL-4 expression by Th2 cells in splenocytes harvested from experimental mice and kept viably frozen until the time of analysis. To identify activated B cells, freshly thawed splenocytes were stained with B220 and GL7. To identify Th2 cells, splenocytes were cultured for 5 hours in medium in the presence of PMA and ionomycin and then surface stained for CD4, followed by intracellular staining for IL-4 (utilizing a Mouse BD Biosciences Th1/Th2/Th17 Phenotyping Kit). (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.

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