Modulating endothelial cells with EGFL7 to diminish aGVHD after allogeneic bone marrow transplantation in mice

Author:

Dorrance Adrienne1,Moutuou Moutuaata2,Goda Chinmayee1ORCID,Sell Natalie E1,Kalyan Sonu1,Karunasiri Malith3,Kulkarni Rohan1ORCID,Goulard Marie1,Kolovich Sofia4,Rudich Alex1,Naumann Eric1,Ackaoui Antoine5,Bigras Charles-Etienne6,Daudelin Francis6,Garzon Ramiro1,Ranganathan Parvathi1,Guimond Martin7

Affiliation:

1. Ohio State University, Columbus, Ohio, United States

2. University of Montreal

3. The Ohio State University Comprehensive Cancer Center, United States

4. Ohio State University, Bryan, Ohio, United States

5. University of Montreal, Saint-Lazare, Canada

6. Division d'Hématologie-Oncologie, Centre de Recherche de l'Hôpital Maisonneuve-Rosemont, Canada

7. Hopital Maisonneuve-Rosemont, Canada

Abstract

Acute graft versus host (aGVHD) is the second cause of death after allogeneic-hematopoietic stem cell transplant (allo-HSCT) underscoring the need for novel therapies. Based on previous work that endothelial cell dysfunction is present in aGVHD and that epidermal growth factor-like domain 7 (EGFL7) plays a significant role in decreasing inflammation by repressing endothelial cell activation and T cell migration, we hypothesized that increasing EGFL7 levels after allo-HSCT will diminish the severity of aGVHD. Here, we show that treatment with recombinant EGFL7 (rEGFL7) in two different murine models of aGVHD decreases aGVHD severity and improves survival in recipient mice after allogeneic transplantation with respect to controls without affecting graft versus leukemia effect. Furthermore, we showed that rEGFL7 treatment results in higher thymocytes, T, B and dendritic cells in recipient mice after allo-HSCT. This study constitutes a proof of concept of the ability of rEGFL7 therapy to reduce GHVD severity and mortality after allo-HSCT.

Publisher

American Society of Hematology

Subject

Hematology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Role of endothelial cells in graft-versus-host disease;Frontiers in Immunology;2022-11-23

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