Enforced gut homing of murine regulatory T cells reduces early graft-versus-host disease severity

强制小鼠调节性T细胞归巢至肠道可降低早期移植物抗宿主病的严重程度

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作者:Jemma H Larson,Sujeong Jin,Michael Loschi,Sara Bolivar Wagers,Govindarajan Thangavelu,Michael C Zaiken,Cameron McDonald-Hyman,Asim Saha,Ethan G Aguilar,Brent Koehn,Mark J Osborn,Angela Panoskaltsis-Mortari,Kelli P A Macdonald,Geoffrey R Hill,William J Murphy,Jonathan S Serody,Ivan Maillard,Leslie S Kean,Sangwon V Kim,Dan R Littman,Bruce R Blazar

Abstract

Damage to the gastrointestinal tract following allogeneic hematopoietic stem cell transplantation is a significant contributor to the severity and perpetuation of graft-versus-host disease. In preclinical models and clinical trials, we showed that infusing high numbers of regulatory T cells reduces graft-versus-host disease incidence. Despite no change in in vitro suppressive function, transfer of ex vivo expanded regulatory T cells transduced to overexpress G protein-coupled receptor 15 or C-C motif chemokine receptor 9, specific homing receptors for colon or small intestine, respectively, lessened graft-versus-host disease severity in mice. Increased regulatory T cell frequency and retention within the gastrointestinal tissues of mice that received gut homing T cells correlated with lower inflammation and gut damage early post-transplant, decreased graft-versus-host disease severity, and prolonged survival compared with those receiving control transduced regulatory T cells. These data provide evidence that enforced targeting of ex vivo expanded regulatory T cells to the gastrointestinal tract diminishes gut injury and is associated with decreased graft-versus-host disease severity.

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