Inhibiting retinoic acid signaling ameliorates graft-versus-host disease by modifying T-cell differentiation and intestinal migration

K Aoyama, A Saha, J Tolar, MJ Riddle… - Blood, The Journal …, 2013 - ashpublications.org
K Aoyama, A Saha, J Tolar, MJ Riddle, RG Veenstra, PA Taylor, R Blomhoff…
Blood, The Journal of the American Society of Hematology, 2013ashpublications.org
Graft-versus-host disease (GVHD) is a critical complication after allogeneic bone marrow
transplantation. During GVHD, donor T cells are activated by host antigen-presenting cells
and differentiate into T-effector cells (Teffs) that migrate to GVHD target organs. However,
local environmental factors influencing Teff differentiation and migration are largely
unknown. Vitamin A metabolism within the intestine produces retinoic acid, which
contributes to intestinal homeostasis and tolerance induction. Here, we show that the …
Abstract
Graft-versus-host disease (GVHD) is a critical complication after allogeneic bone marrow transplantation. During GVHD, donor T cells are activated by host antigen-presenting cells and differentiate into T-effector cells (Teffs) that migrate to GVHD target organs. However, local environmental factors influencing Teff differentiation and migration are largely unknown. Vitamin A metabolism within the intestine produces retinoic acid, which contributes to intestinal homeostasis and tolerance induction. Here, we show that the expression and function of vitamin A–metabolizing enzymes were increased in the intestine and mesenteric lymph nodes in mice with active GVHD. Moreover, transgenic donor T cells expressing a retinoic acid receptor (RAR) response element luciferase reporter responded to increased vitamin A metabolites in GVHD-affected organs. Increasing RAR signaling accelerated GVHD lethality, whereas donor T cells expressing a dominant-negative RARα (dnRARα) showed markedly diminished lethality. The dnRARα transgenic T cells showed reduced Th1 differentiation and α4β7 and CCR9 expression associated with poor intestinal migration, low GVHD pathology, and reduced intestinal permeability, primarily via CD4+ T cells. The inhibition of RAR signaling augmented donor-induced Treg generation and expansion in vivo, while preserving graft-versus-leukemia effects. Together, these results suggested that reagents blunting donor T-cell RAR signaling may possess therapeutic anti-GVHD properties.
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