The Absence of IL-12Rβ2 Expression on Recipient Nonhematopoietic Cells Diminishes Acute Graft-versus-Host Disease in the Gastrointestinal Tract.
David BastianXiaohui SuiHee-Jin ChoiYongxia WuLinlu TianKaipo YangChen LiuYuejun LiuXue-Zhong YuPublished in: Journal of immunology (Baltimore, Md. : 1950) (2023)
The gastrointestinal (GI) tract is a frequent target organ in acute graft-versus-host disease (aGVHD), which can determine the morbidity and nonrelapse mortality after allogeneic hematopoietic cell transplantation (allo-HCT). Donor T cells recognize allogeneic Ags presented by host APCs, proliferate, and differentiate into Th1 and Th17 cells that drive GVHD pathogenesis. IL-12 has been shown to play an important role in amplifying the allogeneic response in preclinical and clinical studies. This study demonstrates that IL-12Rβ2 expression on recipient nonhematopoietic cells is required for optimal development of aGVHD in murine models of allo-HCT. aGVHD attenuation by genetic depletion of IL-12R signaling is associated with reduced MHC class II expression by intestinal epithelial cells and maintenance of intestinal integrity. We verified IL-12Rβ2 expression on activated T cells and in the GI tract. This study, to our knowledge, reveals a novel function of IL-12Rβ2 in GVHD pathogenesis and suggests that selectively targeting IL-12Rβ2 on host nonhematopoietic cells may preserve the GI tract after allo-HCT.
Keyphrases
- cell cycle arrest
- induced apoptosis
- poor prognosis
- stem cell transplantation
- bone marrow
- healthcare
- liver failure
- endoplasmic reticulum stress
- oxidative stress
- binding protein
- signaling pathway
- drug delivery
- acute lymphoblastic leukemia
- mesenchymal stem cells
- allogeneic hematopoietic stem cell transplantation
- high dose
- cancer therapy
- copy number
- aortic dissection