Translational Clinical Strategies for the Prevention of Gastrointestinal Tract Graft Versus Host Disease

被引:3
|
作者
Rayasam, Aditya [1 ]
Drobyski, William R. [1 ,2 ]
机构
[1] Med Coll Wisconsin, Dept Med, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Bone Marrow Transplant Program, Milwaukee, WI 53226 USA
来源
FRONTIERS IN IMMUNOLOGY | 2021年 / 12卷
基金
美国国家卫生研究院;
关键词
graft versus host disease; inflammatory cytokines; gastrointestinal tract; translational clinical trials; allogeneic hematopoietic stem cell transplantation; mouse models; REGULATORY T-CELLS; INTERLEUKIN-1 RECEPTOR ANTAGONIST; HISTONE-DEACETYLASE INHIBITORS; BONE-MARROW-TRANSPLANTATION; NF-KAPPA-B; MURINE ACUTE; ACUTE GVHD; PROTEASOME INHIBITION; RADIATION PROTOCOLS; AUTOIMMUNE-DISEASES;
D O I
10.3389/fimmu.2021.779076
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Graft versus host disease (GVHD) is the major non-relapse complication associated with allogeneic hematopoietic stem cell transplantation (HSCT). Unfortunately, GVHD occurs in roughly half of patients following this therapy and can induce severe life-threatening side effects and premature mortality. The pathophysiology of GVHD is driven by alloreactive donor T cells that induce a proinflammatory environment to cause pathological damage in the skin, gastrointestinal (GI) tract, lung, and liver during the acute phase of this disease. Recent work has demonstrated that the GI tract is a pivotal target organ and a primary driver of morbidity and mortality in patients. Prevention of this complication has therefore emerged as an important goal of prophylaxis strategies given the primacy of this tissue site in GVHD pathophysiology. In this review, we summarize foundational pre-clinical studies that have been conducted in animal models to prevent GI tract GVHD and examine the efficacy of these approaches upon subsequent translation into the clinic. Specifically, we focus on therapies designed to block inflammatory cytokine pathways, inhibit cellular trafficking of alloreactive donor T cells to the GI tract, and reconstitute impaired regulatory networks for the prevention of GVHD in the GI tract.
引用
收藏
页数:14
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