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近期代谢进展在预防和治疗急、慢性移植物抗宿主病中的作用

Recent Metabolic Advances for Preventing and Treating Acute and Chronic Graft Versus Host Disease.

机构信息

Department of Pediatrics, Division of Blood & Marrow Transplant & Cellular Therapy, University of Minnesota Cancer Center, Minneapolis, MN, United States.

Renal Division, Transplantation Research Center, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.

出版信息

Front Immunol. 2021 Oct 12;12:757836. doi: 10.3389/fimmu.2021.757836. eCollection 2021.

Abstract

The therapeutic efficacy of allogeneic hematopoietic stem cell transplantation (allo-HSCT) is limited by the development of graft-versus-host disease (GVHD). In GVHD, rigorous pre-conditioning regimen resets the immune landscape and inflammatory milieu causing immune dysregulation, characterized by an expansion of alloreactive cells and a reduction in immune regulatory cells. In acute GVHD (aGVHD), the release of damage- and pathogen- associated molecular patterns from damaged tissue caused by the conditioning regimen sets the stage for T cell priming, activation and expansion further exacerbating tissue injury and organ damage, particularly in the gastrointestinal tract. Studies have shown that donor T cells utilize multiple energetic and biosynthetic pathways to mediate GVHD that can be distinct from the pathways used by regulatory T cells for their suppressive function. In chronic GVHD (cGVHD), donor T cells may differentiate into IL-21 producing T follicular helper cells or tissue resident T helper cells that cooperate with germinal center B cells or memory B cells, respectively, to produce allo- and auto-reactive antibodies with subsequent tissue fibrosis. Alternatively, donor T cells can become IFN- γ/IL-17 cytokine expressing T cells that mediate sclerodermatous skin injury. Patients refractory to the first line standard regimens for GVHD treatment have a poor prognosis indicating an urgent need for new therapies to restore the balance between effector and regulatory immune cells while preserving the beneficial graft-versus-tumor effect. Emerging data points toward a role for metabolism in regulating these allo- and auto-immune responses. Here, we will discuss the preclinical and clinical data available on the distinct metabolic demands of acute and chronic GVHD and recent efforts in identifying therapeutic targets using metabolomics. Another dimension of this review will examine the changing microbiome after allo-HSCT and the role of microbial metabolites such as short chain fatty acids and long chain fatty acids on regulating immune responses. Lastly, we will examine the metabolic implications of coinhibitory pathway blockade and cellular therapies in allo-HSCT. In conclusion, greater understanding of metabolic pathways involved in immune cell dysregulation during allo-HSCT may pave the way to provide novel therapies to prevent and treat GVHD.

摘要

同种异体造血干细胞移植(allo-HSCT)的治疗效果受到移植物抗宿主病(GVHD)的限制。在 GVHD 中,严格的预处理方案重置了免疫景观和炎症环境,导致免疫失调,其特征是同种反应性细胞的扩增和免疫调节细胞的减少。在急性 GVHD(aGVHD)中,预处理方案引起的损伤组织和病原体相关分子模式的释放为 T 细胞启动、激活和扩增奠定了基础,进一步加剧了组织损伤和器官损伤,特别是在胃肠道中。研究表明,供体 T 细胞利用多种能量和生物合成途径来介导 GVHD,这些途径可能与调节性 T 细胞用于其抑制功能的途径不同。在慢性 GVHD(cGVHD)中,供体 T 细胞可能分化为产生 IL-21 的滤泡辅助 T 细胞或组织驻留辅助 T 细胞,分别与生发中心 B 细胞或记忆 B 细胞合作,产生同种和自身反应性抗体,随后发生组织纤维化。或者,供体 T 细胞可以成为 IFN-γ/IL-17 细胞因子表达 T 细胞,介导硬皮病样皮肤损伤。对 GVHD 一线标准治疗方案无反应的患者预后不良,这表明迫切需要新的治疗方法来恢复效应和调节免疫细胞之间的平衡,同时保留有益的移植物抗肿瘤效应。新出现的数据表明代谢在调节这些同种和自身免疫反应中起着作用。在这里,我们将讨论有关急性和慢性 GVHD 的不同代谢需求的临床前和临床数据,以及使用代谢组学识别治疗靶点的最新进展。本综述的另一个方面将检查 allo-HSCT 后的微生物组变化以及微生物代谢物(如短链脂肪酸和长链脂肪酸)在调节免疫反应中的作用。最后,我们将检查协同抑制途径阻断和细胞疗法在 allo-HSCT 中的代谢意义。总之,对 allo-HSCT 期间免疫细胞失调涉及的代谢途径的深入了解可能为提供预防和治疗 GVHD 的新疗法铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f6b/8546182/1b53e9798809/fimmu-12-757836-g001.jpg

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