Purinergic signalling in graft-versus-host disease

IF 4 3区 医学 Q1 PHARMACOLOGY & PHARMACY Current Opinion in Pharmacology Pub Date : 2023-02-01 DOI:10.1016/j.coph.2022.102346
Ronald Sluyter , Peter Cuthbertson , Amal Elhage , Chloe Sligar , Debbie Watson
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引用次数: 2

Abstract

Allogeneic hematopoietic stem cell transplantation is used to treat blood cancers, but often results in lethal graft-versus-host disease (GVHD). GVHD is an inflammatory disorder mediated by donor leukocytes that damage host tissues. Purinergic signalling plays important roles in GVHD development in mice but studies of these pathways in human GVHD remain limited. P2X7 receptor activation by ATP on host antigen presenting cells contributes to the induction of GVHD, while activation of this receptor on regulatory T cells, myeloid-derived suppressor cells and possibly type 3 innate lymphoid cells results in their loss to promote GVHD progression. In contrast, A2A receptor activation by adenosine on donor T cells serves to restrict GVHD development. These and other purinergic signalling molecules remain potential biomarkers and therapeutic targets in GVHD.

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移植物抗宿主病中的嘌呤能信号传导
异基因造血干细胞移植用于治疗血癌,但通常会导致致命的移植物抗宿主病(GVHD)。GVHD是一种由供体白细胞介导的炎症性疾病,可损伤宿主组织。嘌呤能信号传导在小鼠移植物抗宿主病的发展中起着重要作用,但对人类移植物抗逆转录病毒途径的研究仍然有限。宿主抗原呈递细胞上ATP激活P2X7受体有助于GVHD的诱导,而调节性T细胞、髓源性抑制细胞和可能的3型先天性淋巴细胞上该受体的激活导致其丢失以促进GVHD的进展。相反,供体T细胞上腺苷激活的A2A受体可限制移植物抗宿主病的发展。这些和其他嘌呤能信号分子仍然是移植物抗宿主病的潜在生物标志物和治疗靶点。
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来源期刊
CiteScore
8.80
自引率
2.50%
发文量
131
审稿时长
4-8 weeks
期刊介绍: Current Opinion in Pharmacology (COPHAR) publishes authoritative, comprehensive, and systematic reviews. COPHAR helps specialists keep up to date with a clear and readable synthesis on current advances in pharmacology and drug discovery. Expert authors annotate the most interesting papers from the expanding volume of information published today, saving valuable time and giving the reader insight on areas of importance.
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