炎性小体:造血干细胞移植的潜在治疗靶点。

IF 8.2 2区 生物学 Q1 CELL BIOLOGY Cell Communication and Signaling Pub Date : 2024-12-18 DOI:10.1186/s12964-024-01974-3
Jieya Luo, Yunxia Zhou, Mingyang Wang, Junan Zhang, Erlie Jiang
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引用次数: 0

摘要

造血干细胞移植(HSCT)在提高恶性和非恶性血液病患者的治愈率和生存率方面取得了显著进展。然而,相当数量的患者继续面临挑战,包括移植相关并发症、感染、移植失败和死亡。炎性小体是先天免疫系统的多蛋白复合物,通过释放炎症细胞因子甚至介导细胞死亡来响应各种危险信号。适度激活炎性小体对免疫防御和维持体内平衡至关重要,但过度激活会导致炎症损伤。造血干细胞移植和炎性小体之间复杂的相互作用源于它们在免疫反应和炎症中的关键作用。本文综述了各种类型炎性小体的分子结构和组成,重点介绍了它们在造血干细胞移植过程及其相关并发症中的激活和效应机制。此外,我们总结了靶向炎性小体和相关因子在造血干细胞移植中的治疗意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Inflammasomes: potential therapeutic targets in hematopoietic stem cell transplantation.

The realm of hematopoietic stem cell transplantation (HSCT) has witnessed remarkable advancements in elevating the cure and survival rates for patients with both malignant and non-malignant hematologic diseases. Nevertheless, a considerable number of patients continue to face challenges, including transplant-related complications, infection, graft failure, and mortality. Inflammasomes, the multi-protein complexes of the innate immune system, respond to various danger signals by releasing inflammatory cytokines and even mediating cell death. While moderate activation of inflammasomes is essential for immune defense and homeostasis maintenance, excessive activation precipitates inflammatory damage. The intricate interplay between HSCT and inflammasomes arises from their pivotal roles in immune responses and inflammation. This review examines the molecular architecture and composition of various types of inflammasomes, highlighting their activation and effector mechanisms within the context of the HSCT process and its associated complications. Additionally, we summarize the therapeutic implications of targeting inflammasomes and related factors in HSCT.

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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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