免疫微环境对绝经后骨质疏松症的影响
姚琼璐1 杨雨清1 徐涛涛2*
  
DOI:10.3969/j.issn.1006-7108.2023.06.022
中文关键词:  绝经后骨质疏松症  免疫微环境  骨免疫学
英文关键词:postmenopausal osteoporosis  immune microenvironment  osteoimmunology
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作者单位
姚琼璐1 杨雨清1 徐涛涛2* 1.浙江中医药大学第一临床医学院浙江 杭州 310053 2.浙江中医药大学附属第一医院浙江 杭州 310006 
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中文摘要:
      绝经后骨质疏松症(postmenopausal osteoporosis,PMOP)是由于雌激素缺乏导致的、以骨量减少和骨组织微结构破坏为特征的的疾病。近年来,越来越多的观点认为免疫微环境与该病的发生发展密切相关,多种免疫细胞及其分泌的细胞因子通过RANK/RANKL/OPG等信号途径调控成骨细胞和破骨细胞的生物学功能,从而影响骨稳态失衡。因此,基于骨免疫学的免疫微环境逐渐成为PMOP防治研究的主要靶标之一。笔者综述了骨代谢相关的免疫细胞如T细胞、B细胞、巨噬细胞、肥大细胞和单核细胞对PMOP的发生发展以及对骨折愈合的影响,并总结基于骨免疫学的PMOP治疗靶点,以期为未来PMOP的药物开发及临床应用提供新的思路。
英文摘要:
      Postmenopausal osteoporosis (PMOP) is a disease characterized by bone mass reduction and the destruction of bone microstructure, which is caused by the lack of estrogen. In recent years, more and more people believe that the immune microenvironment is closely related to the occurrence and development of this disease. A variety of immune cells and their secreted cytokines regulate the biological functions of osteoblasts and osteoclasts through RANK/RANKL/OPG signaling pathways, thereby affecting the imbalance of bone homeostasis. Therefore, immune microenvironment based on bone immunology have gradually become one of the main targets in the prevention and treatment of PMOP. This article reviews the effects of immune cells related to bone metabolism such as T cells, B cells, macrophages, mast cells and monocytes on the occurrence and development of PMOP and fracture healing, and summarizes the therapeutic targets of PMOP based on bone immunology, in order to provide new ideas for the drug development and clinical application of PMOP in the future.
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