Rauner Martina, Sipos Wolfgang, Pietschmann Peter
Ludwig Boltzmann Institute of Aging Research, Vienna, Austria.
Int Arch Allergy Immunol. 2007;143(1):31-48. doi: 10.1159/000098223. Epub 2006 Dec 22.
Osteoimmunology is an interdisciplinary research field combining the exciting fields of osteology and immunology. An observation that contributed enormously to the emergence of osteoimmunology was the accelerated bone loss caused by inflammatory diseases such as rheumatoid arthritis. Receptor activator of nuclear factor kappaB ligand (RANKL), which is the main regulator of osteoclastogenesis, was found to be the primary culprit responsible for the enhanced activation of osteoclasts: activated T cells directly and indirectly increased the expression of RANKL, and thereby promoted osteoclastic activity. Excessive bone loss is not only present in inflammatory diseases but also in autoimmune diseases and cancer. Furthermore, there is accumulating evidence that the very prevalent skeletal disorder osteoporosis is associated with alterations in the immune system. Meanwhile, numerous connections have been discovered in osteoimmunology beyond merely the actions of RANKL. These include the importance of osteoblasts in the maintenance of the hematopoietic stem cell niche and in lymphocyte development as well as the functions of immune cells participating in osteoblast and osteoclast development. Furthermore, research is being done investigating cytokines, chemokines, transcription factors and co-stimulatory molecules which are shared by both systems. Research in osteoimmunology promises the discovery of new strategies and the development of innovative therapeutics to cure or alleviate bone loss in inflammatory and autoimmune diseases as well as in osteoporosis. This review gives an introduction to bone remodeling and the cells governing that process and summarizes the most recent discoveries in the interdisciplinary field of osteoimmunology. Furthermore, an alternative large animal model will be discussed and the pathophysiological alterations of the immune system in osteoporosis will be highlighted.
骨免疫学是一个跨学科研究领域,它融合了骨学和免疫学这两个令人兴奋的领域。类风湿关节炎等炎症性疾病导致的骨质流失加速,这一观察结果对骨免疫学的出现起到了巨大的推动作用。核因子κB受体活化因子配体(RANKL)是破骨细胞生成的主要调节因子,被发现是破骨细胞活化增强的主要元凶:活化的T细胞直接或间接增加RANKL的表达,从而促进破骨细胞活性。骨质过度流失不仅存在于炎症性疾病中,也存在于自身免疫性疾病和癌症中。此外,越来越多的证据表明,非常普遍的骨骼疾病骨质疏松症与免疫系统的改变有关。与此同时,在骨免疫学中发现了许多联系,不仅仅局限于RANKL的作用。这些联系包括成骨细胞在维持造血干细胞微环境和淋巴细胞发育中的重要性,以及免疫细胞在成骨细胞和破骨细胞发育中的功能。此外,正在对两个系统共有的细胞因子、趋化因子、转录因子和共刺激分子进行研究。骨免疫学的研究有望发现新的策略并开发创新疗法,以治愈或减轻炎症性疾病、自身免疫性疾病以及骨质疏松症中的骨质流失。本综述介绍了骨重塑以及控制该过程的细胞,并总结了骨免疫学这一跨学科领域的最新发现。此外,还将讨论一种替代的大型动物模型,并强调骨质疏松症中免疫系统的病理生理改变。