Institute of Musculoskeletal Sciences, University of Oxford, The Botnar Research Centre, Nuffield Orthopaedic Centre, Headington, Oxford, UK.
J Natl Cancer Inst. 2011 Feb 2;103(3):232-40. doi: 10.1093/jnci/djq516. Epub 2010 Dec 28.
Nitrogen-containing bisphosphonates have been associated with the development of osteonecrosis of the jaws (ONJ), but the lack of reliable epidemiological data and appropriate animal models has restricted our understanding of ONJ pathophysiology and limited its management. The best available information is from histopathologic findings, which implicate bone necrosis and infection, although it is not clear which is primary. However, there are data suggesting that macrophages could well be the central factor in allowing the infection to develop first, followed by local necrosis, which could also account for the development of ONJ in patients treated with denosumab, a human monoclonal antibody to the receptor activator of nuclear factor-κB ligand. This review examines the evidence that macrophages could play a prominent role in development of ONJ and the proposal that it may be more appropriate to view ONJ as a drug and not only a bisphosphonate-related complication.
含氮双膦酸盐与颌骨骨坏死(ONJ)的发生有关,但由于缺乏可靠的流行病学数据和适当的动物模型,限制了我们对 ONJ 病理生理学的理解,并限制了其管理。目前最好的信息来自组织病理学发现,这些发现提示骨坏死和感染,尽管尚不清楚哪个是主要原因。然而,有数据表明,巨噬细胞很可能是允许感染首先发生的核心因素,随后是局部坏死,这也可以解释在接受核因子-κB 配体受体激活剂拮抗剂(一种针对核因子-κB 配体受体的人单克隆抗体)治疗的患者中发生 ONJ 的原因。本综述探讨了巨噬细胞在 ONJ 发展中可能发挥突出作用的证据,并提出将 ONJ 视为一种药物而不仅仅是双膦酸盐相关并发症可能更为恰当。