Li Shuangshuang, Li Shuang, Meng Lingxiao, Gao Ruihan, Liu Hongrui, Li Minqi
Department of Bone Metabolism, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University & Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Research Center of Dental Materials and Oral Tissue Regeneration & Shandong Provincial Clinical Research Center for Oral Diseases, Jinan, Shandong, China.
Department of Stomatology, Shengli Oilfield Central Hospital, Dongying, Shandong, China.
Clin Oral Investig. 2025 Jan 4;29(1):44. doi: 10.1007/s00784-024-06141-z.
This paper aims to review the immunopathogenesis of Diabetes-associated periodontitis (DPD) and to propose a description of the research progress of drugs with potential clinical value from an immunotherapeutic perspective.
A comprehensive literature search was conducted in PubMed, MEDLINE, Embase, Web of Science, Scopus and the Cochrane Library. Inclusion criteria were studies on the association between diabetes and periodontitis using the Boolean operator "AND" for association between diabetes and periodontitis, with no time or language restrictions. Search terms included diabetes mellitus, periodontitis, immunopathogenesis, specific immunity, non-specific immunity, flora, estrogen, pharmacological treatment, immunotherapy.
Alterations in the subgingival flora environment in a hyperglycemic environment elicit an immune response. Overactivity/suppression of nonspecific immune cells and impaired cellular defenses trigger specific immune responses. Epigenetics as well as female hormones also play a role. There is already a small amount of clinical evidence for the role of metronidazole, subantimicrobial doses of doxycycline, minocycline hydrochloride, and metformin in the treatment of DPD. Some preclinical studies have also accumulated experimental evidence for the improved effects of vitamin D3 and other drugs on DPD.
The development of diabetic periodontitis is immunologically linked to a state of immune imbalance and therefore holds great promise for the use of immunotherapeutic drugs.
Immunotherapy with drugs along with periodontal nonsurgical treatment could provide ideas for DPD treatment based on the immunopathogenesis of DPD.
本文旨在综述糖尿病相关性牙周炎(DPD)的免疫发病机制,并从免疫治疗角度对具有潜在临床价值的药物研究进展进行阐述。
在PubMed、MEDLINE、Embase、Web of Science、Scopus和Cochrane图书馆进行全面的文献检索。纳入标准为使用布尔运算符“AND”检索糖尿病与牙周炎之间关联的研究,无时间或语言限制。检索词包括糖尿病、牙周炎、免疫发病机制、特异性免疫、非特异性免疫、菌群、雌激素、药物治疗、免疫治疗。
高血糖环境下龈下菌群环境的改变引发免疫反应。非特异性免疫细胞的过度活跃/抑制以及细胞防御功能受损触发特异性免疫反应。表观遗传学以及女性激素也发挥作用。甲硝唑、亚抗菌剂量的强力霉素、盐酸米诺环素和二甲双胍在治疗DPD中的作用已有少量临床证据。一些临床前研究也积累了维生素D3等药物对DPD有改善作用的实验证据。
糖尿病性牙周炎的发生在免疫方面与免疫失衡状态相关,因此免疫治疗药物具有很大的应用前景。
基于DPD的免疫发病机制,药物免疫治疗联合牙周非手术治疗可为DPD的治疗提供思路。