Zhang Yanjun, Duan Xiaobo, Xue Fei, Zhou Xinyi, Yuan Quan, Yang Xingmei
State Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases & Department of Implants, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Clin Oral Implants Res. 2025 Feb;36(2):265-277. doi: 10.1111/clr.14380. Epub 2024 Nov 19.
To determine the in vitro effects of minocycline on human gingival fibroblasts (HGFs), its clinical impact on early wound healing after implant placement, and its potential mechanism of action.
First, we evaluated the in vitro proliferation, migration, and collagen production of HGFs treated with different concentrations of minocycline, as well as the underlying mechanism. Subsequently, we conducted a clinical trial and randomly assigned 40 partially edentulous patients to either the test (minocycline hydrochloride treatment) or control (blank control) group immediately after implant surgery. The early wound healing score (EHS), pain index, gingival index (GI), modified sulcus bleeding index (mSBI), and peri-implant crevicular fluid samples were assessed or collected 3 and/or 7 days after surgery.
In vitro, 1 μg/mL minocycline promoted the proliferation, migration, and collagen production of HGFs. Minocycline inhibited collagen degradation by downregulating the expression of matrix metalloproteinase-2 (MMP-2) and MMP-14 and upregulating tissue inhibitors of metalloproteinases-2. However, higher concentrations of minocycline, 10 and 100 μg/mL, exhibited adverse effects. In the randomised clinical trial, the test group showed significantly better clinical outcomes compared to the control group, with higher EHS and lower GI, mSBI, concentrations of IL-1β, IL-10, and TNF-α, and relative abundance of Streptococcus and gram-negative anaerobic bacteria.
Small doses of minocycline (1 μg/mL) promoted the proliferation and migration of HGFs and inhibited collagen degradation in vitro. Locally delivered minocycline after implant surgery improves clinical outcomes by promoting early wound healing, relieving the inflammatory response, and decreasing early colonisation of gram-negative anaerobic bacteria.
This clinical trial was registered in the Chinese Clinical Trial Registry (registration number: ChiCTR2100044680).
确定米诺环素对人牙龈成纤维细胞(HGFs)的体外作用、其对种植体植入后早期伤口愈合的临床影响及其潜在作用机制。
首先,我们评估了用不同浓度米诺环素处理的HGFs的体外增殖、迁移和胶原生成情况以及潜在机制。随后,我们进行了一项临床试验,在种植手术后立即将40例部分牙列缺损患者随机分为试验组(盐酸米诺环素治疗)或对照组(空白对照)。在术后3天和/或7天评估或收集早期伤口愈合评分(EHS)、疼痛指数、牙龈指数(GI)、改良龈沟出血指数(mSBI)和种植体周围龈沟液样本。
在体外,1μg/mL米诺环素促进了HGFs的增殖、迁移和胶原生成。米诺环素通过下调基质金属蛋白酶-2(MMP-2)和MMP-14的表达以及上调金属蛋白酶组织抑制剂-2来抑制胶原降解。然而,更高浓度的米诺环素,即10和100μg/mL,表现出不利影响。在随机临床试验中,试验组的临床结果明显优于对照组,EHS更高,GI、mSBI、白细胞介素-1β、白细胞介素-10和肿瘤坏死因子-α浓度以及链球菌和革兰氏阴性厌氧菌的相对丰度更低。
小剂量米诺环素(1μg/mL)促进了HGFs的增殖和迁移,并在体外抑制了胶原降解。种植手术后局部应用米诺环素可通过促进早期伤口愈合、减轻炎症反应和减少革兰氏阴性厌氧菌的早期定植来改善临床结果。
本临床试验在中国临床试验注册中心注册(注册号:ChiCTR2100044680)。