Golub Lorne M, Elburki Muna S, Walker Clay, Ryan Maria, Sorsa Timo, Tenenbaum Howard, Goldberg Michael, Wolff Mark, Gu Ying
Department of Oral Biology and Pathology, School of Dental Medicine, Stony Brook University, Stony Brook, NY, USA.
Department of Periodontics, Faculty of Dentistry, Benghazi University, Benghazi, Libya.
Int Dent J. 2016 Jun;66(3):127-35. doi: 10.1111/idj.12221. Epub 2016 Mar 23.
Traditionally, the dental profession has primarily treated periodontitis using a mechanical/surgical, rather than a pharmaceutical, approach. However, based on experiments several decades ago which demonstrated that tetracyclines, unexpectedly, inhibit collagen- and bone-destructive mammalian-derived enzymes (e.g. the collagenases), and through non-antibiotic mechanisms, the concept of host-modulation therapy (HMT) was developed. Accordingly, two drug-development strategies evolved: (i) the development of non-antimicrobial formulations of doxycycline; and (ii) the chemical modification of tetracyclines to eliminate their antibiotic activity but retain (or even enhance) their anti-collagenase properties. Regarding the latter, these chemically modified tetracyclines (CMTs) showed efficacy in vitro, in animal models of periodontal (and relevant systemic) disease, and in preliminary clinical trials on patients with Kaposi's sarcoma (however, at the high doses used, photosensitivity was a significant side-effect). In the first strategy, subantimicrobial-dose doxycycline (SDD) demonstrated safety and efficacy in human clinical trials and was approved by the U S Food and Drug Administration (U S FDA) and in other countries for the treatment of periodontitis (20 mg, twice daily, i.e. once every 12 hours) adjunctive to scaling and root planing, and for chronic inflammatory skin diseases (40-mg sustained-release 'beads'). SDD also showed efficacy in patients with systemic diseases relevant to periodontitis, including diabetes mellitus and arthritis, and in postmenopausal women with local and systemic bone loss. Importantly, long-term administration of SDD, of up to 2 years, in clinical trials did not produce antibiotic side-effects. SDD (and in the future, new HMTs, such as low-dose CMT-3, resolvins and chemically modified curcumins) may shift the paradigm of periodontal therapy from a predominantly surgical approach to the greater use of medicinal/pharmacologic strategies, ultimately to benefit larger numbers of patients.
传统上,牙科行业主要采用机械/手术方法而非药物方法来治疗牙周炎。然而,基于几十年前的实验,这些实验意外地证明四环素能抑制胶原蛋白和骨破坏性哺乳动物衍生酶(如胶原酶),并且通过非抗生素机制,宿主调节疗法(HMT)的概念得以发展。因此,出现了两种药物开发策略:(i)开发强力霉素的非抗菌制剂;(ii)对四环素进行化学修饰,以消除其抗生素活性,但保留(甚至增强)其抗胶原酶特性。关于后者,这些化学修饰的四环素(CMTs)在体外、牙周(及相关全身性)疾病动物模型以及卡波西肉瘤患者的初步临床试验中均显示出疗效(然而,在使用的高剂量下,光敏性是一个显著的副作用)。在第一种策略中,亚抗菌剂量的强力霉素(SDD)在人体临床试验中证明了安全性和有效性,并获得了美国食品药品监督管理局(US FDA)及其他国家的批准,用于治疗牙周炎(20毫克,每日两次,即每12小时一次),作为龈下刮治和根面平整的辅助治疗,以及用于慢性炎症性皮肤病(40毫克缓释“微珠”)。SDD在与牙周炎相关的全身性疾病患者中也显示出疗效,包括糖尿病和关节炎患者,以及患有局部和全身性骨质流失的绝经后女性。重要的是,在临床试验中,长达2年的SDD长期给药并未产生抗生素副作用。SDD(以及未来的新HMTs,如低剂量CMT - 3、消退素和化学修饰的姜黄素)可能会将牙周治疗的模式从主要的手术方法转变为更多地使用药物/药理学策略,最终使更多患者受益。