Current understanding of periodontal disease pathogenesis and targets for host-modulation therapy

被引:293
作者
Hajishengallis, George [1 ]
Chavakis, Triantafyllos [2 ]
Lambris, John D. [3 ]
机构
[1] Univ Penn, Dept Basic & Translat Sci, Penn Dent Med, 240 South 40th St, Philadelphia, PA 19104 USA
[2] Tech Univ Dresden, Fac Med, Inst Clin Chem & Lab Med, Dept Clin Pathobiochem, Dresden, Germany
[3] Univ Penn, Perelman Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
complement; cytokines; dysbiosis; inflammation; inhibitors; host modulation; periodontitis; resolution; therapeutics; NECROSIS-FACTOR-ALPHA; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; DEVELOPMENTAL ENDOTHELIAL LOCUS-1; PROLIFERATOR-ACTIVATED RECEPTOR; GINGIVAL CREVICULAR FLUID; LACTOBACILLUS-BREVIS CD2; GENOME-WIDE ASSOCIATION; INNATE IMMUNE-SYSTEM; QUALITY-OF-LIFE; PORPHYROMONAS-GINGIVALIS;
D O I
10.1111/prd.12331
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Recent advances indicate that periodontitis is driven by reciprocally reinforced interactions between a dysbiotic microbiome and dysregulated inflammation. Inflammation is not only a consequence of dysbiosis but, via mediating tissue dysfunction and damage, fuels further growth of selectively dysbiotic communities of bacteria (inflammophiles), thereby generating a self-sustained feed-forward loop that perpetuates the disease. These considerations provide a strong rationale for developing adjunctive host-modulation therapies for the treatment of periodontitis. Such host-modulation approaches aim to inhibit harmful inflammation and promote its resolution or to interfere directly with downstream effectors of connective tissue and bone destruction. This paper reviews diverse strategies targeted to modulate the host periodontal response and discusses their mechanisms of action, perceived safety, and potential for clinical application.
引用
收藏
页码:14 / 34
页数:21
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