Immunomicrobial pathogenesis of periodontitis: keystones, pathobionts, and host response

被引:767
作者
Hajishengallis, George [1 ]
机构
[1] Univ Penn, Sch Dent Med, Dept Microbiol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
dysbiosis; inflammation; keystone pathogen; pathobiont; periodontitis; PORPHYROMONAS-GINGIVALIS; T-CELLS; SIGNALING MECHANISMS; FILIFACTOR-ALOCIS; TH17; PATHWAY; BONE LOSS; DISEASE; INNATE; NEUTROPHILS; HEALTH;
D O I
10.1016/j.it.2013.09.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent studies have uncovered novel mechanisms underlying the breakdown of periodontal host microbe homeostasis, which can precipitate dysbiosis and periodontitis in susceptible hosts. Dysbiotic microbial communities of keystone pathogens and pathobionts are thought to exhibit synergistic virulence whereby not only can they endure the host response but can also thrive by exploiting tissue-destructive inflammation, which fuels a self-feeding cycle of escalating dysbiosis and inflammatory bone loss, potentially leading to tooth loss and systemic complications. Here, I discuss new paradigms in our understanding of periodontitis, which may shed light into other polymicrobial inflammatory disorders. In addition, I highlight gaps in knowledge required for an integrated picture of the interplay between microbes and innate and adaptive immune elements that initiate and propagate chronic periodontal inflammation.
引用
收藏
页码:3 / 11
页数:9
相关论文
共 83 条
[31]   Beyond the red complex and into more complexity: the polymicrobial synergy and dysbiosis (PSD) model of periodontal disease etiology [J].
Hajishengallis, G. ;
Lamont, R. J. .
MOLECULAR ORAL MICROBIOLOGY, 2012, 27 (06) :409-419
[32]   Too old to fight? Aging and its toll on innate immunity [J].
Hajishengallis, G. .
MOLECULAR ORAL MICROBIOLOGY, 2010, 25 (01) :25-37
[33]   Role of complement in host-microbe homeostasis of the periodontium [J].
Hajishengallis, George ;
Abe, Toshiharu ;
Maekawa, Tomoki ;
Hajishengallis, Evlambia ;
Lambris, John D. .
SEMINARS IN IMMUNOLOGY, 2013, 25 (01) :65-72
[34]   The keystone-pathogen hypothesis [J].
Hajishengallis, George ;
Darveau, Richard P. ;
Curtis, Michael A. .
NATURE REVIEWS MICROBIOLOGY, 2012, 10 (10) :717-725
[35]   Low-Abundance Biofilm Species Orchestrates Inflammatory Periodontal Disease through the Commensal Microbiota and Complement [J].
Hajishengallis, George ;
Liang, Shuang ;
Payne, Mark A. ;
Hashim, Ahmed ;
Jotwani, Ravi ;
Eskan, Mehmet A. ;
McIntosh, Megan L. ;
Alsam, Asil ;
Kirkwood, Keith L. ;
Lambris, John D. ;
Darveau, Richard P. ;
Curtis, Michael A. .
CELL HOST & MICROBE, 2011, 10 (05) :497-506
[36]   Microbial manipulation of receptor crosstalk in innate immunity [J].
Hajishengallis, George ;
Lambris, John D. .
NATURE REVIEWS IMMUNOLOGY, 2011, 11 (03) :187-200
[37]   Porphyromonas gingivalis Infection-Associated Periodontal Bone Resorption Is Dependent on Receptor Activator of NF-κB Ligand [J].
Han, Xiaozhe ;
Lin, Xiaoping ;
Yu, Xiaoqian ;
Lin, Jiang ;
Kawai, Toshihisa ;
LaRosa, Karen B. ;
Taubman, Martin A. .
INFECTION AND IMMUNITY, 2013, 81 (05) :1502-1509
[38]   Mobile Microbiome: Oral Bacteria in Extra-oral Infections and Inflammation [J].
Han, Y. W. ;
Wang, X. .
JOURNAL OF DENTAL RESEARCH, 2013, 92 (06) :485-491
[39]  
Hasturk H, 2012, FRONT ORAL BIOL, V15, P160, DOI 10.1159/000329678
[40]   Th17 cells can provide B cell help in autoantibody induced arthritis [J].
Hickman-Brecks, Cynthia L. ;
Racz, Jennifer L. ;
Meyer, Debra M. ;
LaBranche, Timothy P. ;
Allen, Paul M. .
JOURNAL OF AUTOIMMUNITY, 2011, 36 (01) :65-75