期刊
JOURNAL OF DENTAL RESEARCH
卷 89, 期 12, 页码 1349-1363出版社
SAGE PUBLICATIONS INC
DOI: 10.1177/0022034510376402
关键词
periodontal disease; innate immunity; adaptive immunity; T-helper; cytokines; inflammation; bone resorption; infection
资金
- CNPq (National Council for Scientific and Technological Development)
- FAPESP (Sao Paulo State Research Funding Agency)
Periodontal diseases (PD) are chronic infectious inflammatory diseases characterized by the destruction of tooth-supporting structures, being the presence of periodontopathogens required, but not sufficient, for disease development. As a general rule, host inflammatory mediators have been associated with tissue destruction, while anti-inflammatory mediators counteract and attenuate disease progression. With the discovery of several T-cell subsets bearing distinct immunoregulatory properties, this pro- vs. anti-inflammatory scenario became more complex, and a series of studies has hypothesized protective or destructive roles for Th1, Th2, Th17, and Treg subpopulations of polarized lymphocytes. Interestingly, the protective vs. destructive archetype is usually considered in a framework related to tissue destruction and disease progression. However, it is important to remember that periodontal diseases are infectious inflammatory conditions, and recent studies have demonstrated that cytokines (TNF-alpha and IFN-gamma) considered harmful in the context of tissue destruction play important roles in the control of periodontal infection. Therefore, in this review, the state-of-the-art knowledge concerning the protective and destructive roles of host inflammatory immune response will be critically evaluated and discussed from the tissue destruction and control-of-infection viewpoints.
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