Aging Aggravates Periodontal Inflammatory Responses and Alveolar Bone Resorption by Infection.

Periodontitis is a chronic inflammatory disease driven by periodontal pathogens such as and its prevalence increases with age. However, little is known about the effect of immunosenescence on inflammatory response to infection. In the present study, 16S rDNA sequencing analysis showed the relative abundance of was significantly higher in periodontitis patients than healthy group, but there was no difference between the young (20 to 40 years old) and old (65 to 86 years old) periodontitis groups. Furthermore, the cytotoxic effect of P. gingivalis was greater on old THP-1 macrophages and on bone mar-row-derived cells (BMDMs) from old mice, and levels of interleukin (IL)-1β, tumor necrosis factor (TNF)-α, and IL-12 were higher in old than in young THP-1 macrophages. Furthermore, the activations of inflammasome components for IL-1β production by infection were greater in old THP-1 macrophages. Finally, bone loss was significantly greater in -infected aged mice than in young mice. These findings indicate that aging aggravates -induced inflammatory cytokine secretion and inflammasome activation. The study enhances understanding of the relationship between periodontal immunosenescence and inflammatory response in the elderly.