牙龈卟啉单胞菌
医学
载脂蛋白E
牙周病原体
先天免疫系统
免疫系统
免疫学
炎症
脂多糖
牙周炎
疾病
病理
内科学
作者
Frank C. Gibson,Charles C. Hong,Hsin‐Hua Chou,Hiromichi Yumoto,Jiqiu Chen,Egil Lien,Jodie Wong,Caroline A. Genco
出处
期刊:Circulation
[Lippincott Williams & Wilkins]
日期:2004-05-04
卷期号:109 (22): 2801-2806
被引量:328
标识
DOI:10.1161/01.cir.0000129769.17895.f0
摘要
Background— Infectious diseases have emerged as potential risk factors for cardiovascular disease (CVD). Epidemiological studies support a connection between periodontal disease, a chronic inflammatory disease of the supporting tissues of the teeth, and CVD. Methods and Results— To directly test the connection between periodontal disease and atherosclerosis, apoE −/− mice were orally challenged with the periodontal disease pathogen Porphyromonas gingivalis or an invasion-impaired P gingivalis fimbriae-deficient mutant (FimA−). Both wild-type P gingivalis and the FimA− mutant were detected in blood and aortic arch tissue of apoE −/− mice by PCR after challenge. ApoE −/− mice challenged with wild-type P gingivalis presented with increased atherosclerotic plaque and expressed the innate immune response markers Toll-like receptor (TLR)-2 and TLR-4 in aortic tissue. Despite detection of the FimA− mutant in the blood and in aortic arch tissue, apoE −/− mice challenged with the FimA− mutant did not present with periodontal disease, upregulation of TLRs, or accelerated atherosclerosis. Furthermore, we demonstrate that immunization to control P gingivalis -elicited periodontal disease concomitantly prevents P gingivalis -accelerated atherosclerosis. Conclusions— We conclude that invasive P gingivalis accelerates atherosclerosis.
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