Chlamydia pneumoniae Seropositivity Is Associated With Increased Plasma Levels of Soluble Cellular Adhesion Molecules in Community-Dwelling Subjects: The Shimanami Health Promoting Program (J-SHIPP) Study
K. Kohara, Y. Tabara, Yoshikuni Yamamoto, M. Igase, T. Miki
{"title":"Chlamydia pneumoniae Seropositivity Is Associated With Increased Plasma Levels of Soluble Cellular Adhesion Molecules in Community-Dwelling Subjects: The Shimanami Health Promoting Program (J-SHIPP) Study","authors":"K. Kohara, Y. Tabara, Yoshikuni Yamamoto, M. Igase, T. Miki","doi":"10.1161/01.STR.0000018974.05768.FB","DOIUrl":null,"url":null,"abstract":"Background and Purpose— In vitro studies have demonstrated that Chlamydia pneumoniae infection of the endothelium increases the expression of adhesion molecules and chemokines, indicating that C pneumoniae infection affects the adhesion and recruitment of leukocytes to the endothelium, which is believed to be involved in the initial steps of atherosclerosis. However, whether chronic C pneumoniae infection increases these molecules in vivo has not been elucidated. Methods— The association between C pneumoniae seropositivity and plasma concentrations of soluble adhesion molecules and a chemokine was investigated in 200 community-dwelling residents free from cardiovascular diseases and medication. Plasma levels of IgA and IgG antibodies to C pneumoniae were measured by enzyme-linked immunosorbent assay. Indices of IgG and IgA antibodies were determined as the ratio to the standardized positive control. The subjects were divided into 3 groups according to the indices of antibodies:C pneumoniae seronegative (n=57, IgA<1.0 and IgG<1.0), C pneumoniae intermediate (n=81, 1.0≤IgA≥1.1 or 1.0≤IgG≥1.1), and C pneumoniae seropositive (n=62, IgA>1.1 and IgG>1.1). Plasma concentrations of soluble forms of intercellular adhesion molecule-1 (ICAM-1), vascular cellular adhesion molecule-1, and monocyte chemoattractant protein-1 were determined by enzyme-linked immunosorbent assay. Results— Plasma concentrations of ICAM-1 (392±118, 398±94, 470±154 ng/mL, P =0.0004) and vascular cellular adhesion molecule-1 (402±146, 419±130, 472±181 ng/mL, P =0.03) were significantly different among the C pneumoniae seronegative, intermediate, and seropositive groups respectively. However, plasma monocyte chemoattractant protein-1 was not significantly different among the 3 groups. Stepwise regression analysis showed that plasma concentration of ICAM-1 was significantly associated with C pneumoniae seropositivity, independent of other known risk factors for atherosclerosis and carotid intima-media thickness. Conclusion— These findings indicate that C pneumoniae seropositivity is associated with higher plasma concentrations of soluble forms of adhesion molecules in the general population. The increase in circulating adhesion molecules may underlie the mechanisms linking C pneumoniae infection and atherosclerosis in vivo.","PeriodicalId":22274,"journal":{"name":"Stroke: Journal of the American Heart Association","volume":"20 1","pages":"1474-1479"},"PeriodicalIF":0.0000,"publicationDate":"2002-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"15","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Stroke: Journal of the American Heart Association","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1161/01.STR.0000018974.05768.FB","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 15
Abstract
Background and Purpose— In vitro studies have demonstrated that Chlamydia pneumoniae infection of the endothelium increases the expression of adhesion molecules and chemokines, indicating that C pneumoniae infection affects the adhesion and recruitment of leukocytes to the endothelium, which is believed to be involved in the initial steps of atherosclerosis. However, whether chronic C pneumoniae infection increases these molecules in vivo has not been elucidated. Methods— The association between C pneumoniae seropositivity and plasma concentrations of soluble adhesion molecules and a chemokine was investigated in 200 community-dwelling residents free from cardiovascular diseases and medication. Plasma levels of IgA and IgG antibodies to C pneumoniae were measured by enzyme-linked immunosorbent assay. Indices of IgG and IgA antibodies were determined as the ratio to the standardized positive control. The subjects were divided into 3 groups according to the indices of antibodies:C pneumoniae seronegative (n=57, IgA<1.0 and IgG<1.0), C pneumoniae intermediate (n=81, 1.0≤IgA≥1.1 or 1.0≤IgG≥1.1), and C pneumoniae seropositive (n=62, IgA>1.1 and IgG>1.1). Plasma concentrations of soluble forms of intercellular adhesion molecule-1 (ICAM-1), vascular cellular adhesion molecule-1, and monocyte chemoattractant protein-1 were determined by enzyme-linked immunosorbent assay. Results— Plasma concentrations of ICAM-1 (392±118, 398±94, 470±154 ng/mL, P =0.0004) and vascular cellular adhesion molecule-1 (402±146, 419±130, 472±181 ng/mL, P =0.03) were significantly different among the C pneumoniae seronegative, intermediate, and seropositive groups respectively. However, plasma monocyte chemoattractant protein-1 was not significantly different among the 3 groups. Stepwise regression analysis showed that plasma concentration of ICAM-1 was significantly associated with C pneumoniae seropositivity, independent of other known risk factors for atherosclerosis and carotid intima-media thickness. Conclusion— These findings indicate that C pneumoniae seropositivity is associated with higher plasma concentrations of soluble forms of adhesion molecules in the general population. The increase in circulating adhesion molecules may underlie the mechanisms linking C pneumoniae infection and atherosclerosis in vivo.
背景与目的——体外研究表明,肺炎衣原体感染内皮细胞后,黏附分子和趋化因子的表达增加,表明肺炎衣原体感染影响白细胞对内皮细胞的黏附和募集,被认为参与了动脉粥样硬化的初始阶段。然而,慢性肺炎C菌感染是否会在体内增加这些分子尚不清楚。方法-对200名无心血管疾病和无药物治疗的社区居民进行肺炎C血清阳性与血浆可溶性粘附分子和趋化因子浓度之间的关系调查。采用酶联免疫吸附法检测血浆中抗肺炎C的IgA和IgG抗体水平。IgG、IgA抗体指标与标准化阳性对照的比值。根据抗体指标分为3组:肺炎C血清阴性(n=57, IgA1.1和IgG>1.1)。采用酶联免疫吸附法测定血浆中可溶性细胞间黏附分子-1 (ICAM-1)、血管细胞黏附分子-1和单核细胞趋化蛋白-1的浓度。结果-血浆ICAM-1浓度(392±118、398±94、470±154 ng/mL, P =0.0004)和血管细胞粘附分子-1浓度(402±146、419±130、472±181 ng/mL, P =0.03)在肺炎C血清阴性、中间和血清阳性组中分别有显著差异。血浆单核细胞趋化蛋白-1在3组间差异无统计学意义。逐步回归分析显示,血浆ICAM-1浓度与肺炎链球菌血清阳性显著相关,独立于动脉粥样硬化和颈动脉内膜-中膜厚度的其他已知危险因素。结论:这些发现表明,在一般人群中,肺炎C血清阳性与较高的血浆可溶性黏附分子浓度有关。循环黏附分子的增加可能是体内C肺炎感染和动脉粥样硬化联系机制的基础。