Mancini Fabiola, Savarino Andrea, Losardo Maria, Cassone Antonio, Ciervo Alessandra
Department of Infectious, Parasitic and Immune-mediated Diseases, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy.
Microbes Infect. 2009 Mar;11(3):367-73. doi: 10.1016/j.micinf.2008.12.015. Epub 2009 Jan 31.
The purpose of this study was to evaluate the serological response to the recombinant phospholipase D protein of Chlamydophila pneumoniae (CpPLD) in patients with acute coronary syndromes (ACS) and infected by C. pneumoniae. We assessed 100 serum samples from ACS patients and 100 sera from healthy blood donors, all categorized by microimmunefluorescence (MIF) into subjects with presumptive C. pneumoniae infection or past exposure (only specific IgG), chronic infection (presence of specific IgG and IgA), and uninfected, unexposed subjects (MIF titer <1:32). None of the MIF-negative sera showed antibodies against CpPLD. Among MIF-positive subjects, antibodies to CpPLD were consistently found in sera of ACS patients but not in those of healthy subjects, and their titers in ACS patients were higher in subjects with both MIF IgG and IgA than in those with MIF IgG only. Additionally, we recognized an immunodominant P5 epitope in position 233-252 aa of the CpPLD protein which strongly reacted with ACS sera. These data suggest that CpPLD is a protein potentially implicated in the pathogenesis of C. pneumoniae infection. The CpPLD protein and its P5 peptide could be plausible antigens for the diagnosis of C. pneumoniae chronic infections in ACS patients.
本研究旨在评估急性冠脉综合征(ACS)且感染肺炎衣原体(C. pneumoniae)的患者对重组肺炎衣原体磷脂酶D蛋白(CpPLD)的血清学反应。我们评估了100份ACS患者的血清样本和100份健康献血者的血清,所有样本均通过微量免疫荧光法(MIF)分类为推定感染肺炎衣原体或既往暴露(仅特异性IgG)、慢性感染(存在特异性IgG和IgA)以及未感染、未暴露的受试者(MIF滴度<1:32)。所有MIF阴性血清均未显示出抗CpPLD抗体。在MIF阳性受试者中,ACS患者的血清中始终能检测到抗CpPLD抗体,而健康受试者的血清中则未检测到,并且在同时具有MIF IgG和IgA的ACS患者中,其抗体滴度高于仅具有MIF IgG的患者。此外,我们在CpPLD蛋白的233 - 252位氨基酸中识别出一个免疫显性P5表位,它与ACS血清强烈反应。这些数据表明CpPLD是一种可能与肺炎衣原体感染发病机制有关的蛋白。CpPLD蛋白及其P5肽可能是用于诊断ACS患者肺炎衣原体慢性感染的合理抗原。