Postgraduate Program in Health Sciences, Federal University of Bahia School of Medicine, Salvador, Brazil.
Postgraduate Program in Health Sciences, Federal University of Bahia School of Medicine, Salvador, Brazil.
J Immunol Methods. 2018 Sep;460:72-78. doi: 10.1016/j.jim.2018.06.011. Epub 2018 Jun 20.
The aim of this study was to compare the results of serological assays using pneumococcal proteins or polysaccharides for the detection of pneumococcal infection in childhood pneumonia. Serological assays measured IgG against eight pneumococcal proteins (Ply,CbpA,PspA1,PspA2,PcpA,PhtD,StkP-C,PcsB-N), C-polysaccharide [in the whole study population, n = 183], or 19 pneumococcal capsular polysaccharides (1,2,4,5,6B,7F,8,9 V,10A,11A,12F,14,15B,17F,18C,19F,20,23F,33F) [only in a subgroup of patients, n = 53] in paired serum samples of children aged <5 years-old hospitalized with clinical and radiological diagnosis of community-acquired pneumonia. We also performed an inhibition of binding test with the anti-capsular polysaccharide assay in order to confirm the specificity of the antibody responses detected. Invasive pneumococcal pneumonia was investigated by blood culture and PCR (ply-primer). Among 183 children, the anti-protein assay detected antibody response in 77/183(42.1%) patients and the anti-C-polysaccharide assay in 28/183(15.3%) patients. In a subgroup of 53 children, the anti-protein assay detected response in 32/53(60.4%) patients, the anti-C-polysaccharide assay in 11/53(20.8%) patients, and the anti-capsular polysaccharide in 25/53(47.2%) patients. Simultaneous antibody responses against ≥2 different capsular polysaccharides were detected in 11/53(20.8%) patients and this finding could not be explained by cross-reactivity between different serotypes. Among 13 patients with invasive pneumococcal pneumonia, the sensitivity of the anti-protein assay was 92.3%(12/13), of the anti-C-polysaccharide assay 30.8%(4/13), and of the anti-capsular polysaccharide assay 46.2%(6/13). The serological assay using pneumococcal proteins is more sensitive for the detection of pneumococcal infection in children with pneumonia than the assay using pneumococcal polysaccharides. Future studies on childhood pneumonia aetiology should consider applying serological assays using pneumococcal proteins.
本研究旨在比较使用肺炎球菌蛋白或多糖的血清学检测方法在儿童肺炎中检测肺炎球菌感染的结果。血清学检测方法测量了针对 8 种肺炎球菌蛋白(Ply、CbpA、PspA1、PspA2、PcpA、PhtD、StkP-C、PcsB-N)、C 多糖[在整个研究人群中,n=183]或 19 种肺炎球菌荚膜多糖(1、2、4、5、6B、7F、8、9V、10A、11A、12F、14、15B、17F、18C、19F、20、23F、33F)[仅在患者亚组中,n=53]的配对血清样本中针对肺炎球菌的 IgG 抗体。我们还使用荚膜多糖抗血清抑制结合试验来确认检测到的抗体反应的特异性。通过血培养和 PCR(ply 引物)检测侵袭性肺炎球菌肺炎。在 183 名儿童中,抗蛋白检测在 77/183(42.1%)名患者中检测到抗体反应,抗 C 多糖检测在 28/183(15.3%)名患者中检测到抗体反应。在 53 名儿童的亚组中,抗蛋白检测在 32/53(60.4%)名患者中检测到抗体反应,抗 C 多糖检测在 11/53(20.8%)名患者中检测到抗体反应,抗荚膜多糖检测在 25/53(47.2%)名患者中检测到抗体反应。在 53 名患者中有 11 名(20.8%)同时检测到针对≥2 种不同荚膜多糖的抗体反应,这种发现不能用不同血清型之间的交叉反应来解释。在 13 名侵袭性肺炎球菌肺炎患者中,抗蛋白检测的敏感性为 92.3%(12/13),抗 C 多糖检测的敏感性为 30.8%(4/13),抗荚膜多糖检测的敏感性为 46.2%(6/13)。在儿童肺炎中,使用肺炎球菌蛋白的血清学检测方法比使用肺炎球菌多糖的检测方法更能敏感地检测到肺炎球菌感染。未来对儿童肺炎病因的研究应考虑使用肺炎球菌蛋白的血清学检测方法。