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首页> 外文期刊>Clinical and vaccine immunology: CVI >Kinetics of the Human Antibody Response against Salmonella enterica Serovars Enteritidis and Typhimurium Determined by Lipopolysaccharide Enzyme-Linked Immunosorbent Assay
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Kinetics of the Human Antibody Response against Salmonella enterica Serovars Enteritidis and Typhimurium Determined by Lipopolysaccharide Enzyme-Linked Immunosorbent Assay

机译:脂多糖酶联免疫吸附测定法测定人针对肠炎沙门氏菌肠炎沙门氏菌和鼠伤寒沙门氏菌的抗体反应动力学。

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Two indirect enzyme-linked immunosorbent assays (ELISAs) were employed to measure levels of immunoglobulin G (IgG), IgM, and IgA antibodies against Salmonella in sera from 303 Danish patients diagnosed by fecal culture with either Salmonella enterica serovar Enteritidis or Salmonella enterica serovar Typhimurium infections. The ELISAs were based on serovar Enteritidis lipopolysaccharide (LPS) and serovar Typhimurium LPS. The antibody levels were assessed approximately 1, 3, 6, and 12 months after the onset of salmonellosis. Sera from 164 healthy blood donors were analyzed to establish cutoff values for each analysis. One month after the onset of symptoms, the sensitivities of the assays were 95% for patients recovering from a serovar Enteritidis infection and 89% for patients recovering from a serovar Typhimurium infection. Three months after the onset of symptoms, these values had decreased to 85% and 55%. At 6 months they were 62% and 40%, and at 12 months they were 40% and 16%, respectively. The specificities of the assays were 97% for the serovar Enteritidis LPS ELISA and 94% for the serovar Typhimurium LPS ELISA. The high values for both sensitivity and specificity make these two ELISAs useful for serodiagnoses of Salmonella infection shortly after the acute phase of the infection and of Salmonella-associated reactive arthritis, as well as for seroepidemiological studies. A mixed ELISA consisting of both antigens, i.e., serovar Enteritidis and serovar Typhimurium LPS, was developed as a diagnostic tool with very high values for both specificity and sensitivity.
机译:两次间接酶联免疫吸附试验(ELISA)用于测量303名丹麦人经粪便培养诊断为 Salmonella 的血清中针对 Salmonella 的免疫球蛋白G(IgG),IgM和IgA抗体的水平>肠炎沙门氏菌血清型肠炎沙门氏菌或肠炎沙门氏菌血清型鼠伤寒感染。 ELISA基于血清型肠炎沙门氏菌脂多糖(LPS)和血清型鼠伤寒LPS。在沙门氏菌病发作后大约1、3、6和12个月评估抗体水平。分析了来自164名健康献血者的血清,以建立每次分析的临界值。症状发作一个月后,从肠炎肠炎血清感染恢复的患者中检测的灵敏度为95%,从鼠伤寒血清感染中恢复的患者为89%。症状发作三个月后,这些值分别下降到85%和55%。在6个月时分别为62%和40%,在12个月时分别为40%和16%。肠炎血清LPS ELISA测定的特异性为97%,鼠伤寒血清LPS ELISA测定的特异性为94%。灵敏性和特异性均很高,这两种酶联免疫吸附测定法可在感染急性期后不久对沙门氏菌感染和沙门氏菌相关反应性关节炎进行血清学诊断至于血清流行病学研究。开发了由两种抗原即血清肠炎沙门氏菌和血清鼠伤寒沙门氏菌LPS组成的混合ELISA作为诊断工具,具有很高的特异性和敏感性。

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