Baughman Andrew L, Bisgard Kristine M, Edwards Kathryn M, Guris Dalya, Decker Michael D, Holland Kathy, Meade Bruce D, Lynn Freyja
National Immunization Program, Centers for Disease Control and Prevention, 1600 Clifton Rd., NE, Mailstop E-61, Atlanta, GA 30333, USA.
Clin Diagn Lab Immunol. 2004 Nov;11(6):1045-53. doi: 10.1128/CDLI.11.6.1045-1053.2004.
Numerous reports have documented that serologic methods are much more sensitive than culture for the diagnosis of pertussis in adolescents and adults. However, a standardized serologic test for pertussis is not routinely available to most clinicians, and the serologic test levels or cutoff points correlated with diseases have not been determined. The goal of the present study was to examine the distribution of immunoglobulin G (IgG) levels against three Bordetella pertussis antigens (pertussis toxin [PT], filamentous hemagglutinin [FHA], and fimbria types 2 and 3 [FIM]) and to determine population-based antibody levels for the purpose of establishing such diagnostic cutoff points. Enzyme-linked immunosorbent assays (ELISAs) were performed with sera from >6,000 U.S. residents aged 6 to 49 years who participated in the Third National Health and Nutrition Examination Survey. Mixture models were developed to identify hypothesized exposure groups and establish diagnostic cutoffs. Quantifiable (>20 ELISA units/ml [EU]) anti-FHA and anti-FIM IgG antibodies were common (65 and 62% of individuals, respectively), but quantifiable anti-PT IgG antibodies were less frequent (16%). Given the distributions of antibody levels, an anti-PT IgG level of > or =94 EU was proposed as the diagnostic cutoff point. Application of this cutoff point to culture-confirmed illness in a prior study investigating cough illness yielded a high diagnostic sensitivity (80%) and specificity (93%). A standardized ELISA for anti-PT IgG with a single serum sample appears to be useful for the identification of recent B. pertussis infection in adolescents and adults with cough illness. The PT cutoff point will be further evaluated in prospective studies of confirmed B. pertussis infection.
大量报告表明,在青少年和成年人百日咳诊断中,血清学方法比培养法敏感得多。然而,大多数临床医生无法常规获得标准化的百日咳血清学检测,且与疾病相关的血清学检测水平或临界值尚未确定。本研究的目的是检测针对三种百日咳博德特氏菌抗原(百日咳毒素[PT]、丝状血凝素[FHA]以及2型和3型菌毛[FIM])的免疫球蛋白G(IgG)水平分布,并确定基于人群的抗体水平,以建立此类诊断临界值。对参与第三次全国健康和营养检查调查的6000多名6至49岁美国居民的血清进行了酶联免疫吸附测定(ELISA)。开发了混合模型以识别假设的暴露组并建立诊断临界值。可量化(>20 ELISA单位/毫升[EU])的抗FHA和抗FIM IgG抗体很常见(分别占个体的65%和62%),但可量化的抗PT IgG抗体较少见(16%)。鉴于抗体水平分布,建议将抗PT IgG水平≥94 EU作为诊断临界值。在先前一项调查咳嗽疾病的研究中,将此临界值应用于培养确诊的疾病,诊断敏感性高(80%),特异性也高(93%)。使用单一血清样本的标准化抗PT IgG ELISA似乎有助于识别患有咳嗽疾病的青少年和成年人近期的百日咳博德特氏菌感染。PT临界值将在确诊的百日咳博德特氏菌感染前瞻性研究中进一步评估。