Suppr超能文献

评估菌株特异性抗原变异对幽门螺杆菌感染血清学诊断准确性的影响。

Evaluation of the effects of strain-specific antigen variation on the accuracy of serologic diagnosis of Helicobacter pylori infection.

作者信息

Marchildon Patrice A, Sugiyama Toshiro, Fukuda Yoshihiro, Peacock Jeffrey S, Asaka Masahiro, Shimoyama Takashi, Graham David Y

机构信息

Enteric Products, Inc., Stony Brook, New York, USA.

出版信息

J Clin Microbiol. 2003 Apr;41(4):1480-5. doi: 10.1128/JCM.41.4.1480-1485.2003.

Abstract

It has been suggested that enzyme immunoassay (EIA) kits validated in one region may yield variable diagnostic performance results in different regions, possibly due to strain-specific differences in antibody responses in different populations. We tested (13)C-urea breath test-characterized serum samples from 109 U.S. patients and 288 Japanese patients using enzyme immunoassay with different preparations of high-molecular-weight cell-associated (HM-CAP) antigens that are conserved across Helicobacter pylori strains. Replicate antigens were prepared from five H. pylori clinical isolates. Eight antigen preparations were evaluated: two of U.S. origin and six of Japanese origin. The accuracies achieved with the eight antigen preparations ranged from 94.4 to 96.3% with the U.S. samples. With the Japanese samples the accuracies achieved ranged from 92.3 to 97.2%. Use of a pool of HM-CAP antigens prepared from isolates from Japan resulted in a higher median enzyme immunoassay value and slightly fewer samples with indeterminate results compared to the results obtained by use of the U.S. standard HM-CAP antigen for H. pylori-positive patients (accuracies, 97.2 and 92.3%, respectively), suggesting that variations in performance between both antigen source and patient population might be reduced by using antigens pooled from several strains.

摘要

有人提出,在一个地区经验证的酶免疫分析(EIA)试剂盒在不同地区可能会产生不同的诊断性能结果,这可能是由于不同人群抗体反应的菌株特异性差异所致。我们使用酶免疫分析法,对来自109名美国患者和288名日本患者的经¹³C - 尿素呼气试验表征的血清样本进行检测,所用的抗原是不同制备方法的高分子量细胞相关(HM - CAP)抗原,这些抗原在幽门螺杆菌菌株中是保守的。从五株幽门螺杆菌临床分离株制备了重复抗原。评估了八种抗原制剂:两种源自美国,六种源自日本。对于美国样本,八种抗原制剂的准确率在94.4%至96.3%之间。对于日本样本,准确率在92.3%至97.2%之间。与使用美国标准的幽门螺杆菌HM - CAP抗原相比,使用从日本分离株制备的HM - CAP抗原池导致幽门螺杆菌阳性患者的酶免疫分析值中位数更高,结果不确定的样本略少(准确率分别为97.2%和92.3%),这表明通过使用从多个菌株汇集的抗原,抗原来源和患者群体之间的性能差异可能会减少。

相似文献

10

引用本文的文献

3
Serodiagnosis and Bacterial Genome of Infection.血清诊断与感染的细菌基因组。
Toxins (Basel). 2021 Jul 5;13(7):467. doi: 10.3390/toxins13070467.
6
Non-invasive diagnostic tests for Helicobacter pylori infection.幽门螺杆菌感染的非侵入性诊断测试。
Cochrane Database Syst Rev. 2018 Mar 15;3(3):CD012080. doi: 10.1002/14651858.CD012080.pub2.
10
Analysis of Helicobacter pylori genotypes in clinical gastric wash samples.临床胃冲洗样本中幽门螺杆菌基因型分析
Tumour Biol. 2016 Aug;37(8):10123-32. doi: 10.1007/s13277-016-4886-4. Epub 2016 Jan 29.

本文引用的文献

1
Helicobacter pylori in North and South America before Columbus.哥伦布之前南北美洲的幽门螺杆菌。
FEBS Lett. 2002 Apr 24;517(1-3):180-4. doi: 10.1016/s0014-5793(02)02617-0.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验