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采用单克隆抗体检测幽门螺杆菌过氧化氢酶的粪便抗原的特性和用途。

Characterization and usefulness of stool antigen tests using a monoclonal antibody to Helicobacter pylori catalase.

机构信息

Sagami Research Laboratories, Wakamoto Pharmaceutical Co. Ltd, Kanagawa, Japan.

出版信息

J Gastroenterol Hepatol. 2012 Apr;27 Suppl 3:23-8. doi: 10.1111/j.1440-1746.2012.07066.x.

DOI:10.1111/j.1440-1746.2012.07066.x
PMID:22486867
Abstract

BACKGROUND AND AIM

Two types of stool antigen tests have been used in the management of Helicobacter pylori infection. Testmate Pylori Antigen enzyme immunoassay (TPAg EIA) is a direct sandwich enzyme immunoassay (EIA) while Testmate Rapid Pylori Antigen (Rapid TPAg) is performed using immunochromatography. The aim of this study was to study the characterization and usefulness of these tests.

METHODS

Accuracy of both tests was studied using 111 fecal samples obtained from H. pylori-positive or -negative patients. Cross-reactivity was examined with four other Helicobacter spp. and five fecal bacteria in humans. To estimate the sensitivity of both kits, we tested H. pylori clinical strains. We also examined the diagnostic performances of both tests after the storage for 12 months.

RESULTS

The accuracy of both Testmate kits was 100% in fecal samples from 111 patients. No cross-reactivity was observed in both Testmate kits in five fecal bacteria and four other Helicobacter spp. TPAg EIA and Rapid TPAg showed positive results in 1342 of 1344, and 483 of 485 clinical strains, respectively. Diagnostic performances was maintained for 12 months when TPAg EIA was stored at 4°C and Rapid TPAg at 30°C.

CONCLUSIONS

We examined the details of high accuracy of TPAg EIA and Rapid TPAg. The diagnostic performance of both kits was maintained after storage for up to 1 year. The two types of tests would be useful in the management of H. pylori infection.

摘要

背景与目的

两种粪便抗原检测已被用于幽门螺杆菌感染的管理。Testmate 幽门螺杆菌抗原酶免疫测定(TPAg EIA)是一种直接的夹心酶免疫测定(EIA),而 Testmate 快速幽门螺杆菌抗原(Rapid TPAg)则采用免疫层析法进行。本研究旨在研究这些检测方法的特征和实用性。

方法

使用从幽门螺杆菌阳性或阴性患者中获得的 111 份粪便样本研究了这两种检测方法的准确性。用另外四种幽门螺杆菌和五种人体肠道细菌检测交叉反应性。为了估计这两种试剂盒的敏感性,我们测试了幽门螺杆菌临床株。我们还检查了两种试剂盒在储存 12 个月后的诊断性能。

结果

两种 Testmate 试剂盒在 111 名患者的粪便样本中的准确性均为 100%。两种 Testmate 试剂盒在五种肠道细菌和四种其他幽门螺杆菌中均未观察到交叉反应性。TPAg EIA 和 Rapid TPAg 分别在 1342 株和 483 株临床菌株中呈阳性结果。当 TPAg EIA 储存在 4°C 时,Rapid TPAg 储存在 30°C 时,12 个月后诊断性能保持不变。

结论

我们详细检查了 TPAg EIA 和 Rapid TPAg 高准确性的细节。两种试剂盒的诊断性能在储存长达 1 年后仍保持不变。这两种类型的检测方法将有助于幽门螺杆菌感染的管理。

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