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Blood group antigen-Binding Adhesion2 (BabA2) gene in gastric tissue biopsies as a diagnostic biomarker for Helicobacter pylori infection

机译:血型抗原结合粘附2(BABA2)基因在胃组织活检中作为幽门螺杆菌感染的诊断生物标志物

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BACKGROUND: The Lewis (b) blood group antigen-Binding Adhesion2 (BabA2) has been reported to mediate the attachment of H. pylori to human. AIM: assessment the diagnostic potential of detection of (BabA2) gene compared with immunostaining of Lewis (b) by specific mouse monoclonal antibodies in gastric biopsies from Egyptian Patients as a diagnostic maker for Helicobacter pylori infection. MATERIALS AND METHODS: Fifty untreated patients suffering from dyspeptic complaints were enrolled in this study and underwent for upper gastro-duodenal endoscopy. Biopsies were taken for histological examination by (HE) and immunohistochemical analysis for Lewis b by specific mouse monoclonal antibodies, and scoring of Lewis b expression in gastric tissue biopsy as well as molecular detection of BabA2 gene of H. pylori by PCR. Biochemical analysis was performed to detect the presence of H. pylori urease activity using Rapid Urease Test (RUT). RESULTS : Out of 50 gastric biopsies, 41?biopsies were positive for histological, Immunostaining for Lewis b expression and urease activity test (RUT) for H pylori. RUT showed a sensitivity of 87.8%, specificity 88.9%, positive predictive value (PPV) 97.2%, and negative predictive value (NPV) 61.5%. BabA2 gene results revealed that, out of 41 positive biopsied cases, 39 (95.1%) were positive by the PCR test for BabA2 gene. And all 9 negative biopsies (100%) for H pylori negative for BabA2gene so the sensitivity and specificity of BabA2 gene detection in gastric biopsies by PCR were 95.1% and 100%; respectively. CONCLUSION : BabA2 gene detection in gastric tissue biopsies could be suggested as a diagnostic biomarker to be included among the other biomarkers routinely performed for clinical diagnosis of H. pylori infection.
机译:背景:据报道,Lewis(B)血液组抗原结合粘附2(巴巴2)介导H.Pylori对人的附着。目的:评估(Baba2)基因的检测诊断潜力与埃及患者胃活组织检查中的胃活组织检查中的特定小鼠单克隆抗体相比,作为埃及患者作为幽门螺杆菌感染的诊断制造商。材料和方法:患有消化不良抱怨的五十个未经处理的患者纳入本研究,并进行上胃 - 十二指肠内镜检查。通过(He)和通过特定小鼠单克隆抗体的Lewis B的(He)和免疫组织化学分析,以及胃组织活检中的Lewis B表达的分析以及PCR的分子检测。进行生化分析以检测快速脲酶试验(RUT)的幽门螺杆菌脲酶活性的存在。结果:50个胃生物检查,41个?活组织检查对于Hewis B表达和脲酶活性试验(Rut)的组织学,免疫抑制的阳性,用于H幽门螺杆菌。车辙显示敏感性为87.8%,特异性88.9%,阳性预测值(PPV)97.2%,负预测值(NPV)61.5%。 BABA2基因结果显示,在41例阳性活检病例中,BAB2基因的PCR试验为39例(95.1%)阳性。所有9个阴性活组织检查(100%)对于Baba2庚烯的H幽门螺杆菌阴性,因此PCR胃生物检查中的巴巴2基因检测的敏感性和特异性为95.1%和100%;分别。结论:胃组织活检中的Baba2基因检测可以提出作为诊断生物标志物,以包括用于临床诊断H. Pylori感染的其他生物标志物。

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