免疫组织化学在幽门螺杆菌鉴定中的应用

R. Patnayak, V. Reddy, A. Jena, N. Rukmangadha, S. Parthasarathy, M. Reddy
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引用次数: 14

摘要

背景:幽门螺杆菌是慢性活动性胃炎、十二指肠溃疡以及胃腺癌、黏膜相关淋巴组织淋巴瘤等恶性肿瘤的致病菌。在胃活检中提到幽门螺杆菌的存在是必要的,因为它在病人护理中起着重要的作用。虽然有几种特殊的染色方法可以在组织学切片上检测幽门螺杆菌,但它们的特异性和敏感性差异很大。免疫组化检测幽门螺杆菌可以使用抗幽门螺杆菌抗体,该抗体与整个细菌的体细胞抗原反应。本研究的目的是比较常规苏木精和伊红(H和E)、Giemsa、warlin - starry (WS)银染色和免疫组织化学技术诊断幽门螺杆菌的可靠性。材料与方法:本研究是一项为期1年(2009年)的回顾性研究,对组织病理学诊断为胃炎的患者在胃肠内镜下的胃活检进行研究。每个标本石蜡块取5 μm切片进行标准H、E染色。在常规H和E染色中显示胃炎组织病理学特征的患者活检标本的显微镜切片以及怀疑存在幽门螺杆菌的患者,也使用纯化的多克隆幽门螺杆菌抗血清(BioGenex)进行Giemsa, WS和免疫组织化学(IHC)染色。我们的研究中没有包括胃切除术标本。结果:29例患者中,H、E、Giemsa、WS染色检出幽门螺杆菌26例(32.9%),IHC染色检出幽门螺杆菌49例(62.0%)。结论:免疫组化检测幽门螺杆菌优于常规H、E染色。然而,在财政拮据的发展中国家,常规H和E染色结合特殊染色在显示幽门螺杆菌方面是相当可靠的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Utility of immunohistochemistry in demonstrating Helicobacter pylori
Background: Helicobacter pylori is the causative organism for chronic active gastritis, duodenal ulcer and also for malignancies like gastric adenocarcinoma and mucosa associated lymphoid tissue lymphoma. It is essential to mention the presence of H. pylori in gastric biopsies as it has an important role in patient care. Though there are several special stains to detect H. pylori in histological sections, their specificity and sensitivity vary greatly. Immunohistochemically H. pylori can be detected by using anti H. pylori antibody, which reacts with somatic antigens of the whole bacteria. The aim of this study was to compare the reliability of routine hematoxylin and eosin (H and E), Giemsa, Warthin-Starry (WS) silver stain and immunohistochemical technique in diagnosing H. pylori. Materials and Methods: In this retrospective 1-year (2009) study, endoscopic gastric biopsies taken from patients during gastrointestinal-endoscopy with histopathological diagnosis of gastritis were studied. Standard H and E staining was performed on 5-μm-sections from paraffin block of each specimen. Microscopic sections of biopsy specimens of patients showing features of gastritis histopathologically in routine H and E stain and where the presence of H. pylori was suspected were also stained with Giemsa, WS, and immunohistochemistry (IHC) using purified polyclonal H. pylori antiserum (BioGenex). We have not included gastric resection specimens in our study. Results: Of the 29 cases, 26 (32.9%) showed presence of H. pylori on H and E, Giemsa and WS stains, whereas 49 (62.0%) cases demonstrated H. pylori on IHC stain. Conclusion: We conclude that H. pylori detection by IHC has advantage over routine H and E staining. However, in the developing countries with financial constraints, routine H and E staining in combination with special staining are fairly reliable in demonstrating H. pylori.
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