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幽门螺杆菌黏附因子血型抗原结合黏附素在慢性胃炎症中的关键重要性。

Key importance of the Helicobacter pylori adherence factor blood group antigen binding adhesin during chronic gastric inflammation.

作者信息

Prinz C, Schöniger M, Rad R, Becker I, Keiditsch E, Wagenpfeil S, Classen M, Rösch T, Schepp W, Gerhard M

机构信息

Department of Medicine II and Gastroenterology, Bogenhausen Academic Teaching Hospital, Technical University, Munich, Germany.

出版信息

Cancer Res. 2001 Mar 1;61(5):1903-9.

Abstract

Helicobacter pylori has been assigned as a class I carcinogen because of its relation to gastric adenocarcinoma. Chronic H. pylori infection may lead to severe gastritis, glandular atrophy (AT), and intestinal metaplasia (IM). Strains secreting the vacuolating toxin VacA and producing the cytotoxin-associated antigen CagA (type 1 strains), as well as the blood group antigen binding adhesin (BabA) targeting Lewis(b) antigens, have been associated previously with distal gastric adenocarcinoma (M. Gerhard et al., Proc. Natl. Acad. Sci. USA, 96: 12778-12783, 1999) and may therefore also be related to lesions preceding gastric cancer. Antral and corpus biopsies were collected from 451 patients; 151 were H. pylori positive, as determined by PCR. Gastric biopsies were histologically evaluated for activity of gastritis (G0-G3, granulocyte infiltration), chronicity of gastritis (L1-L3, lymphocyte infiltration), and the presence of IM and/or AT according to the Sydney classification. Simultaneously, the presence of bacterial genes encoding virulence and adherence factors (racAs1/s2, cagA, and babA2) was determined by PCR. The presence of cagA+ and vacAs1 (alone or combined) both correlated with activity and chronicity of gastritis (P < 0.05); however, the overall prevalence of these genes was 60 or 72%, respectively, and was thus relatively frequent. The babA2 gene, encoding the adhesin BabA, was detected in 38% of infected patients and was correlated with the activity of gastritis in antrum and corpus (P < 0.005). cagA+/vacAs1+ strains (suggesting the presence of type 1 strains) that were also babA2 positive were detected more frequently in patients with severe histological alterations (such as G3, IM, or AT) compared with subjects without these changes (P < 0.01). cagA+/vacAs1+ strains that were babA2 negative, however, lacked a significant correlation with severe histological changes, activity, or chronicity of gastritis in antrum and corpus. Adherence of H. pylori via BabA appears to be of importance for efficient delivery of VacA and CagA and may play a special role in the pathogenesis of severe histological changes.

摘要

幽门螺杆菌因其与胃腺癌的关系已被列为I类致癌物。幽门螺杆菌慢性感染可能导致严重胃炎、腺体萎缩(AT)和肠化生(IM)。分泌空泡毒素VacA并产生细胞毒素相关抗原CagA的菌株(1型菌株),以及靶向Lewis(b)抗原的血型抗原结合黏附素(BabA),此前已被证实与远端胃腺癌有关(M. Gerhard等人,《美国国家科学院院刊》,96: 12778 - 12783, 1999),因此也可能与胃癌前期病变有关。从451名患者中采集了胃窦和胃体活检样本;经聚合酶链反应(PCR)检测,其中151名患者幽门螺杆菌呈阳性。根据悉尼分类法,对胃活检样本进行组织学评估,以确定胃炎的活动程度(G0 - G3,粒细胞浸润)、胃炎的慢性程度(L1 - L3,淋巴细胞浸润)以及IM和/或AT的存在情况。同时,通过PCR检测编码毒力和黏附因子的细菌基因(racAs1/s2、cagA和babA2)的存在情况。cagA+和vacAs1(单独或联合)的存在均与胃炎的活动程度和慢性程度相关(P < 0.05);然而,这些基因的总体患病率分别为60%或72%,因此相对较高。在38%的感染患者中检测到编码黏附素BabA的babA2基因,且该基因与胃窦和胃体胃炎的活动程度相关(P < 0.005)。与无这些变化的受试者相比,在有严重组织学改变(如G3、IM或AT)的患者中,同时为babA2阳性的cagA+/vacAs1+菌株(提示存在1型菌株)检测频率更高(P < 0.01)。然而,babA2阴性的cagA+/vacAs1+菌株与胃窦和胃体胃炎的严重组织学改变、活动程度或慢性程度缺乏显著相关性。幽门螺杆菌通过BabA的黏附似乎对于VacA和CagA的有效传递很重要,并且可能在严重组织学改变的发病机制中起特殊作用。

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