Mizukami T, Osawa T, Niwa M, Oya A, Masubuchi N, Takahashi S
Technology Development Division, BML Inc., Kawagoe.
Rinsho Byori. 1994 Nov;42(11):1188-93.
We have developed an enzyme-linked immunosorbent assay (ELISA) for the detection of IgG antibodies against Helicobacter pylori (HP) using purified HP urease as an antigen. The urease was purified from ultrasonicated extract of HP by NaCl linear gradient system on DEAE-Sepharose 4B chromatography. Two molecular weight bands, 65kD and 27kD were observed on a SDS-PAGE gel in the purified urease sample. The urease antigen did not crossreact to rabbit antibodies prepared against Campylobacter coli and Campylobacter jejuni. Out of 93 gastric biopsy patients, sixty nine patients (74.2%) were positive in HP culture test. Serum HP antibody titers (AU: arbitrary unit) of HP culture positive and negative patients were 42.9 +/- 47.4 and 16.7 +/- 25.7 (mean +/- SD), respectively (p < 0.05). The ELISA system have sensitivity of 72.5% and specificity of 70.8%. We believe that the ELISA system is useful for diagnosis and monitoring of HP infection.
我们已经开发出一种酶联免疫吸附测定(ELISA)法,以纯化的幽门螺杆菌(HP)脲酶作为抗原,用于检测抗幽门螺杆菌的IgG抗体。脲酶是通过在DEAE-琼脂糖4B柱上用NaCl线性梯度系统从幽门螺杆菌超声提取物中纯化得到的。在纯化的脲酶样品的SDS-PAGE凝胶上观察到两条分子量条带,分别为65kD和27kD。脲酶抗原与针对结肠弯曲菌和空肠弯曲菌制备的兔抗体无交叉反应。在93例胃活检患者中,69例(74.2%)幽门螺杆菌培养试验呈阳性。幽门螺杆菌培养阳性和阴性患者的血清幽门螺杆菌抗体滴度(AU:任意单位)分别为42.9±47.4和16.7±25.7(平均值±标准差)(p<0.05)。该ELISA系统的灵敏度为72.5%,特异性为70.8%。我们认为该ELISA系统对幽门螺杆菌感染的诊断和监测有用。