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Evaluation of HER2 Protein Expression Using 2 New Monoclonal Antibodies

机译:使用2种新型单克隆抗体评估HER2蛋白的表达

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This study describes the performance of 2 new mouse anti-HER2 monoclonal antibodies (Abs), clones 33F and 410G, in evaluating HER2 overexpression in a series of 123 invasive breast carcinoma cases. In-house immunohistochemistry (IHC) was performed and the results were compared with those for the SP3 and A0485 anti-HER2 Abs. Chromogenic in situ hybridization was used to detect ERBB2 amplification and its concordance with IHC was analyzed. Comparison of IHC results for 33F with SP3 and A0485 yielded concordance rates (A) of 0.81 and 0.75, respectively; the same concordance rates were found when comparing results for 410G with SP3 and A0485. Compared with SP3 and A0485, 33F and 410G specificities were 98.6% and 98.6%, and 100% and 100%, respectively, whereas the sensitivities were 80% and 74.1%, and 78% and 72.2%, respectively. The K values between 33F and 410G HER2+ expression and chromogenic in situ hybridization-positive amplification were 1 and 0.96, respectively. These concordance rates were reproduced in another production batch (K = 0.96 and K = 0.96). Together, these results show that the tested monoclonal Abs would be well suited for detecting HER2 protein overexpression by IHC.
机译:这项研究描述了2种新型小鼠抗HER2单克隆抗体(Abs)(克隆33F和410G)在一系列123例浸润性乳腺癌病例中评估HER2过表达的性能。进行了内部免疫组织化学(IHC),并将结果与​​SP3和A0485抗HER2 Abs的结果进行了比较。用生色原位杂交检测ERBB2扩增,并分析其与IHC的一致性。比较33F与SP3和A0485的IHC结果,得出的一致率(A)分别为0.81和0.75;将410G与SP3和A0485的结果进行比较时,发现相同的一致性率。与SP3和A0485相比,33F和410G的特异性分别为98.6%和98.6%,以及100%和100%,而敏感性分别为80%和74.1%,78%和72.2%。在33F和410G HER2 +表达和显色原位杂交阳性扩增之间的K值分别为1和0.96。这些一致性比率在另一个生产批次中复制(K = 0.96和K = 0.96)。总之,这些结果表明,所测试的单克隆抗体绝对适合用于检测IHC过量表达的HER2蛋白。

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