Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Curr Mol Med. 2010 Mar;10(2):115-22. doi: 10.2174/156652410790963259.
Malignant tumors induce humoral immune response in cancer patients, although the incidence of such autoantibody responses against individual tumor-associated antigens (TAA) is rather low. To increase predictive value of TAA-recognizing autoantibodies as potential cancer biomarkers, TAAs should be combined into protein arrays. Here we review recent advances in the application of such arrays and summarize data concerning most promising antigens. We also review the methods of cloning TAA-recognizing autoantibodies, generation of human hybridomas and screening of recombinant human immunoglobulin libraries.
恶性肿瘤会在癌症患者体内诱导体液免疫应答,尽管针对个别肿瘤相关抗原(TAA)的自身抗体反应发生率相当低。为了提高 TAA 识别自身抗体作为潜在癌症生物标志物的预测价值,TAA 应组合到蛋白质阵列中。本文综述了此类阵列应用的最新进展,并总结了有关最有前途抗原的相关数据。我们还回顾了克隆 TAA 识别自身抗体、生成人杂交瘤和筛选重组人免疫球蛋白文库的方法。