Cekaite Lina, Haug Ola, Myklebost Ola, Aldrin Magne, Østenstad Bjørn, Holden Marit, Frigessi Arnoldo, Hovig Eivind, Sioud Mouldy
Department of Tumor Biology, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo, Norway.
Proteomics. 2004 Sep;4(9):2572-82. doi: 10.1002/pmic.200300768.
We describe a novel approach for high-throughput analysis of the immune response in cancer patients using phage-based microarray technology. The recombinant phages used for fabricating phage arrays were initially selected via the use of random peptide phage libraries and breast cancer patient serum antibodies. The peptides displayed by the phages retained their ability to be recognized by serum antibodies after immobilization. The recombinant phage microarrays were screened against either breast cancer or healthy donor serum antibodies. A model-based statistical method is proposed to estimate significant differences in serum antibody reactivity between patients and normals. A significant tumor effect was found with most of the selected phage-displayed peptides, suggesting that recombinant phage microarrays can serve as a tool in monitoring humoral responses towards phage-displayed peptides.
我们描述了一种使用基于噬菌体的微阵列技术对癌症患者免疫反应进行高通量分析的新方法。用于制造噬菌体阵列的重组噬菌体最初是通过使用随机肽噬菌体文库和乳腺癌患者血清抗体来选择的。噬菌体展示的肽在固定后仍保留其被血清抗体识别的能力。重组噬菌体微阵列针对乳腺癌或健康供体血清抗体进行筛选。提出了一种基于模型的统计方法来估计患者和正常人血清抗体反应性的显著差异。发现大多数选定的噬菌体展示肽具有显著的肿瘤效应,这表明重组噬菌体微阵列可作为监测针对噬菌体展示肽的体液反应的工具。