Adler Michael, Wacker Ron, Niemeyer Christof M
Chimera Biotec GmbH, Emil-Figge-Str. 76 A, D-44227, Dortmund, Germany.
Analyst. 2008 Jun;133(6):702-18. doi: 10.1039/b718587c. Epub 2008 Apr 2.
The versatility of immunoassays for the detection of antigens can be combined with the signal amplification power of nucleic acid amplification techniques in a broad range of innovative detection strategies. This review summarizes the spectrum of both, DNA-modification techniques used for assay enhancement and the resulting key applications. In particular, it focuses on the highly sensitive immuno-PCR (IPCR) method. This technique is based on chimeric conjugates of specific antibodies and nucleic acid molecules, the latter of which are used as markers to be amplified by PCR or related techniques for signal generation and read-out. Various strategies for the combination of antigen detection and nucleic acid amplification are discussed with regard to their laboratory analytic performance, including novel approaches to the conjugation of antibodies with DNA, and alternative pathways for signal amplification and detection. A critical assessment of advantages and drawbacks of these methods for a number of applications in clinical diagnostics and research is conducted. The examples include the detection of viral and bacterial antigens, tumor markers, toxins, pathogens, cytokines and other targets in different biological sample materials.
免疫测定法检测抗原的多功能性可与核酸扩增技术的信号放大能力相结合,应用于广泛的创新检测策略中。本综述总结了用于检测增强的DNA修饰技术及其产生的关键应用。特别关注高灵敏度的免疫PCR(IPCR)方法。该技术基于特异性抗体与核酸分子的嵌合缀合物,核酸分子用作标记物,通过PCR或相关技术进行扩增以产生和读取信号。讨论了抗原检测与核酸扩增相结合的各种策略及其实验室分析性能,包括抗体与DNA缀合的新方法,以及信号放大和检测的替代途径。对这些方法在临床诊断和研究中的多种应用的优缺点进行了批判性评估。实例包括在不同生物样品材料中检测病毒和细菌抗原、肿瘤标志物、毒素、病原体、细胞因子及其他靶点。