多路复用
组织微阵列
免疫荧光
病理
免疫组织化学
一级和二级抗体
冰冻切片程序
抗体
染色
生物医学工程
生物
医学
免疫学
生物信息学
作者
Jeffrey Chun Tatt Lim,Joe Yeong,Chun Jye Lim,Clara Chong Hui Ong,Siew Cheng Wong,Valerie Chew,Syed Salahuddin Ahmed,Puay Hoon Tan,Jabed Iqbal
出处
期刊:Pathology
[Elsevier BV]
日期:2018-02-09
卷期号:50 (3): 333-341
被引量:79
标识
DOI:10.1016/j.pathol.2017.11.087
摘要
Multiplex immunofluorescence (mIF) allows simultaneous antibody-based detection and quantification of the expression of up to six markers, plus a nuclear counterstain, on a single tissue section. Recent studies have shown the potential for mIF to advance our understanding of complex disease processes, including cancer. It is important that the technique be standardised and validated to facilitate its transition into clinical use. Traditional approaches to mIF rely on manual processing of sections, which is time-consuming and a source of significant variation between samples/individuals. Here we determined if an automated diagnostic tissue stainer could be used for mIF incorporating tyramide signal amplification (TSA), and how the final image quality compared with sections stained semi-automatically or manually. Using tissue microarrays of fixed human breast tumour sections, we observed comparable antibody labelling between the diagnostic autostainer and manual technique. The diagnostic autostainer produced higher signal intensity with similar spectral unmixing efficiency. We also found that microwave treatment for antibody stripping during TSA labelling could be replaced by the heating option incorporated within the diagnostic-use autostainer. These data show that diagnostic autostainers used for traditional immunohistochemistry protocols can be readily adapted to achieve rapid preparation of high-quality sections using a TSA method for clinical mIF.
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