Nottingham Digestive Diseases Biomedical Research Unit, Queen's Medical Centre, Nottingham, NG7 2UH, UK.
J Immunol Methods. 2013 Aug 30;394(1-2):1-9. doi: 10.1016/j.jim.2013.04.009. Epub 2013 May 1.
Sensitive measurement of multiple cytokine profiles from small mucosal tissue biopsies, for example human gastric biopsies obtained through an endoscope, is technically challenging. Multiplex methods such as Luminex assays offer an attractive solution but standard protocols are not available for tissue samples. We assessed the utility of three commercial Luminex kits (VersaMAP, Bio-Plex and MILLIPLEX) to measure interleukin-17A (IL-17) and interferon-gamma (IFNγ) concentrations in human gastric biopsies and we optimised preparation of mucosal samples for this application. First, we assessed the technical performance, limits of sensitivity and linear dynamic ranges for each kit. Next we spiked human gastric biopsies with recombinant IL-17 and IFNγ at a range of concentrations (1.5 to 1000 pg/mL) and assessed kit accuracy for spiked cytokine recovery and intra-assay precision. We also evaluated the impact of different tissue processing methods and extraction buffers on our results. Finally we assessed recovery of endogenous cytokines in unspiked samples. In terms of sensitivity, all of the kits performed well within the manufacturers' recommended standard curve ranges but the MILLIPLEX kit provided most consistent sensitivity for low cytokine concentrations. In the spiking experiments, the MILLIPLEX kit performed most consistently over the widest range of concentrations. For tissue processing, manual disruption provided significantly improved cytokine recovery over automated methods. Our selected kit and optimised protocol were further validated by measurement of relative cytokine levels in inflamed and uninflamed gastric mucosa using Luminex and real-time polymerase chain reaction. In summary, with proper optimisation Luminex kits (and for IL-17 and IFNγ the MILLIPLEX kit in particular) can be used for the sensitive detection of cytokines in mucosal biopsies. Our results should help other researchers seeking to quantify multiple low concentration cytokines in small tissue samples.
从小的黏膜组织活检中敏感地测量多种细胞因子谱,例如通过内窥镜获得的人类胃活检,在技术上具有挑战性。多指标方法,如 Luminex 分析,提供了一个有吸引力的解决方案,但标准方案不适用于组织样本。我们评估了三种商业 Luminex 试剂盒(VersaMAP、Bio-Plex 和 MILLIPLEX)用于测量人类胃活检中白细胞介素-17A(IL-17)和干扰素-γ(IFNγ)浓度的效用,并优化了这种应用中黏膜样本的制备。首先,我们评估了每个试剂盒的技术性能、灵敏度极限和线性动态范围。接下来,我们在一系列浓度(1.5 至 1000 pg/mL)下用重组白细胞介素-17 和干扰素-γ对人类胃活检进行了加标,并评估了试剂盒对加标细胞因子回收率和内测定精密度的准确性。我们还评估了不同组织处理方法和提取缓冲液对我们结果的影响。最后,我们评估了未加标样本中内源性细胞因子的恢复情况。在灵敏度方面,所有试剂盒在制造商推荐的标准曲线范围内都表现良好,但 MILLIPLEX 试剂盒在低细胞因子浓度下提供了最一致的灵敏度。在加标实验中,MILLIPLEX 试剂盒在最宽的浓度范围内表现最一致。对于组织处理,手动破坏比自动方法提供了显著提高的细胞因子恢复。我们选择的试剂盒和优化的方案进一步通过使用 Luminex 和实时聚合酶链反应测量炎症和非炎症胃黏膜中的相对细胞因子水平进行了验证。总之,通过适当的优化,Luminex 试剂盒(特别是对于 IL-17 和 IFNγ,MILLIPLEX 试剂盒)可用于敏感检测黏膜活检中的细胞因子。我们的结果应该有助于其他研究人员定量分析小组织样本中的多种低浓度细胞因子。