Breidert Matthias, Eftekhari Pierre, Louis François, Rotoiu Claudia, Rath Timo, Neurath Markus F, Atreya Raja
Department of Gastroenterology and Hepatology, City Hospital Waid and Triemli, Zürich, Switzerland.
Inoviem Scientific, BIOPARC 3, Illkirch-Graffenstaden, France.
Crohns Colitis 360. 2020 Apr;2(2):otaa037. doi: 10.1093/crocol/otaa037. Epub 2020 May 24.
We applied for the first time 2 label-free technologies, physiological intermolecular modulation spectroscopy (PIMS) and nematic protein organization technic (NPOT) in anti-tumor necrosis factor (TNF) refractory inflammatory bowel disease (IBD) patients to identify clinical responders to vedolizumab therapy and elucidate their underlying functional molecular network.
PIMS analysis was performed in peripheral blood taken prior to the first vedolizumab application in 20 IBD patients (Crohn disease n = 13; ulcerative colitis n = 7) refractory to at least 1 previous anti-TNF agent therapy. Peripheral blood taken from clinical responders and nonresponders at week 14 of vedolizumab therapy were additionally subjected to NPOT analysis. Response to therapy was assessed by respective clinical disease activity scores (partial Mayo Score and Harvey-Bradshaw Index).
Clinical response to vedolizumab treatment was observed in 7 of 13 Crohn disease and 4 of 7 ulcerative colitis patients at week 14. Response to therapy was accurately predicted by PIMS blood analysis in 100% of ulcerative colitis and 77% of Crohn disease patients. Overall prediction of clinical response with PIMS blood analysis was achieved with a 89% positive predictive value and a 82% negative predictive value. NPOT analysis revealed the heightened expression of the proteins ITGB7, ITGAV, ITG3, PF4, and ASGH in the peripheral blood of vedolizumab responders compared to nonresponders.
PIMS analysis of the blood of anti-TNF refractory IBD patients was able to stratify responders to vedolizumab therapy with high accuracy and specificity. NPOT technology could decipher underling molecular networks in the blood of responders, enabling subsequent personalized therapeutic approaches in IBD.
我们首次将两种无标记技术,即生理分子间调制光谱法(PIMS)和向列型蛋白质组织技术(NPOT)应用于抗肿瘤坏死因子(TNF)难治性炎症性肠病(IBD)患者,以识别维多珠单抗治疗的临床反应者并阐明其潜在的功能分子网络。
对20例IBD患者(克罗恩病n = 13;溃疡性结肠炎n = 7)进行了PIMS分析,这些患者对至少1种先前的抗TNF药物治疗无效,样本为首次使用维多珠单抗前采集的外周血。在维多珠单抗治疗第14周时,从临床反应者和无反应者采集的外周血还进行了NPOT分析。通过各自的临床疾病活动评分(部分梅奥评分和哈维-布拉德肖指数)评估治疗反应。
在第14周时,13例克罗恩病患者中有7例、7例溃疡性结肠炎患者中有4例对维多珠单抗治疗有临床反应。PIMS血液分析在100%的溃疡性结肠炎患者和77%的克罗恩病患者中准确预测了治疗反应。PIMS血液分析对临床反应的总体预测阳性预测值为89%,阴性预测值为82%。NPOT分析显示,与无反应者相比,维多珠单抗反应者外周血中ITGB7、ITGAV、ITG3、PF4和ASGH蛋白的表达升高。
对TNF难治性IBD患者血液进行PIMS分析能够以高精度和特异性对维多珠单抗治疗的反应者进行分层。NPOT技术可以解读反应者血液中的潜在分子网络,从而在IBD中实现后续的个性化治疗方法。