Aghdaei Hamid Asadzadeh, Kadijani Azade Amini, Sorrentino Dario, Mirzaei Alireza, Shahrokh Shabnam, Balaii Hedieh, Geraci Marco, Zali Mohammad Reza
Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
IBD Center, Virginia Tech Carilion School of Medicine, Roanoke, VA, USA.
United European Gastroenterol J. 2018 Aug;6(7):1074-1081. doi: 10.1177/2050640618774637. Epub 2018 May 2.
Predicting the response of inflammatory bowel disease (IBD) patients to infliximab (IFX) is an unmet clinical need. The expression and density of transmembrane tumor necrosis factor-α in circulating leukocytes maybe directly related to response by promoting apoptosis.
We tested the hypothesis that direct apoptosis assessment by real-time polymerase chain reaction evaluation of pro-apoptotic (Bax) and anti-apoptotic (Bcl-2) proteins in peripheral blood mononuclear cells (PBMCs) might be associated with response to IFX.
IFX naïve patients (Crohn's disease, 32 and ulcerative colitis, 20; 35 responders and 17 non-responders) were evaluated for Bax and Bcl-2 mRNA expression levels before and 2 weeks after the first infusion. In a subset of patients, apoptosis was also evaluated using flow cytometry.
After the first infusion, Bax increased more in responders than in non-responders (0.7± 0.38 vs 0.81 ± 0.32 and 0.86 ± 0.37 vs 0.87 ± 0.45, respectively, = 0.071). Bcl-2 decreased more in responders than in non-responders (0.71 ± 0.12 vs 0.63 ± 0.13 and 0.81 ± 0.28 vs 0.77 ± 0.27, respectively, = 0.038). The Bax/Bcl-2 ratio increased more in responders than in non-responders (0.99 ± 0.5 vs 1.3 ± 0.51 and 1.03 ± 0.17 vs 1.1 ± 0.28, respectively, = 0.005). The Bax/Bcl-2 ratio was able to predict response in 33/52 patients and was correlated to flow cytometry-assessed apoptosis ( = 0.911; < 0.001).
An increased Bax/Bcl-2 ratio in PBMCs was associated with therapeutic response to IFX in IBD patients.
预测炎症性肠病(IBD)患者对英夫利昔单抗(IFX)的反应是一项尚未满足的临床需求。循环白细胞中跨膜肿瘤坏死因子-α的表达和密度可能通过促进细胞凋亡与反应直接相关。
我们检验了以下假设,即通过实时聚合酶链反应评估外周血单个核细胞(PBMC)中促凋亡蛋白(Bax)和抗凋亡蛋白(Bcl-2)来直接评估细胞凋亡可能与对IFX的反应相关。
对初治IFX的患者(克罗恩病32例、溃疡性结肠炎20例;35例反应者和17例无反应者)在首次输注前及输注后2周评估Bax和Bcl-2 mRNA表达水平。在一部分患者中,还使用流式细胞术评估细胞凋亡。
首次输注后,反应者的Bax升高幅度大于无反应者(分别为0.7±0.38对0.81±0.32以及0.86±0.37对0.87±0.45,P = 0.071)。反应者的Bcl-2降低幅度大于无反应者(分别为0.71±0.12对0.63±0.13以及0.81±0.28对 0.77±0.27,P = 0.038)。反应者的Bax/Bcl-2比值升高幅度大于无反应者(分别为0.99±0.5对1.3±0.51以及1 .03±0.17对1.1±0.28,P = 0.005)。Bax/Bcl-2比值能够在52例患者中的33例中预测反应,并且与流式细胞术评估的细胞凋亡相关(P = 0.911;P<0.001)。
PBMC中Bax/Bcl-2比值升高与IBD患者对IFX的治疗反应相关。