Algaba Alicia, Linares Pablo M, Encarnación Fernández-Contreras M, Figuerola Ariadna, Calvet Xavier, Guerra Iván, de Pousa Inés, Chaparro María, Gisbert Javier P, Bermejo Fernando
*Department of Gastroenterology, Hospital Universitario de Fuenlabrada, Madrid, Spain; †Gastroenterology Unit, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa, Madrid, Spain; ‡Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas, Madrid, Spain; §Gastroenterology Unit, Hospital de Sabadell, Institut Parc Taulí, Sabadell, Barcelona, Spain; and ‖Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas, Barcelona, Spain.
Inflamm Bowel Dis. 2014 Apr;20(4):695-702. doi: 10.1097/MIB.0000000000000004.
Infliximab and adalimumab effectiveness might be related with changes in angiogenic factors. The aim of the study was to compare the concentrations of angiogenic proteins in patients with inflammatory bowel disease (IBD) and healthy controls and to analyze changes in the levels during infliximab and adalimumab treatment.
A prospective case-control study was conducted in 37 patients with IBD starting treatment with infliximab (16 with Crohn's disease and 6 with ulcerative colitis) or adalimumab (15 with Crohn's disease) and 40 control subjects. Four samples were taken from IBD patients, one before each of the first 3 doses of infliximab/adalimumab and one at week 14. Serum levels of vascular endothelial growth factor (VEGF), placental growth factor, angiopoietin 1 (Ang1), angiopoietin 2, and Tie2 were measured using enzyme-linked immunosorbent assay.
Patients with IBD had higher VEGF levels than control subjects (511.5 ± 255.6 versus 395.5 ± 256.4; P = 0.05). Patients who achieved remission at the third dose of anti-TNF-alpha had lower VEGF levels at baseline (453.5 ± 250.7 versus 667.5 ± 153.9 pg/mL) and before the second (409.7 ± 217 versus 681.3 ± 350.6 pg/mL) and third (400.5 ± 222.8 versus 630.4 ± 243.1 pg/mL) doses compared with those with no remission (P < 0.05). Ang1 levels decreased before each treatment dose in patients who achieved remission (P < 0.05). High baseline VEGF levels predicted for a poor response to anti-TNF-alpha therapy (area under the receiver operating characteristics curve = 0.8), whereas high Ang1 levels were associated with disease remission (area under the receiver operating characteristics curve = 0.7). Concentrations of angiogenic proteins did not correlate with clinical activity scores.
Circulating VEGF and Ang1 levels decrease after anti-TNF-alpha therapy and may predict response to treatment. Whether these changes are a direct effect of anti-TNF-alpha therapy or a sign of disease improvement remains to be elucidated.
英夫利昔单抗和阿达木单抗的疗效可能与血管生成因子的变化有关。本研究的目的是比较炎症性肠病(IBD)患者和健康对照者血管生成蛋白的浓度,并分析英夫利昔单抗和阿达木单抗治疗期间这些水平的变化。
对37例开始接受英夫利昔单抗治疗(16例克罗恩病患者和6例溃疡性结肠炎患者)或阿达木单抗治疗(15例克罗恩病患者)的IBD患者及40名对照者进行了一项前瞻性病例对照研究。从IBD患者身上采集4份样本,在首次3剂英夫利昔单抗/阿达木单抗给药前各采集1份,在第14周采集1份。采用酶联免疫吸附测定法检测血清血管内皮生长因子(VEGF)、胎盘生长因子、血管生成素1(Ang1)、血管生成素2和Tie2的水平。
IBD患者的VEGF水平高于对照者(511.5±255.6对395.5±256.4;P=0.05)。在第三次给予抗TNF-α时达到缓解的患者在基线时(453.5±250.7对667.5±153.9 pg/mL)以及在第二次(409.7±217对681.3±350.6 pg/mL)和第三次(400.5±222.8对630.4±243.1 pg/mL)给药前的VEGF水平低于未缓解的患者(P<0.05)。达到缓解的患者在每次治疗剂量前Ang1水平均下降(P<0.05)。高基线VEGF水平预示着对抗TNF-α治疗反应不佳(受试者工作特征曲线下面积=0.8),而高Ang1水平与疾病缓解相关(受试者工作特征曲线下面积=0.7)。血管生成蛋白的浓度与临床活动评分无关。
抗TNF-α治疗后循环VEGF和Ang1水平下降,可能预测治疗反应。这些变化是抗TNF-α治疗的直接作用还是疾病改善的迹象仍有待阐明。