90K/Mac-2 BP Is a New Predictive Biomarker of Response to Infliximab Therapy in IBD Patients

被引:4
作者
Pesole, Pasqua Letizia [1 ]
Liso, Marina [1 ]
Donghia, Rossella [1 ]
Guerra, Vito [1 ]
Lippolis, Antonio [1 ]
Mastronardi, Mauro [1 ]
Iacovazzi, Palma Aurelia [1 ]
机构
[1] Natl Inst Gastroenterol IRCCS Saverio de Bellis, I-70013 Castellana Grotte, Italy
关键词
inflammatory bowel disease; 90K; Mac-2; BP; galectin-3 binding protein; infliximab; biological drug; biomarkers; Crohn's disease; ulcerative colitis; INFLAMMATORY-BOWEL-DISEASE; FECAL CALPROTECTIN; CROHNS-DISEASE; TROUGH LEVELS; ANTI-TNF; DRUG; SERUM; GLYCOPROTEIN; LEVEL;
D O I
10.3390/ijms24043955
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inflammatory bowel diseases (IBD), comprising Crohn's disease (CD) and Ulcerative Colitis (UC), are multifactorial disorders characterized by a chronic inflammatory status with the secretion of cytokines and immune mediators. Biologic drugs targeting pro-inflammatory cytokines, such as infliximab, are broadly used in the treatment of IBD patients, but some patients lose responsiveness after an initial success. The research into new biomarkers is crucial for advancing personalized therapies and monitoring the response to biologics. The aim of this single center, observational study is to analyze the relationship between serum levels of 90K/Mac-2 BP and the response to infliximab, in a cohort of 48 IBD patients (30 CD and 18 UC), enrolled from February 2017 to December 2018. In our IBD cohort, high 90K serum levels were found at baseline in patients who then developed anti-infliximab antibodies at the fifth infusion (22 weeks after the first), becoming non-responders (9.76 +/- 4.65 mu g/mL compared to 6.53 +/- 3.29 mu g/mL in responder patients, p = 0.005). This difference was significant in the total cohort and in CD, but not significant in UC. We then analyzed the relationship between serum levels of 90K, C-reactive protein (CRP), and Fecal calprotectin. A significant positive correlation was found at baseline between 90K and CRP, the most common serum inflammation marker (R = 0.42, p = 0.0032). We concluded that circulating 90K could be considered a new non-invasive biomarker for monitoring the response to infliximab. Furthermore, 90K serum level determination, before the first infliximab infusion, in association with other inflammatory markers such as CRP, could assist in the choice of biologics for the treatment of IBD patients, thereby obviating the need for a drug switch due to loss of response, and so improving clinical practice and patient care.
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