Peripheral Lymphocytes of Patients with Inflammatory Bowel Disease Have Altered Concentrations of Key Apoptosis Players: Preliminary Results
Open Access
- 1 November 2018
- journal article
- research article
- Published by Wiley in BioMed Research International
- Vol. 2018, 1-10
Abstract
Notwithstanding uncertain pathogenesis of inflammatory bowel disease (IBD), deregulation of adaptive immunity is paramount for the development of inflammation. Essential role in the resolution of inflammation is played by apoptosis, deregulated in lymphocytes isolated from inflamed intestine. Despite IBD being a systemic disease, little is known about apoptosis of peripheral lymphocytes. The concentrations of Bcl-2, cytochrome c, p53, and caspase-9 were determined (ELISA) in lymphocyte-enriched fractions of peripheral blood mononuclear cells (LE-PBMCs) from 64 individuals (42 with IBD) and related to IBD phenotype and activity, treatment, and inflammatory and hematological indices. The diagnostic potential of evaluated markers was determined as well. All evaluated molecules were significantly lower in IBD patients, of which cytochrome c and p53 were significantly lower exclusively in patients with Crohn’s disease (CD) and cytochrome c differed significantly between CD and ulcerative colitis (UC). Caspase 9 was significantly lower in active IBD and Bcl-2 in active UC whereas cytochrome c was higher in active CD. Treatment with corticosteroids affected the concentrations of cytochrome c and p53. Both positively correlated with hsCRP and the concentrations of all markers were interrelated. As IBD markers, Bcl-2 and caspase-9 displayed good accuracy and, as a panel of markers with cytochrome c, their accuracy was excellent (92%). As CD markers Bcl-2, cytochrome c, and p53 displayed fair accuracy but combined determination of Bcl-2 and cytochrome c improved the accuracy to 85%. Taken together, our results imply diminished intrinsic apoptotic capacity of LE-PBMCs in IBD but an upregulation of proapoptotic features parallel to increasing severity of inflammation. Observed abnormalities in intrinsic pathway of apoptosis are more pronounced in CD. Upon positive validation on a larger set of patients, combined quantification of Bcl-2 and cytochrome c might be considered as an adjunct in differential diagnosis of UC and CD of colon and rectum.Keywords
Funding Information
- Wroclaw Medical University (ST-906)
This publication has 48 references indexed in Scilit:
- Enhanced Blood Lymphocytes Apoptosis in Children with Inflammatory Bowel DiseaseISRN Gastroenterology, 2013
- Immunopathogenesis of inflammatory bowel diseaseSelf/Nonself, 2010
- Role of Cytochrome c in Apoptosis: Increased Sensitivity to Tumor Necrosis Factor Alpha Is Associated with Respiratory Defects but Not with Lack of Cytochrome c ReleaseMolecular and Cellular Biology, 2007
- Crohn’s Disease Activity Index and Vienna Classification – Is It Worthwhile to Calculate before Surgery?Digestive Surgery, 2006
- Apoptosis of T cells and the control of inflammatory bowel disease: therapeutic implicationsGut, 2006
- Infliximab for Induction and Maintenance Therapy for Ulcerative ColitisNew England Journal of Medicine, 2005
- Divergent cell cycle kinetics underlie the distinct functional capacity of mucosal T cells in Crohn’s disease and ulcerative colitisGut, 2004
- Decreased Bax expression by mucosal T cells favours resistance to apoptosis in Crohn's diseaseGut, 2001
- Cytochrome c Deficiency Causes Embryonic Lethality and Attenuates Stress-Induced ApoptosisCell, 2000
- Cortisone in Ulcerative ColitisBMJ, 1955