NKT-CSP/MICI: NKT Role in the Regulation of the Inflammatory Bowel Disease

Sponsor
University Hospital, Lille (Other)
Overall Status
Completed
CT.gov ID
NCT02884557
Collaborator
(none)
64
1
2
75.9
0.8

Study Details

Study Description

Brief Summary

Inflammatory bowel diseases (IBD) include Crohn's disease (CD) and ulcerative colitis (UC). These diseases are a public health problem because they concern many patients (1 case in 1000). IBDs are characterized by dysregulated immune response against luminal antigens causing chronic inflammation of the gut in genetically predisposed individuals. Their exact cause is unknown and there is currently no cure. The primary sclerosing cholangitis (PSC) is a liver inflammatory disease of unknown origin that is known to be strongly associated with IBD. An important clinical observation highlights the mild symptoms of IBD when associated to the PSC. Conversely, treating PSC by liver transplant or immunosuppressive drugs is associated with a progression of intestinal inflammation.

Based, on these clinical findings that suggest a protective effect regulator of liver inflammation on intestinal inflammation, and on the results obtained by our group in mouse models that identified the natural killer T cell (NKT) as essential in control of experimental colitis, the project aims to determine, using PCR, if the expression of NKT cell markers are increased in the colon of patients with PSC+IBD compared to patients with IBD alone or PSC alone.

Condition or Disease Intervention/Treatment Phase
  • Other: collection of gut biopsies collection of blood samples
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
64 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Evaluation of the Expression of Natural Killer T Cells (NKT) Marker in the Gut of Patients With Primary Sclerosing Cholangitis (PSC) Complicated by an Inflammatory Bowel Disease (IBD)
Actual Study Start Date :
May 1, 2013
Actual Primary Completion Date :
Aug 27, 2019
Actual Study Completion Date :
Aug 28, 2019

Arms and Interventions

Arm Intervention/Treatment
Other: PSC + IBD group

collection of gut biopsies collection of blood samples in patients with PSC and IBD

Other: collection of gut biopsies collection of blood samples
Four to eight colon biopsies will be sampled during endoscopy. Thirty milliliters of blood will be sampled.

Other: IBD alone group

collection of gut biopsies collection of blood samples in patients with IBD alone

Other: collection of gut biopsies collection of blood samples
Four to eight colon biopsies will be sampled during endoscopy. Thirty milliliters of blood will be sampled.

Outcome Measures

Primary Outcome Measures

  1. The increase in the expression of the NKT marker Valpha24 mRNA by PCR in the colon of patients with PSC alone, PSC + IBD compared to patients with IBD alone [Through study completion, an average of 1 year]

Secondary Outcome Measures

  1. The number of NKT infiltrating colonic biopsies, using immunohistochemical staining [Through study completion, an average of 1 year]

  2. The percentage of NKT cells among the peripheral blood lymphocytes by flow cytometry [At the time of the inclusion]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with PSC alone, IBD alone or PSC + IBD

  • Obtention of oral and written consent

  • Patients affiliated with the social security system

Exclusion Criteria:
  • Minor patient

  • Suspicion of malignant lesion of the colon

  • Inability for information

  • person unable to consent, and not benefiting from a legal protection regimen

  • Person deprived of liberty

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHRU, Hôpital Claude Huriez Lille France

Sponsors and Collaborators

  • University Hospital, Lille

Investigators

  • Principal Investigator: Pierre Desreumeaux, MD, PhD, University Hospital, Lille

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Lille
ClinicalTrials.gov Identifier:
NCT02884557
Other Study ID Numbers:
  • 2011_06
  • 2012-A00493-40
First Posted:
Aug 31, 2016
Last Update Posted:
Aug 27, 2020
Last Verified:
Mar 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 27, 2020