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Differential EBI2 Expression Upon Allelic Status of the rs9557195 Polymorphism

Differential EBI2 Expression Upon Allelic Status of the rs9557195 Polymorphism

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03633409
Enrollment
340
Registered
2018-08-16
Start date
2017-11-01
Completion date
2018-12-01
Last updated
2018-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammatory Bowel Diseases

Keywords

IBD, EBI2, G protein coupled receptor, FACS, UBAC2, lymphocyte migration, single nucleotide polymorphism

Brief summary

EBI2 is a risk gene for inflammatory bowel diseases (rs9557195). Patients of the Swiss IBD cohort study have been genotyped for the allelic status of EBI2. The investigators will test the influence of rs9557195 genoty (TT or CC allel), inflammatory activity and current treatment (infliximab vs. vedolizumab) on expression and activity of EBI2 on blood lymphocytes, mRNA expression of EBI2 and UBAC2 (located on the opposite DNA strand of EBI2) and activity of lymphocytes on a migraton assay.

Detailed description

EBI2 is a risk gene for inflammatory bowel diseases (rs9557195). EBI2 is a G protein coupled receptors expressed on the immune cells. EBI2 directs migration and activity of immune cells. Patients of the Swiss IBD cohort study have been genotyped for the allelic status of EBI2. The investigators will recruit patients with Crohn's disease and ulcerative colitis, assess epidemiological and clinical parameters (including clinical activity of IBD) draw blood, isolate lymphocytes, DNA and RNA. The investigators will test the influence of rs9557195 genotype (TT or CC allel), inflammatory activity and current treatment (infliximab vs. vedolizumab) on expression and activity of EBI2 on blood lymphocytes (by FACS using an EBI2-antibody), mRNA expression (by qPCR) of EBI2 and UBAC2 (located on the opposite DNA strand of EBI2) and activity of lymphocytes on a migration assay.

Interventions

None listed

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years

Inclusion criteria

* Patient with IBD OR healthy volunteer * No major uncontrolled medical/ surgical/ psychiatric condition requiring ongoing management besides IBD in the respective study groups. Well controlled conditions (i.e. medically controlled arterial hypertension, occupational asthma) may be present

Exclusion criteria

none

Design outcomes

Primary

MeasureTime frameDescription
EBI2 expression - dependent on rs9557195 allele status (FACS)at time of inclusion into the studyEBI2 levels in PBMCs will be determined by FACS, and compared according to allele status of rs9557195

Secondary

MeasureTime frameDescription
EBI2 expression - dependent on rs9557195 allele status (RT-PCR)at time of inclusion into the studyEBI2 levels in PBMCs will be determined by RT-PCR, and compared according to EBI2 levels in PBMCs will be determined by RT-PCR, and compared according to allele status of rs9557195
UBAC2 expression - dependent on rs9557195 allele status (RT-PCR)at time of inclusion into the studyUBAC2 levels in PBMCs will be determined by RT-PCR, and compared according to 2 levels in PBMCs will be determined by RT-PCR, and compared according to allele status of rs9557195
Motility of PBMCs dependent on rs9557195 allele status (Boyden chamber)at time of inclusion into the studymotility of PBMCs will be assessed using the Boyden chamber and compared according to allele status of rs9557195
EBI2-expression (FACS) in individuals treated with infliximab vs. vedolizumabat time of inclusion into the studyWe will compare EBI2 expression as determined by FACS in individuals with infliximab and vedolizumab treatment
EBI2-expression (FACS) according to gut inflammationat time of inclusion into the studyWe will compare EBI2 expression (determined by FACS) in IBD patients with severe disease, in remission and in healthy volunteers

Countries

Switzerland

Contacts

Primary ContactBenjamin Misselwitz, MD
benjamin.misselwitz@usz.ch+41 44 255 1111
Backup ContactRene Roth, MD
rene.roth@usz.ch+41 44 255 1111

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026