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Clinical Trials/NCT00368784
NCT00368784CompletedNot Applicable

T Cell Repertoire Analysis of Immune Mediated Skin Diseases

University of California, Davis1 site in 1 country426 target enrollmentStarted: January 2007Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
426
Locations
1
Primary Endpoint
Peripheral blood will be collected from adults ages 18-85.

Study Overview

Brief Summary

This study is designed to identify the cells of the immune system that cause skin disease such as psoriasis and mycosis fungoides. Blood samples from many patients will be compared in hopes of finding common cells and molecules responsible for skin diseases. Results of this study will increase our knowledge about immune mediated skin disease.

Detailed Description

The aim of the study is to characterized the T cell repertoire of individuals with immune mediated skin disease (e.g. psoriasis and mycosis fungoides). Peripheral blood with be collected from volunteers with psoriasis, mycosis fungoides and age matched controls. Fifteen tablespoons of blood will be collected prior to the initiation of treatment and again after the patient shows a clinical response to treatment. The time between blood draws will be no less than 3 months. There will be no more than two blood draws per patient. Blood samples will be used to determine the patient's HLA haplotype via PCR and DNA sequencing. After the patient's haplotype has been established the activated T cell repertoire will be analyzed for clonal expansions. Clonal expansions in the T cell repertoire will be determined by immunoscope analysis, which is a PCR based technique.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Have an immune mediated skin disease, such as psoriasis or mycosis fungoides
  • Are not taking immunosuppressive medications, which may interfere with T cell analysis.

Exclusion Criteria

  • are taking immunosuppressive medications, which may interfere with T cell analysis

Outcomes

Primary Outcomes

Peripheral blood will be collected from adults ages 18-85.

Time Frame: 2 Years

These samples will then be used for PCR analysis and T cell cloning.

Secondary Outcomes

  • T cell repertoire(2 Years)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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