Role of Altered CD40-Ligand Gene Transcription in Systemic Lupus Erythematosus
Sponsor
National Center for Research Resources (NCRR) (NIH)
Overall Status
Unknown status
CT.gov ID
NCT00008749
Collaborator
Arthritis Foundation (Other)
1
Study Details
Study Description
Brief Summary
Systemic lupus erythematosus is an often devastating autoimmune disease which affects 1 in 2,000 women in the United States. Recently, several research laboratories have reported that a protein, named CD40-ligand (CD154), is overexpressed by a subset of white blood cells, called lymphocytes, in patients with lupus. Expression of CD154 appears critical to the generation of antibodies that cause disease in lupus. Blocking CD154 interactions in the immune system has been shown to decrease disease activity in animal models of lupus. We propose to study the regulation of CD154 in patients with lupus in hopes of inhibiting its abnormal and deleterious expression.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Observational Model:
Case-Control
Official Title:
Role of Altered CD40-Ligand Gene Transcription in Systemic Lupus Erythematosus
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
13 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion:
A diagnosis of systemic lupus erythematosus
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Children's Hospital of Philadelphia | Philadelphia | Pennsylvania | United States | 19104-4318 |
Sponsors and Collaborators
- National Center for Research Resources (NCRR)
- Arthritis Foundation
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT00008749
Other Study ID Numbers:
- NCRR-M01RR00240-1736
First Posted:
Jan 18, 2001
Last Update Posted:
Jun 24, 2005
Last Verified:
Dec 1, 2003
Additional relevant MeSH terms: