Systemic Lupus Erythematosus Clinical Trial
Official title:
Study of CD184 in Systemic Lupus Erythematosus
NCT number | NCT04799730 |
Other study ID # | Soh-Med-21-03-01 |
Secondary ID | |
Status | Not yet recruiting |
Phase | |
First received | |
Last updated | |
Start date | May 2021 |
Est. completion date | May 2022 |
The objective of this study is to estimate the possible role of CD184 in the pathogenesis of SLE; comparing its level among SLE cases to healthy controls.
Status | Not yet recruiting |
Enrollment | 100 |
Est. completion date | May 2022 |
Est. primary completion date | November 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 16 Years to 60 Years |
Eligibility | Inclusion Criteria: - Confirmed SLE patients diagnosed and fulfilled the SLE classification criteria according to the 2019 ACR/EULAR classification criteria for SLE (Aringer et al., 2019) - Willing and agreed to be included in the study. Exclusion Criteria: - Childhood SLE. - SLE-patients will refuse to consent to this study. - Other autoimmune diseases. - Known or suspected malignancies, especially B cell lymphoma. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Sohag University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | changes in the expression of CD184(CXCR4) expression in circulating B cells | Flow cytometry analysis of chemokine receptor (CXCR4):Human peripheral-blood mononuclear cells (PBMCs) labeling with CXCR4 antibody will be performed in the same day after taking blood samples and subsequent measurement of the CXCR4 mean fluorescence intensity (MFI) by flow cytometry. MFI of the anti-chemokine receptor (CXCR4) staining will be calculated according to statistical thresholds set in reference to staining with negative control antibodies. The patient's CXCR4 on CD19+ B cells expression or mean MFI will be further compared to the MFI of the simultaneously performed age-matched controls samples and other subgroups of SLE patients. | 6 months |
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