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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.
Detection of CXCR4 (CD184) expression on CD19+ B cells by flow cytometry in patients of SLE, comparing its level in the development of lupus activity and pathogenic process of SLE internal organ involvement/ mucocutaneus and/or musculoskeletal involvement. Identify this correlation will be useful for clarifying other accessory factors to improve the diagnosis, better treatment strategy, follow up as well as prognosis for these patients
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| SLE cases in remission | according to SLE Disease Activity Index (SLEDAI) inactive disease will be considered as SLEDAI <5 | ||
| SLE cases in activity | according to SLE Disease Activity Index (SLEDAI) Active disease will be defined as SLEDAI ≥ 5 | ||
| Control group | Healthy age and sex matched subjects. |
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| Measure | Description | Time Frame |
|---|---|---|
| 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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Inclusion Criteria:
Exclusion Criteria:
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Study population will be classified into two group:
Then SLE group I patients will be subdivided according to the disease activity to three subgroups:
I. Group A: SLE cases in remission II. Group B: SLE cases in activity, but no internal organ involvement (i.e. only mucocutaneus and/or musculoskeletal involvement).
III. Group C: SLE cases in activity, and with internal organ involvement (renal, neuropsychiatric, hematological or cardiopulmonary).
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Asmaa A Ibrahim, Master | Contact | 01032138809 | smaibrahim2019@gmail.com | |
| Shereen Philip Aziz, Professor | Contact | 01033386104 |
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| Type | Date | Date Unknown |
|---|---|---|
| Release | Mar 6, 2024 | |
| Reset | Aug 14, 2024 |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Mar 6, 2024 | Aug 14, 2024 |
| ID | Term |
|---|---|
| D008180 | Lupus Erythematosus, Systemic |
| ID | Term |
|---|---|
| D003240 | Connective Tissue Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |
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patient's peripheral-blood mononuclear cells (PBMCs) will be isolated from heparinized venous blood