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Isolation of CD4+ T-cells and Analysis of Circulating T-follicular Helper (cTfh) Cell Subsets from Peripheral Blood Using 6-color Flow Cytometry
Published on: January 7, 2019
Relationship between T lymphocyte subsets and cortisol in systemic lupus erythematosus
1Department of Biochemistry, Basic Medical Science Block, Panjab University, Chandigarh, India.
Kathmandu University Medical Journal (KUMJ)
|January 15, 2010
Summary
Low cortisol and high CD8(+) T cells are linked to Systemic Lupus Erythematosus (SLE) disease activity in North India. These factors may play a role in the development of SLE.
Area of Science:
- Immunology
- Endocrinology
- Rheumatology
Background:
- Systemic Lupus Erythematosus (SLE) is a chronic autoimmune disease marked by heightened B cell activity and aberrant T cell function.
- Understanding the interplay of immune cells and hormones is crucial for managing SLE.
Purpose of the Study:
- To examine the association between T lymphocyte subsets, serum cortisol levels, and disease activity in North Indian SLE patients.
- To identify potential biomarkers for SLE progression and severity.
Main Methods:
- Flow cytometry was used to quantify CD4(+) and CD8(+) T cell percentages in SLE patients and healthy controls.
- Serum cortisol levels were measured using enzyme-linked immunosorbent assay (ELISA).
Main Results:
- SLE patients exhibited significantly lower CD4(+) T cells and higher CD8(+) T cells compared to controls.
- A reduced CD4(+)/CD8(+) T cell ratio and lower serum cortisol were observed in SLE patients.
- CD8(+) T cell counts and the CD4(+)/CD8(+) ratio correlated with SLE disease activity scores (SLEDAI) and erythrocyte sedimentation rate (ESR).
Conclusions:
- Low serum cortisol and elevated CD8(+) T cell percentages are implicated in the pathogenesis of SLE.
- These findings suggest potential therapeutic targets for managing SLE.
- Further research is warranted to elucidate the precise mechanisms involved.
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