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Published on: October 14, 2021
Lymphocyte subpopulations in Sheehan's syndrome
Hulusi Atmaca1, Mehmet Araslı, Zihni Acar Yazıcı
1Department of Endocrinology and Metabolism, Ondokuz Mayis University Medical School, Kurupelit 55139, Samsun, Turkey. hatmaca@yahoo.com
Sheehan's syndrome patients show altered immune cell profiles, including higher CD3(+)DR(+) expression, suggesting ongoing inflammation. These changes may indicate immune dysregulation in pituitary dysfunction.
Area of Science:
- Endocrinology
- Immunology
- Clinical Medicine
Background:
- Sheehan's syndrome (pituitary dysfunction post-partum hemorrhage) has an unclear autoimmune link.
- Limited research exists on immunological alterations in Sheehan's syndrome patients.
- Investigating lymphocyte subsets can elucidate potential autoimmune involvement.
Purpose of the Study:
- To evaluate lymphocyte subsets in patients with Sheehan's syndrome.
- To compare immune cell profiles between Sheehan's syndrome patients and healthy controls.
- To explore correlations between immune alterations and disease duration.
Main Methods:
- Cross-sectional clinical study involving 15 Sheehan's syndrome patients and 25 healthy controls.
- Immunophenotyping of peripheral blood leukocytes using cytofluorometry.
- Analysis of various lymphocyte subsets, including CD3, CD4, CD8, CD19, CD16/56, CD25, and DR expression.
Main Results:
- Sheehan's patients had significantly higher leucocyte counts, CD3(+)DR(+) expression, CD8(+)28(+) cells, CD4(+)CD25(+) cells, and CD3(+)DR(+)/CD3 ratio compared to controls.
- Patients exhibited lower percentages of CD3, CD4, and a lower CD4/CD8 ratio.
- A positive correlation was found between illness duration and CD3(+)DR(+) expression (r=0.53, p=0.03).
Conclusions:
- Peripheral lymphocyte subsets show significant variations in Sheehan's syndrome patients, suggesting altered immune regulation.
- Elevated CD3(+)DR(+) expression, correlating with illness duration, indicates persistent inflammation in Sheehan's syndrome.
- The precise role of these cellular alterations in the cause or consequence of pituitary deficiency remains to be determined.
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