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Immunomodulating Effects Depend on Prolactin Levels in Patients with Hyperprolactinemia
Lea Ewerman1, Eva Landberg2, Sandra Hellberg3
1Department of Endocrinology, and Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden.
Non-pregnancy related hyperprolactinemia alters immune markers. Moderate prolactin increases Th2/Th17 chemokines and B cell attraction, but very high levels normalize these, with high prolactin decreasing T-helper cell activation in vitro.
Area of Science:
- Immunology
- Endocrinology
Background:
- Prolactin influences immune cells via prolactin receptors.
- Chemokines shape T helper (Th) cell responses.
- Hyperprolactinemia (elevated prolactin) may impact immune function.
Purpose of the Study:
- To investigate the association between non-pregnancy related hyperprolactinemia and circulating levels of chemokines and immunological markers.
- To assess potential dose-dependent effects of prolactin on immune responses.
Main Methods:
- Cross-sectional study comparing 35 hyperprolactinemia patients with 102 healthy controls.
- Assessed serum levels of Th1, Th2, Th17 chemokines (CCL22, CXCL1), B cell chemokine (CXCL13), C-reactive protein, and immunoglobulins.
- Utilized an in vitro model to evaluate prolactin's effect on T-helper cell activation.
Main Results:
- Hyperprolactinemia group showed significantly higher levels of CCL22, CXCL1, CXCL13, and C-reactive protein compared to controls.
- These markers positively correlated with prolactin levels.
- Differences were observed at low/moderate hyperprolactinemia but not at high levels (>3600 mU/l).
- In vitro studies indicated prolactin increased T-helper cell activation at moderate levels but decreased it at high levels.
Conclusions:
- Hyperprolactinemia exhibits immunomodulatory effects, increasing Th2/Th17-associated chemokines and B cell attraction markers.
- A threshold effect exists, with very high prolactin levels not showing these elevations.
- In vitro data suggest a biphasic effect of prolactin on T-helper cell activation, potentially explaining the in vivo findings.
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