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Updated: Nov 6, 2025

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Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture
Published on: April 8, 2016
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CORRELATION OF CD4+Т LYMPHOCYTES ACTIVATION WITH INTERLEUKIN IL-9, IL-17, IL- 22 PROFILES IN THE PERIPHERAL BLOOD OF
N Mitskevich1, T Tsertsvadze1, N Maisuradze1
11Ivane Javakhishvili Tbilisi State University, Division of Immunology and Microbiology; Georgia.
Georgian Medical News
|May 8, 2021
Summary
Psoriasis patients show altered T cell profiles, with decreased IL-9 and IL-17 in peripheral blood, suggesting cell migration to skin lesions. This impacts the IL-23/Th17 immune axis in chronic skin inflammation.
Area of Science:
- Immunology
- Dermatology
- Cell Biology
Background:
- Psoriasis is a T cell-mediated chronic inflammatory skin disease.
- The IL-23/Th17 immune axis is central to psoriasis pathogenesis.
- Th1, Th17, Th22, and Th9 cells are implicated in psoriasis inflammation and memory.
Purpose of the Study:
- To evaluate T cell profiles and the IL-23/Th17 axis in moderate to severe plaque psoriasis.
- To assess levels of IL-17A, IL-22, and IL-9 in peripheral blood of psoriasis patients.
- To analyze the expression of the T helper cell activation marker CD69.
Main Methods:
- Compared peripheral blood from psoriasis patients (n=18) with healthy controls (n=15).
- Measured IL-17A, IL-22, and IL-9 levels using flow cytometry (FACScan).
- Assessed CD69 expression on T helper cells.
Main Results:
- Reduced CD4+ T cell expression and decreased CD69 activation marker expression in psoriasis patients.
- Significantly increased IL-22 levels observed in psoriasis patients.
- Decreased IL-9 and IL-17 levels in peripheral blood Th cells of psoriasis patients.
Conclusions:
- Peripheral blood T cell profiles and IL-23/Th17 axis activity differ significantly in psoriasis patients compared to controls.
- Lower IL-9 and IL-17 in peripheral blood suggest their mobilization to psoriatic skin lesions.
- These findings highlight altered immune cell dynamics in psoriasis pathogenesis.
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