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Altered circulating memory T cells in vitiligo cases followed NB-UVB therapy
Fuquan Lin1, Xiukun Sun1, Jiehao Lei1
1Department of Dermatology, Hangzhou Third People's Hospital, Affiliated Hangzhou Dermatology Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Photodermatology, Photoimmunology & Photomedicine
|July 15, 2021
Summary
Vitiligo patients have reduced CD4+ and CD8+ central memory T cells. Narrowband UVB therapy decreases these cells and related chemokines, suggesting an immunosuppressive effect and a potential new treatment avenue.
Area of Science:
- Immunodermatology
- Autoimmune disease research
- T cell subset analysis
Background:
- Vitiligo is an autoimmune condition causing melanocyte loss.
- T cell subsets, including memory T cells, are implicated in vitiligo pathogenesis.
Purpose of the Study:
- To quantify CD4+ and CD8+ memory T cell subsets in vitiligo patients' blood.
- To assess changes in these T cell subsets after narrowband ultraviolet B (NB-UVB) therapy.
Main Methods:
- Flow cytometry was used to analyze T cell subsets (TCM and TEM) in 33 vitiligo patients and 16 healthy controls.
- Peripheral blood levels of related chemokines were also measured.
Main Results:
- Vitiligo patients showed reduced CD4+ and CD8+ central memory T (TCM) cell counts, with higher levels in active disease.
- NB-UVB therapy significantly decreased CD4+ and CD8+ TCM frequencies and CXCL9/CXCL10 chemokine levels in vitiligo patients.
Conclusions:
- NB-UVB therapy may exert immunosuppressive effects by reducing circulating memory T cells.
- CXCL9 and CXCL10 chemokines appear to mediate the homing of T cells to skin lesions.
- Targeting these chemokines could offer new therapeutic strategies for vitiligo.
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