CXCL9 as a key biomarker of vitiligo activity and prediction of the success of cultured melanocyte transplantation

Author:

Lin Fuquan,Hu Wenting,Xu Wen,Zhou Miaoni,Xu Ai‑E.

Abstract

AbstractThis study aimed to investigate the potential biomarkers of vitiligo by evaluating the disease activity and curative effect of autologous cultured pure melanocyte transplantation (CMT) on patients. Altogether, 36patients with stable vitiligo were treated with CMT. Blister fluid samples were collected from patients with stable vitiligo. Patients with active vitiligo were matched with healthy controls. The chemokine levels in the serum and blister fluid samples were measured using Luminex. The curative effect on patients with stable vitiligo was evaluated 6 months after treatment. Treatment responses were defined according to the extent of repigmentation as effective (if 50% or more repigmentation was achieved) or ineffective (if less than 50% or worse repigmentation was achieved). Patients received re-transplantation if the initial treatment was ineffective. The levels of C-X-C motif chemokine ligand (CXCL)9 and CXCL10 in blister fluid samples were significantly lower in stable patients than in active participants. Receiver operating characteristic analysis revealed that the levels of CXCL9 and CXCL10 were sensitive and specific in diagnosing active vitiligo. Further, 65.6% (21/32) of patients who received CMT had effective treatment responses. The high CXCL9 level in the blister fluid was a significant predictor of ineffective treatment responses. The treatment response was significantly enhanced after treatment. Four patients with ineffective treatment responses received anti-inflammatory treatment and re-transplantation. The CXCL9 and CXCL10 levels in the blister fluid were related to the presence of active vitiligo. Also, the CXCL9 level was a predictor of the effectiveness of CMT in treating vitiligo.

Funder

National Natural Science Foundation of China

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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1. Ritlecitinib, a JAK3/TEC family kinase inhibitor, stabilizes active lesions and repigments stable lesions in vitiligo;Archives of Dermatological Research;2024-07-18

2. Vitiligo;The Rose and Mackay Textbook of Autoimmune Diseases;2024

3. Research Progress on Cellular Immunology Pathogenesis of Vitiligo;Advances in Clinical Medicine;2024

4. The IFN‐γ‐CXCL9/CXCL10‐CXCR3 axis in vitiligo: pathological mechanism and treatment;European Journal of Immunology;2023-11-08

5. Management of Stable Vitiligo—A Review of the Surgical Approach;Journal of Clinical Medicine;2023-03-02

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