» Articles » PMID: 34377130

Comparison of Tyrosinase Antibody, Tyrosinase-related Protein-1 and -2 Antibodies, Melanin-concentrating Hormone Receptor Antibody Levels with Autologous Serum Skin Test and Autologous Plasma Skin Test Results in Patients with Vitiligo

Overview
Publisher Termedia
Date 2021 Aug 11
PMID 34377130
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: Although the exact etiopathogenesis of vitiligo is unknown, the autoimmunity hypothesis is much in evidence. The autologous serum skin test (ASST) and autologous plasma skin test (APST) are methods used in the diagnosis of some autoimmune diseases, which are easy and inexpensive to perform.

Aim: In this study, we investigated whether or not ASST and APST could determine autoimmunity in patients with vitiligo.

Material And Methods: In this study, 30 vitiligo patients presenting to the dermatology outpatient clinic and 30 healthy volunteers without any known autoimmune diseases were included. Antibodies such as tyrosinase, tyrosinase-related protein-1 (TYRP1), tyrosinase-related protein-2 (TYRP2) and melanin-concentrating hormone receptor 1 (MCHR1) antibodies determined to be associated with vitiligo were examined. In addition, the association of these antibodies with the positivity of ASST and APST, which were suggested to be associated with autoimmunity, were examined.

Results: In our study, tyrosinase antibody was found to be significantly higher in vitiligo patients. ASST was positive in 12 (40%) patients with vitiligo and 8 (26.6%) control subjects. APST was positive in 8 (26.6%) of the patients with vitiligo and in 2 (6.6%) of the controls, and there was a significant difference between the groups in terms of APST positivity ( = 0.032). In addition, in our study, a significant correlation was found between TYRP1 antibody positivity and APST positivity in the patient group ( = 0.005).

Conclusions: These findings suggest that we may use APST to investigate the autoimmune etiopathogenesis of vitiligo.

Citing Articles

Melanogenesis and Hypopigmentation: The Case of Vitiligo.

Vinardell M, Maddaleno A, Mitjans M Indian J Dermatol. 2023; 67(5):524-530.

PMID: 36865864 PMC: 9971791. DOI: 10.4103/ijd.ijd_1067_21.

References
1.
Rocha I, Oliveira L, De Castro L, de Araujo Pereira L, Chaul A, Guerra J . Recognition of melanoma cell antigens with antibodies present in sera from patients with vitiligo. Int J Dermatol. 2000; 39(11):840-3. DOI: 10.1046/j.1365-4362.2000.00089.x. View

2.
Ravetch J, Clynes R . Divergent roles for Fc receptors and complement in vivo. Annu Rev Immunol. 1998; 16:421-32. DOI: 10.1146/annurev.immunol.16.1.421. View

3.
Cui T, Yi X, Zhang W, Wei C, Zhou F, Jian Z . miR-196a-2 rs11614913 polymorphism is associated with vitiligo by affecting heterodimeric molecular complexes of Tyr and Tyrp1. Arch Dermatol Res. 2015; 307(8):683-92. DOI: 10.1007/s00403-015-1563-1. View

4.
Kemp E, Waterman E, Gawkrodger D, Watson P, Weetman A . Autoantibodies to tyrosinase-related protein-1 detected in the sera of vitiligo patients using a quantitative radiobinding assay. Br J Dermatol. 1999; 139(5):798-805. DOI: 10.1046/j.1365-2133.1998.02503.x. View

5.
Huggins R, Schwartz R, Janniger C . Vitiligo. Acta Dermatovenerol Alp Pannonica Adriat. 2006; 14(4):137-42, 144-5. View