RESUMO
INTRODUCTION: Occurence of vitiligo lesions is caused by the destruction of melanocytes in a ected skin and therefore by the re- duction of pigment melanin content. Questions remain about the presence of residual melanocytes in the depigmented skin and optimal methods of their identi cation. METHODS: Skin biopsy samples from 16 patients with non-segmental vitiligo and from 10 healthy volunteers were investigated for Melan-A (A103 clone)+ melanocytes expression by immunohistochemical analysis and for melanin by histochemical studies with section staining by Fontana-Masson method. RESULTS: For some patients including those with long-standing disease (up to 40 years) Melan-A+ cells and melanin granules were detected in depigmented skin as indication that the residual melanocytes are preserved in vitiligo lesions. More than three-fold decrease of Melan-A+ melanocytes amount was revealed in perilesional normally pigmented skin of vitiligo patients (P < 0.001) compared with the skin of healthy volunteers. Clinically intact skin involvement in the pathological process should be taken into consideration if local treatment methods are prescribed. CONCLUSION: In some vitiligo patients the residual melanocytes are preserved in depigmented skin. Melan-A marker is useful for identi cation of melanocytes in vitiligo patients' skin.
Assuntos
Antígeno MART-1/metabolismo , Melanócitos/fisiologia , Vitiligo/metabolismo , Vitiligo/patologia , Adulto , Biomarcadores/metabolismo , Estudos de Casos e Controles , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto JovemRESUMO
It was demonstrated that all vitiligo patients, independently of the disease stage, have a significant decrease in the total number of T cells and an elevated level of peripheral blood lymphocytes and activated natural killers (CD56). The low level of T lymphocytes is associated with the increase in the number of CD3(+)4(+)8(+) cells, which are characterized by a faster apoptosis induction. The elevated level of B lymphocytes in peripheral blood in vitiligo is due to the significant increase in the number of B cells of all the stages of differentiation, suggesting a general activation of the whole B-cell immunity. Perhaps, it is associated with the continuous stimulations of B cells by the type 2 helper lymphocytes. The Th2 lymphocyte mediators, including IL-4, do not only stimulate of B-cell immunity, but also regulate maturation of NK cells. It is typical for vitiligo that the level of mature B cells responsible for Ig synthesis (CD38(+), mIgM(+), mIgG(+)) stays elevated even in remission. Moreover, a considerable increase in the number of peripheral blood lymphocytes expressing the adhesion receptor CD54 is observed, which most likely reflects that the blood lymphocytes are highly prepared for tissue migration.