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J Allergy Clin Immunol ; 105(1 Pt 1): 157-65, 2000 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-10629466

RESUMO

BACKGROUND: Toxic epidermal necrolysis is a severe reaction with skin involvement induced by different drugs and other agents. The mechanisms implicated in the induction of the reaction are poorly understood. OBJECTIVE: Our purpose was to study the involvement of T lymphocytes and other immunocompetent cells in the peripheral blood, blister fluid, and affected skin of 3 patients who had a severe reaction after receiving anticonvulsant medication. METHODS: Quantification of T lymphocytes expressing the skin-homing receptor (cutaneous lymphocyte-associated antigen ¿CLA) in peripheral blood, skin, and skin blister fluid and assessment of other adhesion molecules, activation markers, and inflammatory interleukins by flow cytometry, immunohistochemistry, and reverse transcription-PCR. RESULTS: An increase in CD3(+)CLA(+) cells paralleling the severity of the disease was observed in both peripheral blood and skin, tending to normalize as soon as patient's conditions improved. E-selectin was detected in endothelial vessels in parallel with CLA expression on lymphocytes. An overexpression of TNFalpha, IFN-gamma, and IL-2 was also observed in PBMCs. The expression of the different markers changed over the course of the disease. CONCLUSIONS: These data show an increase in activated T cells expressing the skin-homing receptor in both tissue and peripheral blood accompanying clinical symptoms, with a recruitment of macrophages and an overexpression of cytokines. All these results suggest an important role for T cells in the production of toxic epidermal necrolysis.


Assuntos
Anticonvulsivantes/efeitos adversos , Síndrome de Stevens-Johnson/imunologia , Adulto , Formação de Anticorpos , Células Sanguíneas/metabolismo , Células Sanguíneas/patologia , Complexo CD3/análise , Carbamazepina/efeitos adversos , Citocinas/metabolismo , Selectina E/metabolismo , Endotélio/metabolismo , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fenitoína/efeitos adversos , Receptores de Retorno de Linfócitos/metabolismo , Pele/metabolismo , Pele/patologia , Síndrome de Stevens-Johnson/metabolismo , Síndrome de Stevens-Johnson/patologia , Síndrome de Stevens-Johnson/fisiopatologia
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