Evidence that Singlet Oxygen-induced Human T Helper Cell Apoptosis Is the Basic Mechanism of Ultraviolet-A Radiation Phototherapy

Author:

Morita Akimichi1,Werfel Thomas1,Stege Helger1,Ahrens Constanze1,Karmann Karin1,Grewe Markus1,Grether-Beck Susanne1,Ruzicka Thomas1,Kapp Alexander1,Klotz Lars-Oliver1,Sies Helmut1,Krutmann Jean1

Affiliation:

1. From Clinical and Experimental Photodermatology, Department of Dermatology, Heinrich-Heine-University of Düsseldorf, D-40225 Düsseldorf; Department of Dermatology, Hannover Medical School, D-30625 Hannover; and Institute of Physiological Chemistry I, Heinrich-Heine-University, D-40225 Düsseldorf, Germany

Abstract

Ultraviolet A (UVA) irradiation is effectively used to treat patients with atopic dermatitis and other T cell mediated, inflammatory skin diseases. In the present study, successful phototherapy of atopic dermatitis was found to result from UVA radiation-induced apoptosis in skin-infiltrating T helper cells, leading to T cell depletion from eczematous skin. In vitro, UVA radiation-induced human T helper cell apoptosis was mediated through the FAS/FAS-ligand system, which was activated in irradiated T cells as a consequence of singlet oxygen generation. These studies demonstrate that singlet oxygen is a potent trigger for the induction of human T cell apoptosis. They also identify singlet oxygen generation as a fundamental mechanism of action operative in phototherapy.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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