The Journal of Experimental Medicine · 1998 · 462 citations · 29 references
Life SciencesDermatologyImmunologyAutoimmunityClinical ImmunologyImmunopathologyAutoimmune DiseasesAutoimmune Skin DiseasesCytotoxic T Lymphocyte ResponsesHuman Leukocyte Antigen SystemT Cell ActivationT Cell BiologyAntigen Recognition By Cytotoxic T LymphocytesAutoimmune Cytotoxic T Lymphocyte ResponsesEx Vivo ModelsMelanoma-associated AntigensSkin-homing LymphocytesT-cell Mediated AutoimmunityT-cell Mediated ImmunityT-cell Mediated Skin Disease
Vitiligo is an autoimmune condition characterized by loss of epidermal melanocytes. Using tetrameric complexes of human histocompatibility leukocyte antigen (HLA) class I to identify antigen-specific T cells ex vivo, we observed high frequencies of circulating MelanA-specific, A*0201-restricted cytotoxic T lymphocytes (A2-MelanA tetramer+ CTLs) in seven of nine HLA-A*0201-positive individuals with vitiligo. Isolated A2-MelanA tetramer+ CTLs were able to lyse A*0201-matched melanoma cells in vitro and their frequency ex vivo correlated with extent of disease. In contrast, no A2-MelanA tetramer+ CTL could be identified ex vivo in all four A*0201-negative vitiligo patients or five of six A*0201-positive asymptomatic controls. Finally, we observed that the A2-MelanA tetramer+ CTLs isolated from vitiligo patients expressed high levels of the skin homing receptor, cutaneous lymphocyte-associated antigen, which was absent from the CTLs seen in the single A*0201-positive normal control. These data are consistent with a role of skin-homing autoreactive melanocyte-specific CTLs in causing the destruction of melanocytes seen in autoimmune vitiligo. Lack of homing receptors on the surface of autoreactive CTLs could be a mechanism to control peripheral tolerance in vivo.
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