In recent years, increasing evidence has indicated an important role for T cells in various
drug-induced diseases. A detailed analysis of patients with various
drug allergies revealed the existence of
drug-specific T cells in the circulation or in eluate from skin infiltration in bullous, pustular, and
maculopapular drug eruptions. The
drug-specific T cells use the ab-
T cell receptor CD4+ or CD8+ and react with drugs acting as
haptens (covalently bound to larger molecules, such as
penicillins), but also recognize drugs if they are bound only in a labile way to major histocompatibility complex molecules (noncovalent
drug presentation). Functional analysis revealed a predominant
IL-5 production by
drug-specific CD4+ T cells in maculopapular
exanthema (MPE) and
bullous skin diseases, while patients with
acute generalized exanthematous pustulosis have a peculiar T cell subset secreting high amounts of
IL-8. Moreover, in MPE CD4+, perforin+ T cells were found in vitro and in immunohistology that had cytotoxic potential and killed keratinocytes in vitro and in vivo.