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Department of Dermatology, Hamamatsu University School of Medicine, Hamamatsu, Japan
Phenobarbital has a high potential to elicit adverse reactions
including severe skin eruptions and systemic involvements among the
worldwide-prescribed drugs. Although phenobarbital hypersensitivity is
thought to be mediated by T cells specific to the drug, its precise
mechanism remains not fully elucidated. To characterize T cells
reactive with phenobarbital, we generated drug-specific T cell clones
and lines from PBMCs of patients with phenobarbital hypersensitivity
showing various degrees of cutaneous and extracutaneous involvements.
Although the TCR V
repertoire and phenotype in the T cell clones/T
cell lines were heterogeneous among the patients, V
13.1+
and V
5.1+ clones or lines were raised from the
individuals examined who possessed different HLA haplotypes.
Histopathological examination suggested that
V
5.1+CD8+ T cells and V
13.1+
T cells played a role in cutaneous and extracutaneous involvements,
respectively. A V
13.1+CD4+ clone was found
to proliferate in response to the Ag with processing-impaired, fixed
APCs. Most of the clones and lines belonged to the Th2 phenotype,
producing IL-4 and IL-5 but not IFN-
upon phenobarbital stimulation.
Clones/lines with Th1 or Th0 phenotypes also constituted minor
populations. These observations clearly indicate the heterogeneity and
a marked individual deviation of reactive T cell subsets among the
patients in terms of CD4/8 phenotype, V
repertoire, Ag recognition
pattern, and cytokine production; and thus provide evidence whereby
each pathogenic T cell subset contributes to special elements of
clinical presentation.
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