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Cutaneous adverse reaction
to ciprofloxacin: demonstration of specific lymphocyte proliferation
and cross-reactivity to ofloxacin in vitro.
Ronnau AC, Sachs B, von Schmiedeberg S, Hunzelmann N, Ruzicka T,
Gleichmann E, Schuppe HC.
Medical Institute of Environmental Hygiene at Heinrich-Heine-University,
Department of Dermatology, Duesseldorf, Germany.
Ciprofloxacin (CPFX) is a widely used fluoroquinolone antibiotic,
inducing cutaneous adverse drug reactions in about 1 to 2% of the
treated patients. Conclusive diagnosis of drug allergy, however, still
remains a major problem in daily clinical practice. Here, we present 2
patients with drug allergy to CPFX. In both cases the clinical
suspicion for CPFX as the causative agent was confirmed in vitro by
means of the lymphocyte transformation test, whereas epicutaneous
patch tests remained negative. In vivo, a small percentage of the drug
is biotransformed to the three major metabolites desethylene-, sulfo-
and oxociprofloxacin. Though structurally closely related to their
mother compound, these metabolites failed to induce in vitro
lymphocyte proliferation in both patients. On the other hand, in vitro
crossreactivity to ofloxacin, another fluorinated quinolone, could be
demonstrated, which to our knowledge has not previously been reported.
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