Diagnosis of Sulfonamide Hypersensitivity Reactions by In-Vitro "Rechallenge" with Hydroxylamine Metabolites

Abstract

Study Objective: To determine whether differences in in-vitro detoxification of sulfonamide-reactive metabolites can be detected among the lymphocytes from controls, patients with sulfonamide hypersensitivity reactions, and patients with nonhypersensitivity reactions to the sulfonamide agents.

Design: In-vitro toxicity assay on lymphocytes.

Setting: Clinics for adverse drug reactions in an adult and pediatric tertiary care center.

Patients: Peripheral blood lymphocytes were obtained from 46 normal volunteers and 76 patients referred to the clinic for assessment of adverse drug reactions to sulfonamide agents. Thirty-one patients had clinical histories consistent with a diagnosis of hypersensitivity reaction, whereas 45 patients had clinical histories felt to be inconsistent with a diagnosis of hypersensitivity reaction.

Interventions: Lymphocytes were assayed with tetrazolium to determine toxicity from the hydroxylamine of sulfamethazole.

Measurements and Main Results: The lymphocytes from patients with a history of hypersensitivity reactions showed markedly increased toxicity across a tenfold-concentration toxicity-concentration curve compared with those from controls and patients with a history of nonhypersensitivity reactions. These differences were highly significant (P < 0.01). No difference was found between the toxicity shown by the lymphocytes from controls and that shown by the lymphocytes from patients with a history of nonhypersensitivity reactions.

Conclusions: Metabolic differences in the production and detoxification of reactive metabolites of sulfonamide agents are important determinants of hypersensitivity reactions to these agents. These results suggest that the hydroxylamine derivative of sulfamethoxazole may be a reactive metabolite mediating these reactions. Sulfonamide hydroxylamines are useful in the diagnosis and study of the pathogenesis of hypersensitivity reactions to sulfonamide agents.

Article and Author Information

  • From the Hospital for Sick Children, Sunnybrook Medical Centre, and University of Toronto, Toronto, Ontario. For current author addresses, see end of text.

  • †Deceased.

  • Grant Support: Partial support by grants MT7489, MA10036, and MA9716 from the Medical Research Council of Canada. Dr. Rieder is a Centennial Fellow of the Medical Research Council of Canada, and Dr. Shear is a Career Scientist of the Ontario Ministry of Health.

  • Requests for Reprints: Stephen P. Spielberg, MD, Division of Clinical Pharmacology, Department of Paediatrics, Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8.

  • Current Author Address: Dr. Rieder: Division of Clinical Pharmacology, Department of Paediatrics, Children's Hospital of Western Ontario, London, Ontario N6C 2V5.

    Drs. Spielberg and Shear and Ms. Miller: Division of Clinical Pharmacology, Hospital for Sick Children, Toronto, Ontario M5G 1X8. Dr. Uetrecht: Faculty of Pharmacy, University of Toronto, Toronto, Ontario.

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