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Likelihood and Mechanisms of Cross‐Allergenicity Between Sulfonamide Antibiotics and Other Drugs Containing a Sulfonamide Functional Group
Author(s) -
Brackett Carolyn C.,
Singh Harleen,
Block John H.
Publication year - 2004
Publication title -
pharmacotherapy: the journal of human pharmacology and drug therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.227
H-Index - 109
eISSN - 1875-9114
pISSN - 0277-0008
DOI - 10.1592/phco.24.9.856.36106
Subject(s) - sulfonamide , antibiotics , sulfadiazine , chemistry , immunology , medicine , stereochemistry , biochemistry
Concerns about cross‐allergenicity between sulfonamide antibiotics and nonantibiotic, sulfonamide‐containing drugs persist and can complicate patients' drug therapy unnecessarily. No interaction between the human immune system and the sulfonamide functional group has been demonstrated. The immunologic determinant of type I, immediate hypersensitivity responses to sulfonamide antibiotics is the N1 heterocyclic ring. Nonantibiotic sulfonamides do not contain this structural feature. Non‐type I hypersensitivity responses to sulfonamide antibiotics are largely attributable to reactive metabolites that may cause either direct cytotoxicity or immunologic response. Formation of these metabolites is a stereospecific process that occurs at the N4 amino nitrogen of the sulfonamide antibiotics, a structure also not found on any nonantibiotic sulfonamide drugs. The stereospecificity of these reactions implies that cross‐reactivity with nonantibiotic sulfonamide‐containing drugs is highly unlikely; this assertion is supported by recent literature. However, T‐cell recognition of unmetabolized, nonhaptenated parent sulfonamide antibiotic appears to occur in a small subset of hypersensitive patients. Several of the severe cutaneous reactions associated with sulfonamide antibiotics are mediated by T cells. It is not known whether T‐cell recognition of antibiotic is related to the sulfonamide functional group. Until the mechanism of this recognition is elucidated, cross‐reactivity with nonantibiotic sulfonamides appears to remain at least theoretically possible.

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