T Cell-Mediated Hypersensitivity Reactions to Drugs
The immunological mechanisms driving delayed hypersensitivity reactions (HSRs) to drugs mediated by drug-reactive T lymphocytes are exemplified by several key examples and their human leukocyte antigen (HLA) associations: abacavir and HLA-B*57:01 , carbamazepine and HLA-B*15:02 , allo-purinol and HL...
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Veröffentlicht in: | Annual review of medicine 2015-01, Vol.66 (1), p.439-454 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The immunological mechanisms driving delayed hypersensitivity reactions (HSRs) to drugs mediated by drug-reactive T lymphocytes are exemplified by several key examples and their human leukocyte antigen (HLA) associations: abacavir and
HLA-B*57:01
, carbamazepine and
HLA-B*15:02
, allo-purinol and
HLA-B*58:01
, and both amoxicillin-clavulanate and nevirapine with multiple class I and II alleles. For HLA-restricted drug HSRs, specific class I and or II HLA alleles are necessary but not sufficient for tissue specificity and the clinical syndrome. Several models have been proposed to explain the immunopathogenesis of severe T cell-mediated drug HSRs, and our increased understanding of the risk factors and mechanisms involved in the development of these reactions will further the development of sensitive and specific strategies for preclinical screening that will lead to safer and more cost-effective drug design. |
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ISSN: | 0066-4219 1545-326X |
DOI: | 10.1146/annurev-med-050913-022745 |