Pharmacogenetics of hypersensitivity to abacavir: from PGx hypothesis to confirmation to clinical utility
The hypersensitivity (HSR) to abacavir (ABC) pharmacogenetics (PGx) program represents the progression from an exploratory discovery to a validated biomarker. Within the program, two retrospective PGx studies were conducted to identify HIV-1 patients at increased risk for ABC HSR, a treatment-limiti...
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Veröffentlicht in: | The pharmacogenomics journal 2008-12, Vol.8 (6), p.365-374 |
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Hauptverfasser: | , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
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Zusammenfassung: | The hypersensitivity (HSR) to abacavir (ABC) pharmacogenetics (PGx) program represents the progression from an exploratory discovery to a validated biomarker. Within the program, two retrospective PGx studies were conducted to identify HIV-1 patients at increased risk for ABC HSR, a treatment-limiting and potentially life-threatening adverse event. A strong statistical association between the major histocompatibility complex allele,
HLA-B*5701
, and clinically diagnosed ABC HSR was identified but varied between racial populations. Subsequently, ABC skin patch testing was introduced as a research tool to supplement clinical case ascertainment. In a randomized, prospective study evaluating the clinical utility of
HLA-B*5701
screening, avoidance of ABC in
HLA-B*5701
-positive patients significantly reduced clinically diagnosed ABC HSR and eliminated patch test-positive ABC HSR. Finally, a retrospective PGx study supports the generalizability of the association across races. Prospective
HLA-B*5701
screening should greatly reduce the incidence of ABC HSR by identifying patients at high risk for ABC HSR before they are treated. |
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ISSN: | 1470-269X 1473-1150 |
DOI: | 10.1038/tpj.2008.3 |