Pharmacogenetics of hypersensitivity to abacavir: from PGx hypothesis to confirmation to clinical utility

Pharmacogenomics J. 2008 Dec;8(6):365-74. doi: 10.1038/tpj.2008.3. Epub 2008 Mar 11.

Abstract

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.

Publication types

  • Review

MeSH terms

  • Dideoxynucleosides / adverse effects*
  • Drug Hypersensitivity / genetics*
  • HLA-B Antigens / genetics
  • Humans
  • Patch Tests
  • Pharmacogenetics*
  • Reverse Transcriptase Inhibitors / adverse effects*

Substances

  • Dideoxynucleosides
  • HLA-B Antigens
  • Reverse Transcriptase Inhibitors
  • abacavir