z-logo
open-access-imgOpen Access
HLA-B*5701 screening for susceptibility to abacavir hypersensitivity
Author(s) -
Andrew Lucas,
David Nolan,
S. Mallal
Publication year - 2007
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkl557
Subject(s) - abacavir , medicine , nevirapine , pharmacogenetics , human leukocyte antigen , drug , immunology , pharmacotherapy , adverse effect , intensive care medicine , antiretroviral therapy , human immunodeficiency virus (hiv) , pharmacology , viral load , genotype , biology , genetics , antigen , gene
The introduction of highly active antiretroviral therapy (also known as combination therapy) has transformed the nature of HIV infection from a severe and ultimately fatal disease to that of a manageable chronic condition. HIV drugs are highly efficacious, but their use comes at the cost of a range of drug-related adverse events, including severe drug hypersensitivity reactions (HSRs) that have been most notably associated with abacavir and nevirapine therapy. This article discusses the issues of pharmacogenetic screening, in the light of the strong genetic association of the HLA-B*5701 allele and the susceptibility to developing abacavir HSRs. It also presents the screening's impact on clinical practice and discusses the practical considerations that influence the introduction and cost-effectiveness of such screening.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom