Journal
JOURNAL OF CLINICAL INVESTIGATION
Volume 128, Issue 7, Pages 2819-2832Publisher
AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI99321
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Funding
- FDA Intramural Research Program
- NIAID, NIH
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Adverse drug reactions (ADRs) are a major obstacle to drug development, and some of these, including hypersensitivity reactions to the HIV reverse transcriptase inhibitor abacavir (ABC), are associated with HLA alleles, particularly HLA-B*57:01. However, not all HLA-B*57:01' patients develop ADRs, suggesting that in addition to the HLA genetic risk, other factors may influence the outcome of the response to the drug. To study HLA-linked ADRs in vivo, we generated HLA-B*57:01-Tg mice and show that, although ABC activated Tg mouse CD8(+) T cells in vitro in a HLA-B*57:01-dependent manner, the drug was tolerated in vivo. In immunocompetent Tg animals, ABC induced CD8(+) T cells with an anergy-like phenotype that did not lead to ADRs. In contrast, in vivo depletion of CD4(+) T cells prior to ABC administration enhanced DC maturation to induce systemic ABC-reactive CD8(+) T cells with an effector-like and skin-homing phenotype along with CD8(+) T infiltration and inflammation in drug-sensitized skin. B7 costimulatory molecule blockade prevented CD8(+) T cell activation. These Tg mice provide a model for ABC tolerance and for the generation of HLA-B*57:01-restricted, ABC-reactive CD8(+) T cells dependent on both HLA genetic risk and immunoregulatory host factors.
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