Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis

被引:238
作者
Kindmark, A. [2 ]
Jawaid, A. [1 ]
Harbron, C. G. [1 ]
Barratt, B. J. [1 ]
Bengtsson, O. F. [2 ]
Andersson, T. B. [2 ]
Carlsson, S. [2 ]
Cederbrant, K. E. [3 ]
Gibson, N. J. [1 ]
Armstrong, M. [1 ]
Lagerstrom-Fermer, M. E. [2 ]
Dellsen, A.
Brown, E. M. [1 ]
Thornton, M. [1 ]
Dukes, C. [1 ]
Jenkins, S. C. [1 ]
Firth, M. A. [1 ]
Harrod, G. O. [1 ]
Pinel, T. H. [1 ]
Billing-Clason, S. M. E. [2 ]
Cardon, L. R. [4 ]
March, R. E. [1 ]
机构
[1] AstraZeneca, Macclesfield SK10 4TG, Cheshire, England
[2] AstraZeneca, R&D, Molndal, Sweden
[3] AstraZeneca, R&D, Sodertalje, Sweden
[4] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England
关键词
pharmacogenetics; pharmacogenomics; adverse event; immune system; liver injury;
D O I
10.1038/sj.tpj.6500458
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
One of the major goals of pharmacogenetics is to elucidate mechanisms and identify patients at increased risk of adverse events (AEs). To date, however, there have been only a few successful examples of this type of approach. In this paper, we describe a retrospective case-control pharmacogenetic study of an AE of unknown mechanism, characterized by elevated levels of serum alanine aminotransferase (ALAT) during long-term treatment with the oral direct thrombin inhibitor ximelagatran. The study was based on 74 cases and 130 treated controls and included both a genome-wide tag single nucleotide polymorphism and large-scale candidate gene analysis. A strong genetic association between elevated ALAT and the MHC alleles DRB1*07 and DQA1*02 was discovered and replicated, suggesting a possible immune pathogenesis. Consistent with this hypothesis, immunological studies suggest that ximelagatran may have the ability to act as a contact sensitizer, and hence be able to stimulate an adaptive immune response.
引用
收藏
页码:186 / 195
页数:10
相关论文
共 30 条
[1]   HLA-DR predicts the prognosis in Scandinavian patients with pulmonary sarcoidosis [J].
Berlin, M ;
FogdellHahn, A ;
Olerup, O ;
Eklund, A ;
Grunewald, J .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 156 (05) :1601-1605
[2]   Molecular aspects of drug recognition by specific T cells [J].
Britschgi, M ;
von Greyerz, S ;
Burkhart, C ;
Pichler, WJ .
CURRENT DRUG TARGETS, 2003, 4 (01) :1-11
[3]   Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium [J].
Carlson, CS ;
Eberle, MA ;
Rieder, MJ ;
Yi, Q ;
Kruglyak, L ;
Nickerson, DA .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (01) :106-120
[4]  
Castell J. V., 1998, Clinical and Experimental Allergy, V28, P13
[5]   Immunomics: discovering new targets for vaccines and therapeutics [J].
De Groot, AS .
DRUG DISCOVERY TODAY, 2006, 11 (5-6) :203-209
[6]   Genomic control to the extreme [J].
Devlin, B ;
Bacanu, SA ;
Roeder, K .
NATURE GENETICS, 2004, 36 (11) :1129-1130
[7]   The structure of haplotype blocks in the human genome [J].
Gabriel, SB ;
Schaffner, SF ;
Nguyen, H ;
Moore, JM ;
Roy, J ;
Blumenstiel, B ;
Higgins, J ;
DeFelice, M ;
Lochner, A ;
Faggart, M ;
Liu-Cordero, SN ;
Rotimi, C ;
Adeyemo, A ;
Cooper, R ;
Ward, R ;
Lander, ES ;
Daly, MJ ;
Altshuler, D .
SCIENCE, 2002, 296 (5576) :2225-2229
[8]   Noncovalent interactions of drugs with immune receptors may mediate drug-induced hypersensitivity reactions [J].
Gerber, BO ;
Pichler, WJ .
AAPS JOURNAL, 2006, 8 (01) :E160-E165
[9]   Geographic patterns of functional categories of HLA-DRB1 alleles: a new approach to analyse associations between HLA-DRB1 and disease [J].
Gibert, M ;
Sanchez-Mazas, A .
EUROPEAN JOURNAL OF IMMUNOGENETICS, 2003, 30 (05) :361-374
[10]   Major histocompatibility complex haplotypes in Spanish immunoglobulin A deficiency patients:: a comparative fine mapping microsatellite study [J].
Gual, L ;
Martínez, A ;
Fernández-Arquero, M ;
García-Rodríguez, MC ;
Ferreira, A ;
Fontán, G ;
de la Concha, EG ;
Urcelay, E .
TISSUE ANTIGENS, 2004, 64 (06) :671-677