Are drug metabolites able to cause T-cell-mediated hypersensitivity reactions?

被引:17
作者
Sullivan, Andrew [1 ]
Gibson, Andrew [1 ]
Park, Brian Kevin [2 ]
Naisbitt, Dean J. [1 ]
机构
[1] Univ Liverpool, Dept Clin & Mol Pharmacol, Liverpool L69 3GE, Merseyside, England
[2] Univ Liverpool, Inst Translat Med, Dept Clin & Mol Pharmacol, Liverpool L69 3GE, Merseyside, England
基金
英国医学研究理事会;
关键词
chemically reactive metabolite; drug hypersensitivity; drug metabolism; T lymphocytes; BIOACTIVATION IN-VITRO; HIV-POSITIVE PATIENTS; HUMAN CYTOCHROME-P450 ENZYMES; REDUCED GLUTATHIONE; GENE POLYMORPHISMS; SULFAMETHOXAZOLE; CARBAMAZEPINE; ACTIVATION; ABACAVIR; ANTIGEN;
D O I
10.1517/17425255.2015.992780
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Adverse drug reactions with an immune pathogenesis are a problem in the clinic and an impediment to drug development. T lymphocytes are believed to play a role in the pathogenesis; however, the nature of the drug interaction with immune receptors remains an area of debate. Areas covered: This article reviews recent advances in our understanding of drug hypersensitivity focusing specifically on the way in which drugs are displayed in MHC molecules. Most drugs associated with a high incidence of reactions have been shown to form protein-reactive metabolites. Hence, the relationship between drug metabolism and T-cell activation is discussed in detail. Expert opinion: The role of metabolism in pathogenesis of immunological drug reactions has only been studied with a small number of drugs where synthetic metabolites are available for functional studies. In each case, metabolite-responsive T cells have been detected. However, the field is skewed by the fact that most research is conducted using the parent compound in metabolically inert cell systems. We propose that research efforts are directed towards the synthesis of drug metabolites and/or drug-protein conjugates. Furthermore, analytical methods need to be developed to relate metabolite exposure to the T-cell response. For now, our understanding of the chemical basis of drug hypersensitivity is incomplete.
引用
收藏
页码:357 / 368
页数:12
相关论文
共 91 条
  • [11] BRANDER C, 1995, J IMMUNOL, V155, P2670
  • [12] Influence of reduced glutathione on the proliferative response of sulfamethoxazole-specific and sulfamethoxazole-metabolite-specific human CD4+T-cells
    Burkhart, C
    Von Greyerz, S
    Depta, JPH
    Naisbitt, DJ
    Britschgi, M
    Park, KB
    Pichler, WJ
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2001, 132 (03) : 623 - 630
  • [13] Stimulation of human T cells with sulfonamides and sulfonamide metabolites
    Castrejon, J. Luis
    Berry, Neil
    El-Ghaiesh, Sabah
    Gerber, Basil
    Pichler, Werner J.
    Park, B. Kevin
    Naisbitt, Dean J.
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2010, 125 (02) : 411 - 418
  • [14] Human leukocyte antigen class I-restricted activation of CD8+ T cells provides the immunogenetic basis of a systemic drug hypersensitivity
    Chessman, Diana
    Kostenko, Lyudmila
    Lethborg, Tessa
    Purcell, Anthony W.
    Williamson, Nicholas A.
    Chen, Zhenjun
    Kjer-Nielsen, Lars
    Mifsud, Nicole A.
    Tait, Brian D.
    Holdsworth, Rhonda
    Almeida, Coral Ann
    Nolan, David
    Macdonalds, Whitney A.
    Archbold, Julia K.
    Kellerher, Anthony D.
    Marriott, Debbie
    Mallal, Simon
    Bharadwaj, Mandvi
    Rossjohn, Jamie
    McCluskey, James
    [J]. IMMUNITY, 2008, 28 (06) : 822 - 832
  • [15] A marker for Stevens-Johnson syndrome
    Chung, WH
    Hung, SI
    Hong, HS
    Hsih, MS
    Yang, LC
    Ho, HC
    Wu, JY
    Chen, YT
    [J]. NATURE, 2004, 428 (6982) : 486 - 486
  • [16] Coombs P. R., 1968, CLASSIFICATION ALLER
  • [17] CRIBB AE, 1991, DRUG METAB DISPOS, V19, P900
  • [18] CRIBB AE, 1995, DRUG METAB DISPOS, V23, P406
  • [19] CRIBB AE, 1990, DRUG METAB DISPOS, V18, P784
  • [20] Adverse Drug Reactions in Hospital In-Patients: A Prospective Analysis of 3695 Patient-Episodes
    Davies, Emma C.
    Green, Christopher F.
    Taylor, Stephen
    Williamson, Paula R.
    Mottram, David R.
    Pirmohamed, Munir
    [J]. PLOS ONE, 2009, 4 (02):