Institute for Immunology and Infectious Diseases, Murdoch University, Murdoch, Western Australia.
Institute for Immunology and Infectious Diseases, Murdoch University, Murdoch, Western Australia; Vanderbilt University School of Medicine, Nashville, Tenn.
J Allergy Clin Immunol Pract. 2014 Jan-Feb;2(1):21-33. doi: 10.1016/j.jaip.2013.11.005.
Drug hypersensitivity syndromes such as abacavir hypersensitivity and the severe cutaneous adverse drug reactions have been associated with significant short- and long-term morbidity and mortality. More recently, these immunologically mediated and previously unpredictable diseases have been shown to be associated with primarily class I but also class II HLA alleles. The case of the association of HLA-B*57:01 and abacavir hypersensitivity has created a translational roadmap for how this knowledge can be used in the clinic to prevent severe reactions. Although many hurdles exist to the widespread translation of such HLA screening approaches, our understanding of how drugs interact with the major histocompatibility complex has contributed to the discovery of new models that have provided considerable insights into the immunopathogenesis of severe cutaneous adverse drug reactions and other T-cell-mediated drug hypersensitivity syndromes. Future translation of this knowledge will facilitate the development of preclinical toxicity screening to significantly improve efficacy and safety of drug development and design.
药物超敏反应综合征,如阿巴卡韦超敏反应和严重皮肤不良反应,与显著的短期和长期发病率和死亡率相关。最近,这些免疫介导的、以前不可预测的疾病已被证明与主要的 I 类但也有 II 类 HLA 等位基因相关。HLA-B*57:01 与阿巴卡韦超敏反应的关联为如何将这一知识应用于临床以预防严重反应提供了一个转化途径。尽管 HLA 筛选方法的广泛转化存在许多障碍,但我们对药物如何与主要组织相容性复合体相互作用的理解,有助于发现新的模型,这些模型为严重皮肤不良反应和其他 T 细胞介导的药物超敏反应综合征的免疫发病机制提供了重要的见解。这方面知识的未来转化将促进临床前毒性筛选的发展,从而显著提高药物开发和设计的疗效和安全性。