Severe cutaneous adverse reactions

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Chung, W. H. et al. Granulysin is a key mediator for disseminated keratinocyte death in Stevens-Johnson syndrome and toxic epidermal necrolysis. Nat. Med. 14, 1343–1350 (2008). Study reporting that granulysin triggers keratinocyte death in SJS/TEN.

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Pan, R. Y., Chu, M. T., Wang, C. W., Lee, Y. S. & Lemonnier, F. Identification of drug-specific public TCR driving severe cutaneous adverse reactions. Nat. Commun. 10, 3569 (2019).

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Villani, A. P. et al. Massive clonal expansion of polycytotoxic skin and blood CD8+ T cells in patients with toxic epidermal necrolysis. Sci. Adv. 7, eabe001 (2021).

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Chung, W. H. et al. Medical genetics: a marker for Stevens-Johnson syndrome. Nature 428, 486 (2004). Study reporting the association between HLA-B*15:02 and carbamazepine SJS/TEN.

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Hung, S. I. et al. HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol. Proc. Natl Acad. Sci. USA 102, 4134–4139 (2005). Study reporting the association between HLA-B*58:01 and risk of allopurinol SCARs.

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Lonjou, C. et al. A European study of HLA-B in Stevens-Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs. Pharmacogenet. Genomics 18, 99–107 (2008).

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Chung, W. H. et al. Genetic variants associated with phenytoin-related severe cutaneous adverse reactions. JAMA 312, 525–534 (2014). Article discussing impaired drug metabolism and SCARs.

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Su, S. C. et al. HLA alleles and CYP2C9*3 as predictors of phenytoin hypersensitivity in East Asians. Clin. Pharmacol. Ther. 105, 476–485 (2019).

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Viard, I. et al. Inhibition of toxic epidermal necrolysis by blockade of CD95 with human intravenous immunoglobulin. Science 282, 490–493 (1998). Study reporting that FASL-mediated cell apoptosis could be inhibited by IVIg therapy for SJS/TEN.

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Nassif, A. et al. Toxic epidermal necrolysis: effector cells are drug-specific cytotoxic T cells. J. Allergy Clin. Immunol. 114, 1209–1215 (2004).

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Picard, D. et al. Drug reaction with eosinophilia and systemic symptoms (DRESS): a multiorgan antiviral T cell response. Sci. Transl. Med. 2, 46ra62 (2010).

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Kardaun, S. H. et al. Drug reaction with eosinophilia and systemic symptoms (DRESS): an original multisystem adverse drug reaction. Results from the prospective RegiSCAR study. Br. J. Dermatol. 169, 1071–1080 (2013).

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Wei, B. M. et al. Drug-induced hypersensitivity syndrome / drug reaction with eosinophilia and systemic symptoms. Part I. Epidemiology, pathogenesis, clinicopathological features, and prognosis. J. Am. Acad. Dermatol. https://doi.org/10.1016/j.jaad.2023.02.072 (2023).

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Shiohara, T. & Mizukawa, Y. Drug-induced hypersensitivity syndrome (DiHS)/drug reaction with eosinophilia and systemic symptoms (DRESS): an update in 2019. Allergol. Int. 68, 301–308 (2019).

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Bluestein, S. B., Yu, R., Stone, C. Jr. & Phillips, E. J. Reporting of drug reaction with eosinophilia and systemic symptoms from 2002 to 2019 in the US Food and Drug Administration Adverse Event Reporting System. J. Allergy Clin. Immunol. Pract. 9, 3208–3211.e1 (2021).

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Hetherington, S. et al. Genetic variations in HLA-B region and hypersensitivity reactions to abacavir. Lancet 359, 1121–1122 (2002).

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Mallal, S. et al. Association between presence of HLA-B*5701, HLA-DR7, and HLA-DQ3 and hypersensitivity to HIV-1 reverse-transcriptase inhibitor abacavir. Lancet 359, 727–732 (2002). Study reporting an association between HLA-B*57:01 and abacavir hypersensitivity.

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Hung, S. I. et al. Genetic susceptibility to carbamazepine-induced cutaneous adverse drug reactions. Pharmacogenet. Genomics 16, 297–306 (2006).

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McCormack, M. et al. HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans. N. Engl. J. Med. 364, 1134–1143 (2011). Study reporting an association between HLA-A*31:01 and carbamazepine hypersensitivity.

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Genin, E. et al. HLA-A*31:01 and different types of carbamazepine-induced severe cutaneous adverse reactions: an international study and meta-analysis. Pharmacogenomics J. 14, 281–288 (2014).

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Zhang, F. R. et al. HLA-B*13:01 and the dapsone hypersensitivity syndrome. N. Engl. J. Med. 369, 1620–1628 (2013). Study reporting an associaton between HLA-B*13:01 and dapsone hypersensitivity syndrome.

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Konvinse, K. C. et al. HLA-A*32:01 is strongly associated with vancomycin-induced drug reaction with eosinophilia and systemic symptoms. J. Allergy Clin. Immunol. 144, 183–192 (2019).

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