An association study of HLA with levofloxacin-induced severe cutaneous adverse drug reactions in Han Chinese

被引:2
|
作者
Jiang, Menglin [1 ,2 ]
Yang, Jin [3 ,4 ]
Yang, Linlin [5 ]
Wang, Lina [5 ]
Wang, Ting [1 ,2 ]
Han, Shengna [5 ]
Cheng, Ye [1 ,2 ]
Chen, Zihua [3 ,4 ]
Su, Yu [1 ,2 ]
Zhang, Lirong [5 ]
Yang, Fanping [3 ,4 ]
Chen, Sheng-an [3 ,4 ]
Zhang, Jin [1 ,2 ]
Xiong, Hao [3 ,4 ]
Wang, Lanting [3 ,4 ]
Zhang, Zhen [3 ,4 ]
Ma, Li [3 ,4 ]
Luo, Xiaoqun [3 ,4 ]
Xing, Qinghe [1 ,2 ]
机构
[1] Fudan Univ, Childrens Hosp, Shanghai 200032, Peoples R China
[2] Fudan Univ, Inst Biomed Sci, Shanghai 200032, Peoples R China
[3] Fudan Univ, Huashan Hosp, Dept Allergy & Immunol, Shanghai 200040, Peoples R China
[4] Fudan Univ, Huashan Hosp, Dept Dermatol, Shanghai 200040, Peoples R China
[5] Zhengzhou Univ, Sch Basic Med Sci, Dept Pharmacol, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
TOXIC EPIDERMAL NECROLYSIS; STEVENS-JOHNSON SYNDROME; HYPERSENSITIVITY REACTIONS; SYSTEMIC SYMPTOMS; RISK; HLA-B-ASTERISK-1301; EOSINOPHILIA; ALLOPURINOL; PEPTIDES; ALLELE;
D O I
10.1016/j.isci.2023.107391
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Levofloxacin-induced severe cutaneous adverse drug reactions (LEV-SCARs) remain unexplored. An association study of human leukocyte antigen (HLA) alleles with LEV-SCARs among 12 patients, 806 healthy subjects, and 100 levofloxacin-tolerant individuals was performed. The carrier frequencies of HLA-B*13:01 (odds ratio [OR]: 4.50; 95% confidence interval [CI]: 1.15-17.65; p = 0.043), HLA-B*13:02 (OR: 6.14; 95% CI: 1.73-21.76; p = 0.0072), and serotype B13 (OR: 17.73; 95% CI: 3.61-86.95; p = 4.85 x 10(-5)) in patients with LEV-SCARs were significantly higher than those of levofloxacin-tolerant individuals. Molecular docking analysis suggested that levofloxacin formed more stable binding models with HLA-B*13:01 and HLA-B*13:02 than with non-risk HLA-B*46:01. Mass spectrometry revealed that nonapeptides bound to HLA-B*13:02 shifted at several positions after exposure to levofloxacin. Prospective screening for serotype B13 (sensitivity: 83%, specificity: 78%) and alternative drug treatment for carriers may significantly decrease the incidence of LEV-SCARs.
引用
收藏
页数:14
相关论文
共 50 条
  • [31] Association between HLA-B*1502 allele and antiepileptic drug-induced cutaneous reactions in han Chinese
    Man, Celeste B. L.
    Kwan, Patrick
    Baum, Larry
    Yu, Evelyn
    Lau, K. M.
    Cheng, Alice S. H.
    Ng, Margaret H. L.
    EPILEPSIA, 2007, 48 (05) : 1015 - 1018
  • [32] The association between HLA-B*15:02 and phenytoin-induced severe cutaneous adverse reactions: a meta-analysis
    Thanh Huong Phung
    Khanh Ngoc Cong Duong
    Gloria, Mac Ardy Junio
    Thien Khac Nguyen
    PHARMACOGENOMICS, 2021, 23 (01) : 49 - 59
  • [33] Updates on the immunopathology and genomics of severe cutaneous adverse drug reactions
    Gibson, Andrew
    Deshpande, Pooja
    Campbell, Chelsea N.
    Krantz, Matthew S.
    Mukherjee, Eric
    Mockenhaupt, Maja
    Pirmohamed, Munir
    Palubinsky, Amy M.
    Phillips, Elizabeth J.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2023, 151 (02) : 289 - +
  • [34] Severe Cutaneous Adverse Drug Reactions in Pediatric Patients: A Multicenter Study
    Misirlioglu, Emine Dibek
    Guvenir, Hakan
    Bahceci, Semiha
    Abul, Mehtap Haktanir
    Can, Demet
    Guc, Belgin Emine Usta
    Erkocoglu, Mustafa
    Toyran, Muge
    Nacaroglu, Hikmet Tekin
    Civelek, Ersoy
    Buyuktiryaki, Betul
    Ginis, Tayfur
    Orhan, Fazil
    Kocabas, Can Naci
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2017, 5 (03) : 757 - 763
  • [35] Drug-induced liver injury associated with severe cutaneous adverse drug reactions: A nationwide study in Taiwan
    Huang, Yi-Shin
    Wu, Chen-Yi
    Chang, Ting-Tsung
    Peng, Cheng-Yuan
    Lo, Gin-Ho
    Hsu, Chao-Wei
    Hu, Chi-Tan
    Huang, Yi-Hsiang
    LIVER INTERNATIONAL, 2021, 41 (11) : 2671 - 2680
  • [36] Pharmacogenomics of severe cutaneous adverse reactions and drug-induced liver injury
    Kaniwa, Nahoko
    Saito, Yoshiro
    JOURNAL OF HUMAN GENETICS, 2013, 58 (06) : 317 - 326
  • [37] HLA Genotype and Carbamazepine-Induced Cutaneous Adverse Drug Reactions: A Systematic Review
    Yip, V. L.
    Marson, A. G.
    Jorgensen, A. L.
    Pirmohamed, M.
    Alfirevic, A.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2012, 92 (06) : 757 - 765
  • [38] Genetic Association of Co-Trimoxazole-Induced Severe Cutaneous Adverse Reactions Is Phenotype-Specific: HLA Class I Genotypes and Haplotypes
    Sukasem, Chonlaphat
    Pratoomwun, Jirawat
    Satapornpong, Patompong
    Klaewsongkram, Jettanong
    Rerkpattanapipat, Ticha
    Rerknimitr, Pawinee
    Lertpichitkul, Pattamon
    Puangpetch, Apichaya
    Nakkam, Nontaya
    Konyoung, Parinya
    Khunarkornsiri, Usanee
    Disphanurat, Wareeporn
    Srisuttiyakorn, Chutika
    Pattanacheewapull, Oranuch
    Kanjanawart, Sirimas
    Kongpan, Thachanan
    Chumworathayi, Pansu
    Saksit, Niwat
    Bruminhent, Jackrapong
    Tassaneeyakul, Wichittra
    Chantratita, Wasun
    Pirmohamed, Munir
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2020, 108 (05) : 1078 - 1089
  • [39] Immunohistopathological Findings of Severe Cutaneous Adverse Drug Reactions
    Orime, Mari
    JOURNAL OF IMMUNOLOGY RESEARCH, 2017, 2017
  • [40] Association between HLA-B*1502 allele and carbamazepine-induced severe cutaneous adverse reactions in Han people of southern China mainland
    Wang, Qian
    Zhou, Jue-qian
    Zhou, Lie-min
    Chen, Zi-yi
    Fang, Zi-yan
    Chen, Shu-da
    Yang, Li-bai
    Cai, Xiao-dong
    Dai, Qi-lin
    Hong, Hua
    Wang, Hong-xuan
    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2011, 20 (06): : 446 - 448