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Variation at HLA-DRB1 is associated with resistance to enteric fever

Cited 76 time in Web of Science Cited 71 time in Scopus
Authors

Dunstan, Sarah J.; Nguyen Thi Hue; Buhm Han; Li, Zheng; Trinh Thi Bich Tram; Sim, Kar Seng; Parry, Christopher M.; Nguyen Tran Chinh; Ha Vinh; Nguyen Phu Huong Lan; Nga Tran Vu Thieu; Phat Voong Vinh; Koirala, Samir; Dongol, Sabina; Arjyal, Amit; Karkey, Abhilasha; Shilpakar, Olita; Dolecek, Christiane; Foo, Jia Nee; Le Thi Phuong; Mai Ngoc Lanh; Tan Do; Aung, Tin; Do Nu Hon; Teo, Yik Ying; Hibberd, Martin L.; Anders, Katherine L.; Okada, Yukinori; Raychaudhuri, Soumya; Simmons, Cameron P.; Baker, Stephen; de Bakker, Paul I. W.; Basnyat, Buddha; Tran Tinh Hien; Farrar, Jeremy J.; Khor, Chiea Chuen

Issue Date
2014-12
Publisher
Nature Publishing Group
Citation
Nature Genetics, Vol.46, pp.1333-1336
Abstract
Enteric fever affects more than 25 million people annually and results from systemic infection with Salmonella enterica serovar Typhi or Paratyphi pathovars A, B or C-1. We conducted a genome-wide association study of 432 individuals with blood culture-confirmed enteric fever and 2,011 controls from Vietnam. We observed strong association at rs7765379 (odds ratio (OR) for the minor allele = 0.18, P = 4.5 x 10(-10)), a marker mapping to the H LA class II region, in proximity to HLA-DQB1 and HLA-DRB1. We replicated this association in 595 enteric fever cases and 386 controls from Nepal and also in a second independent collection of 151 cases and 668 controls from Vietnam. Imputation-based fine-mapping across the extended MHC region showed that the classical HLA-DRB1*04:05 allele (OR = 0.14, P = 2.60 x 10(-11)) could entirely explain the association at rs7765379, thus implicating HLA-DRB1 as a major contributor to resistance against enteric fever, presumably through antigen presentation.
ISSN
1061-4036
URI
https://hdl.handle.net/10371/191600
DOI
https://doi.org/10.1038/ng.3143
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  • College of Medicine
  • Department of Medicine
Research Area Bioinformatics, Computational Biology, Genomics, Human Leukocyte Antigen, Statistical Genetics

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