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A TNF region haplotype offers protection from typhoid fever in Vietnamese patients
Authors:Sarah J. Dunstan  Nguyen Thi Hue  Kirk Rockett  Julian Forton  Andrew P. Morris  Mahamadou Diakite  Mai Ngoc Lanh  Le Thi Phuong  Deborah House  Christopher M. Parry  Ha Vinh  Nguyen T. Hieu  Gordon Dougan  Tran Tinh Hien  Dominic Kwiatowski  Jeremy J. Farrar
Affiliation:(1) Oxford University Clinical Research Unit, Hospital for Tropical Diseases, 190 Ben Ham Tu, Quan 5, District 5, Ho Chi Minh City, Vietnam;(2) Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, Oxford University, OX3 7LJ Oxford, United Kingdom;(3) Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam;(4) Wellcome Trust Centre for Human Genetics, Oxford University, OX3 7BN Oxford, UK;(5) Dong Thap Provincial Hospital, Dong Thap, Vietnam;(6) Wellcome Trust Sanger Centre Hinxton, Cambridge, UK;(7) Department of Medical Microbiology and Genitourinary Medicine, University of Liverpool, Liverpool, UK;(8) Hung Vuong Hospital, Ho Chi Minh City, Vietnam
Abstract:The genomic region surrounding the TNF locus on human chromosome 6 has previously been associated with typhoid fever in Vietnam (Dunstan et al. in J Infect Dis 183:261–268, 2001). We used a haplotypic approach to understand this association further. Eighty single nucleotide polymorphisms (SNPs) spanning a 150 kb region were genotyped in 95 Vietnamese individuals (typhoid case/mother/father trios). A subset of data from 33 SNPs with a minor allele frequency of >4.3% was used to construct haplotypes. Fifteen SNPs, which tagged the 42 constructed haplotypes were selected. The haplotype tagging SNPs (T1–T15) were genotyped in 380 confirmed typhoid cases and 380 Vietnamese ethnically matched controls. Allelic frequencies of seven SNPs (T1, T2, T3, T5, T6, T7, T8) were significantly different between typhoid cases and controls. Logistic regression results support the hypothesis that there is just one signal associated with disease at this locus. Haplotype-based analysis of the tag SNPs provided positive evidence of association with typhoid (posterior probability 0.821). The analysis highlighted a low-risk cluster of haplotypes that each carry the minor allele of T1 or T7, but not both, and otherwise carry the combination of alleles *12122*1111 at T1–T11, further supporting the one associated signal hypothesis. Finally, individuals that carry the typhoid fever protective haplotype *12122*1111 also produce a relatively low TNF-α response to LPS.
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