Genetic variation at the Th2 immune gene IL13 is associated with IgE-mediated paediatric food allergy

被引:29
作者
Ashley, S. E. [1 ,2 ]
Tan, H-T. T. [1 ,3 ]
Peters, R. [1 ,4 ]
Allen, K. J. [1 ,4 ,5 ,6 ]
Vuillermin, P. [1 ,7 ,8 ]
Dharmage, S. C. [1 ,9 ]
Tang, M. L. K. [1 ,4 ,5 ]
Koplin, J. [1 ,9 ]
Lowe, A. [1 ,9 ]
Ponsonby, A. -L. [1 ,4 ]
Molloy, J. [1 ,7 ,8 ]
Matheson, M. C. [1 ,4 ]
Saffery, R. [1 ,2 ,4 ]
Ellis, J. A. [1 ,4 ,10 ]
Martino, D. [1 ,4 ,11 ]
机构
[1] Royal Childrens Hosp, Murdoch Childrens Res Inst, Murdoch, WA, Australia
[2] Monash Univ, MTHP, Hudson Inst, Clayton, Vic, Australia
[3] Univ Sains Malaysia, Sch Med Sci, Dept Immunol, Kubang Kerian, Malaysia
[4] Univ Melbourne, Dept Paediat, Parkville, Vic, Australia
[5] Royal Childrens Hosp, Dept Allergy & Immunol, Parkville, Vic, Australia
[6] Univ Manchester, Inst Inflammat & Repair, Manchester, Lancs, England
[7] Child Hlth Res Unit, Barwon Hlth, Geelong, Vic, Australia
[8] Deakin Univ, Waurn Ponds, Australia
[9] Univ Melbourne, Sch Populat & Global Hlth, Ctr Epidemiol & Biostat, Melbourne, Vic, Australia
[10] Deakin Univ, Fac Hlth, Ctr Social & Early Emot Dev, Waurn Ponds, Australia
[11] Univ Western Australia, Dept Paediat, Perth, WA, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
food allergy; food sensitization; IL13; Immunoglobulin E; interleukin-13; single nucleotide polymorphism; GERMAN MULTICENTER ATOPY; INTERLEUKIN-13; GENE; COHORT PROFILE; ASTHMA; POLYMORPHISM; POPULATION; PEANUT; INFLAMMATION; PREVALENCE; PREDICTORS;
D O I
10.1111/cea.12942
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Food allergies pose a considerable world-wide public health burden with incidence as high as one in ten in 12-month-old infants. Few food allergy genetic risk variants have yet been identified. The Th2 immune gene IL13 is a highly plausible genetic candidate as it is central to the initiation of IgE class switching in B cells. Objective: Here, we sought to investigate whether genetic polymorphisms at IL13 are associated with the development of challenge-proven IgE-mediated food allergy. Method: We genotyped nine IL13 "tag" single nucleotide polymorphisms (tag SNPs) in 367 challenge-proven food allergic cases, 199 food-sensitized tolerant cases and 156 non-food allergic controls from the HealthNuts study. 12-month-old infants were phenotyped using open oral food challenges. SNPs were tested using Cochran-Mantel-Haenszel test adjusted for ancestry strata. A replication study was conducted in an independent, co-located sample of four paediatric cohorts consisting of 203 food allergic cases and 330 non-food allergic controls. Replication sample phenotypes were defined by clinical history of reactivity, 95% PPV or challenge, and IL13 genotyping was performed. Results: IL13 rs1295686 was associated with challenge-proven food allergy in the discovery sample (P=.003; OR=1.75; CI=1.20-2.53). This association was also detected in the replication sample (P=.03, OR=1.37, CI=1.03-1.82) and further supported by a meta-analysis (P=.0006, OR=1.50). However, we cannot rule out an association with food sensitization. Carriage of the rs1295686 variant A allele was also associated with elevated total plasma IgE. Conclusions and Clinical Relavance: We show for the first time, in two independent cohorts, that IL13 polymorphism rs1295686 (in complete linkage disequilibrium with functional variant rs20541) is associated with challenge-proven food allergy.
引用
收藏
页码:1032 / 1037
页数:6
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