Inserm U-954, Faculté de Médecine, University of Lorraine and University Hospital Center (CHU) of Nancy, Nancy, France.
Department of Internal Medicine and Geriatrics, UCSC-Allergy Unit, Complesso Integrato Columbus, Rome, Italy; IRCCS of Mental Retardation and Brain Aging, Oasi Maria S.S., Troina, Italy.
J Allergy Clin Immunol. 2015 Jan;135(1):253-9. doi: 10.1016/j.jaci.2014.07.047. Epub 2014 Sep 12.
Immediate reactions to β-lactams are the most common causes of anaphylactic reactions and can be life-threatening. The few known genetic factors influencing these reactions suggest a link with atopy and inflammation.
We performed a fine-mapping genome-wide association study of the genetic predictors of β-lactam allergy to better understand the underlying mechanisms.
We studied 387 patients with immediate allergic reactions to β-lactams and 1124 paired control subjects from Spain. We replicated the results in 299 patients and 362 paired control subjects from Italy.
We found significant associations with the single nucleotide polymorphisms rs4958427 of ZNF300 (c.64-471G>A, P = 9.9 × 10(-9)), rs17612 of C5 (c.4311A>C [p.Glu1437Asp], P = 7.5 × 10(-7)), rs7754768 and rs9268832 of the HLA-DRA | HLA-DRB5 interregion (P = 1.6 × 10(-6) and 4.9 × 10(-6)), and rs7192 of HLA-DRA (c.724T>G [p.Leu242Val], P = 7.4 × 10(-6)) in an allelic model, with similar results in an additive model. Single nucleotide polymorphisms of HLA-DRA and ZNF300 predicted skin test positivity to amoxicillin and other penicillins but not to cephalosporins. A haplotype block in HLA-DRA and the HLA-DRA | HLA-DRB5 interregion encompassed a motif involved in balanced expression of the α- and β-chains of MHC class II, whereas rs7192 was predicted to influence α-chain conformation. HLA-DRA rs7192 and rs8084 were significantly associated with allergy to penicillins and amoxicillin (P = 6.0 × 10(-4) and P = 4.0 × 10(-4), respectively) but not to cephalosporins in the replication study.
Gene variants of HLA-DRA and the HLA-DRA | HLA-DRB5 interregion were significant predictors of allergy to penicillins but not to cephalosporins. These data suggest complex gene-environment interactions in which genetic susceptibility of HLA type 2 antigen presentation plays a central role.
β-内酰胺类抗生素的即刻反应是引起过敏反应的最常见原因,且可能危及生命。少数已知的影响此类反应的遗传因素提示其与过敏和炎症有关。
我们进行了一项β-内酰胺类抗生素过敏遗传预测因子的精细定位全基因组关联研究,以更好地了解其潜在机制。
我们研究了来自西班牙的 387 例β-内酰胺类抗生素即刻过敏反应患者和 1124 例配对对照者。我们在来自意大利的 299 例患者和 362 例配对对照者中对结果进行了复制。
我们发现 ZNF300 的单核苷酸多态性 rs4958427(c.64-471G>A,P=9.9×10(-9))、C5 的 rs17612(c.4311A>C[p.Glu1437Asp],P=7.5×10(-7))、HLA-DRA|HLA-DRB5 间隔区的 rs7754768 和 rs9268832(P=1.6×10(-6)和 4.9×10(-6))和 HLA-DRA 的 rs7192(c.724T>G[p.Leu242Val],P=7.4×10(-6))在等位基因模型中与即刻过敏反应显著相关,在加性模型中也有类似的结果。HLA-DRA 和 ZNF300 的单核苷酸多态性预测了对阿莫西林和其他青霉素的皮试阳性,但不能预测对头孢菌素的皮试阳性。HLA-DRA 中的单核苷酸多态性和 HLA-DRA|HLA-DRB5 间隔区的单核苷酸多态性包含一个与 MHC Ⅱ类α和β链平衡表达有关的基序,而 rs7192 则预测影响α链构象。HLA-DRA 的 rs7192 和 rs8084 与青霉素和阿莫西林过敏显著相关(P=6.0×10(-4)和 P=4.0×10(-4)),但在复制研究中与头孢菌素过敏不相关。
HLA-DRA 和 HLA-DRA|HLA-DRB5 间隔区的基因变异是青霉素过敏的重要预测因子,但不能预测头孢菌素过敏。这些数据表明 HLA Ⅱ类抗原呈递的遗传易感性在其中发挥核心作用的复杂基因-环境相互作用。