Department of Clinical Biochemistry and Immunology, Statens Serum Institut.
J Infect Dis. 2014 Jan 15;209(2):285-9. doi: 10.1093/infdis/jit422. Epub 2013 Aug 9.
Immunoglobulin G (IgG) cross-linking with Fc gamma receptor IIIB (FcγRIIIB) triggers neutrophil degranulation, releasing reactive oxygen species with high levels associated with protection against malaria. The FCGR3B-c.233C>A polymorphism thought to influence the interaction between IgG and FcγRIIIB was recently associated with malaria. We studied the statistical interaction between glutamate rich protein antibodies and FCGR3B-c.233C>A genotypes on risk of malaria in a cohort of Ghanaian children. The absolute risk of malaria decreased more rapidly with increasing antibody levels for 233AA/AC individuals compared with 233CC children. This genotype related effect modification may significantly influence malaria sero-epidemiological and vaccine trial studies.
免疫球蛋白 G(IgG)与 Fc 受体 IIIB(FcγRIIIB)交联触发中性粒细胞脱颗粒,释放具有高水平的活性氧,与对疟疾的保护有关。最近,FcGR3B-c.233C>A 多态性被认为会影响 IgG 与 FcγRIIIB 之间的相互作用,与疟疾有关。我们研究了在加纳儿童队列中,富谷氨酸蛋白抗体与 FCGR3B-c.233C>A 基因型之间的统计学相互作用对疟疾风险的影响。与 233CC 儿童相比,233AA/AC 个体的抗体水平越高,疟疾的绝对风险下降得越快。这种与基因型相关的效应修饰可能会显著影响疟疾血清流行病学和疫苗试验研究。