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Genome-wide association study of antibody responses to Plasmodium falciparum candidate vaccine antigens

机译:对恶性疟原虫候选疫苗抗原的抗体应答的全基因组关联研究

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We conducted a genome-wide association study (GWAS) of antibody responses directed to three Plasmodium falciparum vaccine candidate antigens (MSP1, MSP2 and GLURP) previously associated with different patterns of protection against malaria infection in Senegalese children. A total of 174 950 single-nucleotide polymorphisms (SNPs) were tested for association with immunoglobulin G1 (IgG1) responses directed to MSP1 and to GLURP and with IgG3 responses to MSP2 FC27 and to MSP2 3D7. We first performed a single-trait analysis with each antibody response and then a multiple-trait analysis in which we analyzed simultaneously the three immune responses associated with the control of clinical malaria episodes. Suggestive associations (P < 1x10(-4)) were observed for 25 SNPs in MSP1 antibody response analysis or in multiple-trait analysis. According to the strength of their observed associations and their functional role, the following genes are of particular interest: RASGRP3 (2p22.3, P = 7.6 x 10(-6)), RIMS1 (6q13, P = 2.0 x 10(-5)), MVB12B (9q33.3, P = 8.9 x 10(-5)) and GNPTAB (12q23.2, P = 7.4 x 10(-5)). Future studies will be required to replicate these findings in other African populations. This work will contribute to the elucidation of the host genetic factors underlying variable immune responses to P. falciparum.
机译:我们进行了针对三项恶性疟原虫疫苗候选抗原(MSP1,MSP2和GLURP)的抗体应答的全基因组关联研究(GWAS),该抗原先前与塞内加尔儿童的疟疾感染保护作用不同。测试了总共174950个单核苷酸多态性(SNP)与针对MSP1和GLURP的免疫球蛋白G1(IgG1)反应以及与针对MSP2 FC27和MSP2 3D7的IgG3反应的关联。我们首先对每种抗体反应进行了单性状分析,然后进行了多性状分析,其中我们同时分析了与临床疟疾发作控制相关的三种免疫反应。在MSP1抗体反应分析或多特征分析中观察到25个SNP的暗示性关联(P <1x10(-4))。根据它们观察到的关联的强度及其功能作用,下列基因特别受关注:RASGRP3(2p22.3,P = 7.6 x 10(-6)),RIMS1(6q13,P = 2.0 x 10(-5) )),MVB12B(9q33.3,P = 8.9 x 10(-5))和GNPTAB(12q23.2,P = 7.4 x 10(-5))。将需要进一步的研究来在其他非洲人口中复制这些发现。这项工作将有助于阐明对恶性疟原虫的可变免疫反应基础的宿主遗传因素。

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