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喀麦隆五种艾滋病相关基因在母婴传播及人类免疫缺陷病毒1型感染中的作用

IMPLICATION OF FIVE AIDS RELATED GENES IN MOTHER-TO-CHILD TRANSMISSION AND ACQUISITION OF HUMAN IMMUNODEFICIENCY VIRUS 1 IN CAMEROON.

作者信息

Mekue Linda Mouafo, Nkenfou Céline Nguefeu, Dambaya Beatrice, Fotso Idriss, Nguefack Felicitée, Fainguem Nadine, Lobè Elise Elong, Kuiaté Jules Roger, Ndjolo Alexis

机构信息

Faculty of Science, University of Dschang, P.O. Box 56, Dschang, Cameroon.

Chantal BIYA International Reference Centre, P.O. Box 3077, Yaounde, Cameroon.

出版信息

Afr J Infect Dis. 2018 Dec 12;13(1):1-10. doi: 10.21010/ajid.v13i1.1. eCollection 2019.

Abstract

BACKGROUND

Genetic variants in the mother and/or infant have been described with evidence to be associated with mother-to-child transmission of HIV, but somehow with contradictory results depending on ethnic or geographic populations. We aimed at looking at the association between the allelic frequency of some genes with vertical transmission or acquisition of HIV in Cameroon.

METHODOLOGY

A total of 262 mothers (212 HIV-infected and 50 HIV non-infected) with their babies (270 in total, 42 HIV exposed-infected, 178 HIV exposed non-infected and 50 HIV non-exposed) were recruited in Yaounde-Cameroon. Their genotypes for , , , and were analyzed using polymerase chain reaction and restriction fragment length polymorphisms.

RESULTS

Allelic frequencies were 14.7%, 41.9%, 9.5% and 14.7% for , respectively in the mothers and 18.8%, 35.9%, 11.3% and 20.5% in the babies. No delta 32 mutation in the gene was found. The mutant genotype was most significantly frequent in the non-transmitter than in the transmitter (p= 0.005) for the . [Odd ratio = 1.69; 95% confidence interval: 0.1158 to 0.7277); was associated to MTCT, = 0.008.The homozygote mutants for the were significantly higher in the infected than in the exposed uninfected babies (p=0.04). The mutations in the other genes were neither implicated in the acquisition nor in the transmission.

CONCLUSION

was associated to the reduction of MTCT. The favored acquisition of HIV by babies. Our study showed that polymorphisms in chemokine ligand may be involved in MTCT.

摘要

背景

已有证据表明母亲和/或婴儿的基因变异与HIV母婴传播有关,但因种族或地理人群的不同,结果存在矛盾。我们旨在研究喀麦隆某些基因的等位基因频率与HIV垂直传播或感染之间的关联。

方法

在喀麦隆雅温得招募了262名母亲(212名感染HIV,50名未感染HIV)及其婴儿(共270名,42名暴露于HIV并感染,178名暴露于HIV但未感染,50名未暴露于HIV)。使用聚合酶链反应和限制性片段长度多态性分析她们的 、 、 、 和 基因的基因型。

结果

母亲中 、 、 、 的等位基因频率分别为14.7%、41.9%、9.5%和14.7%,婴儿中分别为18.8%、35.9%、11.3%和20.5%。未发现 基因的delta 32突变。对于 ,突变基因型在未传播者中比在传播者中更为常见(p = 0.005)。[比值比 = 1.69;95%置信区间:0.1158至0.7277];与母婴传播相关, = 0.008。感染婴儿中 纯合子突变体显著高于暴露但未感染的婴儿(p = 0.04)。其他基因的突变与感染或传播均无关。

结论

与母婴传播减少有关。 有利于婴儿感染HIV。我们的研究表明趋化因子配体的多态性可能与母婴传播有关。

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