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MBL2 genetic polymorphisms and HIV-1 mother-to-child transmission in Zambia
- Publication Year :
- 2016
-
Abstract
- Since antiretroviral drugs have been introduced to prevent mother-to-child transmission, the risk of HIV-1 infection in infants has decreased considerably worldwide. Nevertheless, many factors are involved in viral transmission and host susceptibility to infection. The immune system and its components, including mannose binding protein C (encoding by MBL2 gene), are already known to play an important role in this scenario. In the present study, 313 children and 98 of their mothers from Zambia were genotyped for the MBL2 promoter HL (rs11003125) and XY (rs7096206) polymorphisms and exon 1 D (rs5030737, at codon 52) B (rs1800450, at codon 54) and C (rs1800451, at codon 57) polymorphisms in order to investigate the potential role of these genetic variants in HIV-1 mother-to-child transmission. No statistical significant association was observed comparing transmitter and non-transmitter mothers and also confronting HIV-positive and HIV-negative children. The findings of the current study obtained on mother and children from Zambia evidence lack of association between MBL2 functional polymorphisms and HIV-1 mother-to-child transmission.
- Subjects :
- 0301 basic medicine
Adult
Male
Mother to child transmission
Adolescent
Genotype
Immunology
Human immunodeficiency virus (HIV)
Mannose-Binding Protein C
Zambia
HIV Infections
Mbl2 gene
medicine.disease_cause
Mannose-Binding Lectin
Polymorphism, Single Nucleotide
03 medical and health sciences
Exon
Young Adult
0302 clinical medicine
Immune system
medicine
Humans
Promoter Regions, Genetic
Genetic Association Studies
Genetics
Innate immunity
Innate immune system
Transmission (medicine)
business.industry
Mother-to-child transmission
Infant, Newborn
Middle Aged
Infectious Disease Transmission, Vertical
030104 developmental biology
MBL2
HIV-1
Female
business
030215 immunology
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....53bc577c42b4462d8a6a2e763b71c9c5
- Full Text :
- https://doi.org/10.1007/s12026-015-8779-1