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Tytuł pozycji:

Genetic variation in toll like receptors 2, 7, 9 and interleukin-6 is associated with cytomegalovirus infection in late pregnancy

Tytuł:
Genetic variation in toll like receptors 2, 7, 9 and interleukin-6 is associated with cytomegalovirus infection in late pregnancy
Autorzy:
Doreen Z. Mhandire
Kudakwashe Mhandire
Mulalo Magadze
Ambroise Wonkam
Andre P. Kengne
Collet Dandara
Temat:
Cytomegalovirus
Toll-like receptors
Interleukins
CMV DNA
Zimbabwe
Internal medicine
RC31-1245
Genetics
QH426-470
Źródło:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
Wydawca:
BMC, 2020.
Rok publikacji:
2020
Kolekcja:
LCC:Internal medicine
LCC:Genetics
Typ dokumentu:
article
Opis pliku:
electronic resource
Język:
English
ISSN:
1471-2350
Relacje:
http://link.springer.com/article/10.1186/s12881-020-01044-8; https://doaj.org/toc/1471-2350
DOI:
10.1186/s12881-020-01044-8
Dostęp URL:
https://doaj.org/article/9295c5ac947f4d3e8f00fd47ea887aca  Link otwiera się w nowym oknie
Numer akcesji:
edsdoj.9295c5ac947f4d3e8f00fd47ea887aca
Czasopismo naukowe
Abstract Background Maternal cytomegalovirus (CMV) infection and/or reactivation in pregnancy is associated with a myriad of adverse infant outcomes. However, the role of host genetic polymorphisms in modulating maternal CMV status is inconclusive. This study investigated the possible association of single nucleotide polymorphisms in toll-like receptor (TLR) and cytokine genes with maternal plasma CMV DNA status in black Zimbabweans. Methods In a cross-sectional study, 110 women in late gestation who included 36 CMV infected cases and 74 CMV uninfected, age and HIV status matched controls were enrolled. Twenty single nucleotide polymorphisms in 10 genes which code for proteins involved in immunity against CMV were genotyped using Iplex GOLD SNP genotyping protocol on the Agena MassARRAY® system. Statistical analyses were performed using Stata SE and the ‘Genetics’ and ‘SNPassoc’ packages of the statistical package R. Results The TLR7 rs179008A > T (p C (p = 0.049) polymorphism was on the borderline for association with CMV positive (CMV+) status. In contrast, the interleukin (IL)-6 rs10499563T > C (p T (p = 0.001) polymorphisms were associated with CMV negative (CMV-) status. Furthermore, allele frequencies of SNPs in TLR2, TLR4, TLR9, TLR7, IL-6, IL-10, IL-28B, IL-1A and interferon AR1 (IFNAR1) genes are being reported here for the first time in a Zimbabwean population. The allele frequencies in the Zimbabwean population are generally comparable to other African populations but different when compared to European and Asian populations. Conclusions Toll-like receptor and interleukin genetic polymorphisms influence CMV status in late gestation among black Zimbabweans. This is attributable to possible modulation of immune responses to CMV reactivation in a population previously exposed to CMV infection.
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