A single-nucleotide polymorphism in TLR4 is linked with the risk of HIV-1 infection. Issue 2 (3rd April 2019)

• Record Type: Journal Article
• Authors: Vidyant, S; Chatterjee, A; Dhole, TN
• Is Part Of: British journal of biomedical science. Volume 76:Issue 2(2019)
• Page Start: 59
• Page End: 63
• Publication Date: 2019-04-03
• Subjects: TLR 4 -- polymorphism -- HIV -- disease susceptibility; Medical sciences -- Periodicals; Medical technology -- Periodicals; Biological Science Disciplines; Clinical Laboratory Techniques; Medical Laboratory Science; Anatomie pathologique; Medical sciences; Medical technology; Klinische chemie; Laboratoriumonderzoek; Periodicals; Periodicals; 616.0756; 610.07 M489L
• DOI: 10.1080/09674845.2018.1559486
• Languages: English
• ISSNs: 0967-4845

Abstract

ABSTRACT: Introduction : Toll-like receptors (TLRs) are pattern recognition receptors that play a role in innate immunity. Mounting evidence shows that single-nucleotide polymorphisms (SNPs) in TLRs link to various infectious diseases, including human immunodeficiency virus (HIV). We hypothesized links between two TLR4 SNPs (rs4986790 leading to Asp299Gly and rs4986791 leading to Thr399Ile) and HIV, to investigate the frequency of TLR4 polymorphism and its role in patients infected with HIV. Materials and methods : We recruited 160 HIV-1 seropositive patients, who were further divided on disease severity based on CD4 count (stages I, II and III), and 270 age- and sex matched healthy HIV-1 seronegative individuals. Subjects were genotyped for TLR4 gene polymorphism by polymerase chain reaction restriction fragment length polymorphism. Results : The TLR4 Asp299Gly heterozygous genotype (OR=2.160; p=0.004) and the mutant allele G (OR=2.051; p=0.002) was higher in HIV-1 infection than healthy controls and also in stage I (OR=2.559; p=0.034) compared to different clinical stages of infection. There was no link between the Thr399Ile polymorphism and HIV infection. Conclusion : The TLR4 (Asp299Gly) SNP is a risk factor in HIV-1 disease susceptibility.