The investigation of host genetic variants of toll-like receptor 7 and 8 in COVID-19

Toll-like receptors (TLRs) recognize infectious agents and play an important role in the innate immune system. Studies have suggested that TLR single nucleotide polymorphisms (SNPs) are associated with poor antiviral responses against SARS-CoV-2. Therefore, we aimed to investigate the relationship of TLR7 and TLR8 (SNPs) with COVID-19 disease prognosis. A total of 120 COVID-19 patients, 40 outpatients, 40 clinical ward patients and 40 intensive care unit (ICU) patients were included in the study. TLR7 (rs179009), TLR8-129 C/G (rs3764879) and TLR8 Met1Val (rs3764880) SNPs were genotyped using the PCR-RFLP method. In female patients, individuals carrying AG genotype and G allele for TLR8 Met1Val SNP were found at a higher frequency in patients hospitalized in the ICU than in patients followed in the clinical ward (p < 0.05). In terms of the other two SNPs, no significant difference was found between the groups in females. Furthermore, in male patients, A allele of TLR7 rs179009 SNP was at a higher frequency in patients who have at least one comorbidity than in patients who have no comorbidity (p < 0.05). Our results suggest that TLR8 Met1Val SNP is important in the COVID-19 disease severity in females. Furthermore, TLR7 rs179009 SNP is important in male patients in the presence of comorbid diseases.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:42

Enthalten in:

Nucleosides, nucleotides & nucleic acids - 42(2023), 8 vom: 14., Seite 586-602

Sprache:

Englisch

Beteiligte Personen:

Bagci, Gokhan [VerfasserIn]
Gundogdu, Oguz [VerfasserIn]
Pektas, Ayse Nur [VerfasserIn]
Bagci, Binnur [VerfasserIn]
Avci, Onur [VerfasserIn]
Gursoy, Sinan [VerfasserIn]
Kaygusuz, Kenan [VerfasserIn]
Elaldi, Nazif [VerfasserIn]

Links:

Volltext

Themen:

COVID-19
Journal Article
Single nucleotide polymorphism
TLR7
TLR8
Toll-Like Receptor 7
Toll-Like Receptor 8
Toll-like receptor

Anmerkungen:

Date Completed 23.06.2023

Date Revised 23.06.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1080/15257770.2023.2176515

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM352937963