Toll Like Receptor-4 Gene Polymorphism and Susceptibility to Pulmonary Tuberculosis
THE EGYPTIAN JOURNAL OF IMMUNOLOGY • 2019
Publication Information
Authors
Nehad A. Fouad¹, Amal M. Saeed¹, Ahmed W Mahedy
Keywords
Not Available
Journal
THE EGYPTIAN JOURNAL OF IMMUNOLOGY
Publisher
Not Available
Volume
Vol. 26 (2),
Issue
Vol. 26 (2),
Pages
01-10
publication.type
International
Paper Link
Not Available
Supplementary Materials
Not Available
Abstract
Tuberculosis (TB) affects human life globally for a long time. The difference in clinical outcome of
infection suggests that host genetic makeup is responsible for such variability. Toll like receptors (TLRs)
are pattern recognition receptors and have a significant role in mycobacterial recognition by the innate
immune system. TLR-4 is the key receptor in initiation of innate immunity against M. tuberculosis. This
study investigated whether variants in TLR-4 896A/G (Asp299Gly) and TLR-4 1196C/T (Thr399Ile) genes
are related with susceptibility or resistance to pulmonary tuberculosis (PTB) in Saudi population.
Genotyping of TLR-4 896A/G, TLR-4 1196C/T gene was performed by polymerase chain reaction followed
by restriction fragment length polymorphism (PCR –RFLP) in 60 PTB patients and 60 control subjects.
The A allele at (896A/G) was more frequent in the control group while G allele was more common in PTB
patients. The frequency of T allele of (1196C/T) polymorphism was significantly increased in PTB patients
as compared to the control group (P
infection suggests that host genetic makeup is responsible for such variability. Toll like receptors (TLRs)
are pattern recognition receptors and have a significant role in mycobacterial recognition by the innate
immune system. TLR-4 is the key receptor in initiation of innate immunity against M. tuberculosis. This
study investigated whether variants in TLR-4 896A/G (Asp299Gly) and TLR-4 1196C/T (Thr399Ile) genes
are related with susceptibility or resistance to pulmonary tuberculosis (PTB) in Saudi population.
Genotyping of TLR-4 896A/G, TLR-4 1196C/T gene was performed by polymerase chain reaction followed
by restriction fragment length polymorphism (PCR –RFLP) in 60 PTB patients and 60 control subjects.
The A allele at (896A/G) was more frequent in the control group while G allele was more common in PTB
patients. The frequency of T allele of (1196C/T) polymorphism was significantly increased in PTB patients
as compared to the control group (P
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