AI Article Synopsis
- - The study investigated the impact of genetic variations in Toll-like receptors (TLRs) on the progression of HIV disease, particularly in patients with and without tuberculosis (TB) co-infection.
- - Involving 373 HIV-positive participants over two years, the research found that 98 patients developed active TB/AIDS and had a higher frequency of the AA genotype of TLR9 compared to those who did not progress to TB/AIDS.
- - The findings suggest that HIV-positive individuals with the AA genotype of TLR9 have a higher susceptibility to developing TB during HIV disease progression.
Article Abstract
Background: Toll-like receptors (TLRs) are identified as one of the key components of the innate immune system. The objective of this study was to explore the influence of genetic variability in these TLRs on human immunodeficiency virus (HIV) disease progression with and without tuberculosis (TB) co-infection.
Materials And Methods: This prospective, cross-sectional, and longitudinal study included 373 HIV-positive patients without TB infection. This study aimed to examine the genetic variation in TLRs (TLR2, TLR4, and TLR9) between patients with HIV-1 infection and those who progressed to active TB during the two years of follow-up.
Results: During the two year follow-up of 373 positive patients, 98 patients progressed to active TB/AIDS (acquired immunodeficiency syndrome). When comparing 98 HIV patients who developed active TB/AIDS to 275 HIV patients who did not, it was discovered that the frequency of the A allele in TLR9 was considerably higher ( <0.001) in HIV patients progressed to active TB/AIDS. Ninety eight HIV individuals who advanced to active TB/AIDS showed a significantly higher frequency of the AA genotype in TLR9 than did in HIV patients who had no TB/AIDS (p <0.001).
Conclusion: The increased association of the AA genotype of TLR9 in HIV patients who progressed to active TB during follow-up suggests that HIV-positive patients with the AA genotype of TLR9 have increased susceptibility towards TB during the disease progression.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11128240 | PMC |
| http://dx.doi.org/10.2147/JIR.S451431 | DOI Listing |
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