AI Article Synopsis

  • There is a pressing need for better diagnostic tools to differentiate between latent tuberculosis infection (LTBI) and active tuberculosis (TB).
  • Recent studies indicate that specific cytokines could act as biomarkers to track the progression of TB disease.
  • In research conducted in Durban, South Africa, certain proteins (IL-1RA, IL-6, and IP-10) were found at higher levels in individuals with active TB, suggesting their potential use as indicators for diagnosing TB.

Article Abstract

There is an urgent need for accurate and sensitive diagnostic tools that can overcome the current challenge to distinguish individuals with latent tuberculosis infection (LTBI) from individuals with active tuberculosis (TB). Recent literature has suggested that a group of cytokines may serve as biomarkers of TB disease progression. Using a multiplex ELISA, we quantified 27 circulatory markers present within the unstimulated plasma of individuals in Durban, South Africa who were healthy (n=20), LTBI (n=13), or had active TB (n=30). RT-qPCR was performed to measure gene expression of the cytokines of interest, using RNA isolated from healthy (n=20), LTBI (n=20), or active TB (n=30). We found that at the protein level, IL-1RA, IL-6, and IP-10 were significantly more abundant in participants with active TB (p< 0.05) compared to those with LTBI individuals. IP-10 also showed the strongest association with active TB compared to healthy and LTBI at mRNA level. Our data shows that these proteins may serve as biomarkers of TB at both the protein and gene level.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184682PMC
http://dx.doi.org/10.3389/fcimb.2022.908144DOI Listing

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