Frontiers in Immunology (Sep 2023)

Serum pro-inflammatory biomarkers associated with improvement in quality of life in pulmonary tuberculosis

  • Laura E. Carreto-Binaghi,
  • Luis Gustavo Sartillo-Mendoza,
  • Luis Gustavo Sartillo-Mendoza,
  • Luis Gustavo Sartillo-Mendoza,
  • Marcela Muñoz-Torrico,
  • Silvia Guzmán-Beltrán,
  • Claudia Carranza,
  • Martha Torres,
  • Yolanda González,
  • Esmeralda Juárez

DOI
https://doi.org/10.3389/fimmu.2023.1241121
Journal volume & issue
Vol. 14

Abstract

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IntroductionPulmonary dysfunction is an underestimated complication in tuberculosis (TB) infection, affecting quality of life (QoL). Although respiratory function tests objectively reflect lung disturbances in a specific moment, predictors of illness severity at the time of diagnosis are still lacking.MethodsWe measured serum pro-inflammatory cytokines (TNF-α and IL-8), eicosanoids (PGE2, LTB4, RvD1, Mar1, and LXA4), a marker of tissue damage (cell-free nucleosomes), and indicators of redox status (malonaldehyde, 8-isoprostane, total oxidants, and antioxidants), as well as a score of radiological abnormalities (SRA) and a QoL questionnaire, in 25 patients with pulmonary TB at the time of diagnosis (t0) and two months after the initiation of treatment (t2).ResultsWe found higher antioxidant levels in the patients with the worst QoL at t0, and all the indicators of the prooxidant state were significantly reduced at t2, while the total antioxidant levels increased. LTB4, a pro-inflammatory eicosanoid, was diminished at t2, while all the pro-resolutory lipids decreased substantially. Significant correlations between the SRA and the QoL scores were observed, the latter showing a substantial reduction at t2, ranking it as a reliable tool for monitoring disease evolution during TB treatment.DiscussionThese results suggest that evaluating a combination of these markers might be a valuable predictor of QoL improvement and a treatment response indicator; in particular, the oxidation metabolites and eicosanoid ratios could also be proposed as a future target for adjuvant therapies to reduce inflammation-associated lung injury in TB disease.

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