The role of soluble toll-like receptor-2 and 4 in children with pneumonia: a combined analysis of saliva and serum samples

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Authors: Özlem Necipoğlu Banak, Osman Oguz Demir, Kübra Aykaç, Sevilay Karahan, Ali Bülent Cengiz, Malik Aydin, Yasemin Özsürekçi
Cited by: 0
References: 54

Abstract

Background Since rapid and accurate diagnosis of pneumonia and determination of its severity remain challenging, particularly in childhood, we aimed to evaluate the role of toll-like receptors (TLR) in pneumonia, which has been limited in animal and adult studies. Methods In this study, TLR-2, TLR-4, interleukin (IL)-1β, IL-4, IL-6, IL-10, interferon (IFN)-α, and tumor necrosis factor (TNF)-α levels were measured in serum samples of n = 67 pediatric patients with community acquired pneumonia (CAP) (43 inpatients and 24 outpatients) and 22 healthy pediatric controls. Saliva samples of n = 30 pediatric patients with CAP (19 inpatients and 11 outpatients) and 19 healthy pediatric controls were also investigated to analyze the expression of these cytokines and TLRs. Results In saliva samples taken at the time of diagnosis, threshold levels of TLR-2 were 1.16 2 -ΔΔ Ct and of TLR-4 1.28 2 -ΔΔ Ct differentiating patients with and without pneumonia. The sensitivity of salivary TLR-2 and TLR-4 tests were found to be 0.80 and 0.86, respectively. In serum samples, soluble TLR-2 and TLR-4, IL-1β, IL-4, IL-6, Il-10, IFN-α, and TNF-α levels were significantly decreased in patients with coronavirus disease-19 (COVID-19) as compared with other viruses ( p < 0.05 in each). Only one mortal case was present in the inpatient group during the study period. Conclusion This study demonstrates that salivary TNF-α, soluble TLR-2 and TLR-4 may serve as promising non-invasive biomarkers for diagnosing and stratifying pediatric pneumonia.

Fields of Study & Subjects

Pneumonia and Respiratory Infections Immune Response and Inflammation Inflammation biomarkers and pathways

Publication details

Journal / source
Frontiers in Immunology
Volume
17
Pages
1657027–1657027
Publication date
13 February 2026
Language
EN