Diagnostic Efficacy and Prognostic Recurrence Prediction Effect of Regulatory T Cells plus TGF-β1 in Pediatric Patients with Allergic Rhinitis and Concurrent Adenoid Hypertrophy
Abstract
Objective: The co-occurrence of adenoid hypertrophy (AH) and allergic rhinitis (AR) is known to be linked to immune microenvironment disruptions. This research was designed to assess how regulatory T cells (Treg) and transforming growth factor-β1 (TGF-β1) perform in diagnosing AH in pediatric AR cases and in predicting the likelihood of post-treatment recurrence.
Methods: From February 2023 to June 2024, 127 children diagnosed with AR alone (AR group) and 134 children with AR-AH comorbidity (AR+AH group) were recruited. All participants were followed prospectively for a 12-month period. Peripheral blood Treg counts were measured using flow cytometry, while serum TGF-β1 concentrations were determined via enzyme-linked immunosorbent assay (ELISA). Diagnostic effectiveness was evaluated using receiver operating characteristic (ROC) curves. A Logistic regression model was developed to forecast recurrence risk, with model parameters refined by incorporating relevant clinical features.
Results: AR+AH cases exhibited statistically lower Treg counts and TGF-β1 levels than their AR counterparts (P<0.001). When Treg and TGF-β1 were combined for prediction, the area under the curve (AUC) reached 0.858, along with 91.04% sensitivity and 71.65% specificity—performance that outperformed either marker used individually (P<0.001). Following treatment, the increases in Treg and TGF-β1 levels were less pronounced in the AR+AH group than in the AR group (P<0.001). The follow-up data indicated 42 cases of recurrence, whose post-treatment Treg and TGF-β1 levels remained lower relative to those who did not experience a recurrence (P<0.05). A composite predictive model, integrating age, adenoid-to-nasopharynx (A/N) ratio, Treg, and TGF-β1, yielded an AUC of 0.869, with sensitivity and specificity being 95.24% and 68.48%, respectively.
Conclusion: A synergistic effect is observed when Tregs and TGF-β1 are measured together, enhancing the diagnostic accuracy for AR-AH co-occurrence. Furthermore, their combination with clinical characteristics optimizes stratification of recurrence risk.
Copyright (c) 2025 Ning Lan, Weibin Chen, Lingyun Guo, Yongping Huang

This work is licensed under a Creative Commons Attribution 4.0 International License.
The published articles will be distributed under the Creative Commons Attribution 4.0 International License (CC BY). It is allowed to copy and redistribute the material in any medium or format, and remix, transform, and build upon it for any purpose, even commercially, as long as appropriate credit is given to the original author(s), a link to the license is provided and it is indicated if changes were made. Users are required to provide full bibliographic description of the original publication (authors, article title, journal title, volume, issue, pages), as well as its DOI code. In electronic publishing, users are also required to link the content with both the original article published in Journal of Medical Biochemistry and the licence used.
Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
