Identification of circulating Tfh/Th subsets as a biomarker of developed hospital-acquired pneumonia

BackgroundThis study aimed to explore the possible value of follicular helper T (Tfh) cells in hospital-acquired pneumonia (HAP).MethodsFlow cytometry was used to measure circulating Tfh and helper T cell (Th) cells in 62 HAP patients and 16 healthy individuals. HAP patients were further categorized...

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Main Authors: Yuan Peng, Tao Tao, Ni-Wen Yu, Chenyang Xu, Cheng Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Immunology
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Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2025.1513939/full
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author Yuan Peng
Tao Tao
Ni-Wen Yu
Chenyang Xu
Cheng Chen
author_facet Yuan Peng
Tao Tao
Ni-Wen Yu
Chenyang Xu
Cheng Chen
author_sort Yuan Peng
collection DOAJ
description BackgroundThis study aimed to explore the possible value of follicular helper T (Tfh) cells in hospital-acquired pneumonia (HAP).MethodsFlow cytometry was used to measure circulating Tfh and helper T cell (Th) cells in 62 HAP patients and 16 healthy individuals. HAP patients were further categorized into uncontrolled and controlled groups, in accordance with relevant guidelines. Subgroup analyses were additionally conducted based on the pathogen and the presence of bloodstream infections (BSIs) and the incidence of septic shock. Kaplan-Meier survival analysis and ROC analysis were performed to estimate the prognostic value of the combination of Tfh/Th ratios and PCT levels.ResultsThe Tfh/Th ratio was notably higher in uncontrolled HAP patients than in controls (P<0.05). Specifically, either the Klebsiella pneumoniae (K.p) -positive HAP or BSIs subgroups or septic shock subgroups showed significantly increased Tfh/Th ratios (P<0.05). PCT level in BSIs and septic shock subgroups was significantly increased. However, there were no significant differences in PCT level between K.p-infected and non-K.p-infected patients. So, the Tfh/Th ratio is a good supplement to PCT for distinguishing between the K.p and non-K.p groups. The Tfh/Th ratio also demonstrated a strong correlation with procalcitonin (PCT) levels (P<0.05). Accordingly, the combination of Tfh/Th and PCT could serve as a more effective predictive marker for HAP deterioration and survival prediction. HAP patients with a high Tfh/Th ratio along with high PCT levels had a lower 28-day survival rate.ConclusionThe circulating Tfh/Th ratio, instrumental in gauging the severity of patients with HAP, could be employed as a prognostic biomarker for HAP.
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spelling doaj-art-384d4807d3c74ac5be827ae3183e7a742025-01-22T07:13:20ZengFrontiers Media S.A.Frontiers in Immunology1664-32242025-01-011610.3389/fimmu.2025.15139391513939Identification of circulating Tfh/Th subsets as a biomarker of developed hospital-acquired pneumoniaYuan Peng0Tao Tao1Ni-Wen Yu2Chenyang Xu3Cheng Chen4Intensive Care Unit, The First People’ ‘s Hospital of Kunshan Affiliated with Jiangsu University, Kunshan, ChinaIntensive Care Unit, The First People’ ‘s Hospital of Kunshan Affiliated with Jiangsu University, Kunshan, ChinaRespiratory Department, The First People’ ‘s Hospital of Kunshan Affiliated with Jiangsu University, Kunshan, ChinaIntensive Care Unit, The First People’ ‘s Hospital of Kunshan Affiliated with Jiangsu University, Kunshan, ChinaRespiratory Department, The First Affiliated Hospital of Soochow University, Suzhou, ChinaBackgroundThis study aimed to explore the possible value of follicular helper T (Tfh) cells in hospital-acquired pneumonia (HAP).MethodsFlow cytometry was used to measure circulating Tfh and helper T cell (Th) cells in 62 HAP patients and 16 healthy individuals. HAP patients were further categorized into uncontrolled and controlled groups, in accordance with relevant guidelines. Subgroup analyses were additionally conducted based on the pathogen and the presence of bloodstream infections (BSIs) and the incidence of septic shock. Kaplan-Meier survival analysis and ROC analysis were performed to estimate the prognostic value of the combination of Tfh/Th ratios and PCT levels.ResultsThe Tfh/Th ratio was notably higher in uncontrolled HAP patients than in controls (P<0.05). Specifically, either the Klebsiella pneumoniae (K.p) -positive HAP or BSIs subgroups or septic shock subgroups showed significantly increased Tfh/Th ratios (P<0.05). PCT level in BSIs and septic shock subgroups was significantly increased. However, there were no significant differences in PCT level between K.p-infected and non-K.p-infected patients. So, the Tfh/Th ratio is a good supplement to PCT for distinguishing between the K.p and non-K.p groups. The Tfh/Th ratio also demonstrated a strong correlation with procalcitonin (PCT) levels (P<0.05). Accordingly, the combination of Tfh/Th and PCT could serve as a more effective predictive marker for HAP deterioration and survival prediction. HAP patients with a high Tfh/Th ratio along with high PCT levels had a lower 28-day survival rate.ConclusionThe circulating Tfh/Th ratio, instrumental in gauging the severity of patients with HAP, could be employed as a prognostic biomarker for HAP.https://www.frontiersin.org/articles/10.3389/fimmu.2025.1513939/fullhospital-acquired pneumoniaTfh cellThprognosisPCT
spellingShingle Yuan Peng
Tao Tao
Ni-Wen Yu
Chenyang Xu
Cheng Chen
Identification of circulating Tfh/Th subsets as a biomarker of developed hospital-acquired pneumonia
Frontiers in Immunology
hospital-acquired pneumonia
Tfh cell
Th
prognosis
PCT
title Identification of circulating Tfh/Th subsets as a biomarker of developed hospital-acquired pneumonia
title_full Identification of circulating Tfh/Th subsets as a biomarker of developed hospital-acquired pneumonia
title_fullStr Identification of circulating Tfh/Th subsets as a biomarker of developed hospital-acquired pneumonia
title_full_unstemmed Identification of circulating Tfh/Th subsets as a biomarker of developed hospital-acquired pneumonia
title_short Identification of circulating Tfh/Th subsets as a biomarker of developed hospital-acquired pneumonia
title_sort identification of circulating tfh th subsets as a biomarker of developed hospital acquired pneumonia
topic hospital-acquired pneumonia
Tfh cell
Th
prognosis
PCT
url https://www.frontiersin.org/articles/10.3389/fimmu.2025.1513939/full
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AT niwenyu identificationofcirculatingtfhthsubsetsasabiomarkerofdevelopedhospitalacquiredpneumonia
AT chenyangxu identificationofcirculatingtfhthsubsetsasabiomarkerofdevelopedhospitalacquiredpneumonia
AT chengchen identificationofcirculatingtfhthsubsetsasabiomarkerofdevelopedhospitalacquiredpneumonia