Recurrent pulmonary infection, a vicious cycle of multifactorial interactions, and prevention/treatment strategies
4 affiliations
- 1Department of Pharmacy, Jiaxing Hospital of Traditional Chinese Medicine
- 2Department of Pharmacy, Jiaxing Hospital of Traditional Chinese Medicine Affiliated to Jiaxing University
- 3Department of Pharmacy, Guangyuan Central Hospital
- 4Department of Obstetrics and Gynecology, The Second People's Hospital of Lizhou District
Abstract
Recurrent pulmonary infection (RPI) refers to the frequent and repeated episodes of lower respiratory tract infections. At its core, it represents a vicious cycle arising from the disruption of the homeostatic balance among pathogens, host immunity, and pulmonary architecture. RPI accounts for a considerable proportion of pediatric pneumonia cases, and the cumulative incidence among elderly patients hospitalized for pneumonia is also markedly elevated, imposing a substantial disease burden. The etiologies are notably diverse, beyond common pathogens such as bacteria and viruses, the ubiquity of asymptomatic colonization, underlying comorbidities, immune deficiencies, medication-related factors, and aspiration all constitute critical predisposing factors. This review summarizes the pathogenic characteristics of RPI, host-related factors, and the mechanistic roles of structural lung damage in infection recurrence. It further focuses on the current advances and limitations of precision diagnostic approaches (metagenomic sequencing), immunomodulatory and microbiome-targeted interventions, and vaccination strategies. Existing evidence suggests that the clinical benefits of these interventions in RPI remain to be validated by more high-quality studies. The aim of this article is to provide a reference for the clinical management of RPI and to inform future research directions.
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BibTeX
@article{shen2026recurrent,
title = {{Recurrent pulmonary infection, a vicious cycle of multifactorial interactions, and prevention/treatment strategies}},
author = {Chaojie Shen and Yuhuan Li and Zongjun Xiang and Min Zhao and Jingsong Wang and Xutao Wang},
journal = {Frontiers in Immunology},
year = {2026},
month = oct,
doi = {10.3389/fimmu.2026.1945273},
url = {https://www.frontiersin.org/articles/10.3389/fimmu.2026.1945273/full},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Recurrent pulmonary infection, a vicious cycle of multifactorial interactions, and prevention/treatment strategies
AU - Chaojie Shen
AU - Yuhuan Li
AU - Zongjun Xiang
AU - Min Zhao
AU - Jingsong Wang
AU - Xutao Wang
PY - 2026
DA - 2026/10/29
JO - Frontiers in Immunology
DO - 10.3389/fimmu.2026.1945273
UR - https://www.frontiersin.org/articles/10.3389/fimmu.2026.1945273/full
AB - Recurrent pulmonary infection (RPI) refers to the frequent and repeated episodes of lower respiratory tract infections. At its core, it represents a vicious cycle arising from the disruption of the homeostatic balance among pathogens, host immunity, and pulmonary architecture. RPI accounts for a considerable proportion of pediatric pneumonia cases, and the cumulative incidence among elderly patients hospitalized for pneumonia is also markedly elevated, imposing a substantial disease burden. The etiologies are notably diverse, beyond common pathogens such as bacteria and viruses, the ubiquity of asymptomatic colonization, underlying comorbidities, immune deficiencies, medication-related factors, and aspiration all constitute critical predisposing factors. This review summarizes the pathogenic characteristics of RPI, host-related factors, and the mechanistic roles of structural lung damage in infection recurrence. It further focuses on the current advances and limitations of precision diagnostic approaches (metagenomic sequencing), immunomodulatory and microbiome-targeted interventions, and vaccination strategies. Existing evidence suggests that the clinical benefits of these interventions in RPI remain to be validated by more high-quality studies. The aim of this article is to provide a reference for the clinical management of RPI and to inform future research directions.
SN - 1664-3224
ER -