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An In vitro Model to Study Immune Responses of Human Peripheral Blood Mononuclear Cells to Human Respiratory Syncytial Virus Infection
Published on: December 10, 2013
Increased T cell activation in BALF from children with Mycoplasma pneumoniae pneumonia
Li Guo1, Fang Liu2,3, Mei-Ping Lu1,2
1Department of Rheumatology Immunology & Allergy, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310003, China.
Background And Objective:
The mechanisms of Mycoplasma pneumoniae induced lung inflammation are not clearly understood yet. This study investigated whether activated T cells in the airway contributed to the pulmonary inflammation in patients with severe Mycoplasma pneumoniae pneumonia (MPP).
Methods:
BALF were collected in all 45 patients with MPP (MPP, n = 45), including mild (Mild, n = 20) and severe (Severe, n = 25) group. BALF in 20 of all 25 severe cases with MPP at the recovery stage (Rec-severe, n = 20) were collected again. The control group consisted of 20 patients with airway foreign body aspiration (Con., n = 20). CD3+ T cells, CD69+, HLA-DR+, CD25+ on CD3+ T cells in BALF were determined by flow cytometry. Levels of IL-6, IL-10 in BALF were determined by ELISA, and percentage of neutrophils was counted.
Results:
A significant increased percentage of neutrophils and levels of IL-6 and IL-10, decreased percentage of CD3+ T cells, increased expressions of CD69+, HLA-DR+ or CD25+ on CD3+ T cells were observed in children with MPP compared with the control group (P < 0.05 or 0.01). Compared to mild group, the percentage of neutrophils, CD3+ CD25+, IL-6, and IL-10 were increased in children with severe MPP (P < 0.01 or 0.05). Compared to acute stage, an increased percentage of CD3+ T cells, decreased percentage of neutrophils and IL-6 level, and expressions of CD3+ CD69+ or CD3+ CD25+ were observed at the recovery stage in children with severe MPP (P < 0.01 or 0.05).
Conclusions:
Increased activation of T cell in BALF may play an important role in the inflammatory response of acute and severe MPP. IL-6 may predict the severity and prognosis and provide a better assessment for patient care. However, the underlying mechanism awaits further detailed investigations.
Insights
Activated T cells in the airways contribute to lung inflammation in severe Mycoplasma pneumoniae pneumonia (MPP). Elevated IL-6 levels may indicate disease severity and prognosis in pediatric MPP patients.
Area of Science:
- Pulmonary Medicine
- Immunology
- Pediatric Infectious Diseases
Background:
- The precise mechanisms driving Mycoplasma pneumoniae-induced lung inflammation remain incompletely understood.
- Investigating the role of airway-activated T cells in severe Mycoplasma pneumoniae pneumonia (MPP) is crucial for understanding disease pathogenesis.
Purpose of the Study:
- To determine if activated T cells in the airway contribute to pulmonary inflammation in children with severe MPP.
- To explore the correlation between T cell activation markers, inflammatory cytokines, and disease severity in MPP.
Main Methods:
- Bronchoalveolar lavage fluid (BALF) was collected from 45 children with MPP (mild and severe), 20 severe cases at recovery, and 20 controls with foreign body aspiration.
- Flow cytometry was used to analyze CD3+ T cells and their activation markers (CD69+, HLA-DR+, CD25+).
- ELISA measured IL-6 and IL-10 levels, and neutrophil percentages were quantified.
Main Results:
- Children with MPP showed increased neutrophils, IL-6, IL-10, and activated T cells (CD69+, HLA-DR+, CD25+) compared to controls.
- Severe MPP cases exhibited higher neutrophils, CD3+ CD25+ T cells, IL-6, and IL-10 than mild cases.
- During recovery from severe MPP, T cell percentages increased, while neutrophils and IL-6 decreased, with reduced CD69+ and CD25+ expression on T cells.
Conclusions:
- Activated T cells in BALF are implicated in the inflammatory response during acute and severe MPP.
- Interleukin-6 (IL-6) may serve as a predictive marker for MPP severity and patient prognosis.
- Further research is needed to elucidate the detailed underlying mechanisms of T cell involvement in MPP pathogenesis.
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