CD8+ T lymphocytes in bronchoalveolar lavage in idiopathic pulmonary fibrosis
2007

CD8+ T Lymphocytes in Bronchoalveolar Lavage and Idiopathic Pulmonary Fibrosis

Sample size: 27 publication Evidence: moderate

Author Information

Author(s): Spyros A. Papiris, Androniki Kollintza, Marilena Karatza, Effrosyni Manali, Christina Sotiropoulou, Joseph Milic-Emili, Charis Roussos, Zoe Daniil

Primary Institution: National and Kapodistrian University of Athens, Greece

Hypothesis

The study investigates the relationship between bronchoalveolar lavage (BAL) cell types and clinical indices of disease severity in patients with idiopathic pulmonary fibrosis (IPF).

Conclusion

The associations of BAL CD8+ T lymphocytes with physiological and clinical indices suggest their role in the pathogenesis of IPF.

Supporting Evidence

  • CD8+ T lymphocytes correlated positively with breathlessness as measured by the MRC scale.
  • The CD4+/CD8+ ratio correlated negatively with breathlessness severity.
  • Neutrophils were positively correlated with breathlessness and negatively with lung function measures.

Takeaway

Doctors studied cells from the lungs of patients with a lung disease called idiopathic pulmonary fibrosis to see how they relate to symptoms like breathlessness. They found that certain immune cells are linked to how bad the disease is.

Methodology

The study involved 27 patients with IPF, analyzing bronchoalveolar lavage fluid for immune cell types and correlating these with clinical measures of lung function and breathlessness.

Potential Biases

Potential biases may arise from the selection of patients and the reliance on clinical measures for assessing disease severity.

Limitations

The study is limited by its small sample size and the observational nature of the data.

Participant Demographics

The mean age of participants was 63 years, with 65% male, and included current and ex-smokers.

Statistical Information

P-Value

p = 0.02

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1476-9255-4-14

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