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CD8+ T lymphocytes in bronchoalveolar lavage in idiopathic pulmonary fibrosis

Spyros A Papiris1,7 email, Androniki Kollintza2 email, Marilena Karatza3 email, Effrosyni D Manali1 email, Christina Sotiropoulou4 email, Joseph Milic-Emili5 email, Charis Roussos2 email and Zoe Daniil6 email

2nd Pulmonary Department, National and Kapodistrian University of Athens, "Attikon" University Hospital, Athens, Greece

Department of Critical Care and Pulmonary Services, National and Kapodistrian University of Athens, "Evangelismos" Hospital, Athens, Greece

Hematology Department "Evangelismos" Hospital, Athens, Greece

Applied Biomedical Research & Training Laboratory "Marianthi Simou", National and Kapodistrian University of Athens, Greece

Meakins-Cristie Laboratories, McGill University, Montreal, Quebec, Canada

Medical School, University of Thessaly, 41222 Larissa, Greece

Associate Professor of Medicine and Chairman, 2nd Pulmonary Department, National and Kapodistrian University of Athens, Medical School of Athens, "ATTIKON" University Hospital 1 Rimini Street, 12462 Haidari, Athens, Greece

author email corresponding author email

Journal of Inflammation 2007, 4:14doi:10.1186/1476-9255-4-14

Published: 19 June 2007

Abstract

Background

Recently it was shown that in Idiopathic Pulmonary Fibrosis (IPF) tissue infiltrating CD8+ T lymphocytes (TLs) are associated with breathlessness and physiological indices of disease severity, as well as that CD8+ TLs recovered by bronchoalveolar lavage (BAL) relate to those infiltrating lung tissue. Since BAL is a far less invasive technique than tissue biopsy to study mechanisms in IPF we further investigated the usefulness offered by this means by studying the relationship between BAL macrophages, neutrophils, eosinophils, CD3+, CD4+, CD8+, CD8+/38+ TLs and CD4+/CD8+ ratio with breathlessness and physiological indices.

Patients and methods

27 IPF patients, 63 ± 9 years of age were examined. Cell counts were expressed as percentages of total cells and TLs were evaluated by flow cytometry. FEV1, FVC, TLC, RV, DLCO, PaO2, and PaCO2 were measured in all. Breathlessness was assessed by the Medical Research Council (MRC) chronic dyspnoea scale.

Results

CD8+ TLs correlated positively (rs = 0.46, p = 0.02), while CD4+/CD8+ ratio negatively (rs = -0.54, p = 0.006) with the MRC grade. CD8+ TLs correlated negatively with RV (rs = -0.50, p = 0.017). CD8+/38+ TLs were negatively related to the FEV1 and FVC (rs = -0.53, p = 0.03 and rs = -0.59, p = 0.02, respectively). Neutrophils correlated positively with the MRC grade (rs = 0.42, p = 0.03), and negatively with the DLCO (rs = -0.54, p = 0.005), PaO2 (rs = -0.44, p = 0.03), and PaCO2 (rs = -0.52, p = 0.01).

Conclusion

BAL CD8+ TLs associations with physiological and clinical indices seem to indicate their implication in IPF pathogenesis, confirming our previous tissue study.


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