×
Home
Current Archive Submission Guidelines
News Contact
Original article

Lymphocyte Subsets in Bronchoalveolar Lavage Fluid of Children with Lung Infiltrates

By
Amina Selimović ,
Amina Selimović
Senka Dinarević ,
Senka Dinarević
Tatjana Pejčić ,
Tatjana Pejčić
Ermina Mujičić ,
Ermina Mujičić
Aida Hasanović ,
Aida Hasanović
Siniša Ristić ,
Siniša Ristić
Nataša Banjac ,
Nataša Banjac
Željko Pavlović
Željko Pavlović

Abstract

The analysis of the subpopulation of lymphocytes - CD4+, CD8+ lymphocytes in bronchoalveolar lavage (BAL) of paediatric patients can provide useful information related the lung parenchyma.  The aim of the paper was to analyze the results of bronchoscopy of patients presenting with persistent lung infiltrates and to find out of the diagnostic yield and complication rate of this procedure. The study is a retrospective one. The data related to paediatric findings and BAL results of the bronchoscopies were retrieved from the hospital records. BAL was performed in tracheobronchial airways (middle lobe) by bronchoscope and sent to analysis of CD4+, CD8+ lymphocytes. Bronchoscopy was performed under general anesthesia (sedation, propofol, midazolam, morphium).  The records of seven patients were analyzed. All patients presented with persistent lung infiltrate (atelectasis and pneumonia). 71% of the patients with lung infiltrates in our study were below the age of 5. Our study results showed that CD4+, CD8+ lymphocytes in BAL in the studied group showed a small percentage of CD8+ lymphocytes as an immune response in 8-10% of patients, while the cellular response of CD4 +lymphocytes in the sample itself was present up to 14% in the entire group of the diseased children. There was no serious desaturation during bronchoscopy.  Bronchoscopy with BAL findings of lymphocyte populations is important in the early identification of inflammation and it helps in therapeutic strategies and monitoring of inflammatory response to the given therapy. 

References

1.
Wood RE. THE EMERGING ROLE OF FLEXIBLE BRONCHOSCOPY IN PEDIATRICS. Clinics in Chest Medicine. 2001;22(2):311–7.
2.
Don M, Canciani M, Korppi M. Community‐acquired pneumonia in children: what’s old? What’s new? Acta Paediatrica. 2010;99(11):1602–8.
3.
Wang YH, Voo KS, Liu B, Chen CY, Uygungil B, Spoede W, et al. A novel subset of CD4+ TH2 memory/effector cells that produce inflammatory IL-17 cytokine and promote the exacerbation of chronic allergic asthma. Journal of Experimental Medicine. 2010;207(11):2479–91.
4.
Heidema J, Lukens MV, van Maren WWC, van Dijk MEA, Otten HG, van Vught AJ, et al. CD8+ T Cell Responses in Bronchoalveolar Lavage Fluid and Peripheral Blood Mononuclear Cells of Infants with Severe Primary Respiratory Syncytial Virus Infections. The Journal of Immunology. 2007;179(12):8410–7.
5.
Moumouni H, Garaud P, Diot P, Lemarie E, Anthonioz P. Quantification of cell loss during bronchoalveolar lavage fluid processing. Effects of fixation and staining methods. American Journal of Respiratory and Critical Care Medicine. 1994;149(3):636–40.
6.
Nguyen ET, Kanne JP, Hoang LMN, Reynolds S, Dhingra V, Bryce E, et al. Community-acquired Methicillin-resistant Staphylococcus aureus Pneumonia. Journal of Thoracic Imaging. 2008;23(1):13–9.
7.
Kuwano K, Miyazaki H, Hagimoto N, Kawasaki M, Fujita M, Kunitake R, et al. The Involvement of Fas–Fas Ligand Pathway in Fibrosing Lung Diseases. American Journal of Respiratory Cell and Molecular Biology. 1999;20(1):53–60.

Citation

Article metrics

Google scholar: See link

The statements, opinions and data contained in the journal are solely those of the individual authors and contributors and not of the publisher and the editor(s). We stay neutral with regard to jurisdictional claims in published maps and institutional affiliations.