Optimising the yield from bronchoalveolar lavage on human participants in infectious disease immunology research

Bronchoalveolar lavage (BAL) is becoming a common procedure for research into infectious disease immunology. Little is known about the clinical factors which influence the main outcomes of the procedure. In research participants who underwent BAL according to guidelines, the BAL volume yield, and ce...

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Veröffentlicht in:Scientific reports 2023-05, Vol.13 (1), p.8859-8859, Article 8859
Hauptverfasser: Shaw, Jane Alexandra, Meiring, Maynard, Allies, Devon, Cruywagen, Lauren, Fisher, Tarryn-Lee, Kasavan, Kesheera, Roos, Kelly, Botha, Stefan Marc, MacDonald, Candice, Hiemstra, Andriёtte M., Simon, Donald, van Rensburg, Ilana, Flinn, Marika, Shabangu, Ayanda, Kuivaniemi, Helena, Tromp, Gerard, Malherbe, Stephanus T., Walzl, Gerhard, du Plessis, Nelita
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Sprache:eng
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Zusammenfassung:Bronchoalveolar lavage (BAL) is becoming a common procedure for research into infectious disease immunology. Little is known about the clinical factors which influence the main outcomes of the procedure. In research participants who underwent BAL according to guidelines, the BAL volume yield, and cell yield, concentration, viability, pellet colour and differential count were analysed for association with important participant characteristics such as active tuberculosis (TB) disease, TB exposure, HIV infection and recent SARS-CoV-2 infection. In 337 participants, BAL volume and BAL cell count were correlated in those with active TB disease, and current smokers. The right middle lobe yielded the highest volume. BAL cell and volume yields were lower in older participants, who also had more neutrophils. Current smokers yielded lower volumes and higher numbers of all cell types, and usually had a black pellet. Active TB disease was associated with higher cell yields, but this declined at the end of treatment. HIV infection was associated with more bloody pellets, and recent SARS-CoV-2 infection with a higher proportion of lymphocytes. These results allow researchers to optimise their participant and end assay selection for projects involving lung immune cells.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-023-35723-2