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. 2002 Mar;57(3):277–280. doi: 10.1136/thorax.57.3.277

BAL findings in a patient with pulmonary alveolar proteinosis successfully treated with GM-CSF

O Schoch 1, U Schanz 1, M Koller 1, K Nakata 1, J Seymour 1, E Russi 1, A Boehler 1
PMCID: PMC1746271  PMID: 11867836

Abstract

Methods: Clinical, functional, and bronchoalveolar lavage (BAL) findings were prospectively evaluated in a patient with PAP treated with daily subcutaneous GM-CSF 8 µg/kg for 12 weeks.

Results: Treatment resulted in improvements in dyspnoea, lung function, and peak cycle ergometry performance. In serum and BAL fluid the titre of anti-GM-CSF autoantibodies was raised at baseline and markedly reduced on treatment. At baseline the BAL fluid cellular profile showed a decrease in the absolute number and the percentage of macrophages (50%) and an increase in lymphocytes (45%), predominantly CD4+. This cellular distribution remained unchanged after 6 and 12 weeks of treatment while macrophages became morphologically normal and functionally improved. Extracellular proteinaceous material completely disappeared.

Conclusions: Clinically successful treatment of PAP with GM-CSF was associated with a profound reduction in GM-CSF neutralising autoantibodies, improvement in alveolar macrophage morphology and function, but persistent BAL lymphocytosis.

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