Serial Anti-GM-CSF Autoantibody Levels Reflect Disease Activity in Hypersensitivity Pneumonitis with Autoimmune Pulmonary Alveolar Proteinosis: Case Report

Autoimmune pulmonary alveolar proteinosis (aPAP) is characterized by the accumulation of phospholipids and surfactant proteins in the peripheral air spaces due to alveolar macrophage dysfunction caused by anti-granulocyte-macrophage colony-stimulating factor (GM-CSF) autoantibodies (GMAb). Hypersens...

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Principais autores:	Toru Arai, Masaki Hirose, Eiji Sugimoto, Takayuki Takimoto, Yoshikazu Inoue, Hiromitsu Sumikawa, Tamiko Takemura, Shigeki Shimizu
Formato:	Artigo
Idioma:	Inglês
Publicado em:	MDPI AG 2025-09-01
coleção:	Pathophysiology
Assuntos:	autoimmune pulmonary alveolar proteinosis granulocyte-macrophage colony-stimulating factor hypersensitivity pneumonitis
Acesso em linha:	https://www.mdpi.com/1873-149X/32/3/47
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