Response to inhaled granulocyte‐macrophage colony‐stimulating factor in patient with mild‐to‐moderate autoimmune pulmonary alveolar proteinosis—24 months of follow‐up

INTRODUCTION: Autoimmune pulmonary alveolar proteinosis (aPAP) is a disease caused by IgG antibodies against granulocyte‐macrophage colony‐stimulating factor (GM‐CSF). Whole lung lavage (WLL) allows to remove the lipo‐proteinaceous material accumulated by the poor clearance of alveolar surfactant. H...

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Detalles Bibliográficos
Autores principales: Oterino‐Moreira, Iván, Linares‐Asensio, María‐Jesús, Sanz‐Márquez, Sira, Pérez‐Encinas, Montserrat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Brief Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542988/
https://www.ncbi.nlm.nih.gov/pubmed/37300395
http://dx.doi.org/10.1111/crj.13650

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542988/
https://www.ncbi.nlm.nih.gov/pubmed/37300395
http://dx.doi.org/10.1111/crj.13650

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