Idiopathic Pulmonary Alveolar Proteinosis as an Autoimmune Disease with Neutralizing Antibody against Granulocyte/Macrophage Colony-Stimulating Factor

Idiopathic pulmonary alveolar proteinosis (I-PAP) is a rare disease of unknown etiology in which the alveoli fill with lipoproteinaceous material. We report here that I-PAP is an autoimmune disease with neutralizing antibody of immunoglobulin G isotype against granulocyte/macrophage colony-stimulati...

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Detalles Bibliográficos
Autores principales: Kitamura, Takayuki, Tanaka, Naohiko, Watanabe, Junichi, Uchida, Kanegasaki, Shiro, Yamada, Yoshitsugu, Nakata, Koh
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1999
Materias:
Brief Definitive Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2195627/
https://www.ncbi.nlm.nih.gov/pubmed/10499925

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2195627/
https://www.ncbi.nlm.nih.gov/pubmed/10499925

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