Abstract |
Autoimmune pulmonary alveolar proteinosis ( aPAP) is the most common(around 90%) type of pulmonary alveolar proteinosis, characterized by the presence of granulocyte-macrophage colony-stimulating factor ( GM-CSF) autoantibody. Accumulating evidence has demonstrated the effectiveness of inhaled recombinant human GM-CSF for aPAP. Such a therapy has not been approved in China yet and has been classified off-label and unusual route of administration. Our expert consensus group evaluated the current knowledge with the methods of grading of recommendation assessment, development and evaluation (GRADE). The current evidence-based consensus statement covers the suitable population for inhaled GM-CSF therapy, details of prescription, usage during pregnancy and lactation, adverse effects and other suggestions in clinical usage. This consensus statement provides a clinical practice guideline of inhaled GM-CSF for aPAP in China and hopefully will accelerate basic and clinical research of aPAP.
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Authors | Expert Consensus Group of Pulmonary Alveolar Proteinosis, Rare Lung Disease Alliance, China Alliance of Rare Diseases |
Journal | Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases
(Zhonghua Jie He He Hu Xi Za Zhi)
Vol. 45
Issue 9
Pg. 865-871
(Sep 12 2022)
ISSN: 1001-0939 [Print] China |
PMID | 36097923
(Publication Type: Journal Article)
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Chemical References |
- Granulocyte-Macrophage Colony-Stimulating Factor
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Topics |
- Female
- Humans
- Administration, Inhalation
- Autoimmune Diseases
- Granulocyte-Macrophage Colony-Stimulating Factor
(therapeutic use)
- Pulmonary Alveolar Proteinosis
(drug therapy)
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