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Published in 2025 at "Immunotherapy"
DOI: 10.1080/1750743x.2025.2571020
Abstract: Autoimmune Pulmonary Alveolar Proteinosis (aPAP) is a rare disease characterized by myeloid cell dysfunction, abnormal pulmonary surfactant accumulation, and innate immune deficiency. Pathogenesis is driven by GM-CSF neutralizing autoantibodies (GMAbs) present in high titer in…
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Keywords:
drug evaluation;
rgm csf;
csf;
csf drug ... See more keywords