Pulmonary alveolar proteinosis (PAP) is a rare lung disease characterized by the accumulation of pulmonary surfactant in alveolar macrophages and alveoli, resulting in respiratory impairment and an in
Bold typeface indicates the frequency of IgG responses were associated to the particular HLA-DRB1* or HLA-DQB1* allelic group by the bipartition χ2 test (PEach studied individual contributed two HLA a
This dataset includes: Supplementary Materials and Methods, Supplementary Table I: The clinical information and results in each case, Supplementary Table II: Summary of clinical characteristics in ICI
