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Humoral Immune Status in Relation to Outcomes in Patients with Idiopathic Pulmonary Fibrosis.

Thijs W HoffmanC H M van MoorselK M KazemierD H BiesmaJ C GruttersD A van Kessel
Published in: Lung (2021)
The prevalence of humoral immunodeficiencies was low in patients with IPF and not associated with AE-IPF or survival. Elevated lymphocytes in BAL were associated with the development of AE-IPF and worse survival. Higher serum immunoglobulins and immune cells in blood were also associated with worse survival. The local immune response in the lungs may be a target for future therapies.
Keyphrases
  • idiopathic pulmonary fibrosis
  • immune response
  • interstitial lung disease
  • free survival
  • risk factors
  • toll like receptor
  • type diabetes