Surfactant protein D in serum from patients with allergic bronchopulmonary aspergillosis

M Krane1, M Griese

  • 1Children's Hospital, Ludwig Maximilians University of Munich, Munich, Germany.

Insights

Surfactant protein D (SP-D) is elevated in cystic fibrosis (CF) patients and correlates with lung function decline. However, serum SP-D levels do not aid in diagnosing or monitoring allergic bronchopulmonary aspergillosis (ABPA) in CF patients.

Area of Science:

  • Pulmonary Medicine
  • Immunology
  • Biochemistry

Background:

  • Surfactant protein D (SP-D) plays a role in immune responses to Aspergillus fumigatus.
  • Allergic bronchopulmonary aspergillosis (ABPA) is a common complication in cystic fibrosis (CF).
  • Previous animal studies suggest SP-D may be involved in ABPA.

Purpose of the Study:

  • To investigate serum SP-D concentrations in CF patients with and without ABPA.
  • To assess the potential of serum SP-D as a diagnostic or monitoring biomarker for ABPA in CF.
  • To explore the relationship between serum SP-D levels and lung function in CF patients.

Main Methods:

  • Serum SP-D levels were measured using enzyme immunoassay in 22 CF patients (11 with ABPA, 11 without) and 19 controls.
  • Lung function was assessed by forced expiratory volume in one second (FEV1) and forced vital capacity (FVC).
  • Serum SP-D levels were compared between groups and correlated with lung function parameters.

Main Results:

  • Serum SP-D levels were significantly higher in CF patients compared to controls.
  • Serum SP-D levels did not change significantly during ABPA episodes.
  • A negative correlation was observed between serum SP-D concentration and lung function (FEV1 and FVC).

Conclusions:

  • Serum SP-D levels may serve as a marker for lung injury and to monitor pulmonary function in CF patients.
  • Serum SP-D is not a reliable biomarker for the diagnosis or follow-up of ABPA episodes in CF.
  • Findings contrast with expectations from animal studies regarding SP-D's role in ABPA diagnosis.