Surfactant protein-D, a potential mediator of inflammation in axial spondyloarthritis

Heidi L Munk, Dalia Fakih, Lene Christiansen, Qihua Tan, Anne F Christensen, Leif Ejstrup, Anne G Loft, Kirsten Junker, Kirsten O Kyvik, Rania Jounblat, Uffe Holmskov, Grith L Sorensen, Peter Junker

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

Objectives: Surfactant protein-D (SP-D), an innate immune defence molecule of the collectin family, is expressed in lungs and additional extrapulmonary epithelia. SP-D has immune modulatory and anti-microbial effects depending on its oligomerization. The ratio of high molecular weight (HMW): low molecular weight (LMW) SP-D in serum is mainly determined by the Met11Thr polymorphism (SNP rs721917). We aimed to study the SP-D serum level and the molecular size distribution in patients with untreated axial spondyloarthritis (axSpA) as compared with control subjects.

Methods: Thirty-four patients with disease modifier untreated axSpA according to the ASAS criteria, age 19-63 years, disease duration 3.9 (2.2-5.6) years were included. Demographics, smoking habits, HLA-B27 status, ASDAS, BASDAI, BASFI, BASMI and visual analogue scale scores were recorded. SP-D in serum was measured by ELISA. DNA was isolated from whole blood and single nucleotide polymorphism rs721917 was genotyped. SP-D molecular size distribution was determined using gel filtration chromatography.

Results: SP-D in serum did not differ between patients with axSpA and healthy controls, 1177 (869, 1536) vs 910 (494, 1682) (P = 0.35) and SP-D did not correlate with disease activity. However, the HMW/LMW ratio of SP-D in serum was significantly lower in axSpA, 0.38 (0.18, 0.53) compared with controls 1.49 (0.37, 3.24) when adjusting for the Met11Thr polymorphism, gender, age, BMI and smoking (P = 0.0004). There was no correlation between HMW/LMW ratio and CRP or composite diseases outcome measures.

Conclusion: We suggest that predominance of LMW oligomeric variants of SP-D may enhance local or systemic inflammatory responses in axSpA.

Original languageEnglish
JournalRheumatology
Volume57
Issue number10
Pages (from-to)1861–1865
ISSN1462-0324
DOIs
Publication statusPublished - 1. Oct 2018

Keywords

  • innate immune defence
  • multimerization
  • single nucleotide polymorphism (SNP)
  • spondyloarthritis
  • surfactant protein-D (SP-D)
  • Pulmonary Surfactant-Associated Protein D/blood
  • Spondylarthritis/blood
  • Humans
  • Middle Aged
  • Protein Multimerization
  • Genotype
  • Male
  • Case-Control Studies
  • Young Adult
  • Inflammation Mediators/blood
  • HLA-B27 Antigen
  • Adult
  • Female
  • Polymorphism, Single Nucleotide

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