High maternal expression of SIGLEC1 on monocytes as a surrogate marker of a type I interferon signature is a risk factor for the development of autoimmune congenital heart block

Ann Rheum Dis. 2017 Aug;76(8):1476-1480. doi: 10.1136/annrheumdis-2016-210927. Epub 2017 May 13.

Abstract

Objectives: Autoimmune congenital heart block (CHB) is associated with placental transcytosis of maternal autoantibodies directed against Ro/SS-A and La/SS-B. However, only about 2% of children born to mothers with the respective antibodies are affected, indicating that further risk factors exist, which are not yet fully understood. In this study, we investigated whether a maternal type I interferon (IFN) signature represents a risk factor for the development of CHB.

Methods: Blood samples, clinical data and serological parameters from 9 women with CHB pregnancies, 14 pregnant women with antibodies against Ro/SS-A but without a CHB complication and another 30 healthy pregnant women as controls were studied. SIGLEC1 expression was measured by flow cytometry and was correlated to plasma IFN-α levels measured by ELISA, and IFN-γ-induced protein 10 (IP-10) levels measured by Bio-Plex technique.

Results: Mothers of affected children had a significantly higher expression of SIGLEC1 (p=0.0034) and IFN-α (p=0.014), but not of IP-10 (p=0.14, all MWU) compared to mothers of unaffected children. SIGLEC1 and IFN-α expression were reduced by hydroxychloroquine and oral glucocorticoids.

Conclusions: High expression of SIGLEC1 in pregnant women with autoantibodies against Ro/SS-A indicates an enhanced risk for CHB development, and these women may benefit especially from IFN-α directed therapy, for example with hydroxychloroquine.

Keywords: SIGLEC1; congenital heart block; interferon-α; neonatal lupus syndrome; sialoadhesin.

MeSH terms

  • Adult
  • Antibodies, Antinuclear / immunology
  • Antirheumatic Agents / therapeutic use
  • Autoimmune Diseases / epidemiology
  • Autoimmune Diseases / immunology*
  • Case-Control Studies
  • Chemokine CXCL10 / immunology*
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Glucocorticoids / therapeutic use
  • Heart Block / congenital*
  • Heart Block / epidemiology
  • Heart Block / immunology
  • Humans
  • Hydroxychloroquine / therapeutic use
  • Infant, Newborn
  • Interferon Type I / immunology
  • Interferon-alpha / immunology*
  • Lupus Erythematosus, Systemic / drug therapy
  • Lupus Erythematosus, Systemic / epidemiology
  • Lupus Erythematosus, Systemic / immunology
  • Maternal-Fetal Exchange / immunology*
  • Monocytes / immunology*
  • Pregnancy
  • Pregnancy Complications / drug therapy
  • Pregnancy Complications / epidemiology
  • Pregnancy Complications / immunology*
  • Risk Factors
  • Sialic Acid Binding Ig-like Lectin 1 / immunology*
  • Sjogren's Syndrome / drug therapy
  • Sjogren's Syndrome / epidemiology
  • Sjogren's Syndrome / immunology
  • Transcytosis

Substances

  • Antibodies, Antinuclear
  • Antirheumatic Agents
  • Chemokine CXCL10
  • Glucocorticoids
  • Interferon Type I
  • Interferon-alpha
  • SIGLEC1 protein, human
  • SS-A antibodies
  • SS-B antibodies
  • Sialic Acid Binding Ig-like Lectin 1
  • Hydroxychloroquine

Supplementary concepts

  • Congenital heart block