Inflammasome-targeted therapy might prevent adverse perinatal outcomes of recurrent chronic intervillositis of unknown etiology

Nat Commun. 2024 Oct 30;15(1):9396. doi: 10.1038/s41467-024-53591-w.

Abstract

Chronic histiocytic intervillositis of unknown origin (CHI) is a rare placental disorder associated with adverse pregnancy outcomes, frequent recurrence, and a lack of effective preventive strategies. Recent insights indicate a potential link between CHI-associated inflammatory lesions and the inflammasome pathway, suggesting innovative therapeutic avenues. Here we show a potential role of the inflammasome pathway in CHI through comprehensive transcriptomic analysis of grade 2 or 3 histopathologic CHI samples, paired with placental controls. Additionally, we present case studies of three individuals with recurrent CHI, who have undergone treatment with anakinra and colchicine throughout pregnancy, resulting in improved perinatal outcomes. Notably, all cases are characterized by the birth of healthy, full-term infants, with reduced or absent intervillositis recurrence. Placental assessment unveils heightened activation of the NLRP3-PYCARD inflammasome pathway and IL-1β processing in CHI samples, with downregulation observed in treated pregnancy samples, devoid of intervillositis. Collectively, these findings suggest a potential therapeutic role for targeting the inflammasome pathway in preventing recurrent CHI in pregnant individuals.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • CARD Signaling Adaptor Proteins / genetics
  • CARD Signaling Adaptor Proteins / metabolism
  • Chorionic Villi / metabolism
  • Chorionic Villi / pathology
  • Chronic Disease
  • Female
  • Humans
  • Infant, Newborn
  • Inflammasomes* / metabolism
  • Interleukin 1 Receptor Antagonist Protein* / therapeutic use
  • Interleukin-1beta / genetics
  • Interleukin-1beta / metabolism
  • NLR Family, Pyrin Domain-Containing 3 Protein* / genetics
  • NLR Family, Pyrin Domain-Containing 3 Protein* / metabolism
  • Placenta / metabolism
  • Placenta / pathology
  • Placenta Diseases* / drug therapy
  • Placenta Diseases* / pathology
  • Pregnancy
  • Pregnancy Outcome
  • Recurrence

Substances

  • Inflammasomes
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Interleukin 1 Receptor Antagonist Protein
  • Interleukin-1beta
  • NLRP3 protein, human
  • CARD Signaling Adaptor Proteins
  • PYCARD protein, human