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Prolonged activation of innate antiviral gene signature after childbirth is determined by IFNL3 genotype

Proc Natl Acad Sci U S A. 2016 Sep 20;113(38):10678-83. doi: 10.1073/pnas.1602319113. Epub 2016 Sep 6.

Abstract

Maternal innate and adaptive immune responses are modulated during pregnancy to concurrently defend against infection and tolerate the semiallogeneic fetus. The restoration of these systems after childbirth is poorly understood. We reasoned that enhanced innate immune activation may extend beyond gestation while adaptive immunity recovers. To test this hypothesis, the transcriptional profiles of total peripheral blood mononuclear cells following delivery in healthy women were compared with those of nonpregnant control subjects. Interestingly, interferon-stimulated genes (ISGs) encoding proteins such as IFIT1, IFIT2, and IFIT3, as well as signaling proteins such as STAT1, STAT2, and MAVS, were enriched postpartum. Antiviral genes were primarily expressed in CD14(+) cells and could be stratified according to genetic variation at the interferon-λ3 gene (IFNL3, also named IL28B) SNP rs12979860. Antiviral gene expression was sustained beyond 6 mo following delivery in mothers with a CT or TT genotype, but resembled baseline nonpregnant control levels following delivery in mothers with a CC genotype. CT and TT IFNL3 genotypes have been associated with persistent elevated ISG expression in individuals chronically infected with hepatitis C virus. Together, these data suggest that postpartum, the normalization of the physiological rheostat controlling IFN signaling depends on IFNL3 genotype.

Keywords: CD14; antiviral genes; innate immunity; interferon; postpartum.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Adult
  • Apoptosis Regulatory Proteins
  • Carrier Proteins / genetics
  • Female
  • Gene Expression Regulation / immunology
  • Genotype
  • Hepacivirus / genetics
  • Hepacivirus / immunology*
  • Hepacivirus / pathogenicity
  • Hepatitis C / genetics
  • Hepatitis C / immunology*
  • Hepatitis C / virology
  • Humans
  • Immunity, Innate / genetics*
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Intracellular Signaling Peptides and Proteins / immunology
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / metabolism
  • Lipopolysaccharide Receptors / immunology
  • Maternal-Fetal Relations
  • Polymorphism, Single Nucleotide
  • Postpartum Period
  • Pregnancy
  • Proteins / genetics
  • RNA-Binding Proteins

Substances

  • Adaptor Proteins, Signal Transducing
  • Apoptosis Regulatory Proteins
  • Carrier Proteins
  • IFIT1 protein, human
  • IFIT2 protein, human
  • IFIT3 protein, human
  • Intracellular Signaling Peptides and Proteins
  • Lipopolysaccharide Receptors
  • Proteins
  • RNA-Binding Proteins