Cytokine dysregulation in early- and late-term placentas from feline immunodeficiency virus (FIV)-infected cats

Am J Reprod Immunol. 2011 May;65(5):480-91. doi: 10.1111/j.1600-0897.2010.00919.x. Epub 2010 Sep 6.

Abstract

Problem: Experimental infection of cats with FIV-B-2542 produces high rates of fetal infection and reproductive failure. We hypothesized that dysregulation of placental cytokine expression occurs in FIV-infected queens, and aberrant expression potentiates inflammation and impacts pregnancy outcome. Our purpose was to quantify expression of representative pro-inflammatory cytokines (IL-6, IL-12p35, and IL-1β), IL-10 (anti-inflammatory), and the chemokine SDF-1α in early- and late-term placental tissues.

Method of study: Real-time reverse transcriptase PCR was used to measure gene expression in placental tissues.

Results: Increased expression of IL-6 and IL-12p35 and decreased expression of IL-10 occurred in FIV-infected tissues at early pregnancy; at late gestation, IL-6 expression increased and IL-1β and SDF-1α decreased. At late pregnancy, IL-6 expression positively correlated with FIV load. IL-12:IL-10 ratios were higher in infected tissues at early, but not late pregnancy. Fetal non-viability accompanied decreased IL-12p35 and SDF-1α expression at both stages and decreased IL-12:IL-10 ratio at late pregnancy.

Conclusion: FIV infection caused a pro-inflammatory placental microenvironment at early, but not late pregnancy.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cats
  • Cytokines / genetics
  • Cytokines / immunology
  • Cytokines / metabolism*
  • Disease Models, Animal
  • Feline Acquired Immunodeficiency Syndrome / immunology*
  • Feline Acquired Immunodeficiency Syndrome / pathology
  • Feline Acquired Immunodeficiency Syndrome / virology
  • Female
  • Gene Expression Regulation*
  • Gestational Age
  • Humans
  • Immunodeficiency Virus, Feline / immunology
  • Infectious Disease Transmission, Vertical
  • Inflammation
  • Placenta / immunology*
  • Placenta / metabolism
  • Placenta / virology
  • Pregnancy
  • Pregnancy Complications, Infectious / immunology*
  • Pregnancy Complications, Infectious / pathology
  • Pregnancy Complications, Infectious / virology
  • Pregnancy Outcome
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Cytokines