High tumor necrosis factor alpha (TNF-α) production in Trypanosoma cruzi- infected pregnant mice and increased TNF-α gene transcription in their offspring

M. T. Rivera, S. Marques De Araujo, R. Lucas, J. Deman, C. Truyens, M. P. Defresne -, P. De Baetselier, Y. Carlier

Research output: Contribution to journalArticle

28 Scopus citations

Abstract

Since tumor necrosis factor alpha (TNF-α) is known to be involved in the feto-maternal relationship, this cytokine was studied in Trypanosoma cruzi- infected pregnant BALB/c mice and their fetuses and offspring. Pregnant chronically infected mice displayed significantly higher levels of circulating TNF-α than animals either only infected or only pregnant, TNF- α was undetectable in sera of uninfected and nonpregnant mice as well as in breast milk obtained from infected and uninfected animals. Fetuses from infected mice exhibited significantly more cells containing TNF-α mRNA in their thymus than fetuses from uninfected mothers. When infected 2 months after birth, offspring born to infected and uninfected mothers displayed similar amounts of circulating TNF-α during chronic infection, whereas this cytokine was only weakly detectable during the acute phase of the disease. An intravenous injection of lipopolysaccharide during acute infection strongly increased the production of TNF-α in offspring born to infected mothers to levels higher than those in progeny from uninfected mice. These results suggest that TNF-α is an important cytokine in the feto-maternal relationship during T. cruzi infection and that fetuses and offspring of infected mothers are primed to produce elevated levels of TNF-α.

Original languageEnglish (US)
Pages (from-to)591-595
Number of pages5
JournalInfection and Immunity
Volume63
Issue number2
DOIs
StatePublished - 1995
Externally publishedYes

ASJC Scopus subject areas

  • Parasitology
  • Microbiology
  • Immunology
  • Infectious Diseases

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