Co-infection with distinct Trypanosoma cruzi strains induces an activated immune response in human monocytes

Parasite Immunol. 2019 Nov;41(11):e12668. doi: 10.1111/pim.12668. Epub 2019 Sep 30.

Abstract

Aims: The aim of the study was to evaluate the immune response triggered by the first contact of human monocytes with two T cruzi strains from distinct discrete typing units (DTUs) IV and V, and whether co-infection with these strains leads to changes in monocyte immune profiles, which could in turn influence the subsequent infection outcome.

Methods and results: We evaluated the influence of in vitro single- and co-infection with AM64 and 3253 strains on immunological characteristics of human monocytes. Single infection of monocytes with AM64 or 3253 induced opposing anti-inflammatory and inflammatory responses, respectively. Co-infection was observed in over 50% of monocytes after 15 hours of culture, but this percentage dropped ten-fold after 72 hours. Co-infection led to high monocyte activation and an increased percentage of both IL-10 and TNF. The decreased percentage of co-infected cells observed after 72 hours was associated with a decreased frequency of TNF-expressing cells.

Conclusion: Our results show that the exacerbated response observed in co-infection with immune-polarizing strains is associated with a decreased frequency of co-infected cells, suggesting that the activated response favours parasite control. These findings may have implications for designing new Chagas disease preventive strategies.

Keywords: Trypanosoma cruzi; co-infection; discrete typing units; human; monocytes; parasitemia; strains.

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Cells, Cultured
  • Chagas Disease / immunology*
  • Chagas Disease / parasitology
  • Coinfection
  • Humans
  • Interleukin-10 / metabolism
  • Middle Aged
  • Monocytes / immunology*
  • Trypanosoma cruzi / classification*
  • Trypanosoma cruzi / immunology*
  • Tumor Necrosis Factor-alpha / metabolism
  • Young Adult

Substances

  • IL10 protein, human
  • Tumor Necrosis Factor-alpha
  • Interleukin-10