npj Vaccines (Apr 2017)

Engineered trivalent immunogen adjuvanted with a STING agonist confers protection against Trypanosoma cruzi infection

  • Andrés Sanchez Alberti,
  • Augusto E. Bivona,
  • Natacha Cerny,
  • Kai Schulze,
  • Sebastian Weißmann,
  • Thomas Ebensen,
  • Celina Morales,
  • Angel M. Padilla,
  • Silvia I. Cazorla,
  • Rick L. Tarleton,
  • Carlos A. Guzmán,
  • Emilio L. Malchiodi

DOI
https://doi.org/10.1038/s41541-017-0010-z
Journal volume & issue
Vol. 2, no. 1
pp. 1 – 12

Abstract

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Chagas disease: protecting from chronic parasitic disease An amalgamation of parasitic proteins may be the first effective vaccine against the as yet untreatable chronic phase of Chagas disease. The infliction, caused by the parasite Trypanosoma cruzi (T. cruzi), is the world’s leading cause of infectious cardiac inflammation and puts one-sixth of the population of Latin America at risk of infection. International collaborators led by Emilio Malchiodi, of the University of Buenos Aires, Argentina, constructed a vaccine (dubbed ‘Traspain’) comprised of key T. cruzi proteins alongside a novel ‘adjuvant’—designed to promote the efficacy of a vaccine by activating inflammatory responses. The chimera and adjuvant combination elicited a promising immune response and also showed the capacity to prevent tissue damage caused by chronic infection. Multi-part vaccines such as Traspain offer an attractive direction for research into vaccines against chronic parasitic infections.