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
Affiliations
Andrés Sanchez Alberti
Universidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Cátedra de Inmunología and Instituto de Estudios de la Inmunidad Humoral (IDEHU), UBA-CONICET
Augusto E. Bivona
Universidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Cátedra de Inmunología and Instituto de Estudios de la Inmunidad Humoral (IDEHU), UBA-CONICET
Natacha Cerny
Universidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Cátedra de Inmunología and Instituto de Estudios de la Inmunidad Humoral (IDEHU), UBA-CONICET
Kai Schulze
Department of Vaccinology and Applied Microbiology, Helmholtz Center for Infection Research
Sebastian Weißmann
Department of Vaccinology and Applied Microbiology, Helmholtz Center for Infection Research
Thomas Ebensen
Department of Vaccinology and Applied Microbiology, Helmholtz Center for Infection Research
Celina Morales
Universidad de Buenos Aires, Facultad de Medicina, Departamento de Patología, Instituto de Fisiopatología Cardiovascular
Angel M. Padilla
Center for Tropical and Emerging Global Diseases
Silvia I. Cazorla
Universidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Cátedra de Inmunología and Instituto de Estudios de la Inmunidad Humoral (IDEHU), UBA-CONICET
Rick L. Tarleton
Center for Tropical and Emerging Global Diseases
Carlos A. Guzmán
Department of Vaccinology and Applied Microbiology, Helmholtz Center for Infection Research
Emilio L. Malchiodi
Universidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Cátedra de Inmunología and Instituto de Estudios de la Inmunidad Humoral (IDEHU), UBA-CONICET
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.