Efficacy of a trans-sialidase-ISCOMATRIX subunit vaccine candidate to protect against experimental Chagas disease. Issue 10 (3rd March 2015)

• Record Type: Journal Article
• Authors: Bontempi, Iván Alejandro; Vicco, Miguel Hernán; Cabrera, Gabriel; Villar, Silvina Raquel; González, Florencia Belén; Roggero, Eduardo Angel; Ameloot, Paul; Callewaert, Nico; Pérez, Ana Rosa; Marcipar, Iván Sergio
• Is Part Of: Vaccine. Volume 33:Issue 10(2015)
• Page Start: 1274
• Page End: 1283
• Publication Date: 2015-03-03
• Subjects: Vaccines -- Periodicals; 615.372
• DOI: 10.1016/j.vaccine.2015.01.044
• Languages: English
• ISSNs: 0264-410X

Abstract

<abstract abstract-type="author" id="abs0005"> <title id="sect0005">Abstract</title> <sec> <p id="spar0005">Recombinant protein vaccines are safe but elicit low immunological responses. The new generation of adjuvants is currently reversing this situation. Here, a new antigen–adjuvant combination for protection against experimental Chagas disease was assessed. The antigen used in the formulation was a glycosylated mutant inactive trans-sialidase (mTS) that was previously proven to be highly protective against <italic>Trypanosoma cruzi</italic> infection; here, we show that it can be produced in large quantities and high quality using <italic>Pichia pastoris</italic>. The adjuvant used in the formulation was ISCOMATRIX (IMX), which was found to be effective and safe in human clinical trials of vaccines designed to control other intracellular infections. Fifteen days after the third immunization, mice immunized with mTS-IMX showed a TS-specific IgG response with titers >10<sup>6</sup> and high avidity, an increased IgG<sub>2</sub>a/IgG1 ratio, significant delayed-type hypersensitivity (DTH) reactivity, a balanced production of IFN-γ and IL-10 by splenocytes and a strong IFN-γ secretion by CD8<sup>+</sup> T lymphocytes. When these mice where challenged with 1000 trypomastigotes of <italic>T. cruzi</italic>, all mTS-IMX immunized mice survived, whereas mice immunized with mTS alone, IMX or PBS exhibited high mortality. Remarkably, during acute infection, when the parasitemia is highest in this infection model (day 21), mTS-IMX immunized mice had ∼50 times less parasitemia than non-immunized mice. At this moment and also in the chronic phase, 100 days after infection, tissue presented ∼4.5 times lower parasite load and associated inflammatory infiltrate and lesions. These results indicate that protection against Chagas disease can be achieved by a protein antigen–adjuvant mTS formulation that is compatible with human medicine. Therefore, the current formulation is a highly promising <italic>T. cruzi</italic> vaccine candidate to be tested in clinical trials.</p> </sec> </abstract>