Efficacy of a trans-sialidase-ISCOMATRIX subunit vaccine candidate to protect against experimental Chagas disease

被引:36
作者
Bontempi, Ivan Alejandro [1 ]
Vicco, Miguel Hernan [1 ]
Cabrera, Gabriel [1 ]
Villar, Silvina Raquel [2 ,3 ]
Gonzalez, Florencia Belen [2 ,3 ]
Roggero, Eduardo Angel [2 ,3 ]
Ameloot, Paul [4 ,5 ]
Callewaert, Nico [4 ,5 ]
Perez, Ana Rosa [2 ,3 ]
Marcipar, Ivan Sergio [1 ]
机构
[1] Univ Nacl Litoral, Fac Bioquim & Ciencias Biol, Santa Fe, Argentina
[2] Univ Nacl Rosario, Fac Ciencias Med, IDICER CONICET, RA-2000 Rosario, Santa Fe, Argentina
[3] Univ Nacl Rosario, Fac Ciencias Med, Inst Inmunol, RA-2000 Rosario, Santa Fe, Argentina
[4] Univ Ghent VIB, Inflammat Res Ctr, Med Biotechnol Unit, Ghent, Belgium
[5] Univ Ghent, Dept Biochem & Microbiol, B-9000 Ghent, Belgium
关键词
Trypanosoma cruzi; ISCOM; Trans-sialidase; Vaccine; TRYPANOSOMA-CRUZI INFECTION; IFN-GAMMA; T-CELLS; IMMUNITY; IMMUNIZATION; ADJUVANTS; ANTIGENS; MICE; PATHOGENESIS; MACROPHAGES;
D O I
10.1016/j.vaccine.2015.01.044
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 Trypanosoma cruzi infection; here, we show that it can be produced in large quantities and high quality using Pichia pastoris. 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(6) and high avidity, an increased IgG(2)a/IgG1 ratio, significant delayed-type hypersensitivity (DTH) reactivity, a balanced production of IFN-gamma and IL-10 by splenocytes and a strong IFN-gamma secretion by CD8(+) T lymphocytes. When these mice where challenged with 1000 trypomastigotes of T. cruzi, 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 similar to 50 times less parasitemia than non-immunized mice. At this moment and also in the chronic phase, 100 days after infection, tissue presented similar to 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 T. cruzi vaccine candidate to be tested in clinical trials. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1274 / 1283
页数:10
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