Oral Multicomponent DNA Vaccine Delivered by Attenuated Salmonella Elicited Immunoprotection Against American Trypanosomiasis

被引:30
作者
Cazorla, Silvia I. [1 ,2 ,3 ,4 ]
Matos, Marina N. [1 ,2 ,3 ,4 ]
Cerny, Natacha [1 ,2 ,3 ,4 ]
Ramirez, Carolina [1 ,2 ,3 ,4 ]
Sanchez Alberti, Andres [1 ,2 ,3 ,4 ]
Bivona, Augusto E. [1 ,2 ,3 ,4 ]
Morales, Celina [5 ]
Guzman, Carlos A. [6 ]
Malchiodi, Emilio L. [1 ,2 ,3 ,4 ]
机构
[1] UBA, Catedra Inmunol, Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Fac Farm & Bioquim, CONICET, Inst Estudios Inmunidad Humoral Dr RA Margni, RA-1113 Buenos Aires, DF, Argentina
[3] Univ Buenos Aires, Inst Microbiol & Parasitol Med IMPaM, CONICET, Buenos Aires, DF, Argentina
[4] Univ Buenos Aires, Fac Med, Dept Microbiol Parasitol & Inmunol, Buenos Aires, DF, Argentina
[5] Univ Buenos Aires, Fac Med, Inst Fisiopat Cardiovasc, Dept Patol, Buenos Aires, DF, Argentina
[6] Helmholtz Ctr Infect Res, Dept Vaccinol & Appl Microbiol, Braunschweig, Germany
关键词
Chagas disease; American trypanosomiasis; Trypanosoma cruzi; multicomponent vaccine; DNA delivery system; Salmonella enterica; oral vaccine; CHAGAS-DISEASE; CRUZI INFECTION; TARGETED DELETION; T-CELLS; PROTEIN; ANTIGEN; INDETERMINATE; IMMUNIZATION; CANDIDATES; CHALLENGE;
D O I
10.1093/infdis/jiu480
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have reported that attenuated Salmonella (S) carrying plasmids encoding the cysteine protease cruzipain (Cz) protects against Trypanosoma cruzi infection. Here, we determined whether immunoprotection could be improved by the oral coadministration of 3 Salmonella carrying the plasmids that encode the antigens Cz, Tc52, and Tc24. SCz+STc52+STc24-immunized mice presented an increased antibody response against each antigen compared with those in the single antigen-immunized groups, as well as higher trypomastigotes antibody-mediated lyses and cell invasion inhibition compared with controls. SCz+STc52+STc24-immunized and -challenged mice rendered lower parasitemia. Weight loss after infection was detected in all mice except those in the SCz+STc52+STc24 group. Moreover, cardiomyopathy-associated enzyme activity was significantly lower in SCz+STc24+STc52-immunized mice compared with controls. Few or no abnormalities were found in muscle tissues of SCz+STc24+STc52-immunized mice, whereas controls presented with inflammatory foci, necrosis, and amastigote nests. We conclude that a multicomponent approach that targets several invasion and metabolic mechanisms improves protection compared with single-component vaccines.
引用
收藏
页码:698 / 707
页数:10
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