Chimeric Vaccines Designed by Immunoinformatics-Activated Polyfunctional and Memory T cells that Trigger Protection against Experimental Visceral Leishmaniasis

被引:29
作者
De Brito, Rory Cristiane Fortes [1 ]
Ruiz, Jeronimo Conceicao [2 ,3 ]
Cardoso, Jamille Mirelle de Oliveira [1 ]
Ostolin, Thais Lopes Valentim Di Paschoale [1 ]
Reis, Levi Eduardo Soares [1 ]
Mathias, Fernando Augusto Siqueira [1 ]
Aguiar-Soares, Rodrigo Dian de Oliveira [1 ]
Roatt, Bruno Mendes [1 ,4 ]
Correa-Oliveira, Rodrigo [5 ]
Resende, Daniela de Melo [2 ,3 ]
Reis, Alexandre Barbosa [1 ,4 ]
机构
[1] Univ Fed Ouro Preto, Nucleo Pesquisas Ciencias Biol NUPEB, Lab Imunopatol, BR-35400000 Ouro Preto, Brazil
[2] Fiocruz Minas, Inst Rene Rachou, Grp Informat Biossistemas & Genom, BR-30190002 Belo Horizonte, MG, Brazil
[3] Fiocruz MS, Inst Oswaldo Cruz, Programa Posgrad Biol Computac & Sistemas, BR-21040360 Rio De Janeiro, Brazil
[4] Inst Nacl Ciencia & Tecnol Doencas Trop INCT DT, BR-40110160 Salvador, BA, Brazil
[5] Fiocruz Minas, Inst Rene Rachou, Lab Imunol Celular & Mol, BR-30190002 Belo Horizonte, MG, Brazil
关键词
reverse vaccinology; immunoinformatics; chimera vaccine; Leishmania infantum; polyfunctional T cells; memory T cells; rational design of vaccines; MURINE; VACCINATION; IMMUNITY; MICE; IMMUNIZATION; CHALLENGE; PARASITES; QUALITY; GENOME; WEB;
D O I
10.3390/vaccines8020252
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Many vaccine candidates against visceral leishmaniasis (VL) have been proposed; however, to date, none of them have been efficacious for the human or canine disease. On this basis, the design of leishmaniasis vaccines has been constantly changing, and the use of approaches to select specific epitopes seems to be crucial in this scenario. The ability to predict T cell-specific epitopes makes immunoinformatics an even more necessary approach, as in VL an efficient immune response against the parasite is triggered by T lymphocytes in response toLeishmaniaspp. immunogenic antigens. Moreover, the success of vaccines depends on the capacity to generate long-lasting memory and polyfunctional cells that are able to eliminate the parasite. In this sense, our study used a combination of different approaches to develop potential chimera candidate vaccines against VL. The first point was to identify the most immunogenic epitopes ofLeishmania infantumproteins and construct chimeras composed of Major histocompatibility complex (MHC) class I and II epitopes. For this, we used immunoinformatics features. Following this, we validated these chimeras in a murine model in a thorough memory study and multifunctionality of T cells that contribute to a better elucidation of the immunological protective mechanisms of polyepitope vaccines (chimera A and B) using multicolor flow cytometry. Our results showed that in silico-designed chimeras can elicit polyfunctional T cells producing T helper (Th)1 cytokines, a strong immune response againstLeishmaniaantigen, and the generation of central and effector memory T cells in the spleen cells of vaccinated animals that was able to reduce the parasite burden in this organ. These findings contribute two potential candidate vaccines against VL that can be used in further studies, and help in this complex field of vaccine development against this challenging parasite.
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页数:20
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