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Leishmania LiHyC protein is immunogenic and induces protection against visceral leishmaniasis

Leishmania LiHyC protein is immunogenic and induces protection against visceral leishmaniasis
Leishmania LiHyC protein is immunogenic and induces protection against visceral leishmaniasis

Treatment against visceral leishmaniasis (VL) presents problems by the toxicity of drugs, high cost and/or emergence of resistant strains. The diagnosis is hampered by variable sensitivity and/or specificity of tests. In this context, prophylactic vaccination could represent a control measure against disease. In this study, the protective efficacy of Leishmania LiHyC protein was evaluated in a murine model against Leishmania infantum infection. LiHyC was used as recombinant protein (rLiHyC) associated with saponin (rLiHyC/S) or Poloxamer 407-based polymeric micelles (rLiHyC/M) to immunize mice. Animals received also saline, saponin or empty micelles as controls. The immunogenicity was evaluated before and after the challenge, and results showed that vaccination with rLiHyC/S or rLiHyC/M induced the production of high levels of interferon-gamma (IFN-γ), interleukin (IL)-12 and granulocyte-macrophage colony-stimulating factor in cell culture supernatants, as well as higher IFN-γ expression evaluated by RT-qPCR and involvement from CD4+ and CD8+ T-cell subtypes producing IFN-γ, tumor necrosis factor-α and IL-2. A positive lymphoproliferative response was also found in cell cultures from vaccinated animals, besides high levels of rLiHyC- and parasite-specific nitrite and IgG2a antibodies. Immunological assays correlated with significant reductions in the parasite load in the spleens, livers, bone marrows and draining lymph nodes from vaccinated mice, when compared to values found in the controls. The micellar composition showed slightly better immunological and parasitological data, as compared to rLiHyC/S. Results suggest that rLiHyC associated with adjuvants could be considered for future studies as a vaccine candidate against VL.

LiHyC, immune response, polymeric micelles, recombinant proteins, vaccine, visceral leishmaniasis
0141-9838
Machado, Amanda S.
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Lage, Daniela P.
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Vale, Danniele L.
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Freitas, Camila S.
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Linhares, Flávia P.
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Cardoso, Jamille M.O.
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Oliveira-da-Silva, João A.
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Pereira, Isabela A.G.
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Ramos, Fernanda F.
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Tavares, Grasiele S.V.
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Ludolf, Fernanda
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Bandeira, Raquel S.
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Maia, Luiz G.N.
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Menezes-Souza, Daniel
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Duarte, Mariana C.
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Chávez-Fumagalli, Miguel A.
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Roatt, Bruno M.
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Christodoulides, Myron
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Martins, Vívian T.
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Coelho, Eduardo Antonio Ferraz
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Machado, Amanda S.
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Lage, Daniela P.
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Vale, Danniele L.
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Freitas, Camila S.
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Linhares, Flávia P.
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Cardoso, Jamille M.O.
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Oliveira-da-Silva, João A.
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Pereira, Isabela A.G.
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Ramos, Fernanda F.
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Tavares, Grasiele S.V.
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Ludolf, Fernanda
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Bandeira, Raquel S.
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Maia, Luiz G.N.
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Menezes-Souza, Daniel
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Duarte, Mariana C.
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Chávez-Fumagalli, Miguel A.
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Roatt, Bruno M.
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Christodoulides, Myron
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Martins, Vívian T.
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Coelho, Eduardo Antonio Ferraz
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Machado, Amanda S., Lage, Daniela P., Vale, Danniele L., Freitas, Camila S., Linhares, Flávia P., Cardoso, Jamille M.O., Oliveira-da-Silva, João A., Pereira, Isabela A.G., Ramos, Fernanda F., Tavares, Grasiele S.V., Ludolf, Fernanda, Bandeira, Raquel S., Maia, Luiz G.N., Menezes-Souza, Daniel, Duarte, Mariana C., Chávez-Fumagalli, Miguel A., Roatt, Bruno M., Christodoulides, Myron, Martins, Vívian T. and Coelho, Eduardo Antonio Ferraz (2022) Leishmania LiHyC protein is immunogenic and induces protection against visceral leishmaniasis. Parasite Immunology, 44 (8), [e12921]. (doi:10.1111/pim.12921).

Record type: Article

Abstract

Treatment against visceral leishmaniasis (VL) presents problems by the toxicity of drugs, high cost and/or emergence of resistant strains. The diagnosis is hampered by variable sensitivity and/or specificity of tests. In this context, prophylactic vaccination could represent a control measure against disease. In this study, the protective efficacy of Leishmania LiHyC protein was evaluated in a murine model against Leishmania infantum infection. LiHyC was used as recombinant protein (rLiHyC) associated with saponin (rLiHyC/S) or Poloxamer 407-based polymeric micelles (rLiHyC/M) to immunize mice. Animals received also saline, saponin or empty micelles as controls. The immunogenicity was evaluated before and after the challenge, and results showed that vaccination with rLiHyC/S or rLiHyC/M induced the production of high levels of interferon-gamma (IFN-γ), interleukin (IL)-12 and granulocyte-macrophage colony-stimulating factor in cell culture supernatants, as well as higher IFN-γ expression evaluated by RT-qPCR and involvement from CD4+ and CD8+ T-cell subtypes producing IFN-γ, tumor necrosis factor-α and IL-2. A positive lymphoproliferative response was also found in cell cultures from vaccinated animals, besides high levels of rLiHyC- and parasite-specific nitrite and IgG2a antibodies. Immunological assays correlated with significant reductions in the parasite load in the spleens, livers, bone marrows and draining lymph nodes from vaccinated mice, when compared to values found in the controls. The micellar composition showed slightly better immunological and parasitological data, as compared to rLiHyC/S. Results suggest that rLiHyC associated with adjuvants could be considered for future studies as a vaccine candidate against VL.

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More information

Accepted/In Press date: 13 April 2022
e-pub ahead of print date: 18 April 2022
Published date: August 2022
Additional Information: Funding Information: This work was supported by grant APQ‐02167‐21 from the Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG) and by grant APQ‐408675/2018‐7 from the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Brazil. The authors also thank the Brazilian agencies Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) and CNPq for the student scholarships.
Keywords: LiHyC, immune response, polymeric micelles, recombinant proteins, vaccine, visceral leishmaniasis

Identifiers

Local EPrints ID: 477135
URI: http://eprints.soton.ac.uk/id/eprint/477135
ISSN: 0141-9838
PURE UUID: 147f21ee-488b-4922-9351-adab7041621f
ORCID for Myron Christodoulides: ORCID iD orcid.org/0000-0002-9663-4731

Catalogue record

Date deposited: 30 May 2023 16:34
Last modified: 17 Mar 2024 02:36

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Contributors

Author: Amanda S. Machado
Author: Daniela P. Lage
Author: Danniele L. Vale
Author: Camila S. Freitas
Author: Flávia P. Linhares
Author: Jamille M.O. Cardoso
Author: João A. Oliveira-da-Silva
Author: Isabela A.G. Pereira
Author: Fernanda F. Ramos
Author: Grasiele S.V. Tavares
Author: Fernanda Ludolf
Author: Raquel S. Bandeira
Author: Luiz G.N. Maia
Author: Daniel Menezes-Souza
Author: Mariana C. Duarte
Author: Miguel A. Chávez-Fumagalli
Author: Bruno M. Roatt
Author: Vívian T. Martins
Author: Eduardo Antonio Ferraz Coelho

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