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Immunoinformatics Evaluation of a Fusion Protein Composed of Leishmania infantum LiHyV and Phlebotomus kandelakii Apyrase as a Vaccine Candidate against Visceral Leishmaniasis.
Fayaz, Shima; Bahrami, Fariborz; Fard-Esfahani, Pezhman; Parvizi, Parviz; Bahramali, Golnaz; Ajdary, Soheila.
Afiliación
  • Fayaz S; Department of Biochemistry, Pasteur Institute of Iran, Tehran, Iran.
  • Bahrami F; Department of Immunology, Pasteur Institute of Iran, Tehran, Iran.
  • Fard-Esfahani P; Department of Immunology, Pasteur Institute of Iran, Tehran, Iran.
  • Parvizi P; Department of Biochemistry, Pasteur Institute of Iran, Tehran, Iran.
  • Bahramali G; Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran.
  • Ajdary S; Department of AIDS and Bloodborne Diseases, Pasteur Institute of Iran, Tehran, Iran.
Iran J Parasitol ; 17(2): 145-158, 2022.
Article en En | MEDLINE | ID: mdl-36032738
Background: Visceral leishmaniasis (VL) is a lethal parasitic disease, transmitted by sand fly vectors. Immunomodulatory properties of sand fly saliva proteins and their protective effects against Leishmania infection in pre-exposed animals suggest that a combination of an antigenic salivary protein along with a Leishmania antigen can be considered for designing a vaccine against leishmaniasis. Methods: Three different fusion forms of L. infantum hypothetical protein (LiHyV) in combination with Phlebotomus kandelakii salivary apyrase (PkanAp) were subjected to insilico analyses. Major Histocompatibility Complex (MHC) class I and II epitopes in both humans and BALB/c mice were predicted. Antigenicity, immunogenicity, epitope conservancy, toxicity, and population coverage were also evaluated. Results: Highly antigenic promiscuous epitopes consisting of truncated LiHyV (10-285) and full-length PkanAp (21-329) were identified in human and was named Model 1. This model contained 25 MHC-I and 141 MHC-II antigenic peptides which among them, MPANSDIRI and AQSLFDFSGLALDSN were fully conserved. LALDSNATV, RCSSALVSI, ALVSINVPL, SAVESGALF of MHC-I epitopes, and 28 MHC-II binding epitopes showed 60% conservancy among various clades. A population coverage with a rate of >75% in the Iranian population and >70% in the whole world was also identified. Conclusion: Based on this in-silico approach, the predicted Model 1 could potentially be used as a vaccine candidate against VL.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Iran J Parasitol Año: 2022 Tipo del documento: Article País de afiliación: Irán Pais de publicación: Irán

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Iran J Parasitol Año: 2022 Tipo del documento: Article País de afiliación: Irán Pais de publicación: Irán