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Immunoinformatic construction of an adenovirus-based modular vaccine platform and its application in the design of a SARS-CoV-2 vaccine.
Porto, Pedro Soares; Anjos, Déborah; Dábilla, Nathânia; da Fonseca, Simone Gonçalves; Souza, Menira.
  • Porto PS; Laboratory of Virology and Cell Culture, Instituto de Patologia Tropical e Saúde Pública, Universidade Federal de Goiás, Goiânia, GO, Brazil.
  • Anjos D; Laboratory of Virology and Cell Culture, Instituto de Patologia Tropical e Saúde Pública, Universidade Federal de Goiás, Goiânia, GO, Brazil.
  • Dábilla N; Laboratory of Virology and Cell Culture, Instituto de Patologia Tropical e Saúde Pública, Universidade Federal de Goiás, Goiânia, GO, Brazil.
  • da Fonseca SG; Immunoregulation Laboratory, Instituto de Patologia Tropical e Saúde Pública, Universidade Federal de Goiás, Brazil.
  • Souza M; Laboratory of Virology and Cell Culture, Instituto de Patologia Tropical e Saúde Pública, Universidade Federal de Goiás, Goiânia, GO, Brazil. Electronic address: menirasouza@gmail.com.
Infect Genet Evol ; 85: 104489, 2020 11.
Article in English | MEDLINE | ID: covidwho-692494
ABSTRACT
The current SARS-CoV-2 pandemic has imposed new challenges and demands for health systems, especially in the development of new vaccine strategies. Vaccines for many pathogens were developed based on the display of foreign epitopes in the variable regions of the human adenovirus (HAdV) major capsid proteins (hexon, penton and fiber). The humoral immune response against the HAdV major capsid proteins was demonstrated to play a role in the development of an immune response against the epitopes in display. Through the immunoinformatic profiling of the major capsid proteins of HAdVs from different species, we developed a modular concept that can be used in the development of vaccines based on HAdV vectors. Our data suggests that different immunomodulatory potentials can be observed in the conserved regions, present in the hexon and penton proteins, from different species. Using this modular approach, we developed a HAdV-5 based vaccine strategy for SARS-CoV-2, constructed through the display of SARS-CoV-2 epitopes indicated by our prediction analysis as immunologically relevant. The sequences of the HAdV vector major capsid proteins were also edited to enhance the IFN-gamma induction and antigen presenting cells activation. This is the first study proposing a modular HAdV platform developed to aid the design of new vaccines by inducing an immune response more suited for the epitopes in display.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Vaccines / Epitopes, B-Lymphocyte / Computational Biology / Capsid Proteins Type of study: Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Infect Genet Evol Journal subject: Biology / Communicable Diseases / Genetics Year: 2020 Document Type: Article Affiliation country: J.meegid.2020.104489

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Vaccines / Epitopes, B-Lymphocyte / Computational Biology / Capsid Proteins Type of study: Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Infect Genet Evol Journal subject: Biology / Communicable Diseases / Genetics Year: 2020 Document Type: Article Affiliation country: J.meegid.2020.104489