BCG como plataforma vacinal: da imunidade treinada à análise in sílico de peptídeos do SARS-CoV-2

First identified in 2019, the SARS-CoV-2 is a Betacoronavirus that triggered a global pandemic, resulting in millions of cases and deaths. Characterized by high transmissibility and the ability to evade the acquired immunity, it infects human cells through the interaction between the Spike protein a...

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Detalhes bibliográficos
Autor: Campelo, Thales Alves
Formato: tesis doctoral
Estado:Versión publicada
Fecha de publicación:2025
País:Brasil
Recursos:Universidade Federal do Ceará (UFC)
Repositorio:Repositório Institucional da Universidade Federal do Ceará (UFC)
Idioma:portugués
OAI Identifier:oai:repositorio.ufc.br:riufc/81319
Acesso em linha:http://repositorio.ufc.br/handle/riufc/81319
Access Level:acceso abierto
Palavra-chave:CNPQ::CIENCIAS DA SAUDE::MEDICINA::ANATOMIA PATOLOGICA E PATOLOGIA CLINICA
Imunidade Heteróloga
Imunidade Treinada
SARS-CoV- 2
Immunity, Heterologous
Trained Immunity
SARS-CoV-2
Descrição
Resumo:First identified in 2019, the SARS-CoV-2 is a Betacoronavirus that triggered a global pandemic, resulting in millions of cases and deaths. Characterized by high transmissibility and the ability to evade the acquired immunity, it infects human cells through the interaction between the Spike protein and the ACE2 receptor, initiating complex immune responses. Given the need for alternative vaccines, the Bacillus Calmette-Guérin (BCG) vaccine, widely used against tuberculosis, stands out for its potential to induce innate/trained and adaptive immunities, as well as its application in heterologous protection against viral infections. In this context, this study conducted an in silico analysis to identify and evaluate SARS-CoV-2- immunogenic peptides, with potential for incorporation into a future recombinant BCG (rBCG) to induce a specific and robust immune response against covid-19. Additionally, the immune mechanisms associated with the trained immunity conferred by BCG were revisited, highlighting its ability to reprogram monocytic cells and induce amplified responses to subsequent infections. The results highlighted the identification of immunogenic peptides derived from SARS-CoV-2, with broad population coverage and the ability to stimulate specific immune responses. Furthermore, it was demonstrated that BCG can reprogram innate immune cells through trained immunity, offering cross-protection against viral infections. The rBCG platform was identified as a viable strategy for the development of multivalent vaccines, combining innate/trained and adaptive immunities to induce effective immune responses. Despite challenges such as genetic stability and variability between strains, the findings reinforce the potential of rBCG in combating emerging diseases and pandemics.