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https://www.arca.fiocruz.br/handle/icict/58322
NEXT-GENERATION NEXT-GENERATION LEISHMANIZATION: REVISITING MOLECULAR TARGETS FOR SELECTING GENETICALLY ENGINEERED LIVE-ATTENUATED LEISHMANIA.
Affilliation
Fundação Oswaldo Cruz. Instituto René Rachou. Biotecnologia Aplicada ao Estudo de Patógenos. Belo Horizonte, Brazil.
Fundação Oswaldo Cruz. Instituto René Rachou. Biotecnologia Aplicada ao Estudo de Patógenos. Belo Horizonte, Brazil.
Fundação Oswaldo Cruz. Instituto René Rachou. Biotecnologia Aplicada ao Estudo de Patógenos. Belo Horizonte, Brazil.
Fundação Oswaldo Cruz. Instituto René Rachou. Biotecnologia Aplicada ao Estudo de Patógenos. Belo Horizonte, Brazil.
Fundação Oswaldo Cruz. Instituto René Rachou. Biotecnologia Aplicada ao Estudo de Patógenos. Belo Horizonte, Brazil.
Abstract
CRISPR/Cas; genetic manipulation; leishmanization; live-attenuated Leishmania; vaccine.Despite decades of research devoted to finding a vaccine against leishmaniasis, we are still lacking a safe and effective vaccine for humans. Given this scenario, the search for a new prophylaxis alternative for controlling leishmaniasis should be a global priority. Inspired by leishmanization-a first generation vaccine strategy where live L. major parasites are inoculated in the skin to protect against reinfection-live-attenuated Leishmania vaccine candidates are promising alternatives due to their robust elicited protective immune response. In addition, they do not cause disease and could provide long-term protection upon challenge with a virulent strain. The discovery of a precise and easy way to perform CRISPR/Cas-based gene editing allowed the selection of safer null mutant live-attenuated Leishmania parasites obtained by gene disruption. Here, we revisited molecular targets associated with the selection of live-attenuated vaccinal strains, discussing their function, their limiting factors and the ideal candidate for the next generation of genetically engineered live-attenuated Leishmania vaccines to control leishmaniasis.
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