Structural and immunological principles leading to chemically synthesized, multiantigenic, multistage, minimal subunit-based vaccine development
Identifying the principles and rules for developing a logical, rational vaccine methodology against various diseases, is discussed. SPf66, the first multiantigenic, multistage, minimal subunit-based, chemically synthesized anti-P. falciparum malaria vaccine. A robust, sensitive, and specific methodo...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2011
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/23654
- Acceso en línea:
- https://doi.org/10.1021/cr100223m
https://repository.urosario.edu.co/handle/10336/23654
- Palabra clave:
- Class I
Cloning and sequencing
Cytokines
Falciparum malaria
Genes encoding
Hepatic cells
High affinity
Immune systems
Molecular levels
Vaccine development
Biosynthesis
Cloning
Genes
Vaccines
Subunit vaccine
Vaccine
Chemical structure
Human
Immunization
Immunology
Review
Humans
Immunization
Vaccines
Subunit
Molecular
Models
Vaccines
- Rights
- License
- Abierto (Texto Completo)
Summary: | Identifying the principles and rules for developing a logical, rational vaccine methodology against various diseases, is discussed. SPf66, the first multiantigenic, multistage, minimal subunit-based, chemically synthesized anti-P. falciparum malaria vaccine. A robust, sensitive, and specific methodology is developed for defining the intimate molecular interactions mediating merozoite invasion of RBC by synthesizing short merozoite-derived protein peptides binding specifically and with high affinity (HABP) to RBCs. Conserved HABP-mediated sporozoite binding to hepatic cells is identified in EBA-175 for developing a multiantigenic, multistage, fully protective antimalarial vaccine. for developing a logical and rational vaccine methodology at the molecular level, monkeys' immune system molecules is analyzed by cloning and sequencing the Aotus genes encoding immunoglobulins, cytokines, and Class I and II molecules. |
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