Abstract:
:Twenty years ago we reported the first synthetic peptide-based anti-malarial vaccine named SPf66, which conferred limited protective efficacy in large-scale human field-trials. Our efforts towards a second vaccine generation based on the rational selection of conserved high activity binding peptides (HABPs) whose critical binding residues have to be precisely replaced by others. Introducing peptide bond isosters on these HABPs' critical binding residues constitutes also an important approach. Our results suggest that knowing a parasite's immunologically active peptides, their 3D structure, and their interaction for properly stabilizing MHC-II peptide-TCR complexes constitutes the basis for rationally designing a fully effective, multi-component, multistage subunit-based anti-malarial vaccine.
journal_name
Microbes Infectjournal_title
Microbes and infectionauthors
Lozano JM,Patarroyo MEdoi
10.1016/j.micinf.2007.02.004subject
Has Abstractpub_date
2007-05-01 00:00:00pages
751-60issue
6eissn
1286-4579issn
1769-714Xpii
S1286-4579(07)00084-6journal_volume
9pub_type
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journal_title:Microbes and infection
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journal_title:Microbes and infection
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journal_title:Microbes and infection
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journal_title:Microbes and infection
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journal_title:Microbes and infection
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journal_title:Microbes and infection
pub_type: 杂志文章
doi:10.1016/j.micinf.2007.10.002
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journal_title:Microbes and infection
pub_type: 杂志文章
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更新日期:2008-03-01 00:00:00
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更新日期:2006-08-01 00:00:00
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journal_title:Microbes and infection
pub_type: 杂志文章
doi:10.1016/j.micinf.2004.03.006
更新日期:2004-06-01 00:00:00
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journal_title:Microbes and infection
pub_type: 杂志文章
doi:10.1016/j.micinf.2013.08.004
更新日期:2013-11-01 00:00:00