Abstract:
AIMS:The study was designed to evaluate a novel cationic lipid DNA adjuvant (N3) and its function for HIV-1gp160/rev DNA plasmid delivered intranasally. The primary N3/HIV-DNA plasmid immunizations were boosted intranasally with a gp41 peptide in a anionic L3 adjuvant. This novel prime-boost strategy of mucosal immunization provided a broad HIV-1 envelope specific immunity, and recognition of viruses of subtypes A, B and C. CONCLUSIONS:Intranasal N3-adjuvanted gp160/rev DNA prime followed by one L3-peptide boosting immunization, induced broadly neutralizing antibodies against HIV-1 in the mucosa and systemically. The needle-free intranasal prime-boost strategy using two different adjuvant formulations reduced significantly the dose of DNA needed.
journal_name
Vaccinejournal_title
Vaccineauthors
Hinkula J,Devito C,Zuber B,Benthin R,Ferreira D,Wahren B,Schröder Udoi
10.1016/j.vaccine.2005.08.015subject
Has Abstractpub_date
2006-05-22 00:00:00pages
4494-7issue
21eissn
0264-410Xissn
1873-2518pii
S0264-410X(05)00810-8journal_volume
24pub_type
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