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Safety and immunogenicity of a peptide containing the cross-neutralization epitope of HPV16 L2 administered nasally in healthy volunteers
- Source :
- Vaccine. 21(27-30)
- Publication Year :
- 2003
-
Abstract
- Amino acid (aa) 108-120 of L2 protein of human papillomavirus (HPV) type 16 contains a cross-neutralization epitope against genital HPV. We designed a placebo-controlled trial in healthy adults to evaluate the safety and immunogenicity of a synthetic peptide consisting of the aa 108-120 of HPV16 L2 (L2-108/120) region. A total of 13 volunteers were given nasal inoculations with 0.1 (n=5) or 0.5mg (n=5) doses of the peptides or placebo (n=3) without adjuvant at weeks 0, 4, and 12. Sera were collected before inoculation and at 6, 16 and 36 weeks. The inoculation caused no serious local and systemic complications. The inoculation generated anti-L2 antibodies binding to both HPV16 and 52 L1/L2-capsids in four of the five recipients in the 0.5mg group. Sera of the four recipients showed neutralizing activities against HPV16 and 52. Serological responses to the peptides were not found in the 0.1mg group and the placebo group recipients. This study suggests the L2-108/120 peptide is tolerable in humans and has the potential as a broad-spectrum prophylactic vaccine against genital HPV.
- Subjects :
- Adult
Male
medicine.medical_treatment
Dose-Response Relationship, Immunologic
Pilot Projects
Cross Reactions
Placebo
Epitope
Neutralization
Serology
Epitopes
Neutralization Tests
medicine
Humans
Papillomaviridae
Administration, Intranasal
General Veterinary
General Immunology and Microbiology
biology
business.industry
Immunogenicity
Public Health, Environmental and Occupational Health
Viral Vaccines
Virology
Infectious Diseases
Immunoglobulin G
Immunology
Vaccines, Subunit
biology.protein
Molecular Medicine
Nasal administration
Capsid Proteins
Female
Antibody
business
Adjuvant
Subjects
Details
- ISSN :
- 0264410X
- Volume :
- 21
- Issue :
- 27-30
- Database :
- OpenAIRE
- Journal :
- Vaccine
- Accession number :
- edsair.doi.dedup.....a108d26289aa3f0f6fbbe1b31123cd0b