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Expression of hBD-2 induced by 23-valent pneumococcal polysaccharide vaccine, Haemophilus influenzae type b vaccine and split influenza virus vaccine.
- Source :
-
Molecular medicine reports [Mol Med Rep] 2012 Oct; Vol. 6 (4), pp. 733-8. Date of Electronic Publication: 2012 Jul 26. - Publication Year :
- 2012
-
Abstract
- Human β-defensin-2 (hBD-2) is an antimicrobial peptide with high activity and broad spectrum activity. hBD-2 expression may be highly elevated by microorganisms and inflammation. We reported that the majority of common vaccines used, including 23-valent pneumococcal polysaccharide vaccine, Haemophilus influenzae type b vaccine and split influenza virus vaccine, could induce the expression of hBD-2 in epithelial cells. Among them, the 23-valent pneumococcal polysaccharide vaccine was effective at a lower concentration (0.5 µg/ml), while Haemophilus influenzae type b vaccine and split influenza virus vaccine were effective at the concentration of 1 µg/ml. However, bacteriostatic experiments revealed that the split influenza virus vaccine was capable of inducing the highest antimicrobial activity. The medium of the 23-valent pneumococcal polysaccharide vaccine treatment group had a higher antimicrobial activity than the medium of the Haemophilus influenzae type b vaccine treatment group. The transcriptional regulator of hBD-2, that is, the NF-κB subunit, had a high level of activity, while the normal epithelial cells showed barely detectable activity, indicating that these vaccines have potential for clinical application.
- Subjects :
- Bacterial Capsules
Bronchi cytology
Cells, Cultured
Epithelial Cells drug effects
Epithelial Cells metabolism
Humans
NF-kappa B metabolism
beta-Defensins genetics
Haemophilus Vaccines pharmacology
Influenza Vaccines pharmacology
Pneumococcal Vaccines pharmacology
Transcription, Genetic drug effects
beta-Defensins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1791-3004
- Volume :
- 6
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Molecular medicine reports
- Publication Type :
- Academic Journal
- Accession number :
- 22842707
- Full Text :
- https://doi.org/10.3892/mmr.2012.1005