Unbound MEDLINE

Nasal vaccination with CpG oligodeoxynucleotide induces protective immunity against non-typeable Haemophilus influenzae in the nasopharynx. The Laryngoscope. [Laryngoscope] Journal article

 
TitleNasal vaccination with CpG oligodeoxynucleotide induces protective immunity against non-typeable Haemophilus influenzae in the nasopharynx.
Author(s)Abe N, Kodama S, Hirano T, Eto M, Suzuki M 
InstitutionFrom the Department of Otolaryngology (n.a., s.k., t.h., m.e., m.s.), Oita University Faculty of Medicine, 1-1 Idaigaoka, Hazama-machi, Yufu, Oita, Japan.
SourceLaryngoscope 2006 Mar; 116(3):407-12.
MeSHAdjuvants, Immunologic
Administration, Intranasal
Animals
Antibodies, Anti-Idiotypic
CD4-Positive T-Lymphocytes
CD8-Positive T-Lymphocytes
Comparative Study
Disease Models, Animal
Haemophilus Infections
Haemophilus Vaccines
Haemophilus influenzae
Immunity, Mucosal
Immunoglobulin A
Immunoglobulin G
Interferon Type II
Interleukin-6
Mice
Mice, Inbred BALB C
Nasopharyngeal Diseases
Oligodeoxyribonucleotides
Research Support, Non-U.S. Gov't
Vaccination
AbstractOBJECTIVES: Nasal vaccination is an effective therapeutic regimen for preventing otitis media. Since cholera toxin (CT) is toxic, an alternative adjuvant is required for the development of a nasal vaccine. The efficacy of CpG oligodeoxynucleotide (ODN) as a mucosal adjuvant was examined.
METHODS: Mice were immunized intranasally with P6 protein of non-typeable Haemophilus influenzae (NTHi) and adjuvant, CT, or CpG ODN, and P6-specific antibody responses were examined. The expression of P6-specific cytokine mRNA in splenic CD4 T cells was also determined. In addition, NTHi challenges were performed and the NTHi was quantified in nasal washes.
RESULTS: P6-specific IgA in nasal wash and serum IgG titers were elevated significantly after nasal immunization. The IgG1/IgG2a ratio in serum from P6+CpG-immunized mice was less than that of P6+CT-immunized mice. Although IL-6 was expression similarly in both groups, IFN-gamma expression was greater in P6+CpG-immunized mice than in P6+CT-immunized mice. Enhanced clearance of NTHi from the nasopharynx was also shown equally in both groups.
CONCLUSION: These results indicate that CpG ODN might be an effective mucosal adjuvant, acting by mechanisms that are different from CT. These findings suggest that nasal vaccination with P6 and CpG ODN might be an effective regimen for the induction of NTHi-specific protective immunity.
Languageeng
Pub Type(s)Journal Article
PubMed ID16540899
  
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