Literature DB >> 10722632

Induction of specific immunoglobulin A and Th2 immune responses to P6 outer membrane protein of nontypeable Haemophilus influenzae in middle ear mucosa by intranasal immunization.

S Kodama1, S Suenaga, T Hirano, M Suzuki, G Mogi.   

Abstract

Nontypeable Haemophilus influenzae (NTHI) is a major pathogen of otitis media. One of the outer membrane proteins of NTHI, P6, is an antigen common to all strains and is considered as a candidate for mucosal vaccine. To elucidate the possibility of developing a nasal vaccine against nontypeable Haemophilus influenzae (NTHI) and to investigate mucosal immune responses in the middle ear, mice were immunized intranasally with the P6 outer membrane protein of NTHI, and P6-specific immune responses in the middle ear mucosa were examined. Mice were given with P6 and cholera toxin intranasally as an adjuvant on days 0, 7, and 14 and were killed on day 21. The P6-specific immunoglobulin A (IgA) antibody titer in ear wash was significantly elevated. Mononuclear cells were isolated from middle ear mucosa, and an increase in P6-specific IgA-producing cells was shown with an enzyme-linked immunospot assay. In addition, an increase in memory T cells in middle ear mucosa was detected with flow cytometric analysis after intranasal immunization. Moreover, in vitro stimulation with P6 resulted in proliferation of purified CD4(+) T cells from immunized mice, and these T cells expressed Th2 cytokine mRNA. These results indicate that P6-specific IgA-B-cell immune responses and selected Th2 cytokine expressing Th cells were induced in middle ear mucosa by intranasal immunization. These findings suggest that a nasal vaccine is useful for preventing otitis media with effusion.

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Year:  2000        PMID: 10722632      PMCID: PMC97416          DOI: 10.1128/IAI.68.4.2294-2300.2000

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  46 in total

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2.  Identification of a 16,600-dalton outer membrane protein on nontypeable Haemophilus influenzae as a target for human serum bactericidal antibody.

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3.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.

Authors:  P Chomczynski; N Sacchi
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4.  Recombinant murine IL-5 induces high rate IgA synthesis in cycling IgA-positive Peyer's patch B cells.

Authors:  K W Beagley; J H Eldridge; H Kiyono; M P Everson; W J Koopman; T Honjo; J R McGhee
Journal:  J Immunol       Date:  1988-09-15       Impact factor: 5.422

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Journal:  Int J Pediatr Otorhinolaryngol       Date:  1980-02       Impact factor: 1.675

Review 6.  Nontypable Haemophilus influenzae: a review of clinical aspects, surface antigens, and the human immune response to infection.

Authors:  T F Murphy; M A Apicella
Journal:  Rev Infect Dis       Date:  1987 Jan-Feb

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Authors:  M Takahashi; J Peppard; J P Harris
Journal:  Acta Otolaryngol       Date:  1989 Jan-Feb       Impact factor: 1.494

9.  Induction of antigen-specific IgA-forming cells in the middle ear mucosa.

Authors:  N Watanabe; H Yoshimura; G Mogi
Journal:  Arch Otolaryngol Head Neck Surg       Date:  1988-07

10.  Interleukins and IgA synthesis. Human and murine interleukin 6 induce high rate IgA secretion in IgA-committed B cells.

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Journal:  J Exp Med       Date:  1989-06-01       Impact factor: 14.307

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  14 in total

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2.  Nasal immunity to staphylococcal toxic shock is controlled by the nasopharynx-associated lymphoid tissue.

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3.  Intranasal immunization with recombinant Ascaris suum 14-kilodalton antigen coupled with cholera toxin B subunit induces protective immunity to A. suum infection in mice.

Authors:  N Tsuji; K Suzuki; H Kasuga-Aoki; Y Matsumoto; T Arakawa; K Ishiwata; T Isobe
Journal:  Infect Immun       Date:  2001-12       Impact factor: 3.441

4.  Intranasal vaccination of infant mice induces protective immunity in the absence of nasal-associated lymphoid tissue.

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Journal:  Vaccine       Date:  2008-02-04       Impact factor: 3.641

Review 5.  Mouse models for the study of mucosal vaccination against otitis media.

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Review 6.  Mouse models for human otitis media.

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7.  Promiscuous peptides on the nontypeable Haemophilus influenzae P6 outer membrane protein.

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Journal:  J Clin Immunol       Date:  2008-04-01       Impact factor: 8.317

8.  Antibody in middle ear fluid of children originates predominantly from sera and nasopharyngeal secretions.

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9.  Accumulation of Regulatory T Cells and Chronic Inflammation in the Middle Ear in a Mouse Model of Chronic Otitis Media with Effusion Induced by Combined Eustachian Tube Blockage and Nontypeable Haemophilus influenzae Infection.

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Review 10.  Mouse models as a tool to unravel the genetic basis for human otitis media.

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