Mucosal immunization with filamentous hemagglutinin protects against Bordetella pertussis respiratory infection
- PMID: 1548072
- PMCID: PMC257021
- DOI: 10.1128/iai.60.4.1482-1488.1992
Mucosal immunization with filamentous hemagglutinin protects against Bordetella pertussis respiratory infection
Abstract
Mucosal immunization of mice with purified Bordetella pertussis filamentous hemagglutinin (FHA), by either the respiratory or the gut route, was found to protect against B. pertussis infection of the trachea and lungs. Intranasal immunization of BALB/c and (C57BL/6 x C3H/HeN)F1 adult female mice with FHA prior to B. pertussis aerosol challenge resulted in a 2 to 3 log reduction in number of bacteria recovered from the lungs and the tracheas of immunized mice in comparison to unimmunized controls. Intraduodenal immunization of adult mice with FHA before infection also resulted in approximately a 2 log reduction in the recovery of bacteria from the lungs and the tracheas of immunized mice in comparison to unimmunized controls. Immunoglobulin A and immunoglobulin G anti-FHA were both detected in bronchoalveolar lavage fluids of mucosally immunized mice. Limiting dilution analysis revealed a 60-fold increase in the frequency of FHA-specific B cells isolated from the lungs of mice immunized intranasally with FHA in comparison to unimmunized control mice. These data suggest that both gut and respiratory mucosal immunization with a major adhesin of B. pertussis generates a specific immune response in the respiratory tract that may serve as one means of mitigating subsequent B. pertussis respiratory infection.
Similar articles
-
Bordetella pertussis filamentous hemagglutinin: evaluation as a protective antigen and colonization factor in a mouse respiratory infection model.Infect Immun. 1990 Jan;58(1):7-16. doi: 10.1128/iai.58.1.7-16.1990. Infect Immun. 1990. PMID: 2294058 Free PMC article.
-
Protection of mice against respiratory Bordetella pertussis infection by intranasal immunization with P.69 and FHA.Vaccine. 1993;11(8):866-72. doi: 10.1016/0264-410x(93)90363-3. Vaccine. 1993. PMID: 8356847
-
Mucosal and systemic antibody responses against an acellular pertussis vaccine in mice after intranasal co-administration with recombinant cholera toxin B subunit as an adjuvant.Vaccine. 2003 Mar 7;21(11-12):1165-73. doi: 10.1016/s0264-410x(02)00516-9. Vaccine. 2003. PMID: 12559794
-
Mice are protected against Bordetella pertussis infection by intra-nasal immunization with filamentous haemagglutinin.FEMS Microbiol Lett. 1993 Mar 1;107(2-3):211-6. doi: 10.1111/j.1574-6968.1993.tb06032.x. FEMS Microbiol Lett. 1993. PMID: 8472903
-
Immune responses and protection against Bordetella pertussis infection after intranasal immunization of mice with filamentous haemagglutinin in solution or incorporated in biodegradable microparticles.Vaccine. 1995 Apr;13(5):455-62. doi: 10.1016/0264-410x(94)00008-b. Vaccine. 1995. PMID: 7639014
Cited by
-
Genome rearrangements, deletions, and amplifications in the natural population of Bartonella henselae.J Bacteriol. 2006 Nov;188(21):7426-39. doi: 10.1128/JB.00472-06. Epub 2006 Aug 25. J Bacteriol. 2006. PMID: 16936024 Free PMC article.
-
Intransal or intragastric immunization with proteosome-Shigella lipopolysaccharide vaccines protects against lethal pneumonia in a murine model of Shigella infection.Infect Immun. 1995 Jun;63(6):2382-6. doi: 10.1128/iai.63.6.2382-2386.1995. Infect Immun. 1995. PMID: 7768627 Free PMC article.
-
Orally administered microencapsulated Bordetella pertussis fimbriae protect mice from B. pertussis respiratory infection.Infect Immun. 1996 Feb;64(2):489-94. doi: 10.1128/iai.64.2.489-494.1996. Infect Immun. 1996. PMID: 8550197 Free PMC article.
-
Protective immunity to Bordetella pertussis requires both B cells and CD4(+) T cells for key functions other than specific antibody production.J Exp Med. 2000 Jun 5;191(11):1841-52. doi: 10.1084/jem.191.11.1841. J Exp Med. 2000. PMID: 10839801 Free PMC article.
-
Adjuvanticity and protective immunity elicited by Bordetella pertussis antigens encapsulated in poly(DL-lactide-co-glycolide) microspheres.Infect Immun. 1995 Apr;63(4):1195-200. doi: 10.1128/iai.63.4.1195-1200.1995. Infect Immun. 1995. PMID: 7890372 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical