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Gonococcal transferrin binding protein chimeras induce bactericidal and growth inhibitory antibodies in mice.


ABSTRACT: We have previously demonstrated the full-length gonococcal transferrin binding proteins (TbpA and TbpB) to be promising antigens in the development of a protective vaccine against Neisseria gonorrhoeae. In the current study we employed a genetic chimera approach fusing domains from TbpA and TbpB to the A2 domain of cholera toxin, which naturally binds in a non-covalent fashion to the B subunit of cholera toxin during assembly. For one construct, the N-terminal half of TbpB (NB) was fused to the A2 subunit of cholera toxin. In a second construct, the loop 2 region (L2) of TbpA was genetically fused between the NB domain and the A2 domain, generating a double chimera. Both chimeras were immunogenic and induced serum bactericidal and vaginal growth-inhibiting antibodies. This study highlights the potential of using protective epitopes instead of full-length proteins in the development of an efficacious gonococcal vaccine.

SUBMITTER: Price GA 

PROVIDER: S-EPMC2225598 | biostudies-literature | 2007 Oct

REPOSITORIES: biostudies-literature

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Gonococcal transferrin binding protein chimeras induce bactericidal and growth inhibitory antibodies in mice.

Price Gregory A GA   Masri Heather P HP   Hollander Aimee M AM   Russell Michael W MW   Cornelissen Cynthia Nau CN  

Vaccine 20070806 41


We have previously demonstrated the full-length gonococcal transferrin binding proteins (TbpA and TbpB) to be promising antigens in the development of a protective vaccine against Neisseria gonorrhoeae. In the current study we employed a genetic chimera approach fusing domains from TbpA and TbpB to the A2 domain of cholera toxin, which naturally binds in a non-covalent fashion to the B subunit of cholera toxin during assembly. For one construct, the N-terminal half of TbpB (NB) was fused to the  ...[more]

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