» Articles » PMID: 18008168

Exploiting Cholera Vaccines As a Versatile Antigen Delivery Platform

Overview
Journal Biotechnol Lett
Date 2007 Nov 17
PMID 18008168
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

The development of safe, immunogenic and protective cholera vaccine candidates makes possible their use as a versatile antigen delivery platform. Foreign antigens can be delivered to the immune system with cholera vaccines by expressing heterologous antigens in live attenuated vectors, as fusion proteins with cholera toxin subunits combined with inactivated Vibrio cholerae whole cells or by exposing them on the surface of V. cholerae ghosts. Progress in our understanding of the genes expressed by V. cholerae during infection creates unprecedented opportunities to develop an improved generation of vaccine vectors to induce immune protection against a broad range of pathogenic organisms.

Citing Articles

The Mutagenic Plasticity of the Cholera Toxin B-Subunit Surface Residues: Stability and Affinity.

Au C, Manfield I, Webb M, Paci E, Turnbull W, Ross J Toxins (Basel). 2024; 16(3).

PMID: 38535799 PMC: 10974167. DOI: 10.3390/toxins16030133.


A Self-Assembling Whole-Cell Vaccine Antigen Presentation Platform.

Liao J, Smith D, Brynjarsdottir J, Watnick P J Bacteriol. 2018; 200(15).

PMID: 29483163 PMC: 6040178. DOI: 10.1128/JB.00752-17.


Live bacterial vaccine vectors: an overview.

da Silva A, Zangirolami T, Novo-Mansur M, de Campos Giordano R, Martins E Braz J Microbiol. 2015; 45(4):1117-29.

PMID: 25763014 PMC: 4323283. DOI: 10.1590/s1517-83822014000400001.


Attenuation of bacterial virulence by quorum sensing-regulated lysis.

Silva A, Benitez J, Wu J J Biotechnol. 2010; 150(1):22-30.

PMID: 20673838 PMC: 2974442. DOI: 10.1016/j.jbiotec.2010.07.025.


Use of stabilized luciferase-expressing plasmids to examine in vivo-induced promoters in the Vibrio cholerae vaccine strain CVD 103-HgR.

Morin C, Kaper J FEMS Immunol Med Microbiol. 2009; 57(1):69-79.

PMID: 19678844 PMC: 2906245. DOI: 10.1111/j.1574-695X.2009.00580.x.

References
1.
Osorio C, Crawford J, Michalski J, Martinez-Wilson H, Kaper J, Camilli A . Second-generation recombination-based in vivo expression technology for large-scale screening for Vibrio cholerae genes induced during infection of the mouse small intestine. Infect Immun. 2005; 73(2):972-80. PMC: 546989. DOI: 10.1128/IAI.73.2.972-980.2005. View

2.
Benitez J, Garcia L, Silva A, Garcia H, Fando R, Cedre B . Preliminary assessment of the safety and immunogenicity of a new CTXPhi-negative, hemagglutinin/protease-defective El Tor strain as a cholera vaccine candidate. Infect Immun. 1999; 67(2):539-45. PMC: 96352. DOI: 10.1128/IAI.67.2.539-545.1999. View

3.
Butterton J, Boyko S, Calderwood S . Use of the Vibrio cholerae irgA gene as a locus for insertion and expression of heterologous antigens in cholera vaccine strains. Vaccine. 1993; 11(13):1327-35. DOI: 10.1016/0264-410x(93)90103-5. View

4.
Ghorpade A, Garg L . Efficient expression, processing and secretion of a biologically active mammalian protein by Vibrio cholerae. FEBS Lett. 1996; 387(2-3):167-70. DOI: 10.1016/0014-5793(96)00475-9. View

5.
Eko F, Schukovskaya T, Lotzmanova E, Firstova V, Emalyanova N, Klueva S . Evaluation of the protective efficacy of Vibrio cholerae ghost (VCG) candidate vaccines in rabbits. Vaccine. 2003; 21(25-26):3663-74. DOI: 10.1016/s0264-410x(03)00388-8. View