Intranasal administration of proteoliposome-derived cochleates from Vibrio cholerae O1 induce mucosal and systemic immune responses in mice

Acevedo, Reinaldo; Callico, Adriana; del Campo, Judith; Gonzalez, Elizabeth; Cedre, Barbara; Gonzalez, Lissette; Romeu, Belkis; Zayas, Caridad; Lastre, Miriam; Fernandez, Sonsire; Oliva, Reynaldo; Garcia, Luis; Luis Perez, Jose; Perez, Oliver

Abstract

Conservative estimates place the death toll from cholera at more than 100,000 persons each year. A particulate mucosal vaccine strategy combining antigens and immune stimulator molecules from Vibrio cholerae to overcome this problem is described. Proteoliposomes extracted from V. cholerae O1 were transformed into cochleates (AFCo2, Adjuvant Finlay cochleate 2) through a calcium inducible rotary dialysis method. Light microscopy was carried out and tubules of 16.25 +/- 4.57 pm in length were observed. Western blots were performed to verify the immunochemical properties of the main AFCo2 incorporated antigens, revealing full recognition of the outer membrane protein U (OmpU), lipopolysaccharide (LPS), and mannose-sensitive hemagglutinin (MSHA) antigens. AFCo2 were administered by the intranasal route using a two or three dose schedule and the immune response against V. cholerae antigens was assessed. Three AFCo2 doses were required to induce significant (p 0.05), antigen specific IgA in saliva (1.34 +/- 0.135) and feces (0.60 +/- 0.089). While, two or three doses of AFCo2 or proteoliposomes induce similar specific IgG and vibriocidal activity responses in sera. These results show for the first time that AFCo2 can be obtained from V. cholerae O1 proteoliposomes and have the potential to protect against the pathogen when administered intranasally. (c) 2009 Elsevier Inc. All rights reserved.

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Título según WOS: ID WOS:000272129500003 Not found in local WOS DB
Título de la Revista: METHODS
Volumen: 49
Número: 4
Editorial: ACADEMIC PRESS INC ELSEVIER SCIENCE
Fecha de publicación: 2009
Página de inicio: 309
Página final: 315
DOI:

10.1016/j.ymeth.2009.03.027

Notas: ISI