@article{acevedo_bacterial_2014,
	title = {Bacterial outer membrane vesicles and vaccine applications},
	volume = {5},
	url = {http://journal.frontiersin.org/Journal/10.3389/fimmu.2014.00121/abstract},
	doi = {10.3389/fimmu.2014.00121},
	abstract = {Vaccines based on outer membrane vesicles (OMV) were developed more than 20 years ago against Neisseria meningitidis serogroup B. These nano-sized structures exhibit remarkable potential for immunomodulation of immune responses and delivery of meningococcal antigens or unrelated antigens incorporated into the vesicle structure. This paper reviews different applications in OMV Research and Development (R\&D) and provides examples of OMV developed and evaluated at the Finlay Institute in Cuba. A Good Manufacturing Practice (GMP) process was developed at the Finlay Institute to produce OMV from N. meningitidis serogroup B (dOMVB) using detergent extraction. Subsequently, OMV from N. meningitidis, serogroup A (dOMVA), serogroup W (dOMVW), and serogroup X (dOMVX) were obtained using this process. More recently, the extraction process has also been applied effectively for obtaining OMV on a research scale from Vibrio cholerae (dOMVC), Bordetella pertussis (dOMVBP), Mycobacterium smegmatis (dOMVSM), and BCG (dOMVBCG). The immunogenicity of the OMV has been evaluated for specific antibody induction, and together with functional bactericidal and challenge assays in mice has shown their protective potential. dOMVB has been evaluated with non-neisserial antigens, including with a herpes virus type 2 glycoprotein, ovalbumin, and allergens. In conclusion, OMV are proving to be more versatile than first conceived and remain an important technology for development of vaccine candidates.},
	urldate = {2014-08-26},
	journal = {Immunotherapies and Vaccines},
	author = {Acevedo, Reinaldo and Fernandez, Sonsire and Zayas, Caridad and Acosta, Armando and Sarmiento, Maria Elena and Ferro, Valerie A. and Rosenqvist, Einar and Campa, Concepcion and Cardoso, Daniel and Garcia, Luis and Perez, Jose Luis},
	year = {2014},
	pages = {121},
}

{"_id":"46i65gKnNevjynv82","bibbaseid":"acevedo-fernandez-zayas-acosta-sarmiento-ferro-rosenqvist-campa-etal-bacterialoutermembranevesiclesandvaccineapplications-2014","author_short":["Acevedo, R.","Fernandez, S.","Zayas, C.","Acosta, A.","Sarmiento, M. E.","Ferro, V. A.","Rosenqvist, E.","Campa, C.","Cardoso, D.","Garcia, L.","Perez, J. L."],"bibdata":{"bibtype":"article","type":"article","title":"Bacterial outer membrane vesicles and vaccine applications","volume":"5","url":"http://journal.frontiersin.org/Journal/10.3389/fimmu.2014.00121/abstract","doi":"10.3389/fimmu.2014.00121","abstract":"Vaccines based on outer membrane vesicles (OMV) were developed more than 20 years ago against Neisseria meningitidis serogroup B. These nano-sized structures exhibit remarkable potential for immunomodulation of immune responses and delivery of meningococcal antigens or unrelated antigens incorporated into the vesicle structure. This paper reviews different applications in OMV Research and Development (R&D) and provides examples of OMV developed and evaluated at the Finlay Institute in Cuba. A Good Manufacturing Practice (GMP) process was developed at the Finlay Institute to produce OMV from N. meningitidis serogroup B (dOMVB) using detergent extraction. Subsequently, OMV from N. meningitidis, serogroup A (dOMVA), serogroup W (dOMVW), and serogroup X (dOMVX) were obtained using this process. More recently, the extraction process has also been applied effectively for obtaining OMV on a research scale from Vibrio cholerae (dOMVC), Bordetella pertussis (dOMVBP), Mycobacterium smegmatis (dOMVSM), and BCG (dOMVBCG). The immunogenicity of the OMV has been evaluated for specific antibody induction, and together with functional bactericidal and challenge assays in mice has shown their protective potential. dOMVB has been evaluated with non-neisserial antigens, including with a herpes virus type 2 glycoprotein, ovalbumin, and allergens. In conclusion, OMV are proving to be more versatile than first conceived and remain an important technology for development of vaccine candidates.","urldate":"2014-08-26","journal":"Immunotherapies and Vaccines","author":[{"propositions":[],"lastnames":["Acevedo"],"firstnames":["Reinaldo"],"suffixes":[]},{"propositions":[],"lastnames":["Fernandez"],"firstnames":["Sonsire"],"suffixes":[]},{"propositions":[],"lastnames":["Zayas"],"firstnames":["Caridad"],"suffixes":[]},{"propositions":[],"lastnames":["Acosta"],"firstnames":["Armando"],"suffixes":[]},{"propositions":[],"lastnames":["Sarmiento"],"firstnames":["Maria","Elena"],"suffixes":[]},{"propositions":[],"lastnames":["Ferro"],"firstnames":["Valerie","A."],"suffixes":[]},{"propositions":[],"lastnames":["Rosenqvist"],"firstnames":["Einar"],"suffixes":[]},{"propositions":[],"lastnames":["Campa"],"firstnames":["Concepcion"],"suffixes":[]},{"propositions":[],"lastnames":["Cardoso"],"firstnames":["Daniel"],"suffixes":[]},{"propositions":[],"lastnames":["Garcia"],"firstnames":["Luis"],"suffixes":[]},{"propositions":[],"lastnames":["Perez"],"firstnames":["Jose","Luis"],"suffixes":[]}],"year":"2014","pages":"121","bibtex":"@article{acevedo_bacterial_2014,\n\ttitle = {Bacterial outer membrane vesicles and vaccine applications},\n\tvolume = {5},\n\turl = {http://journal.frontiersin.org/Journal/10.3389/fimmu.2014.00121/abstract},\n\tdoi = {10.3389/fimmu.2014.00121},\n\tabstract = {Vaccines based on outer membrane vesicles (OMV) were developed more than 20 years ago against Neisseria meningitidis serogroup B. These nano-sized structures exhibit remarkable potential for immunomodulation of immune responses and delivery of meningococcal antigens or unrelated antigens incorporated into the vesicle structure. This paper reviews different applications in OMV Research and Development (R\\&D) and provides examples of OMV developed and evaluated at the Finlay Institute in Cuba. A Good Manufacturing Practice (GMP) process was developed at the Finlay Institute to produce OMV from N. meningitidis serogroup B (dOMVB) using detergent extraction. Subsequently, OMV from N. meningitidis, serogroup A (dOMVA), serogroup W (dOMVW), and serogroup X (dOMVX) were obtained using this process. More recently, the extraction process has also been applied effectively for obtaining OMV on a research scale from Vibrio cholerae (dOMVC), Bordetella pertussis (dOMVBP), Mycobacterium smegmatis (dOMVSM), and BCG (dOMVBCG). The immunogenicity of the OMV has been evaluated for specific antibody induction, and together with functional bactericidal and challenge assays in mice has shown their protective potential. dOMVB has been evaluated with non-neisserial antigens, including with a herpes virus type 2 glycoprotein, ovalbumin, and allergens. In conclusion, OMV are proving to be more versatile than first conceived and remain an important technology for development of vaccine candidates.},\n\turldate = {2014-08-26},\n\tjournal = {Immunotherapies and Vaccines},\n\tauthor = {Acevedo, Reinaldo and Fernandez, Sonsire and Zayas, Caridad and Acosta, Armando and Sarmiento, Maria Elena and Ferro, Valerie A. and Rosenqvist, Einar and Campa, Concepcion and Cardoso, Daniel and Garcia, Luis and Perez, Jose Luis},\n\tyear = {2014},\n\tpages = {121},\n}\n\n","author_short":["Acevedo, R.","Fernandez, S.","Zayas, C.","Acosta, A.","Sarmiento, M. E.","Ferro, V. A.","Rosenqvist, E.","Campa, C.","Cardoso, D.","Garcia, L.","Perez, J. L."],"key":"acevedo_bacterial_2014","id":"acevedo_bacterial_2014","bibbaseid":"acevedo-fernandez-zayas-acosta-sarmiento-ferro-rosenqvist-campa-etal-bacterialoutermembranevesiclesandvaccineapplications-2014","role":"author","urls":{"Paper":"http://journal.frontiersin.org/Journal/10.3389/fimmu.2014.00121/abstract"},"metadata":{"authorlinks":{}},"html":""},"bibtype":"article","biburl":"https://bibbase.org/zotero/robin.marlow","dataSources":["ix72eqAAMGCuupBaz"],"keywords":[],"search_terms":["bacterial","outer","membrane","vesicles","vaccine","applications","acevedo","fernandez","zayas","acosta","sarmiento","ferro","rosenqvist","campa","cardoso","garcia","perez"],"title":"Bacterial outer membrane vesicles and vaccine applications","year":2014}