Bacterial outer membrane vesicles and vaccine applications

被引：200

作者：

Acevedo, Reinaldo ^{[1
]}

Fernandez, Sonsire ^{[1
]}

Zayas, Caridad ^{[1
]}

Acosta, Armando ^{[1
]}

Elena Sarmiento, Maria ^{[1
]}

Ferro, Valerie A. ^{[2
]}

Rosenqyise, Einar ^{[3
]}

Campal, Concepcion ^{[1
]}

Cardoso, Daniel ^{[1
]}

Garcia, Luis ^{[1
]}

Luis Perez, Jose ^{[1
]}

机构：

[1] Finlay Inst, Havana, Cuba

[2] Univ Strathclyde, Strathclyde Inst Pharm & Biomed Sci, Glasgow, Lanark, Scotland

[3] Norwegian Inst Publ Hlth, Oslo, Norway

来源：

FRONTIERS IN IMMUNOLOGY | 2014年 / 5卷

关键词：

outer membrane vesicles; vaccines; proteoliposomes; adjuvant; Neisseria meningitidis; Vibrio cholerae; Bordetella pertussis; Mycobacterium tuberculosis; NEISSERIA-MENINGITIDIS; MENINGOCOCCAL DISEASE; OMV VACCINE; CELL-WALL; SEROGROUP; ADJUVANT; IMMUNOGENICITY; PROTEOLIPOSOME; IMMUNIZATION; PERTUSSIS;

D O I：

10.3389/fimmu.2014.00121

中图分类号：

R392 [医学免疫学]; Q939.91 [免疫学];

学科分类号：

100102 ;

摘要：

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 (dOMV(B)) using detergent extraction. Subsequently, OMV from N. meningitidis, serogroup A (dOMV(A)), serogroup W(dOMV(W)), and serogroup X (dOMV(X)) 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 (dOMV(C)), Bordetella pertussis (dOMV(BP)), Mycobacterium smegmatis (dOMV(SM)), and BCG (dOMV(BCG)). 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. dOMV(B) 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.

引用

页数：6

共 54 条

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