Potential Applications of Microparticulate-Based Bacterial Outer Membrane Vesicles (OMVs) Vaccine Platform for Sexually Transmitted Diseases (STDs): Gonorrhea, Chlamydia, and Syphilis

被引:12
作者
Chbib, Christiane [1 ]
Shah, Sarthak M. [2 ]
Gala, Rikhav P. [3 ]
Uddin, Mohammad N. [2 ]
机构
[1] Larkin Univ, Coll Pharm, Dept Pharmaceut Sci, Miami, FL 33169 USA
[2] Mercer Univ, Coll Pharm, Dept Pharmaceut Sci, Atlanta, GA 30341 USA
[3] Fraunhofer USA, Ctr Midatlantic, Biotechnol Div, Newark, DE 19702 USA
关键词
antibiotic; chlamydia; gonorrhea; syphilis; sexually transmitted diseases (STDs); microparticulate; vaccine; outer membrane vesicles (OMV); GRAM-NEGATIVE BACTERIA; PLASMID DNA; DELIVERY; RELEASE; ANTIGEN; PURIFICATION; BIOGENESIS; STRATEGIES; PROTECTION; ANTIBODIES;
D O I
10.3390/vaccines9111245
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Sexually transmitted diseases (STDs) are a major global health issue. Approximately 250 million new cases of STDs occur each year globally. Currently, only three STDs (human papillomavirus (HPV), hepatitis A, and hepatitis B) are preventable by vaccines. Vaccines for other STDs, including gonorrhea, chlamydia, and syphilis, await successful development. Currently, all of these STDs are treated with antibiotics. However, the efficacy of antibiotics is facing growing challenge due to the emergence of bacterial resistance. Therefore, alternative therapeutic approaches, including the development of vaccines against these STDs, should be explored to tackle this important global public health issue. Mass vaccination could be more efficient in reducing the spread of these highly contagious diseases. Bacterial outer membrane vesicle (OMV) is a potential antigen used to prevent STDs. OMVs are released spontaneously during growth by many Gram-negative bacteria. They present a wide range of surface antigens in native conformation that possess interesting properties such as immunogenicity, adjuvant potential, and the ability to be taken up by immune cells, all of which make them an attractive target for application as vaccines against pathogenic bacteria. The major challenge associated with the use of OMVs is its fragile structure and stability. However, a particulate form of the vaccine could be a suitable delivery system that can protect the antigen from degradation by a harsh acidic or enzymatic environment. The particulate form of the vaccine can also act as an adjuvant by itself. This review will highlight some practical methods for formulating microparticulate OMV-based vaccines for STDs.
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页数:11
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共 66 条
[1]   The impact of ExHp-CD (outer membrane vesicles) released from Helicobacter pylori SS1 on macrophage RAW 264.7 cells and their immunogenic potential [J].
Ahmed, Abeer Ahmed Qaed ;
Qi, Fuyu ;
Zheng, Ruizhu ;
Xiao, Lin ;
Abdalla, Ahmed M. E. ;
Mao, Lin ;
Bakadia, Bianza Moise ;
Liu, Li ;
Atta, Omar Mohammad ;
Li, Xiaohong ;
Shi, Zhijun ;
Yang, Guang .
LIFE SCIENCES, 2021, 279
[2]   Vaccines Combined with Immune Checkpoint Antibodies Promote Cytotoxic T-cell Activity and Tumor Eradication [J].
Ali, Omar A. ;
Lewin, Sarah A. ;
Dranoff, Glenn ;
Mooney, David J. .
CANCER IMMUNOLOGY RESEARCH, 2016, 4 (02) :95-100
[3]   Affinity purification of bacterial outer membrane vesicles (OMVs) utilizing a His-tag mutant [J].
Alves, Nathan J. ;
Turner, Kendrick B. ;
DiVito, Kyle A. ;
Daniele, Michael A. ;
Walper, Scott A. .
RESEARCH IN MICROBIOLOGY, 2017, 168 (02) :139-146
[4]  
[Anonymous], 2019, NATL OVERVIEW SEXUAL
[5]   Vaccine delivery: a matter of size, geometry, kinetics and molecular patterns [J].
Bachmann, Martin F. ;
Jennings, Gary T. .
NATURE REVIEWS IMMUNOLOGY, 2010, 10 (11) :787-796
[6]   Biomimetic Delivery with Micro- and Nanoparticles [J].
Balmert, Stephen C. ;
Little, Steven R. .
ADVANCED MATERIALS, 2012, 24 (28) :3757-3778
[7]   Recombinant outer membrane vesicles carrying Chlamydia muridarum HtrA induce antibodies that neutralize chlamydial infection in vitro [J].
Bartolini, Erika ;
Ianni, Elvira ;
Frigimelica, Elisabetta ;
Petracca, Roberto ;
Galli, Giuliano ;
Scorza, Francesco Berlanda ;
Norais, Nathalie ;
Laera, Donatello ;
Giusti, Fabiola ;
Pierleoni, Andrea ;
Donati, Manuela ;
Cevenini, Roberto ;
Finco, Oretta ;
Grandi, Guido ;
Grifantini, Renata .
JOURNAL OF EXTRACELLULAR VESICLES, 2013, 2 (01)
[8]   Purification of outer membrane vesicles from Pseudomonas aeruginosa and their activation of an IL-8 response [J].
Bauman, Susanne J. ;
Kuehn, Meta J. .
MICROBES AND INFECTION, 2006, 8 (9-10) :2400-2408
[9]   Oral delivery of microparticles containing plasmid DNA encoding hepatitis-B surface antigen [J].
Bhowmik, Tuhin ;
D'Souza, Bernadette ;
Uddin, Mohammad N. ;
D'Souza, Martin J. .
JOURNAL OF DRUG TARGETING, 2012, 20 (04) :364-371
[10]   The interaction of plasmid DNA with polyamidoamine dendrimers: mechanism of complex formation and analysis of alterations induced in nuclease sensitivity and transcriptional activity of the complexed DNA [J].
Bielinska, AU ;
KukowskaLatallo, JF ;
Baker, JR .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1997, 1353 (02) :180-190