Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 26
Filter
2.
Methods Mol Biol ; 2197: 207-222, 2021.
Article in English | MEDLINE | ID: mdl-32827139

ABSTRACT

Human papillomavirus (HPV ) has been extensively associated with the development of cervical cancer due to the expression of oncoproteins like E7. This protein can interfere with pRB tumor suppressor activity, enabling the uncontrolled proliferation of abnormal cells. DNA vaccines are known as the third-generation vaccines, providing the ability of targeting viral infections such as HPV in a preventive and therapeutic way. Although current strategies make use of plasmid DNA (pDNA) as the vector of choice to be used as a DNA vaccine, minicircle DNA (mcDNA) has been proving its added value as a non-viral DNA vector by demonstrating higher expression efficiency and increased biosafety than the pDNA. However, due to its innovative profile, few methodologies have been explored and implemented for the manufacture of this molecule. This chapter describes the detailed procedures for the production, extraction, and purification of supercoiled E7-mcDNA vaccine, by using size-exclusion chromatography to obtain mcDNA with a purity degree which meets the regulatory agency criteria. Then, the assessment of E7 antigen expression through immunocytochemistry is also described.


Subject(s)
DNA, Circular/isolation & purification , Papillomavirus Vaccines/isolation & purification , Plasmids/isolation & purification , Vaccines, DNA/isolation & purification , Cell Culture Techniques , Chromatography, Gel , Escherichia coli/genetics , Fermentation , Gene Expression , Immunohistochemistry , Papillomavirus E7 Proteins/genetics , Papillomavirus E7 Proteins/immunology , Papillomavirus Vaccines/genetics , Papillomavirus Vaccines/immunology , Vaccines, DNA/genetics , Vaccines, DNA/immunology
3.
AIDS Rev ; 21(4): 218-232, 2019.
Article in English | MEDLINE | ID: mdl-31834327

ABSTRACT

Virus-like particles (VLPs) are a type of subunit vaccine which resembles viruses but do not contain any genetic material so that they are not infectious. VLPs maintain the same antigenic conformation to the original virus, and they could be a better vaccine candidate than live-attenuated and inactivated vaccines. In addition, compared to other subunit vaccines such as soluble protein, VLPs can stimulate both innate and adaptive immune responses effectively and safely against several pathogens by the closer morphology to its native virus. They have already been licensed as vaccines against Hepatitis B virus, human papillomavirus (HPV), and several veterinary diseases. Moreover, it has been investigated to prevent other viral infections including HIV. While HIV VLP-based vaccines have been studied over 35 years, none of them has been successful enough to reach even Phase III clinical trials. In this review, we summarize: (i) general features of VLPs; (ii) epidemiological data and current status of vaccine research and development on HPV and HIV; and (iii) previous studies held on HPV VLPs, HIV VLPs, and chimeric HPV/HIV VLPs including production methods and different animal immunization assays. Furthermore, we review present state of human clinical trials with VLPs and consider the potential to develop a successful preventive HIV vaccine using HPV VLP models. Finally, we discuss the benefits, limitations, and challenges of developing chimeric VLP-based HPV/HIV vaccines with recent findings, critical issues to improve VLP-based vaccines, and hot topics for the next 5 years to join the global effort to fight against these two pathogens.


Subject(s)
AIDS Vaccines/immunology , AIDS Vaccines/isolation & purification , Papillomavirus Vaccines/immunology , Papillomavirus Vaccines/isolation & purification , Vaccines, Virus-Like Particle/immunology , Vaccines, Virus-Like Particle/isolation & purification , AIDS Vaccines/genetics , Clinical Trials as Topic , Global Health , HIV/genetics , HIV/immunology , HIV Infections/epidemiology , HIV Infections/prevention & control , Humans , Papillomaviridae/genetics , Papillomaviridae/immunology , Papillomavirus Infections/epidemiology , Papillomavirus Infections/prevention & control , Papillomavirus Vaccines/genetics , Vaccines, Virus-Like Particle/genetics
4.
Viral Immunol ; 31(2): 80-85, 2018 03.
Article in English | MEDLINE | ID: mdl-29298130

ABSTRACT

The human papillomavirus (HPV) is an important causal agent of premalignant cervical epithelial changes and cervical cancers. These cancers account for ∼5% of all cancers globally and kill more than a quarter million women annually. HPV infections also associate with certain anogenital and oropharyngeal cancers. Events leading to the development of HPV vaccines to prevent associated cancers are described, with a further discussion of goals that must be met to achieve full virus eradication.


Subject(s)
Drug Discovery/methods , Papillomaviridae/immunology , Papillomavirus Infections/complications , Papillomavirus Vaccines/immunology , Papillomavirus Vaccines/isolation & purification , Uterine Cervical Neoplasms/epidemiology , Uterine Cervical Neoplasms/prevention & control , Anus Neoplasms/epidemiology , Anus Neoplasms/prevention & control , Female , Humans , Male , Oropharyngeal Neoplasms/epidemiology , Oropharyngeal Neoplasms/prevention & control
5.
Electrophoresis ; 38(22-23): 2975-2980, 2017 11.
Article in English | MEDLINE | ID: mdl-28683160

ABSTRACT

Affinity chromatography based on amino acids as interacting ligands was already indicated as an alternative compared to ion exchange or hydrophobic interaction for plasmid DNA purification. Understanding the recognition mechanisms occurring between histidine-based ligands and nucleic acids enables more efficient purification of a DNA vaccine, as the binding and elution conditions can be adjusted in order to enhance the purification performance. Decreasing pH to slightly acidic conditions increases the positive charge of histidine ligand, what influences the type of interaction between chromatographic support and analytes. This was proven in this work, where hydrophobic effects established in the presence of ammonium sulfate were affected at pH 5.0 in comparison to pH 8.0, while electrostatic and cation-π interactions were intensified. Histidine ligand at pH 5.0 interacts with phosphate groups or aromatic rings of plasmid DNA. Due to different responses of RNA and pDNA on mobile phase changes, the elution order between RNA and pDNA was changed with mobile phase pH decrease from 8.0 to 5.0. The phenomenon was more evident with L-histidine ligand due to more hydrophilic character, leading to an improved selectivity of L-histidine-modified chromatographic monolith, allowing the product recovery with 99% of purity (RNA removal). With the 1-benzyl- L-histidine ligand, stronger and less selective interactions with the nucleic acids were observed due to the additional hydrophobicity associated with the phenyl aromatic ring. Optimization of sample displacement chromatography parameters (especially (NH4 )2 SO4 concentration) at slightly acidic pH enabled excellent isolation of pDNA, by the removal of RNA in a negative mode, with binding capacities above 1.5 mg pDNA per mL of chromatographic support.


Subject(s)
Chromatography, Affinity/methods , Histidine/chemistry , Oncogene Proteins, Viral/genetics , Papillomavirus E7 Proteins/genetics , Papillomavirus Vaccines/isolation & purification , Plasmids/isolation & purification , Repressor Proteins/genetics , Vaccines, DNA/isolation & purification , DNA/isolation & purification , Histidine/metabolism , Ligands , Papillomavirus Vaccines/genetics , Plasmids/genetics , Vaccines, DNA/genetics
6.
Hum Vaccin Immunother ; 13(6): 1-4, 2017 06 03.
Article in English | MEDLINE | ID: mdl-28362244

ABSTRACT

The discovery of HPV as the etiological factor for HPV-associated malignancies and disease has opened up several opportunities for prevention and therapy. Current commercially available HPV vaccines (Gardasil, Gardasil 9, and Cervarix) are prophylactic in nature and derived from adjuvanted L1-based virus-like particles of HPV. Globally, through several clinical trials, they were found to be very safe and efficacious. Certain limitations such as cost-effectiveness, low coverage against all HPV types and a 3-dose schedule make these vaccines difficult to use worldwide. Approaches to address these issues involve alternate expression systems using L1 or alternate antigen (L2) as well as optimizing doses and broadening protection to provide cheap and cross-protective vaccines. Additionally, promising preclinical immunogenicity results from our own studies using alternative hosts such as Pichia and an antigen delivery system-based measles vector have potential for development as next generation HPV prophylactic vaccines. Several other therapeutic approaches are also ongoing.


Subject(s)
Drug Discovery/trends , Papillomavirus Infections/prevention & control , Papillomavirus Vaccines/immunology , Global Health , Humans , Papillomavirus Vaccines/administration & dosage , Papillomavirus Vaccines/adverse effects , Papillomavirus Vaccines/isolation & purification
7.
Article in English | MEDLINE | ID: mdl-27037127

ABSTRACT

Quadrivalent human papillomavirus (HPV) vaccine is formulated of four types of non-infectious recombinant virus like particles (VLPs) that are structurally and immunologically similar to the corresponding infectious HPV virus types 6, 11, 16 and 18. With almost identical physical, chemical and structural properties of the four types of VLPs, ELISA remains the only approved in vitro potency testing assay. In this study, an alternative industry-friendly, stability- and potency-indicating assay protocol was developed and validated for the determination of HPV vaccine. Vacuum-driven immunoaffinity extraction (IAE) was employed using type-specific, conformation-dependent antibodies against each type of HPV VLPs. ELISA assay was employed to evaluate the ability of IAE columns to specifically separate each of the four types of VLPs from their quadrivalent mixture. Mean percentage recoveries of 76.76±2.69, 69.12±5.79, 84.86±5.25 and 71.14±4.50% were obtained for VLPs types 6, 11, 16 and 18, respectively with no significant interference in each case. Antigen content was then determined using SE-HPLC over a concentration range of 5.00-20.00µg/mL (r>0.998) for VLPs type 6, 11, 16 and 18, respectively. The SE-HPLC assay was found accurate and precise (RSD<10.00%) with LOD ranging from 1.23-3.85µg/mL. The assay protocol was found superior to conventional ELISA assay with respect to simplicity, total analysis time and cost. Good correlation between the results of analysis obtained using IAE-SE-HPLC and ELISA demonstrated the suitability of the suggested assay protocol for stability and potency assessment with a good potential for implementation for batch release. This approach should be applicable for quality assessment of other vaccine preparations based on VLPs.


Subject(s)
Antibodies, Immobilized/chemistry , Chromatography, Affinity/methods , Chromatography, High Pressure Liquid/methods , Papillomavirus Vaccines/isolation & purification , Vaccines, Virus-Like Particle/isolation & purification , Chromatography, Gel/methods , Humans , Limit of Detection , Papillomavirus Vaccines/chemistry , Vaccines, Virus-Like Particle/chemistry
8.
Expert Rev Vaccines ; 15(7): 853-62, 2016 07.
Article in English | MEDLINE | ID: mdl-26901354

ABSTRACT

Human papillomavirus (HPV) is a worldwide public health problem, particularly in resource-limited countries. Fifteen high-risk genital HPV types are sexually transmitted and cause 5% of all cancers worldwide, primarily cervical, anogenital and oropharyngeal carcinomas. Skin HPV types are generally associated with benign disease, but a subset is linked to non-melanoma skin cancer. Licensed HPV vaccines based on virus-like particles (VLPs) derived from L1 major capsid antigen of key high risk HPVs are effective at preventing these infections but do not cover cutaneous types and are not therapeutic. Vaccines targeting L2 minor capsid antigen, some using capsid display, adjuvant and fusions with early HPV antigens or Toll-like receptor agonists, are in development to fill these gaps. Progress and challenges with L2-based vaccines are summarized.


Subject(s)
Capsid Proteins/immunology , Papillomavirus Infections/prevention & control , Papillomavirus Vaccines/immunology , Papillomavirus Vaccines/isolation & purification , Drug Discovery/trends , Humans , Papillomavirus Infections/epidemiology , Vaccines, Subunit/immunology , Vaccines, Subunit/isolation & purification
9.
Expert Rev Vaccines ; 15(8): 989-1007, 2016 08.
Article in English | MEDLINE | ID: mdl-26901118

ABSTRACT

The identification of human papillomavirus (HPV) as an etiological factor for HPV-associated malignancies creates the opportunity to control these cancers through vaccination. Currently, available preventive HPV vaccines have not yet demonstrated strong evidences for therapeutic effects against established HPV infections and lesions. Furthermore, HPV infections remain extremely common. Thus, there is urgent need for therapeutic vaccines to treat existing HPV infections and HPV-associated diseases. Therapeutic vaccines differ from preventive vaccines in that they are aimed at generating cell-mediated immunity rather than neutralizing antibodies. The HPV-encoded early proteins, especially oncoproteins E6 and E7, form ideal targets for therapeutic HPV vaccines since they are consistently expressed in HPV-associated malignancies and precancerous lesions, playing crucial roles in the generation and maintenance of HPV-associated disease. Our review will cover various therapeutic vaccines in development for the treatment of HPV-associated lesions and cancers. Furthermore, we review strategies to enhance vaccine efficacy and the latest clinical trials on therapeutic HPV vaccines.


Subject(s)
Drug Discovery/trends , Papillomavirus Infections/therapy , Papillomavirus Vaccines/administration & dosage , Papillomavirus Vaccines/immunology , Humans , Papillomavirus Vaccines/isolation & purification
10.
Appl Microbiol Biotechnol ; 100(3): 1231-1240, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26446387

ABSTRACT

Here, we describe a process for expression, purification, and characterization of truncated human papillomavirus type-6 (HPV-6) L1 virus-like particles (VLPs). The scalable cultivation process in a WAVE Bioreactor at the 10-L scale was optimized to express HPV-6 L1 VLPs using the baculovirus insect expression system. A hollow fiber membrane system was used for the integrated operation, including concentration, diafiltration, extraction, and clarification. The HPV-6 L1 protein was further purified by anion-exchange chromatography and hydrophobic chromatography. The HPV-6 L1 protein could self-assemble into VLPs with a diameter of approximately 50-60 nm after removal of the reductant dithiothreitol (DTT). The final purified HPV-6 L1 VLPs product was characterized to estimate yield and purity, and exceeds the requirements for pharmaceutical-grade VLP vaccine. Immunization of mice demonstrated that the vaccine could elicit high titer neutralizing antibodies in vivo. This study confirms the feasibility of producing pharmaceutical-grade HPV type-6 L1 VLPs on an industrial scale for clinical trials.


Subject(s)
Capsid Proteins/metabolism , Industrial Microbiology/methods , Papillomavirus Infections/virology , Papillomavirus Vaccines/metabolism , Animals , Baculoviridae/genetics , Baculoviridae/metabolism , Bioreactors , Capsid Proteins/chemistry , Capsid Proteins/genetics , Capsid Proteins/isolation & purification , Female , Humans , Immunization , Industrial Microbiology/instrumentation , Mice , Mice, Inbred BALB C , Papillomavirus Vaccines/chemistry , Papillomavirus Vaccines/genetics , Papillomavirus Vaccines/isolation & purification , Spodoptera
11.
Vaccine ; 33(46): 6366-70, 2015 Nov 17.
Article in English | MEDLINE | ID: mdl-26368398

ABSTRACT

The success of Gavi, the Vaccine Alliance depends on the vaccine markets providing appropriate, affordable vaccines at sufficient and reliable quantities. Gavi's current supplier base for new and underutilized vaccines, such as the human papillomavirus (HPV), rotavirus, and the pneumococcal conjugate vaccine is very small. There is growing concern that following globalization of laws on intellectual property rights (IPRs) through trade agreements, IPRs are impeding new manufacturers from entering the market with competing vaccines. This article examines the extent to which IPRs, specifically patents, can create such obstacles, in particular for developing country vaccine manufacturers (DCVMs). Through building patent landscapes in Brazil, China, and India and interviews with manufacturers and experts in the field, we found intense patenting activity for the HPV and pneumococcal vaccines that could potentially delay the entry of new manufacturers. Increased transparency around patenting of vaccine technologies, stricter patentability criteria suited for local development needs and strengthening of IPRs management capabilities where relevant, may help reduce impediments to market entry for new manufacturers and ensure a competitive supplier base for quality vaccines at sustainably low prices.


Subject(s)
Intellectual Property , Papillomavirus Vaccines/economics , Papillomavirus Vaccines/isolation & purification , Pneumococcal Vaccines/economics , Pneumococcal Vaccines/isolation & purification , Rotavirus Vaccines/economics , Rotavirus Vaccines/isolation & purification , Brazil , China , Developing Countries , Drug Industry/trends , Humans , India , Technology, Pharmaceutical/economics , Technology, Pharmaceutical/methods
12.
Expert Rev Vaccines ; 14(7): 1031-41, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25882610

ABSTRACT

The available vaccines against human papillomavirus have some limitations such as low coverage due to their high cost, reduced immune coverage and the lack of therapeutic effects. Recombinant vaccines produced in plants (genetically engineered using stable or transient expression systems) offer the possibility to obtain low cost, efficacious and easy to administer vaccines. The status on the development of plant-based vaccines against human papillomavirus is analyzed and placed in perspective in this review. Some candidates have been characterized at a preclinical level with interesting outcomes. However, there is a need to perform the immunological characterization of several vaccine prototypes, especially through the oral administration route, as well as develop new candidates based on new chimeric designs intended to provide broader immunoprotection and therapeutic activity.


Subject(s)
Papillomavirus Infections/prevention & control , Papillomavirus Vaccines/administration & dosage , Papillomavirus Vaccines/isolation & purification , Plants, Genetically Modified , Technology, Pharmaceutical/methods , Drug Discovery/trends , Humans , Papillomavirus Infections/immunology , Papillomavirus Vaccines/genetics , Papillomavirus Vaccines/immunology , Vaccines, Edible/administration & dosage , Vaccines, Edible/genetics , Vaccines, Edible/immunology , Vaccines, Edible/isolation & purification , Vaccines, Synthetic/administration & dosage , Vaccines, Synthetic/genetics , Vaccines, Synthetic/immunology , Vaccines, Synthetic/isolation & purification
13.
J Microbiol Biotechnol ; 25(6): 936-40, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25639723

ABSTRACT

Human papillomavirus (HPV) type 52 is a high-risk HPV responsible for cervical cancer. HPV type 52 is common around the world and is the most common in some Asian regions. The available prophylactic HPV vaccines protect only from HPV types 16 and 18. Supplementing economical vaccines that target HPV type 52 may satisfactorily complement available prophylactic vaccines. A codon-adapted HPV 52 L1 gene was expressed in the methylotrophic yeast Hansenula polymorpha, which is used as an industrial platform for economical hepatitis B surface antigen particle production in China. We found that the recombinant proteins produced in this expression system could form virus-like particles (VLPs) with diameters of approximately 50 nm. This study suggests that the HPV 52 VLPs produced in this platform may satisfactorily complement available prophylactic vaccines in fighting against HPVs prevalent in Asia.


Subject(s)
Oncogene Proteins, Viral/metabolism , Pichia/genetics , Protein Multimerization , Recombinant Proteins/metabolism , Virosomes/metabolism , China , Humans , Oncogene Proteins, Viral/genetics , Papillomavirus Vaccines/isolation & purification , Recombinant Proteins/genetics , Technology, Pharmaceutical/methods
14.
Expert Rev Vaccines ; 14(3): 383-94, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25455657

ABSTRACT

The goal of therapeutic HPV vaccines is the induction of cytotoxic T lymphocyte immunity against HPV-associated cancers. Recombinant proteins and synthetic peptides have high safety profiles but low immunogenicity, which limits their efficacy when used in a vaccine. Self-adjuvanting lipid moieties have been conjugated to synthetic peptides or expressed as lipoproteins to enhance the immunogenicity of vaccine candidates. Mono-, di- and tri-palmitoylated peptides have been demonstrated to activate dendritic cells and induce robust cellular immunity against infectious diseases and cancer. Recently, a platform technology using the high-yield production of recombinant lipoproteins with Toll-like receptor 2 agonist activity was established for the development of novel subunit vaccines. This technology represents a novel strategy for the development of therapeutic HPV vaccines. In this review, we describe recent progress in the design of therapeutic HPV vaccines using lipoimmunogens.


Subject(s)
Antigens, Viral/immunology , Immunotherapy, Active/methods , Lipoproteins/immunology , Papillomavirus Infections/therapy , Papillomavirus Vaccines/immunology , Adjuvants, Immunologic/administration & dosage , Adjuvants, Immunologic/isolation & purification , Antigens, Viral/administration & dosage , Antigens, Viral/isolation & purification , Humans , Lipoproteins/administration & dosage , Lipoproteins/isolation & purification , Papillomaviridae/immunology , Papillomavirus Vaccines/administration & dosage , Papillomavirus Vaccines/isolation & purification , Vaccines, Subunit/administration & dosage , Vaccines, Subunit/immunology , Vaccines, Subunit/isolation & purification
15.
Trends Biotechnol ; 31(11): 654-63, 2013 Nov.
Article in English | MEDLINE | ID: mdl-24125746

ABSTRACT

Human vaccines against three viruses use recombinant virus-like particles (VLPs) as the antigen: hepatitis B virus, human papillomavirus, and hepatitis E virus. VLPs are excellent prophylactic vaccine antigens because they are self-assembling bionanoparticles (20 to 60 nm in diameter) that expose multiple epitopes on their surface and faithfully mimic the native virions. Here we summarize the long journey of these vaccines from bench to patients. The physical properties and structural features of each recombinant VLP vaccine are described. With the recent licensure of Hecolin against hepatitis E virus adding a third disease indication to prophylactic VLP-based vaccines, we review how the crucial quality attributes of VLP-based human vaccines against all three disease indications were assessed, controlled, and improved during bioprocessing through an array of structural and functional analyses.


Subject(s)
Hepatitis B Vaccines/pharmacology , Papillomavirus Vaccines/pharmacology , Technology, Pharmaceutical/methods , Vaccine Potency , Vaccines, Synthetic/pharmacology , Vaccines, Virus-Like Particle/pharmacology , Vaccines, Virus-Like Particle/ultrastructure , Viral Hepatitis Vaccines/pharmacology , Hepatitis B Vaccines/isolation & purification , Humans , Papillomavirus Vaccines/isolation & purification , Vaccines, Synthetic/isolation & purification , Vaccines, Virus-Like Particle/isolation & purification , Viral Hepatitis Vaccines/isolation & purification
16.
Hum Vaccin Immunother ; 9(1): 83-9, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23108357

ABSTRACT

BACKGROUND: Although there are two HPV vaccines have been used to prevent cervical cancer, the cost limits their application in developing countries. The aim of this study was to evaluate the potential value of plant-based HPV16L1 and LTB proteins as a high-efficiency, low-cost and easy-to-use HPV16L1 oral vaccine. RESULTS: Transgenic plant-derived HPV16L1 and LTB were identified, which display potent immunogenicity and biologic activity. Higher levels of specific IgG and IgA levels of HPV16L1 were induced when mice were immunized with L1 combined with LTB by the oral route. The stimulation index (SI) of spleen cells from the L1/LTB-immunized group was significantly higher than that in the L1-immunized group (p < 0.05). The percentage of IFN-γ (+) /IL-4 (+) CD4 (+) T cells from the L1/LTB group was clearly increased compared with that in the L1 and control groups (p < 0.05). METHODS: Plant-expressed HPV16L1 and LTB proteins were extracted from transgenic tobacco leaves, and their biologic characteristics and activity were examined with electron microscopy and GM1-binding assays respectively. Mice were immunized orally with either HPV16L1 or LTB alone or in combination. Induced mucosal and systemic immune responses were detected by ELISA, Hemagglutination inhibition (HAI), lymphocyte proliferation assays and flow cytometry analysis. CONCLUSION: Strong mucosal and systemic immune responses were induced by transgenic tobacco derived HPV16-L1 and LTB combined immunization. This study will lay the foundation for the development of a new type of vaccine to decrease HPV16 infections, which may lead to the prevention of cervical cancer.


Subject(s)
Adjuvants, Immunologic/administration & dosage , Bacterial Toxins/administration & dosage , Capsid Proteins/immunology , Enterotoxins/administration & dosage , Escherichia coli Proteins/administration & dosage , Oncogene Proteins, Viral/immunology , Papillomavirus Vaccines/administration & dosage , Papillomavirus Vaccines/immunology , Plants, Genetically Modified , Vaccination/methods , Adjuvants, Immunologic/genetics , Adjuvants, Immunologic/isolation & purification , Administration, Oral , Animals , Antibodies, Viral/blood , Bacterial Toxins/genetics , Bacterial Toxins/isolation & purification , Capsid Proteins/genetics , Capsid Proteins/isolation & purification , Cell Proliferation , Enterotoxins/genetics , Enterotoxins/isolation & purification , Escherichia coli Proteins/genetics , Escherichia coli Proteins/isolation & purification , Female , Flow Cytometry , Immunity, Mucosal , Immunoglobulin A/analysis , Immunoglobulin G/analysis , Immunoglobulin G/blood , Interferon-gamma/metabolism , Leukocytes, Mononuclear/immunology , Mice , Mice, Inbred BALB C , Oncogene Proteins, Viral/genetics , Oncogene Proteins, Viral/isolation & purification , Papillomavirus Vaccines/genetics , Papillomavirus Vaccines/isolation & purification , Recombinant Proteins/administration & dosage , Recombinant Proteins/genetics , Recombinant Proteins/immunology , Recombinant Proteins/isolation & purification , Spleen/immunology , Nicotiana
17.
Hum Vaccin Immunother ; 8(3): 403-6, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22327500

ABSTRACT

Several types of human papillomavirus (HPV) are causatively associated with cervical cancer, which is the second most common cancer in women worldwide. HPV-16 and 18 are among the high risk types and responsible for HPV infection in more than 70% of the cases. The majority of cervical cancer cases occur in developing countries. Currently available HPV vaccines are expensive and probably unaffordable for most women in low and middle income countries. Therefore, there is a need to develop cost-effective vaccines for these countries. Due to many advantages, plants offer an attractive platform for the development of affordable vaccines. These include low cost of production, scalability, low health risks and the potential ability to be used as unprocessed or partially processed material. Among several techniques, chloroplast transformation is of eminent interest for the production of vaccines because of high yield of foreign protein and lack of transgene transmission through pollen. In this commentary, we focus on the most relevant aspects of plant-derived vaccines that are decisive for the future development of cost-effective HPV vaccines.


Subject(s)
Biotechnology/methods , Papillomavirus Vaccines/immunology , Papillomavirus Vaccines/isolation & purification , Plants, Genetically Modified , Technology, Pharmaceutical/methods , Female , Humans , Papillomavirus Infections/complications , Papillomavirus Infections/prevention & control , Uterine Cervical Neoplasms/prevention & control
18.
Vaccine ; 27(10): 1511-22, 2009 Mar 04.
Article in English | MEDLINE | ID: mdl-19174177

ABSTRACT

HPV 16 L1 capsomeres purified from Escherichia coli represent a promising and potentially cost-effective alternative to the recently licensed VLP-based vaccines for the prevention of cervical cancer. However, recombinant protein preparations from bacteria always bear the risk of contaminating endotoxins which are highly toxic in humans and therefore have to be eliminated from vaccine preparations. In this study, we measured the LPS concentration at various stages of the purification of HPV 16 L1 from E. coli and determined that it enhances the immunogenicity of HPV 16 VLPs and capsomeres. We confirmed the immunogenicity of the L1 capsomeres in TLR4(-/-) mice without the enhancing effect of the LPS and then elaborated a suitable protocol using Triton X-114 phase separation for the removal of LPS without any significant protein loss or influence on the structural integrity of the particles. The LPS-free capsomeres purified from E. coli induced neutralizing L1-specific antibodies. Our results demonstrate the excellent potential of capsomeres as an economically interesting alternative vaccine to prevent cervical cancer that could be made available in developing countries.


Subject(s)
Capsid Proteins/isolation & purification , Human papillomavirus 16/immunology , Oncogene Proteins, Viral/isolation & purification , Animals , Antibodies, Viral/biosynthesis , Capsid Proteins/genetics , Capsid Proteins/immunology , Cell Line , Drug Contamination/prevention & control , Endotoxins/immunology , Endotoxins/isolation & purification , Escherichia coli/genetics , Escherichia coli/immunology , Female , Human papillomavirus 16/genetics , Humans , Mice , Mice, Inbred C57BL , Oncogene Proteins, Viral/genetics , Oncogene Proteins, Viral/immunology , Papillomavirus Infections/immunology , Papillomavirus Infections/prevention & control , Papillomavirus Infections/virology , Papillomavirus Vaccines/genetics , Papillomavirus Vaccines/immunology , Papillomavirus Vaccines/isolation & purification , Recombinant Proteins/genetics , Recombinant Proteins/immunology , Recombinant Proteins/isolation & purification , T-Lymphocytes, Cytotoxic/immunology , Uterine Cervical Neoplasms/immunology , Uterine Cervical Neoplasms/prevention & control , Uterine Cervical Neoplasms/virology
19.
Wei Sheng Wu Xue Bao ; 49(11): 1527-33, 2009 Nov.
Article in Chinese | MEDLINE | ID: mdl-20112683

ABSTRACT

OBJECTIVE: To produce human papillomavirus type 11 virus-like particles (HPV11 VLPs) from Escherichia coli and to investigate its immunogenicity and type cross neutralization nature. METHODS: We expressed the major capsid protein of HPV11 (HPV11-L1) in Escherichia coli ER2566 in non fusion fashion and purified by amino sulfate precipitation, ion-exchange chromatography and hydrophobic interaction chromatography, sequentially. Then we removed the reductant DTT to have the purified HPV11-L1 self-assemble into VLPs in vitro. We investigated the morphology of these VLPs with dynamic light scattering and transmission electron microscopy. We assayed the immunogenicity of the resultant HPV11 VLPs by vaccinations on mice and evaluated by HPV6/11/16/18 pseudovirion neutralization cell models. RESULTS: We expressed HPV11 L1 in Escherichia coli with two forms, soluble and inclusion body. The soluble HPV11 L1 with over 95% purity can self assemble to VLPs in high efficiency. Morphologically, these VLPs were globular, homogeneous and with a diameter of - 50 nm, which is quite similar with native HPV11 virions. The half effective dosage (ED50) of HPV11 VLPs is 0.031 microg, and the maximum titer of neutralizing antibody elicited is averaged to 10(6). The cross neutralization activity (against HPV6/16/18) of the anti-HPV11 serum was found to have exact correlation to the inter-type homology in amino acid alignment. CONCLUSION: We can provide HPV11 VLPs with highly immunogenicity from prokaryote expression system, which may pave a new way for research and development of prophylactic vaccine for HPV11.


Subject(s)
Capsid Proteins/immunology , Capsid Proteins/isolation & purification , Gene Expression , Human papillomavirus 11/immunology , Papillomavirus Infections/immunology , Virion/immunology , Animals , Antibodies, Viral/immunology , Capsid Proteins/metabolism , Escherichia coli/genetics , Escherichia coli/metabolism , Female , Human papillomavirus 11/classification , Human papillomavirus 11/genetics , Humans , Mice , Mice, Inbred BALB C , Papillomavirus Infections/prevention & control , Papillomavirus Infections/virology , Papillomavirus Vaccines/genetics , Papillomavirus Vaccines/immunology , Papillomavirus Vaccines/isolation & purification , Papillomavirus Vaccines/metabolism , Phylogeny , Recombinant Proteins/genetics , Recombinant Proteins/immunology , Recombinant Proteins/isolation & purification , Recombinant Proteins/metabolism , Virion/classification , Virion/genetics
20.
Int J Immunopathol Pharmacol ; 22(4): 967-78, 2009.
Article in English | MEDLINE | ID: mdl-20074460

ABSTRACT

This study reports the immunomodulatory activity on human monocyte derived dendritic cells (MDDCs) of a vaccine preparation shown to be effective against an HPV16-related tumour in an animal model. The vaccine is composed of extract from Nicotiana benthamiana leaves containing HPV16 E7 protein expressed by a potato virus X-derived vector (NbPVX-E7). The effect of the extract was evaluated on MDDC differentiation and maturation by monitoring the phenotypic expression of specific markers. The results show that NbPVX-E7 does not induce monocyte differentiation to dendritic cells, but does induce MDDC maturation. Plant extract does not influence MDDC-uptake of E7-FITC while it significantly improves the Ovalbumin-FITC uptake, considered as a model antigen. Importantly, NbPVX-E7-pulsed MDDCs/PBMCs are able to prime human blood-derived lymphocytes from healthy individuals to induce HPV16 E7-specific cytotoxic activity. This is a propaedeutic study for a possible use of E7-containing plant extract in human immunotherapy of HPV-related lesions.


Subject(s)
Adjuvants, Immunologic/pharmacology , Dendritic Cells/immunology , Lymphocytes/immunology , Nicotiana/metabolism , Oncogene Proteins, Viral/immunology , Papillomavirus Vaccines/immunology , Plant Extracts/immunology , Plants, Genetically Modified , Adjuvants, Immunologic/isolation & purification , Antigen Presentation , Cell Differentiation , Cell Line, Tumor , Cell Survival , Coculture Techniques , Cytotoxicity, Immunologic , Dendritic Cells/drug effects , Dendritic Cells/metabolism , Dose-Response Relationship, Drug , Genetic Vectors , Humans , Lymphocyte Activation , Lymphocytes/drug effects , Male , Oncogene Proteins, Viral/biosynthesis , Oncogene Proteins, Viral/genetics , Oncogene Proteins, Viral/isolation & purification , Ovalbumin/immunology , Ovalbumin/metabolism , Papillomavirus E7 Proteins , Papillomavirus Vaccines/biosynthesis , Papillomavirus Vaccines/genetics , Papillomavirus Vaccines/isolation & purification , Plant Extracts/isolation & purification , Plant Leaves , Potexvirus/genetics , Recombinant Proteins/immunology , Time Factors , Nicotiana/genetics
SELECTION OF CITATIONS
SEARCH DETAIL
...