Chayanika Saha1
James Bojdo1
Nicholas J. Dunne2,3,4,5,6,7,8
Raj Kumar Duary9
Niamh Buckley1
Helen O. McCarthy1,10*- 1School of Pharmacy, Queen’s University of Belfast, Belfast, United Kingdom
- 2School of Mechanical and Manufacturing Engineering, Dublin City University, Dublin, Ireland
- 3Centre for Medical Engineering Research, School of Mechanical and Manufacturing Engineering, Dublin City University, Dublin, Ireland
- 4Department of Mechanical and Manufacturing Engineering, School of Engineering, Trinity College Dublin, Dublin, Ireland
- 5Advanced Manufacturing Research Centre (I-Form), School of Mechanical and Manufacturing Engineering, Dublin City University, Dublin, Ireland
- 6Advanced Materials and Bioengineering Research Centre (AMBER), Royal College of Surgeons in Ireland and Trinity College Dublin, Dublin, Ireland
- 7Advanced Processing Technology Research Centre, Dublin City University, Dublin, Ireland
- 8Trinity Centre for Biomedical Engineering, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland
- 9Department of Food Engineering and Technology, Tezpur University, Tezpur, India
- 10School of Chemical Sciences, Dublin City University, Dublin, Ireland
High grade serous carcinoma (HGSC) is one of the most lethal ovarian cancers that is characterised by asymptomatic tumour growth, insufficient knowledge of malignant cell origin and sub-optimal detection. HGSC has been recently shown to originate in the fallopian tube and not in the ovaries. Conventional treatments such as chemotherapy and surgery depend upon the stage of the disease and have resulted in higher rates of relapse. Hence, there is a need for alternative treatments. Differential antigen expression levels have been utilised for early detection of the cancer and could be employed in vaccination strategies using nucleic acids. In this review the different vaccination strategies in Ovarian cancer are discussed and reviewed. Nucleic acid vaccination strategies have been proven to produce a higher CD8+ CTL response alongside CD4+ T-cell response when compared to other vaccination strategies and thus provide a good arena for antitumour immune therapy. DNA and mRNA need to be delivered into the intracellular matrix. To overcome ineffective naked delivery of the nucleic acid cargo, a suitable delivery system is required. This review also considers the suitability of cell penetrating peptides as a tool for nucleic acid vaccine delivery in ovarian cancer.
1 Introduction
Ovarian Cancer (OC) is a silent gynaecological cancer with approximately 820,000 cases worldwide and ∼4,000 deaths per year in 2020 in the United Kingdom alone (GLOBOCAN, 2020- International Agency for Research on Cancer). Currently, the five-year survival rate for OC is a mere ∼30% for patients with advanced disease and this mortality is attributed to delayed diagnosis, relapse and resistance to standard of care therapies. (Xie et al., 2019) Existing key screening techniques are ineffective to diagnose the disease at an early stage owing to the heterogenous nature of the tumours.
There are several OC tumour subtypes which are categorised as either Type I or Type II based on the cells of origin of the tumour (Figure 1). Type I is mostly benign and shares lineage with the cystic neoplasms and corresponding carcinomas such as endometriomas, cystadenomas. Type I OCs include low-grade endometroid, low-grade serous clear cell and mucinous carcinomas. Type II are the more aggressive OC, evolve more rapidly as a result of genetic instability, and are mostly malignant in nature. Type II tumours include high grade serous carcinoma (HGSC), high-grade endometroid, undifferentiated carcinoma and carcinosarcoma HGSC is the most prevalent of the OC subtypes accounting for approximately 70% of cases. Clinically, HGSC is asymptomatic, which delays diagnosis and this results in high rates of fatality. (Kurman and Shih, 2011; Beirne et al., 2019; Ahmed et al., 2020) The treatment of HGSC has been stagnated because of the lack of research and understanding about the origin of HGSC. Recently, HGSC cells were identified to originate from the fallopian tubes rather than the ovary (Figure 2). Robert et al. proposed a unifying theory for the origin of HGSC suggesting serous tubal intraepithelial carcinoma (STIC), a precursor lesion in the distal, fimbrial end of fallopian tubes, were the cells of origin for HGSC with the involvement of the ovaries only at a secondary stage. (Kurman and Shih, 2010) Immunohistochemical experiments conducted by a group of researchers in the Netherlands provided an early linkage between the neoplastic lesions arising in the fallopian tube to the development of ovarian cancer. (Piek et al., 2001) A recent study on the molecular pathology by Crum et al. (2013) also imply fimbria as the site of origin for the cells of HGSC. This has been widely adopted as a survey conducted by McCluggage et al. (2017) predicts the wide spread acceptance of STIC being the origin of HGSC by 92% of clinicians and 86% of pathologists.
FIGURE 1. Ovarian Cancer types. All tumours associated with OC have been broadly classified into two subtypes: Type I and Type II. Malignant Type II comprises >85% of the total OC.
FIGURE 2. The origin of HGSC OC, most common form of EOC. A precursor lesion known as serous tubal intraepithelial carcinoma (STIC) in the fallopian tube are considered as the site for the origin of the malignant cells and involve the ovaries only secondarily (Created in BioRender.com).
The primary clinical treatment option available for OC patients in the advanced stages is cytoreductive surgery followed by first line of therapy with three weekly intravenous injections of or platinum/taxane chemotherapy (paclitaxel, cisplatin, carboplatin). However the post-primary treatment rate of relapse is very high (>70%) in stage III/IV HGSC patients, which is the main contributor to the high mortality rate in women over 45 years old in Europe and Northern America. (Stuart, 2003) This highlights the urgent need for alternative treatment methods. Immunotherapy is a treatment option that has garnered interest. Immunotherapy can be described as programming the body to eliminate the cancer and this has developed significantly over the past 15 years. Cancer immunotherapy is a broad term to describe the method to induce, enhance or supress the immune response to tumour cells. Targeted therapies such as bevacizumab (VEGF), cetuximab (EGFR) and trastuzumab (HER2) have been used successfully as a combination therapy to combat OC. (Franzese et al., 2019) While, these alternative therapies offer more targeted treatment options with minimal cytotoxicity to the non-cancerous normal healthy cells, the success rate remains sub-optimal and there is a requirement for better therapies. This review examines the options for nucleic acid vaccines along with possible adjuvants that could be used for ovarian cancer.
2 Tumour antigens in ovarian cancer
Development of an immunotherapy requires a target that is either involved in immune tolerance of the cancer, is exclusively expressed, or is overexpressed by the cancer tissue. Tumour antigens (TAs) was coined for the proteins that have abnormal expression in the cancer tissue. (Wang and Wang, 2016; Odunsi, 2017a) TAs can either be mutational antigens/tumour specific antigens (TSAs) or non-mutated overexpressed tumour associated antigens (TAAs). Over the years researchers have measured the expression of different TAs in different OC patient tumour samples with the help of Deoxyribonucleic Acid/Ribonucleic Acid (DNA/RNA) sequencing, Reverse Transcriptase Polymerase Chain Reaction (RT PCR) and Western blotting techniques. Table 1 summarises a list of antigens that are differentially expressed in OC samples.
TABLE 1. Table of identified antigens in Ovarian cancer. These antigens are either mutated or overexpressed in the various types of the ovarian carcinomas and can serve as potential targets for immunotherapy against ovarian cancer cells. The blank spaces indicate that the significance and precise role of the genes in OC is not known and yet to be determined.
Interestingly, over 95% of HGSC cases have multiple mutations in the TP53 gene, mostly in the DNA binding domain. The codons in which these oncogenic mutations are found in HGSC are called the “hotspot” mutations—R175, Y220, G245, R248 and R273. (Deniger et al., 2018) These mutations may be oncogenic due to the loss of wild type variant but much is not known or reported in case of OC. The wild type p53 impacts the cytolytic T-lymphocyte (CTL) response to tumour cells. Transporter associated with Antigen Processing 1 (TAP 1) and Endoplasmic Reticulum Amino Peptidase 1 (ERAP1), miRNA34 and Fas/APO-1 an apoptosis inducing cell surface protein are upregulated in the wild type p53 which are directly involved in upregulation of antigen presentation through the molecular histocompatibility complex I (MHC I) pathway, degradation of Programmed death ligand -1 (PD-L1) transcripts-negative regulators of CTL activation and induction of apoptosis by the CTL after recognition of the antigen on the MHC I. Mutations in the wild type variant lowers the levels of TAP1, ERAP1, miRNA 34 and Fas/APO-1 and thus reduces the interaction between the MHC I on the cancer cells and T-cell receptors (TCR) on the CTLs thereby supressing the recruitment of CD8+ T cells and helping in the growth of the tumours. (Braun and Iwakuma, 2016) The germline mutations of the TSA BRCA1/2 also increase the chances of developing HGSC. BRCA1 and BRCA2 genes play important role in the homologous recombination repair of double strand break of DNA. (Neff et al., 2017) Antoniou et al. (2003) compared the data from four different studies conducted in the United States, Canada, Israel and Poland for ovarian cancer and found the average cumulative risks of developing ovarian cancer by age of 70 years was almost 39% of BRCA1 mutation carriers and 11% of BRCA2 mutation carriers. Other commonly reported TAAs which are over-expressed in ovarian cancer and can serve as potential biomarkers for immunotherapy include Cancer Antigen 125 (CA125) or Mucin 16 (MUC 16), (Leung et al., 2013; Felder et al., 2014; Kloudová et al., 2016; Sallum et al., 2018; Verri et al., 2020) Melanoma Antigen Gene - MAGEA1, MAGEA3, MAGEA4, MAGEC1, MAGEA10 protein family, (Gillespie et al., 1998; Yakirevich et al., 2003; Zhang et al., 2010; Batchu et al., 2014; Daudi et al., 2014; Esfandiary and Ghafouri-Fard, 2015; Srdelić et al., 2019) New York Esophageal squamous cell carcinoma-1 (NY-ESO-1), (Odunsi et al., 2003; Yakirevich et al., 2003) Cancer Testis antigen-45 (CT45), (Chen et al., 2009; Zhang et al., 2015; Coscia et al., 2018; Xie et al., 2019) Folate Receptor alpha (FOLR1), (Leung et al., 2013; Köbel et al., 2014; Kloudová et al., 2016) Epithelial Cellular Adhesion Molecule (EP-CAM), (Van Elssen et al., 2010; van der Gun et al., 2013; Kloudová et al., 2016) Erythroblastic Oncogene B (ERBB) also frequently called Human Epidermal growth factor Receptor 2 (HER-2/neu), (Demir et al., 2014; Wang et al., 2016; Verri et al., 2020) Wilm’s Tumour suppressor gene 1 (WT1), (Hylander et al., 2006; Stewart et al., 2008; Kloudová et al., 2016; Carter et al., 2018; Sallum et al., 2018) Baculoviral IAP repeat containing protein 5 (BIRC-5), (Wang et al., 2018a; Trnski et al., 2019) Preferentially expressed antigen in melanoma (PRAME), (Griffioen et al., 2006; Zhang et al., 2016; Pankov et al., 2017) Trophoblast glycoprotein (TPBG) (Kloudová et al., 2016) and Mucin 1 (MUC-1). (Van Elssen et al., 2010; Kloudová et al., 2016) The expression of Prostate, Ovary, Testes Expressed ankyrin domain family (POTE gene family) in EOC and HGSC has also been studied. POTEs expression in elevated levels was reported for few of the members of the family- POTEs (C, E, F and I) in HGSC. (Bera et al., 2006; Barger et al., 2018; Sharma et al., 2019).
Among the different TAAs the ones belonging to the subset of Cancer testis antigens (CTA) have been explored as potential biomarkers and candidates for vaccine strategies. CTAs are often members of multigene family encoded by ≈ 140 genes and mapped often on the X-chromosome (CTA-X) e.g.,- MAGE, CT45, NY-ESO1 etc., However, some CTA can be mapped in non-X chromosomes as well (non-CTA-X)—e.g., PRAME, BIRC5, BAGE etc., These are mainly expressed in the germ cells of the testes with little or negligible expression in normal healthy cells. (Odunsi, 2017b) CTAs have desirable immunogenicity with abhorrent higher frequency of expression in cancer cells due to DNA methylation or modification within the chromatin network. (Xie et al., 2019) Expression of CTAs is known to be restricted in the sites with privileged immunity such as the testes, fetal ovary and placenta and not in other normal healthy cells which provides a high immunogenicity when these genes are abnormally expressed in tumour cells. They also play an important role in tumour progression (soma-to germline transformation) and as such are the closest match compared to other TAs, for an ideal target for antigen specific immunotherapeutic response.
3 Cancer immune therapy
The immune system is a highly coordinated and complex process that involves interplay between the adaptive and innate immune system, which function to eliminate any foreign antigen that comes in contact with the body and repair damaged tissue or cells. In normal physiological conditions innate immune cells - the dendritic cells (DCs), natural killer cells (NKs), macrophages, neutrophils, basophils, eosinophils, and mast cells, are the first response generated against any foreign antigen during acute inflammation. The innate cells then activate the adaptive immune response by releasing mediators such as cytokines, chemokines and histamines which then retaliates to eliminate any damaged cells, extracellular matrix and invading pathogens.88 However, when tissue homeostasis is perturbed, the balance between both innate and adaptive immune system is lost and initiation of irreparable cell cycles are observed due to the improper engagement and disengagement of the two immune system arms. When a tumour develops in the body it tissue microenvironment consists of the tumour cells, blood vessels, stroma and infiltrating inflammatory immune cells. The host’s immune system tries to get rid of the cells through process of immune surveillance where immune infiltrates attempt to recognise and eliminate the tumour cells. These infiltrates can either be effector innate immune cells such as NK cells and macrophages as well as cells mediating adaptive immunity T-cells, B-cells and DCs. The immune landscape is however, characteristically altered within tumours with an imbalance of the tumour infiltrating lymphocytes (TILs) which are a major part of the tumour infiltrate which help them to evade immune surveillance. These TILs often have impaired T-cell receptor activity and therefore reduced cytotoxic activity and decreased production of cytokines to induce a T-helper cells Th1 stimulation against antigens. A skewed balance of T-helper Th1 cells towards Th2 in the tumour microenvironment is often seen in most tumours during progression. This imbalance dampens the cytolytic activity of the CD8+ CTLs and thus may help tumour growth. Activation of the nuclear factor -κB (NF-κB- a transcription factor) pathway in TILs increases the production of TNF-α as well as other proinflammatory cytokines responsible for cell proliferation in tumour cells. The most common TILs within a tumour are of regulatory (Tregs) or myeloid derived suppressor cells (MDSCs) phenotype which actually aid with immune evasion and promote tumour growth (Figure 3). In normal conditions Tregs help to downregulate the immune system to reduce the risk of autoimmunity but in cancer when their number increases in the tumour microenvironment, they downregulate the functions of effector CD8+ CTLs and CD4+ CD25− T-cells by secretion of inhibitory compounds TGF-β and IL10 and thus help in tumour growth. MDSCs also secrete TGF-β and accumulated levels in the tumour microenvironment which also dampens T-cell responses thus favouring tumour progression. MDSCs in most tumours also produces iNOS along with arginase one enzyme, which dampens the T lymphocyte response by increase in the production of superoxide and Nitric oxide (NO). Another enzyme, indoleamine-2,3-dioxygenase (IDO), produced by MDSCs catabolises tryptophan, which is an essential amino acid for T-cell proliferation and differentiation. Maturation defects in DCs in cancer patients increases the production of vascular endothelial growth factor (VEGF) in the tumours which help in the growth of blood vessels in the tumour aiding to its growth and metastasis. MDSCs are also recruited in the tumour by Granulocyte macrophage colony stimulating factor (GM-CSF) secreted by most tumour cells and thus induces immune suppression and tumour growth. (de Visser et al., 2006) GMCSF in normal physiological conditions help in maintaining homeostasis of immune cells but in tumour cells its presence may be impaired and may promote immune escape. The TILs are reprogrammed to continuously produce these growth factors which benefit the cell differentiation, blood vessel growth and benefit the tumour progression.
FIGURE 3. Cells in the tumour microenvironment. (A) High number of Tregs and MDSCs help in proliferation of the tumour cells evading the immune surveillance (B) Use of immunotherapy can increase the CTL in the tumour microenvironment thereby leading to decrease in the tumour growth by cell apoptosis. (Created with BioRender.com).
Immunotherapy manipulates the complex interaction between the immune cells, cytokines/chemokines and costimulatory substances increasing the immune surveillance to target cancer cells. Better understanding of the tumour tissue environment provides improved strategies to improve the antitumour effects. Higher migration and recruitment of effector CD8+ CTLs, blocking of MDSC activities and other proinflammatory compounds may provide some ideal arenas for antitumour therapies. Immunotherapies in cancer can thus be categorised as 1) immune checkpoint inhibitors with specific antibodies, (Lee and Konstantinopoulos, 2019) 2) monoclonal antibodies against specific tumour antigens, (Hamanishi et al., 2015) 3) adoptive T-cell therapy involving reinfusion of modified autologous T cells, (Tanyi et al., 2018) 4) naturally occurring or genetically modified oncolytic virus therapies, (Fukuhara et al., 2016) 5) Cancer vaccines. (Mittendorf et al., 2008; Mittendorf et al., 2014; Temizoz et al., 2016; Cole et al., 2018a; Kalli et al., 2018) Several recent reviews have discussed these different immune-oncological therapies in detail and so the scope of this review will focus specifically on the recent advancements and challenges of cancer vaccines along with future directions.
4 Cancer vaccines
Cancer vaccines are designed to programme the host’s immune system to detect and kill cancer cells predominantly by inducing a cellular immune response specific to TAA through the activation of APCs along with a lesser antibody response. At present, the vaccine platforms that are used for various trials in OC include - 1) autologous dendritic cell based 2) peptide or protein based, 3) nucleic-acid based.
4.1 The mechanism of cancer vaccines
DCs are considered as the most potent APC among the other immune cells. These cells can be either steady state conventional DC (cDCs—cDC1, cDC2) or non-conventional DCs arising from an inflammatory stimuli termed plasmacytoid DC (pDCs) or monocyte derived DC (MoDCs). The cDCs can further be classified into either migratory or lymphoid DCs. Surface markers on DCs are used to identify the different subsets DC. All DCs express the surface markers CD11c, CD45, MHC II and CD135. The cDC2 subset is CD4+ and expresses CD11b, CD80, CD86 and CD40 but do not express CD8 and CD205 otherwise expressed by cDC1. Unlike lymphoid cDC1 the non-lymphoid migratory cDC1 express CD103 instead of the CD8 and do not express CD11b, SIRPα(CD172A), F4/80 or CD115 which helps to differentiate them from macrophages, cDC2 and monocytes.
APCs take up the foreign antigen and display it in on the MHC I or II pathway depending upon whether the antigen is endogenous or exogenous. In a peptide or protein form the antigens are cleaved in the Endoplasmic Reticulum (ER) and directly represented on the MHC II molecules whereas if the antigens are in nucleic acid form (DNA/RNA) they are further processed and translated into protein inside the cells and then cleaved before presented in the MHC I complex. The activated DCs then migrates to the lymphoid organs such as lymph nodes, thymus, spleen etc., to activate and prime the naïve T cells—CD4+ or CD8+ cells into effector T cells or memory cells.88 Compared to cDC2, cDC1 have the higher ability to cross present antigens and activate a CD8+ cytolytic T cell response. The CD4+ cells detect antigens on the MHC II molecules and differentiate into T helper cells (Th1, Th2, Th17) generating different cytokines (INF-γ, IL-2-Th1; IL-4, IL-5,IL-13- Th2; IL-17,IL-22- Th17) which have proinflammatory and immunoprotective effects. CD8+ cells on the other hand detect antigens presented on the MHC I and generate a cytolytic T cell (CTL) response against the tumour cells. T-cell receptors (TCR) are stimulated by the antigens and are crucial for T-cell proliferation and differentiation which is supported by co stimulatory molecules, such as CD28. Ligands for CD28, CD80 (B7-1), CD86 (B7-2), are expressed by the APCs and are upregulated when these cells encounter an antigen. Different negative regulators e. g Cytotoxic T lymphocyte antigen 4 (CTLA4) and Programmed cell death 1 (PD1) act as checkpoint molecules against the immune response so as to curb the hyperactivation and preserve self-tolerance. These checkpoint molecules have similar characteristics to costimulatory molecules and thus prevent the activation of effector T cells. Tregs (CD4+ CD25+) express the CTLA4 and thus have immunosuppressive effects. Other molecules e.g., CD3, a T cell co receptor, also play a major role in activating a naïve T cell. Upon sufficient downstream stimulation, activated T-cells generate survival cytokines such as IL-2, IL-4 and IL-7 which help them to grow and proliferate. Upon activation, T cells target the cancer so that: 1) restimulation-induced cell death occurs due to strong acute antigenic stimulation, 2) T-cell exhaustion occurs to an unresponsive state as stimulation is weak, 3) decrease of antigen specific T cell population occurs due to diminishing cytokine and antigen stimulation.88 A small number of cells also convert into “Memory T-cells” stimulated by IL-7 and IL-15 and continue to propagate in the immune system to generate a memorised response against future encounters with the same antigen which can be beneficial for the success of prophylactic cancer vaccines in the clinic.
Relatively higher numbers of cDCs cells are found in skin compared to muscle and thus the transdermal route provides an apt delivery route for different cancer vaccines. (Tawde et al., 2016) Of these migratory cDC1 (CD103+) are the most potent target with the ability to acquire the antigens, mature and then migrate from the periphery to the lymphoid site to interact with naïve T-cells to generate CTL effector cells. (Kushwah and Hu, 2011) The dermal Langerin+ CD103+ cDC1s present antigens via MHC I pathway generating elicited CTL levels. (Kushwah and Hu, 2011) A list of cancer vaccines targeting OC that have been completed phase I/II clinical trial with published results is summarised in Table 2. Note that none of these have to date involved non-viral delivery of nucleic acids.
TABLE 2. Table of completed clinical trials showing promising results for various cancer vaccines in OC. All of these vaccines have been used as a second line of treatment after initial cytoreductive debulking of the primary tumours and chemotherapy.
4.2 Dendritic cell vaccines
DC based vaccines use autologous DC cells matured with whole tumour lysate containing the TAA to generate an anti-tumour T-cell response. The most common approach among the clinically registered trials for ex vivo differentiated DC vaccines relies on the methods of extraction and isolation of CD14+ monocytes (MoDCs) by the process of leukapheresis. (Kandalaft et al., 2013; Calmeiro et al., 2020) Immature MoDCs extracted from patients are matured in vitro in presence of IL-4 and GMCSF and exposed to patient specific TAA protein extracted after cytoreductive debulking, which results in the upregulation of the surface markers such as CD80, CD86, CD40 and also lymph node migratory receptors CCR7. These matured antigen presenting DCs are then reinjected into the patients to prime naïve T-cells. (Kandalaft et al., 2013) At present, over 300 clinical trials for DC based anticancer vaccines have been completed or are ongoing for different cancers among which ∼18 are specifically for OC. Based on the positive results in the previous Phase I and IIa trials Gray et al. (2016) conducted a Phase IIb clinical trial of Cvac, (DC-Manan-fusion protein) a MUC-1 autologous dendritic cell vaccine therapy, in multinational patients with confirmed stage III/IV OC. Immunoassay to assess T-cell response suggested a higher CD8+ CTL response than CD4+ T helper cells in patients receiving complete 10 doses of 6 × 10 (Crum et al., 2013) DCs/ml over 56 weeks. Higher MUC-1 specific T-cell responses were detected when compared to basal levels of patients receiving standard of care. They also found improved progression free survival; 13 months compared to 9 months. In Cvac treated patients and overall survival in patients in their 2nd clinical remission (13 months vs. 5 months) was higher compared to the ones in 1st remission (18 months vs. 13 months). (Gray et al., 2016) Even though these DC based vaccines haven been able to show some positive results, their success rates are usually lower than 15%. (Calmeiro et al., 2020) DC-based vaccines are often used as a secondary treatment to prolong the remission after a primary treatment of cytoreductive surgery and chemotherapy. They are based on the patient specific antigens that need to be identified from the debulked tumour to manufacture peptides or nucleic acids to pulse the DC invitro. The limitation associated with using this is that it might extend the time between the first line of treatment and the first dose up to several months. (Gray et al., 2016) They are also a very expensive (∼ £4,000 per single vaccine in European countries), labour intensive process specific to individual patients and the yield of autologous DCs from cancer patients for use in a vaccine is often problematic as during the harvesting process of MoDCs there might be contaminants such as Red blood cells (RBCs) and platelets along with it and also all the DC harvested might not mature during their exposure to the antigen at similar rates. In addition, the procedure requires a high-level clean room with GMP facilities for DC generation, in vitro maturation of the DCs may pose other difficulties such as risk of contamination, improper maturation, decreased cell longevity, inability of the DCs to reach the lymph nodes to elicit proper immune response, etc., (Turnis and Rooney, 2010) Thus, other vaccination methods to induce the naturally circulating DC in the patients could be preferred.
4.3 Peptide vaccines
One of the ways of exploring the immunogenic effects of naturally circulating DCs are peptide vaccines. These vaccines consist of immunogenic short peptide segments (usually of 20–30 amino acid sequence) of whole tumour antigens, which have the potential to initiate an immune response specific to the antigen. (Mittendorf et al., 2008; Brown et al., 2019) These antigenic peptides being exogenous in nature are taken up by the DCs (CD4+ cDC2) and presented on MHC II molecules which prime mostly a humoral response by the CD4+ T-cells. However, a small fraction of these peptides is also cross presented on the MHC I molecules by the CD4+ DCs to induce direct CTL response. These vaccines have been extensively investigated in different cancers. (Mittendorf et al., 2014; de Paula Peres et al., 2015; Kalli et al., 2018; Brown et al., 2019) Some peptides extensively studied in OC include human epidermal growth factor receptor 2 (HER2/neu), CEA and MUC-1 that have been able to show some positive immunogenic results. (de Paula Peres et al., 2015)
A Phase I/IIa clinical study by Brown et al. (2019) suggested reduction in the recurrence risk of ovarian and endometroid cancers when peptide vaccines (E39 plus GM-CSF) specific to folate binding proteins were administered intradermally to patients. A robust, dose-dependent in vivo immune response was seen in vaccinated patients in comparison to the control group. Disease free survival (DFS) was improved in vaccinated patients (55.5%) when compared to the control group (40.0%) after 24 months. The DFS was further seen to improve to 90.0% in patients receiving higher doses of 1,000 µg after receiving treatments of their primary disease but not in recurrent patients. Patients were also given boosters after 6 months to improve the DFS. Thus, the vaccine proved to be safe and was effective to certain extent to prevent recurrence of the disease in high-risk ovarian and endometroid cancer. Another potential target identified by Kalli et al. (2018) for a peptide vaccine that could be used for breast and ovarian cancers is folate receptor alpha (FRα). The peptides chosen were successful in generating a durable T-cell immunity specific to FRα in more than 90% patients (Breast cancer stages II, III and OC stages II- IV) in the phase I clinical trial of the vaccine. Modifications of the peptide with immunoadjuvants have been successful in generating high numbers of long lived CD8 memory T cells. A phase 1 clinical trial on ovarian cancer patients with NY-ESO-1 overlapping peptides (OLP4) revealed that when the peptide was used with adjuvants such as Montanide only and Montanide + polyinosinic-polycytidylic acid (PolyICLC) it elicited a better immune response than when it was used alone. Increased detectable IgG antibody levels after 4 months were seen in almost 91% of the patients receiving the vaccine with both adjuvants when compared 46% with one and 25% with peptide alone. It also showed that the peptide alone generated a CD4+ response in 100% of the cohort while the CD8+ response was seen only in 25% of the patients. However, this increased to 62% and 91% with the adjuvants without effecting the CD4+ response. (Sabbatini et al., 2012) Peptide vaccines have the advantages of relative ease of preparation economically without having the patients go through additional procedures as in the case of DC cell-based vaccines. However, short oligopeptide vaccines might exhibit antigen induced cell death of effector T-cells due to overstimulation by the same immunogenic peptide. (Berry et al., 2017) Also the oligo peptides bind to the MHC I complexes of other somatic cells other than APCs which stimulates suboptimal T-cell priming. Full length protein vaccines however can be processed and presented only by the APC in form of antigenic peptides stimulating optimal T-cell response, but these proteins pose the hindrance of being efficiently chemically produced, endocytosed, and processed inside the APC. Both long and short peptides have limited ability to overcome the biological barriers and are highly sensitive and degradable when exposed to different body fluids and enzymes. (Myc et al., 2011) Another reason for the limited success of peptide vaccines is the high response generation of short lived humoral immunity compared to cellular response because of poor uptake by the cDC1 APC. Also, the naïve T-cell tend to differentiate more into Th2 cells in presence of IL-4 and IL-2 instead of Th1 cells which help in inducing more antibody mediated immunity rather than cell mediated immunity. (Speiser et al., 2002) Thus, nucleic acid vaccines can provide an alternative to generate more cellular cytolytic response against tumour cells.
4.4 Nucleic acid vaccines
Nucleic acid vaccines aim to deliver genetic material that encodes tumour antigens into the host, where they are taken up by innate immune cells and are transcribed and translated (DNA) or translated (mRNA) to produce the antigenic protein. This ultimately leads to the presentation of the tumour antigenic peptide fragments to adaptive immune cells. DNA vaccines use engineered plasmid DNA (pDNA) encoding the antigen that is delivered into the patient, normally via intradermal/subcutaneous or intramuscular injection. However, Intradermal routes have been proven to elicit strong Th1 and CD8+ cytolytic T-cell response along with humoral response when compared to other delivery routes. (Rahman et al., 2000; Constantino et al., 2016) The success rate of these vaccines is highly dependent on the ability of the therapeutic nucleic acid material to overcome the cellular environment to reach the nucleus of the target cell. Cellular barriers include the plasma membrane, endosomal membrane, and the nuclear membrane. Anionic lipophilic cell membranes restrict the entry of the negatively charged hydrophilic genetic cargo such as plasmid DNA. Although endocytosis might aid cellular entry, endosomal entrapment becomes an issue. Nuclear membranes also pose a barrier for pDNA cargos which need to undergo transcription in the nucleus and then transport back to cytosol for translation (Wang et al., 2012).
Once the pDNA enters the cells it may be exposed to one of the following fates (Figure 4): 1) it enters into a APC (preferably cDCs) transported to the nucleus of DCs to initiate the mRNA transcription followed by the synthesis of antigenic protein in the ribosome, degraded in the proteosome and ultimately be presented on the cell surface from the endoplasmic reticulum/golgi bodies in an MHC I (8–10 amino acid lengths) to stimulate antigen specific CD8+ CTL 2) pDNA is taken up by non APCs which then process it and either present it in MHC I molecules subjecting it to apoptosis later and release of the peptides or releases the peptides directly by lysosomal degradation. The released peptides are then either taken up by the DC or B lymphocytes to present it in MHC II (13–25 amino acid length) and later prime CD4+ T helper cell response or generate antibodies for a humoral response. RNA vaccines work in similar pattern except for that they do not require transcription and only require delivery to the cytoplasm to be translated.
FIGURE 4. DNA vaccine targeting DC cells to induce an immune response. The vaccine is delivered intradermally where the immature APC, macrophages and other immune cells are recruited. The cargo enters the immature APC, traffics to the nucleus where the RNA transcription occurs followed by protein translation in the cytoplasm and is then represented on the cellular surface as MHC I and thus matures the DC. These cells then trigger the CD8+CTL response. However, if the plasmid is taken up by the non-APC cells, they either present them in MHC I and subsequently release the antigenic peptide on apoptosis or directly release the peptide by proteolysis by proteosome. These peptides are then taken up by the APC and either cross presented in MHC I or presented on MHC II which stimulates the CD4+ T cell response which further generates CD8+ CTL and memory cells. (Created with BioRender.com).
Unlike peptide vaccines, DNA vaccines are competent in generating both a humoral and cellular immune response in vivo. Alfredo, et al. were able to generate a robust CD4+ and CD8+ cellular immune response against ovarian cancer in murine models with a DNA vaccine targeting follicle-stimulating hormone receptor (FSHR) in an pVAX1 expression vector with three doses administered 2 weeks apart using electroporation. Higher expression of INF-γ, IL-2 and TNF-α was observed after vaccination when compared to empty vector controls. The vaccine was also successful in generating a strong humoral antibody response against the FSHR transmembrane protein and a long-lasting cellular response with CD4+ and CD8+ cells producing INF-γ, IL-2 and TNF-α at equivalent levels even after 3 months of complete immunisation as in the first week after the last vaccination. The study suggested employment of this vaccine as a second line of treatment to prevent recurrence after debulking of the ovaries as primary standard care. (Perales-Puchalt et al., 2019) A randomised phased II trial of PANVAC, a viral DNA vaccine consisting of human genes expressing CEA and MUC-1 and 3 T-cell costimulatory molecules in metastatic breast and ovarian cancer, showed improved progression free survival in patients with metastatic breast cancer and ovarian cancer when used in combination with other chemotherapy. (Heery et al., 2015) The patients with limited disease burden and a less compromised immune system seem to benefit from the vaccine with increased ratio of Teffectors: Tregs. (Mohebtash et al., 2011; Heery et al., 2015) Even though various clinical trials have been ongoing, no nucleic acid based vaccine has been approved for treating ovarian cancer in human as of yet.
Nucleic acid-based vaccines are economic, easy to produce and purify compared to peptide antigenic vaccines. They are easily re-designable, safe to administer and also highly stable (Restifo et al., 2000) with DNA vaccines being more stable than the RNA vaccines. Cold storage is necessary in most of the vaccine strategies to guarantee the stability and longevity of the vaccines. As shown with the recent mRNA vaccines e.g., mRNA-1273 (Moderna Inc. Cambridge, MA, United States) for COVID-19 a cold storage temperature of −20°C is necessary. However, DNA vaccines are more highly durable and require minimal refrigeration temperatures, making them extremely useful. Significant stability for over 24 months was observed with lyophilised pDNA stored at higher temperatures at + 2°C–8°C. (Van der Heijden et al., 2013) Unlike peptide vaccines, DNA vaccines are not Human leukocyte antigen restricted (HLA) and can be presented on the MHC I and MHC II robustly. However, naked nucleic acid vaccines are inefficient to generate the required immunological response as they do not pass through the plasma membrane and into the cells freely. Thus, different gene delivery mechanisms are used to generate an adjuvant effect and enhance the functionality of the DNA vaccines.
4.5 Nucleic acid vaccine delivery
To overcome the biological barriers different methods have been investigated by researchers to assist the transfer of nucleic acid molecules. Physical methods such as electroporation, where pulsed electric fields are applied to increase the permeabilization of the cellular membrane in order to increase the uptake of the therapeutic cargo have proven to be successful. However, intense high voltage pulses may cause irreversible damage to the cells and other important organs in vivo. (Sokołowska and Błachnio-Zabielska, 2019) Other physical methods such as gene gun, (Kandalaft et al., 2013) sonication by ultrasound (Rahman et al., 2000; Wang et al., 2012) etc., have also been used to deliver nucleic acids (DNA) in to cells but have not been fully successful in generating a strong immune response due to lower transfection efficiency in vivo and rapid degradation of DNA by sonication. Thus, use of different vectors to deliver the gene are taken into consideration.
The vectors used for the delivery of the therapeutic nucleic acid must have the ability to condense the nucleic acid cargo protecting it from the degradation, opsonisation and expulsion from the systemic circulation to stimulate cellular internalisation by avoiding endosomal entrapment and promoting nuclear import to the targeted cells. Viral vectors are one of the most widely used delivery mechanisms for gene delivery that have undergone clinical trials for Ovarian cancer (Completed trials with results-NCT00112957, NCT00803569, NCT00088413, NCT02179515- Table 2). However, limitations including toxicity, restriction in nucleic acid loading, immunogenicity and difficulties in mass production have led researchers to search for new alternative non-viral strategies. Table 3 lists the different strategies used to deliver nucleic acid cargo to cells.
TABLE 3. Table of different strategies used to deliver nucleic acid cargo to cells.
4.5.1 Adjuvants for nucleic acids
Adjuvant literally is derived from the word “adjuvare” meaning help in Latin. Thus, an adjuvant may be defined as any substance that aids in the function of the vaccine to enhance its immune response against any antigen by recognising the damage associated molecular patterns (DAMPs) and the pathogen associated molecular patterns (PAMPs) by the pattern recognition receptors (PRRs) of the innate immune cells (Akira et al., 2006; Kawai and Akira, 2010; Takeuchi and Akira, 2010) which surges the antigen specific immune response inducing powerful innate and adaptive responses against any tumour cells or any other pathogen entering the body. Another possible way in which an adjuvant functions may also be as a delivery mechanism to effectively deliver the antigen to the antigen presenting cells (APCs) to increase both the innate and adaptive immune response specific to the antigen.
Advancement in immunological research have been able to establish that the various vaccine adjuvants can act by one or more of the following mechanism to evoke a immune response: 1) it may cause a depot effect to cause a sustained release of the cargo at the injection site; 2) recruitment of immunogenic cells at the injection site; 3) increase the uptake of the cargo and its presentation to the APC; 4) activation and maturation of the APC with expression of MHC class II and other co stimulatory molecules and migration to the lymph nodes; 5) chemokines/cytokine upregulation. (Cox and Coulter, 1997; Hoebe et al., 2004) Some of the examples of nonviral adjuvants include nanoparticles such as gold particles, lipid based vesicles, mineral oil based emulsions, and water based emulsions, alum, empty bacterial cell envelopes etc., (Edelman, 2002; Petrovsky, 2006; Muhammad et al., 2012) Very few of these adjuvants have been used to deliver nucleic acid cargos for OC treatment (Table 4). However, while selecting a suitable adjuvant for a vaccine strategy the following has to be taken into consideration 1) route of delivery of the vaccine 2) immune status of the host 3) timing and dose of the vaccine 4) construction of the antigen to be delivered 5) formulation of the adjuvant, 6) size of the adjuvants.
TABLE 4. Table of clinical trials showing adjuvants used to accelerate Nucleic acid delivery for various cancer vaccines in OC.
4.5.2 Cell penetrating peptides as adjuvants
Cell penetrating peptides (CPP) (Cole et al., 2017; Feni and Neundorf, 2017; Habault and Poyet, 2019) are a lesser known non-viral strategy that can be employed in vaccines to deliver nucleic acids to the target cells. (Lee and Foote, 2009) This alternative mechanism include advantages of easy preparation, low immunogenic and oncogenic characteristics with no potential chance for recombination. They can be considered as a potential adjuvant for a vaccine provided they successfully condense the anionic nucleic acid cargo into a nanoparticle and deliver it successfully into APCs.
Targeting uptake of vaccine cargo into DCs and other cells is heavily dependent on the shape, size and charge of the cargo delivered. The use of nanoparticles is supported by the presumption that a higher cellular uptake of the antigenic cargo and an enhanced interaction with the immune cells can be achieved by an ideal optimised delivery system. (Neek et al., 2019) Degradation of the nucleic acid cargo by internal enzymes such as DNAase and RNAase can be averted by the application of biocompatible nanoparticles which encapsulate the cargo. The particles below 0.5 µm are easily taken up by the DCs (Foged et al., 2005) which then travel to the lymph nodes and induce an adaptive immune response. CPP NPs are self-assembled and have a similar shape and size similar to viral particles with the potential to induce the suitable immune responses. CPPs are small amino acid sequences (5–30 amino acids) with the ability to penetrate through the extra and intracellular barrier of the cells to release the nucleic acid cargo at the destination site. (Feni and Neundorf, 2017; Habault and Poyet, 2019).
The CPP nanocomplexes are easily manufactured to induce the desirable characteristics to the NP by changing their basic amino acid backbone. After the first discovery in 1988, many CPPs have been designed so far in the recent years to act as delivery system for proteins, therapeutic nucleic acid and other small organic molecules. They were often fused with different antigens or are used in DNA vaccines to facilitate the transport of the cargo, increase APC uptake and presentation. CPPs such as TAT, hPP70 have been successful previously in delivering nucleic acid cargos to specific cells for the treatment of various cancers through immunotherapy. (Niu et al., 2018; Ding et al., 2019) Previously, CPPs have also been used as DNA vaccine strategies to deliver DNA cargo to cells. A DC targeting vaccine strategy with microneedles loaded with CPP-PEI1800-Man/DNA complexes encoding Trp2, GMCSF and Fc genes was successful in inducing an elevated GFP+ CD11c+ DC response in lymph nodes (42.2%) and spleen cells (49.6%) of vaccinated BALB/c mice when compared to controls. The mice vaccinated with three doses of the vaccine at weekly intervals were subjected to tumour challenge after 1 week of final immunisation which resulted in 90% survival of all mice during the period with 68.5 % inhibition rate of tumour growth with a reduced tumour volume of 297.2 mm3 (control group tumour volume = 943.8 mm (Ahmed et al., 2020)) after 35 days of the challenge. The INF-γ concentration was also increased almost 4 -fold and a 9-fold increase in levels of IL-2 in vaccinated mice compared to other controls. Therapeutic results of the vaccine with the CCP inhibited growth rate to 48% thereby reducing the tumour volume to almost half as compared to control group. (Mccarthy et al., 2014) Hung et al., used one such CPP VP22, an Herpes simplex Virus (HSV-1) protein to form spherical particles with 0.3–1 µm range to act as a peptide vaccine to deliver DNA encoding antigenic peptide HPV-16 E7 which is associated with most cervical cancers, to target cells. When C57BL/6 mice were vaccinated intradermally via gene gun, a 50-fold increase in the E-7 specific INF-γ+/CD8+ T cell precursors and a very high CTL response as compared to wild type DNA alone controls of E7 was seen. Vaccinated mice remained tumour free even after 63 days of tumour challenge whereas all other controls of unvaccinated mice and E7- DNA alone developed tumour after 14 days of the challenge. The therapeutic effects of the vaccine also exhibited lower number of pulmonary nodules compared to unvaccinated and wild type E-7 DNA controls when it was used to treat tumour metastases in the lungs. (Hung et al., 2022) All these studies thus predict that the use to CPP in vivo models can be successful in delivering a nucleic acid cargo. However, use of these CPP to deliver nucleic acid cargos in human clinical trials has yet to be explored.
4.5.3 RALA as a nucleic acid carrier
RALA is one such synthetic cationic fusogenic CPP which can form self-assembling NPs with a negatively charged nucleic acid cargo (Figure 5). It is composed of 30 amino acid sequence:
N-WEARLARALARALARHLARALARALRACEA
FIGURE 5. RALA Nanoparticle formation. The cationic RALA peptide forms a self-assembled nanoparticle with a negatively charged nucleic acid cargo due to the electrostatic interaction between them. The resultant nanoparticle is expected to have a positive charge due to the neutralization of the negative charge of the nucleic acid by the positively charged RALA.
The amino acids at specific sites have important effects on the CPP characteristics. Arginine sites (R), which are hydrophilic in nature, help to bind nucleic acids, leucine sites (L), which are hydrophobic in nature, bind with the lipid membranes, alanine (A) regions contribute to amphipathicity, tryptophan can be used as a spectroscopic probe and glutamic acid increases solubility in water at a physiological pH. (Mccarthy et al., 2014) The structure allows the peptide to bind with the lipid bilayer of the membrane of an endosome leading to an internal stress to cause pore formation and within the endosome when the pH drops around to 5.5 it adopts an alpha-helical structure by interacting with the phospholipid membrane enabling fusion with the endosome and effective release of the cargo to the cytoplasm. (Mcerlean et al., 2015).
RALA/pDNA nanoparticles with <100 nm size and a positive charge of ∼+ 29 mV were produced successfully by Mccarthy et al. (2014) which were all within the specifications required for optimal cellular uptake of particles by endocytosis repressing the negative cellular membrane barrier. (Foged et al., 2005) RALA/mRNA complexes selectively disrupt membrane at acidic pH and successfully transfected cells in vitro. (Udhayakumar et al., 2017) No significant improvement in transfection efficiency when chloroquine—an endosomal disrupting agent is added is predictive that RALA is able to deliver the mRNA cargo (eGFP) on its own to the cytosol. (Udhayakumar et al., 2017) Characterisation of the particles suggested RALA to be a good nucleic acid carrier with higher α helicity, higher responsiveness to low pH present in the endosome, negligible toxicity effect in vitro and successful delivery of gene in vivo murine models. Negligible effects on circulating IgG, IgM, IL1-β and IL6 in mice was observed with RALA/pEGFP-N1 nanoparticles indicating that RALA itself does not provoke a neutralizing antibody response. (Mccrudden et al., 2018) Studies have also been able to establish functionality of lyophilised RALA nanoparticles which can be stored at room temperature. Cole et al. (2019) successfully delivered RALA/pDNA nanoparticles loaded in dissolvable PVA microneedles generating positive results against cervical and prostate cancer. (Lee and Foote, 2009; Van der Heijden et al., 2013; Cole et al., 2018b) Lyophilisation of RALA-pDNA (pE7) nanoparticles increased the size but kept within >100 nm with minimal change in the positive zeta potential, encapsulation efficiency (>80%), cell viability (80%). These fresh and lyophilised NP showed apparent protein expression when compared to pDNA alone indicating role of RALA to achieve transfection. These RALA NP, when incorporated in the polyvinyl alcohol (PVA) microneedles (MN), used to immunize mice once per 2 weeks (2–3 times), raised levels of anti -E7 IgG (80.06 µg/ml- two doses) compared to naïve controls (25 μg/ml). The splenic T cells from the MN immunized mice showed almost double cytolytic effects on tumour cells when compared to untreated control. RALA/pDNA NP when vaccinated through intramuscular injections and NP loaded in MN were able to reduce the established tumour growth in murine models indicating higher antigen specific cytolytic T-cell response when compared to pDNA on its own. (Cole et al., 2018b)
Udhayakumar et al. (2017) reported that RALA/mRNA OVA complexes were successful to produce elicited antigen specific CD8+ T cell response in vivo in murine models at N:P 5 and 10 when compared to mRNA alone thus indicating the role of RALA in generating a cytolytic cellular immune response. In the preliminary invitro studies mRNA complexed with RALA at N:P 10 was able to promote DC activation and upregulate CD86, CD40 and MHC II when compared to noncomplexed mRNA. DC activated with modified mRNA was less potent in comparison to the unmodified mRNA even though the levels of CD86, CD40 and MHC II were elevated compared to the PBS treated controls. RALA complexes at N:P 10 with modified mRNA reduced levels INF-β while leaving IL-6 levels unaffected with greater ability to elicit CD8+ T cell response and eliminate all target cells compared to unmodified mRNA. RALA/mRNA vaccine was compared with a conventional lipoplex (1,2-dioleoyl-3-trimethylammonium-propane (DOTAP)/1,2- dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE))-based mRNA vaccine for their ability to elicit a CTL response in vivo intradermally in wild type (WT) mice and mice lacking the common INF-α/β receptor (Infar−/−). RALA/mRNA complexes (N:P 10) with unmodified mRNA showed higher responses for CTL after prime-boost immunization in Infar−/− mice and similar levels with modified mRNA when compared with the WT mice indicating the negligible impact of Type I INF with modified mRNA/RALA complexes. Further investigation monitoring INF-β induction in INF-β reporter mice strain revealed a very high INF-β response in noncomplexed and DOTAP/DOPE complexed (N:P 1) modified mRNA explaining the elevated T cell immunity in Infar−/− mice but when it was complexed with RALA (N:P 10) it hardly evoked any INF-β response and thus circumvents any negative effect of the type I INF without any additional augmentation of T-cell immunity in Infar−/− upon vaccination. It was further proven that the non-immunogenic properties of RALA and its ability to induce substantial CD8+ CTL response in vivo is a unique feature which make it an effective delivery system for a vaccine strategy. (Udhayakumar et al., 2017) All the results thus obtained so far indicate RALA to be a strong candidate to act as a nucleic acid vaccine adjuvant.
5 Future perspective and conclusion
HGSC is the most aggressive type of OC, claiming the highest number of lives of the patients with OC, owing to its delayed diagnosis. Advances in sequencing techniques of the tumours are enabling effective identification of tumour antigens and some specific potential neoantigens as well. The genes encoding the overexpressed CTAs can be used as a potential target in a nucleic acid vaccine to induce a strong cytolytic CD8+ T-cell mediated immune response along with some humoral response in HGSC models in vivo. However, the inter and intracellular barrier of the cells pose a significant hindrance in delivering the negatively charged naked nucleic acid cargo to the cells thereby not probing the required immune response. CPPs can act as a potent delivery system required to successfully deliver the cargo and generate the immune response by transfecting the correct DC (cDC). There is no commercially available cancer vaccine to date for ovarian cancer. Nucleic acid vaccines provide platform for future clinical trials in HGSC; however, a non-immunogenic effective delivery system is required so that the immune response comes from the nucleic acid cargo itself.
Author contributions
HM designed the structure and content CS and JB drafted the initial versions of the review CS produced all the figures and tables HM, NB, and RD supervised CS throughout this process ND, HM, and NB rewrote the final drafts, made edits and polished the manuscript.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
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Keywords: ovarian cancer, high grade serous carcinoma, tumour antigens, nucleic acid vaccines, DNA, mRNA
Citation: Saha C, Bojdo J, Dunne NJ, Duary RK, Buckley N and McCarthy HO (2022) Nucleic acid vaccination strategies for ovarian cancer. Front. Bioeng. Biotechnol. 10:953887. doi: 10.3389/fbioe.2022.953887
Received: 26 May 2022; Accepted: 26 October 2022;
Published: 07 November 2022.
Edited by:
Andrea Banfi, University of Basel, SwitzerlandReviewed by:
Ilia Bozo, Federal Medical & Biological Agency of Russia, RussiaMuhammad Nawaz, University of Gothenburg, Sweden
Copyright © 2022 Saha, Bojdo, Dunne, Duary, Buckley and McCarthy. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Helen O. McCarthy, h.mccarthy@qub.ac.uk