Synthesized natural peptides from amphibian skin secretions increase the efficacy of a therapeutic vaccine by recruiting more T cells to the tumour site
Therapeutic vaccines against cervical cancer remain ineffective. Previously, we demonstrated that blocking the signalling of a cytokine, interleukin 10, at the time of immunisation elicited significantly higher numbers of antigen specific T cells and inhibited tumour growth in mice.
In the current paper, we demonstrate, in a HPV16 E6/E7 transformed TC-1 tumour mouse model, that despite increased antigen specific T cell numbers, blocking IL-10 signalling at the time of immunisation does not increase the survival time of the TC-1 tumour bearing mice compared to mice receiving the same immunisation with no IL-10 signalling blockade. Moreover, the function of tumour infiltrating T cells isolated 3 weeks post TC-1 transplantation is more suppressed than those isolated 2 weeks after tumour inoculation. We demonstrate that synthesized caerin peptides, derived from amphibian skin secretions, 1) were able to inhibit TC-1 tumour growth both in vitro and in vivo; 2) are environmentally stable; and 3) promote the secretion of pro-inflammatory interlukine-6 by TC-1 cells. Notably caerin peptides were able to increase the survival time of TC-1 tumour bearing mice after therapeutic vaccination with a HPV16E7 peptide-based vaccine containing IL-10 inhibitor, via recruiting increased levels of T cells to the tumour site.
Caerin peptides increase the efficacy of a therapeutic vaccine by recruiting more T cells to the tumour site.
KeywordsCaerin peptide Therapeutic vaccine Cervical cancer Tumour microenvironment
- Caerin 1.1
- caerin 1.9
Indoleamine-pyrrole 2, 3-dioxygenase
monophosphoryl lipid A
Virus like particles
Cervical cancer is the 2nd most common cancer in woman worldwide, and accounts for around 250,000 deaths each year, especially in developing countries [1, 2]. Cervical cancer results from persistent high-risk human papillomavirus (HPV) infection, mostly HPV subtypes 16 and 18, which are responsible for around 70% of cervical cancers. A prophylactic vaccine, based on the papillomavirus like particles (VLPs), has been available to the public since 2006, but the vaccine is not effective for those already infected [3, 4, 5, 6]. During the past few years, a better understanding of the HPV-host immune system interaction and the development of new therapeutics targeting immune check points have renewed interest in the use of immunotherapy for cervical cancer treatment.
Therapeutic vaccines only target tumour cells but leave normal tissues and organs unaffected. Ideally, therapeutic tumour vaccines should produce sufficient high-quality effector CD8+ T cells that can migrate to the tumour site, overcome the tumour immune suppressive environment and kill the tumour cells . Peptide based therapeutic vaccines are easier to produce with less side effects, and therefore have been studied extensively . In one such study, women with HPV-16-positive, grade 3 vulvar intraepithelial neoplasia were vaccinated with a mix of long peptides from the HPV16 E6 and E7 in incomplete Freund’s adjuvant. Fifteen of 19 patients had a clinical response, with complete viral clearance observed in 9 of 19 patients . Vaccine induced memory CD8+ T cell responses predict the therapeutic efficacy of a therapeutic vaccine . The same vaccine was also able to induce a broad IFNγ-associated T-cell response in patients with advanced or recurrent HPV16-induced gynaecological carcinoma but did not induce tumour regression or prevent progressive disease . Therefore, the efficacy of the therapeutic vaccine against cervical cancer remains to be improved.
Interleukin 10 (IL-10) is a cytokine with multiple biological function . The main function of IL-10 is to limit immune responses against foreign and self-antigens, to avoid excessive immune response damage to self, via inhibiting the function of professional antigen presenting cells . Temporal blockade of IL-10 at the time of immunization drastically increases vaccine-induced CD8+ T cell responses [13, 14]. This phenomenon can be observed when HPV VLPs, soluble antigen, peptide, or DNA are used as immunogens . Compared with vaccination using HPV16 long E7 peptide in incomplete Freund’s adjuvant on its own, blocking IL-10 at the time of immunisation elicits significantly higher numbers of CD8+ T cells and attracts more CD4+ and CD8+ T cells to the tumour site [15, 16]. However, the survival time of HPV16 E6/E7 transformed TC-1 tumour bearing mice is similar between the two immunisation groups. Therefore, the tumour microenvironment is critical and might determine the efficacy of a therapeutic vaccine.
The tumour microenvironment consists of tumour cells, immune suppressive cells such as T Regulatory T cells, tumour associated macrophages, myeloid derived immune suppressive cells, and cytokines with immune suppressive function [17, 18]. Although the presence of T cells within the tumour indicates a better prognosis for the cancer patient, tumour infiltrating T cells are usually anergic, secreting less cytokines and responding poorly to specific and non-specific stimulation . Attempts to overcome the tumour microenvironment have been extensively studied, include targeting the PD-L1–PD-1 axis, Indoleamine-pyrrole 2, 3-dioxygenase (IDO), T regulatory cells, and T cell–intrinsic energy . Monoclonal antibodies targeting PD-1/PD-L1 axis shows efficacy in about one third of melanoma patients. Another example is the use of anaerobic bacteria, which only proliferate in the anoxic environment within the centre of a tumour . Toll like receptor ligands, such as CpG and imiquimod, have also been used to break the immune suppressive microenvironment .
Peptides isolated from amphibians have been shown to lyse bacteria via a unique mechanism possibly involving cell membrane lysis. Some of these peptides are observed to be highly active against cancer cells but not normal mammalian cell. More than 200 host-defence peptides have been isolated and identified from skin secretions of Australian frogs and toads. Many of these peptides have antimicrobial and/or neuropeptide-type activities (27–29). The caerin 1 peptides have previously been shown to be potent membrane-active peptides and to stop the formation of nitric oxide by neuronal nitric oxide synthase. Caerin 1.1 (1GLLSVLGSV10AKHVLPHVLP20HVVPVIAEHL-NH2) has an anti-cancer effect against several human cancer cell lines. The caerin 1.9 peptide (1GLFGVLGSI10AKHVLPHVVP20VIAEKL-NH2) has antimicrobial activity against a wide spectrum of Gram-positive and Gram-negative microbial strains. Caerin 1.1 and 1.9 are originally isolated from skin secretions of Australian tree frog Litoria splendida. Caerin 1.1 and 1.9 inhibit HIV-infected T cells within minutes post-exposure at concentrations non-toxic to T cells and inhibit the transfer of HIV from dendritic cells (DCs) to T cells . We have recently shown that caerin 1.1 and 1.9 have cytotoxicity to HPV 16 early protein E6/E7 transformed TC-1 cells in vitro, and the anti-cancer effects were more profound when caerin 1.1 and 1.9 were used together . Moreover, proteomics analysis showed that caerin 1.9 could stimulate multiple signalling pathways including several pro-inflammatory signalling pathways [20, 23, 24].
In the current paper, we investigated the function of tumour infiltrating T cells at various stages after tumour transplantation in a TC-1 tumour mouse model and showed that caerin 1.1 and 1.9 were able to stimulate the secretion of IL-6 by TC-1 cells. Moreover, caerin 1.1 and 1.9 increased the efficacy of a therapeutic vaccine containing IL-10 inhibitor in the TC-1 mice tumour model by increasing the survival time of TC-1 tumour bearing mice.
Six to eight weeks old, specific pathogen free (SPF) adult female C57BL/6 (H-2b) mice and Nude mice were ordered from the Animal Resource Centre, Sun Yat-Sen University and kept at the Animal Resource Centre, the first affiliated hospital of Guangdong Pharmaceutical University, Guangdong province, China. Experiments were approved by and then performed in compliance with the guidelines of Animal Experimentation Ethics Committee (Ethics Approval Number: FAHGPU20160316) of the aforementioned hospital.
All mice were kept at SPF condition on a 12-h light/12-h dark cycle. The temperature of the animal house was 22 °C and the humidity was 75%. 5 mice were kept each cage, provided with sterilised standard mouse food and water. TC-1 tumour bearing mice were given 1% sodium pentobarbital by i.p. injection when treatment was performed. Mice were sacrificed by CO2 inhalation at the end of each experiment and confirmed by the ceasing of heart beat.
Cell line, peptide synthesis and antibodies
A murine TC-1 cell line transformed with HPV16 E6/E7 was obtained from Shanghai Institute for Cell Resources Centre, Chinese Academy of Sciences, and cultured following the protocols in the product sheets. The culture of TC-1 cells was described elsewhere . Briefly, TC-1 cells were cultured at 37 °C with 5% CO2 in complete RPMI 1640 media (GIBCO) supplemented with 10% heat inactivated fetal calf serum (FCS, GIBCO), 100 U of penicillin/mL and 100 mg of streptomycin/mL (GIBCO), 0.2 mM non-essential amino acid solution, 1.0 mM sodium pyruvate, 2 mM L-glutamine, 0.4 mg/mL G418.
Human cervical cancer cell Hela and stable cell line of T-SV4O immortalized human glomerular mesangial cell (HMC) were purchased from the Shanghai Institute for Biological Sciences, Chinese Academy of Sciences. The cell lines were grown in RPMI 1640 media (GIBCO) supplemented with 10% heat inactivated fatal calf serum (FCS, GIBCO), 100 U of penicillin/mL and 100 mg of streptomycin/mL (GIBCO), in humidified atmosphere of 5% CO2 at 37 °C.
Caerin 1.1 and Caerin 1.9 peptides from Australian tree frog Litoria splendida are synthesized and therefore does not include any actual materials from frogs.
Caerin 1.1 (GLLSVLGSVAKHVLPHVLPHVVPVIAEHL-NH2) and caerin 1.9 (GLFGVLGSIAKHVLPHVVPVIAEKL-NH2), control peptide (GTELPSPPSVWFEAEFK), HPV16 E7 CTL epitope RAHYNIVTF, and four overlapping peptides representing the entire HPV 16 E7 protein, EX (MHGDTPTLHEYMLDLQPETTDLYCYEQLNDSSEEE, LNDSSEEEDEIDGPAGQAEPDRAHYNIVTFCCKC, DRAHYNIVTFCCKCDSTLRLCVQSTHVDIR, CVQSTHVDIRTLEDLLMGTLGIVCPICSQKP were synthesised by Mimotopes Proprietary Limited, Wuxi, China. The purity of the peptides was > 95% as determined by reverse-phase HPLC at Mimotopes. The lipopolysaccharide concentration of F1, F3 and P3 was 0.03EU/ml, 0.03EU/ml and 0.44EU/ml respectively as measured by Kinetic Turbidimetric Assay by Xiamen Bioendo Technology Co., Ltd.
For immunisation, anti-IL10 receptor (1B1.3) monoclonal antibody (MAb) and IgG Isotype control antibody (LTF-2) were purchased from BioXcell, USA and stored at − 80 °C till further use. Anti-Mouse CD3 FITC (17A2) was purchased from BioLegend (San Diego USA). Anti-Mouse IFN-γ PE (XMG1.2), anti-Mouse Granzyme B PE (NG2B), anti-Mouse Perforin PE (eBio0MAK-D), anti-Mouse CD4 PerCP-Cyanine5.5 (RM4–5), anti-Mouse CD8 PerCP-Cyanine5.5 (53–6.7) and anti-Mouse CD279 (PD-1) APC (J43) were purchased from eBioscience (Waltham, USA).
Tumours were excised and cut into small pieces after removal of blood vessels and connective tissue. To isolate blood cells, tumour tissue was incubated for 1 h, with occasional shaking, in an enzyme mixture that consisted of 1 mg /ml of collagenase D, 20 mg /ml of DNase I (Roche), and 10% fetal calf serum in RPMI-1640 at 37 °C. The digested tissue was filtered through a 70 μm nylon mesh, and the resultant cells were washed twice in PBS. Mononuclear cells were obtained with Lymphocyte Separation Medium (Sigma-Aldrich) following centrifugation at 2000 rpm for 25 min. The intra-cellular staining has been described elsewhere . Briefly, mononuclear cells were harvested and incubated with cell stimulation cocktail (eBioscience) in the presence of 2 μM of monensin (eBioscience) at a density of 1 × 106 cells/ml overnight at 37 °C with 5% CO2. Cells were stained with antibody against CD3, CD4 and CD8 and then fixed and permeabilized using permeabilization buffer (Biolegend) before intra-cellularly stained with anti-mouse IFN-γ, anti-Mouse Granzyme B, anti-Mouse Perforin or isotype-matched control mAb for 20 min in the dark at room temperature. Samples were analysed by flow cytometry using a FACS Calibur analyser (Becton Dickinson).
Cell proliferation was determined by MTT assay (ATCC, USA) following the manufacturer instructions as described elsewhere . Briefly, 5 × 103 of TC-1 cells were cultured in flat bottomed 96 well plates before adding approximately 0–15 μg of peptides was added to 5 × 103 TC-1, Hela, or MHC cells and cultured overnight at 37 °C with 5% CO2, followed by adding ten microliters of MTT stock solution and cultured another 4 h. 100 μl of DMSO was added to stop the experiment. Each treatment was performed in triplicate. Results were analysed by an ELISA plate reader (BioTek, USA) at 570 nm according to the manufacturer’s protocol.
Cytokine ELISA kits for the detection of IL-1α and MCP-1, IL-10 and IL-6 were purchased from eBioscience. IL-1α, IL-6, IL-10 and MCP-1 were detected from the supernatants of caerin peptide or as a control imiquimod treated TC-1 cells following the protocols provided by the manufacturer.
TC-1 tumour challenge has been described elsewhere (41). Briefly, TC-1 cells, at approximately 70% confluency, were harvested with 0.25% trypsin and washed repeatedly with PBS. TC-1 tumour cells (3 × 105 /mouse) in 0.1 ml of PBS were injected subcutaneously into the left flank. Tumour sizes were assessed every 3 days using callipers to determine the average diameter of each tumour. Tumour volumes were calculated as width×width×length. Mice were sacrificed when the tumour diameter reached 20 mm. In another experiment, TC-1 tumour bearing mice were sacrificed and the tumour dissected and weighted using an electronic scale (Sartorius, Germany).
Immunization of mice
Four to five days post TC-1-challenge, groups of five to eight mice were immunised subcutaneously (s.c.) with vaccine containing either 40 mg of four overlapping HPV16E7 peptides (EX) (10 μg/each), 15 mg of monophosphoryl lipid A (MPLA) (Sigma-Aldrich), with or without 250 mg of anti-IL10R antibodies, or IgG Isotype Control Antibody (LTF-2), dissolved in PBS. The total injected volume was 100 μL/mouse.
Tumour local administration of caerin peptides
Four to five days post-TC-1-challenge, when the tumours’ diameters reached 3 to 5 mm, the mice either immunised or unimmunised were intratumorally injected with caerin peptides (Caerin 1.1 and Caerin 1.9), or PBS for six consecutive days.
ELISPOT was performed as described previously (37). Briefly, single spleen cell suspensions were added to membrane base 96 well ELISPOT plate (Millipore, Bedford, MA) coated with anti-IFN-γ (BD Harlingen, San Diego, CA). HPV16 E7 CTL epitope RAHYNIVTF was added at various concentrations and cells incubated with the peptide overnight at 37 °C with 5% CO2. The plate was incubated with detection antibody (a biotinylated anti-mouse IFN-γ antibody, BD Harlingen, San Diego, CA) after extensive washing in wash buffer for 2 h at room temperature. Antigen specific IFN-γ secreting cells were detected by sequential exposure of the plate to avidin–horseradish peroxidase (Sigma-Aldrich) and DAB (Sigma-Aldrich). The plate was washed, allowed to air dry overnight, foci of staining were counted by ELISPOT reader system (CTL, Germany).
Data are expressed as the mean ± SD and statistical significance was determined using paired two-tailed Student t test. Survival rate’s comparison between different groups was performed by log rank test, by using Prism 5.0 (Graphpad Software, San Diego). Results were considered significant if P value was less than 0.05.
Blocking IL-10 at the time of immunisation does not increase the survival time of TC-1 tumour bearing mice
Next, C57/BL6 mice were immunised with EX/MPLA twice with an interval of 7 days, with or without IL-10 signalling blockade. Control groups included unimmunised and EX/MPLA immunisation plus a control antibody. Seven days after final immunisation, the mice were challenged subcutaneously with TC-1 tumour cells. Mice that received EX/MPLA and IL-10R antibody immunisation did not have any observable tumour growth, while tumour growth was observed in all other groups after tumour challenge. Moreover, 100% of mice immunised with EX/MPLA together with IL-10R antibody survived 80 days post tumour challenge (Fig. 1b and c). Between 40 and 60% of mice in EX/MPLA only and EX/MPLA control antibody groups survived over 80 days. The survival time was observed to be similar between the EX/MPLA/control antibody and the EX/MPLA only immunisation group 80 days post TC-1 tumour inoculation. All mice from untreated group were dead within 50 days after tumour challenge.
Following this, C57BL/6 mice were subcutaneously inoculated with TC-1 tumour cells. Five days after tumour challenge, TC-1 tumour bearing mice were immunised with EX/MPLA with or without IL-10 signalling blockade, controls include EX/MPLA/control antibody and unimmunised groups. Thirty days after TC-1 tumour inoculation, mice immunised with the EX/MPLA and IL-10 blockade demonstrated increased inhibition of TC-1 tumour growth compared to mice in groups immunised without the IL-10 signalling blockade or with control antibody. However, the survival time among the immunisation groups were similar, whether the tumour bearing mice were immunised with or without the IL-10 signalling blockade (Fig. 1d and e). The survival time of mice immunised with EX/MPLA and anti-IL-10R antibody was statistically longer than that of unimmunised control (P < 0.05).
Tumour infiltrating T cells, isolated 3 weeks were more suppressed compared with those isolated 2 weeks after tumour inoculation
Caerin peptides are stable
Caerin 1.1 and 1.9 inhibit TC-1 growth in vivo
In similar experiment was conducted using intra-tumour injection of Caerin peptides, PBS, 50 μg of imiquimod, or imiquimod/peptides groups. Three days after the final injection, tumours were removed and weighed using an electronic scale. Caerin 1.1 and 1.9 significantly inhibited TC-1 tumour growth compared with PBS or Imiquimod only treated groups. At 50 μg per injection, Imiquimod was unable to inhibit TC-1 growth. However, caerin peptides combined with imiquimod treatment inhibited TC-1 tumour growth, although the inhibition was not statistically significant compared with caerin peptides treatment alone (Fig. 4c). When this experiment was repeated in nude mice, caerin 1.1 and 1.9 lost the ability of inhibiting tumour growth (Fig. 4d).
Caerin 1.1 and 1.9 increase the efficacy of a HPV16 E7 peptide based therapeutic vaccine
We hypothesised that caerin peptides would increase the efficacy of a therapeutic vaccine, based on the observation that they had cytotoxicity on tumour cells and promoted the secretion of pro-inflammatory cytokines using quantitative proteomic analysis . TC-1 tumour bearing mice were divided randomly into 4 groups: 1) Ex/MPLA/anti-IL-10R antibody immunisation and caerin 1.1/1.9 tumour local administration; 2) Ex/MPLA/anti-IL-10R antibody immunisation plus PBS tumour local injection; 3) caerin 1.1/1.9 tumour local injection and 4) PBS tumour local injection. TC-1 tumour bearing mice were immunised twice 7 days apart, followed by intra-tumour injection of caerin 1.1 and 1.9 or PBS. The result clearly showed that immunisation with EX/MPLA/anti-IL-10 antibody plus local administration of caerin peptides significantly increased the survival time of TC-1 tumour bearing mice. Immunisation with EX/MPLA/anti-IL-10R antibody alone, or tumour local injection of caerin peptides alone did not increase the survival time of TC-1 tumour bearing mice compared with PBS treated control group (Fig. 4e). Next, we compared whether caerin peptides local administration combined with EX/MPLA only immunisation also improved the survival time of TC-1 tumour bearing mice. The survival time of caerin treated TC-1 tumour bearing mice was significantly increased compared with PBS treated mice. Mice survived longer when immunised with EX/MPLA/anti-IL-10R antibody plus caerin 1.1/1.9 tumour local injection compared to the EX/MPLA only immunisation group plus caerin 1.1/1.9 local injection, however, there was no statistical difference (Fig. 4f). These results suggest that disturbing the immune suppressive microenvironment is critical for increasing the efficacy of a therapeutic vaccine.
Caerin peptides treated TC-1 cells secrete more IL-6
Caerin 1.1 and 1.9 attract more T cells to the tumour site
Therapeutic vaccines are efficient against HPV infection related pre-cancer conditions, such as VIN3 and CIN3 , but remain to show efficacy against cervical cancer . The low immunogenicity of therapeutic vaccines and the tumour immune suppressive microenvironment are key factors that limit the efficacy of a cancer therapeutic vaccine [1, 14, 17, 19]. To be effective, a therapeutic vaccine should elicit high quality, and sufficient numbers of effector T cells that are able to migrate to the tumour site, overcome the immune suppressive environment and kill tumour or viral infected cells .
In the current study, we demonstrated that immunisation with four overlapping peptides covering entire HPV16 E7 protein (EX) with MPLA as adjuvant elicits significantly greater numbers of E7 specific CD8+ T cells when IL-10 signalling is blocked. However, the EX/MPLA/anti- IL-10 receptor antibody immunisation did not prolong the survival time of TC-1 tumour bearing mice compared with the same vaccine immunisation without IL-10 signalling blockade (Fig. 1). Increased inhibition of TC-1 tumour growth and survival of tumour bearing mice were only observed when tumour challenge was performed after EX/MPLA/anti-IL10R antibody vaccination (Fig. 1). Tumour infiltrating T cells isolated 3 weeks after TC-1 tumour transplantation, secreted less IFNγ, perforin and Granzyme B compared with those isolated 2 weeks after TC-1 tumour inoculation (Fig. 2). We also demonstrated that caerin peptides isolated from the skin secretion of Australian tree frog are able to promote the secretion of pro-inflammatory IL-6 by TC-1 cells (Fig. 5). Moreover, our studies showed the caerin peptides were i) functionally stable (Fig. 4); ii) were able to inhibit TC-1 tumour growth in vivo; iii) that the inhibition require adaptive immune responses (Fig. 4); and iv) increased the efficacy of the Ex/MPLA/anti-IL-10R vaccine (Fig. 4). Finally, we demonstrated a mechanism by which caerin peptides use to enhance the efficacy of the therapeutic vaccine by recruiting more T cells to the tumour site (Fig. 6).
Vaccine induced CD8 + T cells can predict the therapeutic efficacy of a vaccine against the tumour . Great efforts have been made to increase the immunogenicity of therapeutic vaccines. We and others have previously demonstrated that blocking IL-10 at the time of immunisation drastically increase the vaccine induced CD8+ T cell response [14, 25, 26]. Studies also showed that this immunisation strategy better prevents tumour growth than the immunisation without IL-10 signalling blockade, if IL-10 signalling was blocked by i.p. injection of anti-IL-10 receptor antibodies . Subcutaneous administration of vaccine and anti-IL-10 receptor antibodies increases the vaccine induced CD8 T cell responses compared with immunisation without IL-10 signalling blockade, but is not as significant as administration of anti-IL-10 through i.p. injection . In the current study, however, HPV16 E7 peptide-based vaccine was unable to prolong the survival time of TC-1 tumour bearing mice when IL-10 signalling was blocked through subcutaneously administration of anti-IL-10 receptor antibodies at the time of immunisation (Fig. 1). This outcome is similar to most clinical trial results in that therapeutic vaccines are yet to show any clinical efficacy against cervical cancer [1, 27, 28].
Cancer develops after lengthy battle with the human immune system. The tumour microenvironment not only promotes tumour development and metastasis, but also prevents tumour killing by effector cells of the adaptive immune system, mostly T cells . T cells eventually lose their function during chronic viral infection and tumour development . The centre of a solid tumour usually lacks of oxygen, and hypoxia of the solid tumour inhibits CD4+ T cell function . Our results also showed that tumour infiltrating CD4+ and CD8+ T cells isolated 3 weeks after TC-1 tumour inoculation secrete less IFNγ compared with those isolated at 3 weeks, whether or not the T cells express PD-1. Tumour infiltrating CD8+ T cells isolated at 3 weeks also express less Granzyme B and perforin (Fig. 2). These results agree with clinical trial results  in that therapeutic vaccines are not effective against cervical cancer, arguing that when the tumour microenvironment is established, the vaccine-induced T cells will not kill the tumour cells efficiently.
Targeting the tumour microenvironment has recently shown exciting outcomes, from the use of antibody targeting immune-checkpoints, such as anti-PD-1 . Therapeutic vaccines combined with anti-PD-1 enhance the efficacy of the therapeutic vaccines against different solid tumours, both in animal models and clinical trials [32, 33]. Recently, we demonstrated that naturally derived peptides isolated from Australian tree frog are able to inhibit multiple tumour growth in vitro, partially through inducing apoptosis of tumour cells, by penetrating the tumour cell membrane into the cytosol . Proteomic analysis showed that caerin peptides activate multiple cell signalling pathways including NFκB to stimulate pro-inflammatory cytokines and chemokines. These results prompted us to investigate whether caerin peptides can be used to target the tumour microenvironment. Indeed, caerin peptides are able to inhibit both TC-1 in vitro and promote TC-1 cells to secrete more IL-6 (Fig. 5). Caerin peptides are environmentally stable, as their biological activities remaining identical when stored at room temperature, in acidic condition and at high temperatures (100 °C) (Fig. 3), suggesting these peptides are ideal for in vivo administration. Indeed, when combining tumour local administration of caerin peptides with Ex/MPLA vaccine to TC-1 tumour bearing mice, the survival time was significantly extended compared with vaccination alone or caerin peptide treatment alone, whether IL-10 signalling is blocked or not.
Caerin peptides mediated increased efficacy of therapeutic vaccine via recruiting more T cells to the tumour site. After administration of caerin peptide 1.1/1.9, T cell numbers as well as antigen specific CD8+ T cells migrating to TC-1 tumour are significantly increased compared with untreated mice. Moreover, the number of antigen specific CD8+ T cells migrating to TC-1 tumour is significantly increased in vaccine plus caerin treatment group compared with vaccine only group. It is likely that caerin peptides increase the levels of chemokines, which attract T cells to the tumour site.
The efficacy of caerin peptides targeting the tumour microenvironment can be further improved. Previously, we demonstrated that nanomaterial graphene oxide can incorporate IFNγ and anti-IL-10 receptor antibodies . The graphene oxide absorbed antibodies and cytokine retained their biological activities both in vivo and in vitro. They are slowly released to the outside environment compared with free cytokines and antibodies . Graphene oxide absorbed anti-IL10R antibodies are more efficient than free anti-IL10R antibodies at eliciting LPS stimulated CD8 T cell responses. Recently, radioactive iodine 125 (125I) was labelled to the caerin 1.9 peptide. The 125I labelled caerin 1.9 was almost 100 time more efficient at inhibiting tumour growth in vitro compared with non-labelled caerin 1.9, more efficient than free 125 I . Caerin peptides may therefore be used to disturb the tumour microenvironment if properly incorporated in a controlled release reagent, to increase the efficacy of cancer therapeutic vaccines against cancers.
Taken together, caerin peptides are able to boost the efficacy of a HPV16 E7 peptide-based vaccine containing IL-10 signalling inhibitor to better inhibit the HPV16 E6/E7 transformed TC-1 growth and extend the survival time of TC-1 tumour bearing mice. Mechanisms involved include disturbing the tumour microenvironment by recruiting more antigen specific T cells to the tumour site. These results warrant ongoing investigations in a clinical setting.
We thank Mr. Zaowen Liao for the assistance in the experiments.
XP, GN, TW, XL conceived the manuscript; BWM, XCY, JW, SC performed the experiments; TW, SW, XW, GC, WJ analysed the results and provided materials and resources; GN, SC wrote the first draft of the manuscript. XL, SW revised the final draft. All authors read and approve the manuscript.
This project was partly supported by the first affiliated hospital of Guangdong Pharmaceutical University; by Science and Technology Research program of Foshan city (No.: 2012AA100461); Foshan City Council Research Platform Fund (No.: 2015AG1003, FS0AA-KJ218–1301-0039); Science and technology Department of Guangdong province (No.: 2012B03180003), National Natural Science Foundation of China (No: 81472451) and Science and Technology Research program of Guangdong province (No: 2016A020213001). The funding bodies have no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Ethics approval and consent to participate
Experiments were approved by Animal Experimentation Ethics Committee (Ethics Approval Number: FAHGPU20160316) of the First Affiliated Hospital, Guangdong Pharmaceutical University. Consent to participate is not relevant to this manuscript.
Consent for publication
Not relevant to this manuscript.
All authors declare that they have no competing interests.
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