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Original Research ARTICLE

Front. Immunol., 12 June 2019 | https://doi.org/10.3389/fimmu.2019.01349

Immunization With Mycobacterium tuberculosis Antigens Encapsulated in Phosphatidylserine Liposomes Improves Protection Afforded by BCG

Gil R. Diogo1, Peter Hart1, Alastair Copland1, Mi-Young Kim1, Andy C. Tran1, Noemi Poerio2, Mahavir Singh3, Matthew J. Paul1, Maurizio Fraziano2 and Rajko Reljic1*
  • 1Institute for Infection and Immunity, St. George's University of London, London, United Kingdom
  • 2Dipartimento di Biologia, University of Rome Tor Vergata, Rome, Italy
  • 3LIONEX GmbH, Brunswick, Germany

Liposomes have been long considered as a vaccine delivery system but this technology remains to be fully utilized. Here, we describe a novel liposome-based subunit vaccine formulation for tuberculosis (TB) based on phosphatidylserine encapsulating two prominent TB antigens, Ag85B, and ESAT-6. We show that the resulting liposomes (Lipo-AE) are stable upon storage and can be readily taken up by antigen presenting cells and that their antigenic cargo is delivered and processed within endosomal cell compartments. The Lipo-AE vaccine formulation combined with the PolyIC adjuvant induced a mixed Th1/Th17-Th2 immune response to Ag85B but only a weak response to ESAT-6. An immunization regimen based on systemic delivery followed by mucosal boost with Lipo-AE resulted in the accumulation of resident memory T cells in the lungs. Most importantly though, when Lipo-AE vaccine candidate was administered to BCG-immunized mice subsequently challenged with low dose aerosol Mycobacterium tuberculosis, we observed a significant reduction of the bacterial load in the lungs and spleen compared to BCG alone. We therefore conclude that the immunization with mycobacterial antigens delivered by phosphatidylserine based liposomes in combination with Poly:IC adjuvant may represent a novel BCG boosting vaccination strategy.

Introduction

Despite the availability of a vaccine and drug regimens, tuberculosis (TB) remains a major health burden globally. In 2016, there were ~1.3 million deaths from TB among HIV-negative and 374,000 among HIV-positive individuals, making it the 9th cause of death worldwide and the number one due to a single infectious agent (1).

The current vaccine, Bacille Calmette Guérin (BCG), was first administered nearly 100 years ago and is still extensively used today. BCG was first used in children in 1921 and is now given to more than 120 million people worldwide every year, with 4 billion people already immunized (2). It is effective at preventing severe forms of TB in children but provides varying levels of protection against pulmonary TB in adults. Revaccination with BCG has not been shown to be advantageous (3, 4) and is not recommended by the WHO. Coupled with the emergence of multi-drug resistant tuberculosis (MDR-TB) with unsatisfactory treatment rates, it is clear that a more effective TB vaccine is a major healthcare priority.

Although there are several vaccine candidates at various stages of clinical trials and many more at preclinical stage of research and development, it is important to continuously feed the TB vaccine pipeline with both live and subunit vaccines. This is because it may well be that more than a single vaccination strategy will be needed to protect different human populations against TB (e.g., different age groups, HIV status, geographical location etc.). For example, a replacement BCG vaccine is likely to be another live attenuated organism (recombinant BCG or attenuated Mtb) in order to protect young children from severe primary TB infection but a subunit vaccine may be preferable in HIV-positive population due to the host's immunocompromised state. Likewise, it may be preferable to boost BCG with a subunit rather than another attenuated vaccine to avoid excessive delayed hypersensitivity reactions (Koch's phenomenon). Recombinant protein subunit vaccines are inherently safer but are often weakly immunogenic and require adjuvants and/or specialized delivery systems to induce protective immunity.

One such delivery system is liposomes, which were identified as a potential drug delivery platform in the 1970s. However, the discovery that liposomes preferentially target tissue macrophages (5) highlighted their potential also as a vaccine delivery system (6, 7). Subsequently, they have been used in the context of both bacterial (8, 9) and viral infections (10) and even in cancer immunotherapies (11). An attractive characteristic of the liposomal delivery platforms is that they can shelter antigens from degradation, promote phagocytosis by antigen-presenting cells (APCs) (7) and induce phagosome-cytosol cross-presentation pathway of antigenic peptides on MHC Class I molecules (12, 13).

The apoptotic body-like liposomes (ABLs, Figure 1A) used in the present study are prepared from phosphatidylserine (PS), rendering them similar to apoptotic bodies. PS is hydrophilic and appears on the surface of early apoptotic cells (14); this “flags up” the dying cells as a target for APCs such as macrophages and dendritic cells (DC) (15, 16). It is thought that this phenomenon can augment the presentation of the antigens by APCs, leading to improved T cell responses (17). As a cell initiates apoptosis, the PS normally situated on the inner face of the lipid bilayer of the cell membrane is exposed (14). PS is implicated in the detection of apoptotic cells by its interaction with Tim4 and Tim1 on APC, which facilitates phagocytosis (18).

FIGURE 1
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Figure 1. Encapsulation and stability of PS/PS liposomes and their physical characteristics. The stability of PS liposomes carrying Alexafluor488-BSA was assessed for fluorescence intensity by flow cytometry and size distribution by Malverin Zetasizer, immediately and after 30 days from liposome generation and storage at 4°C. (A) Schematic showing PS/PS liposome encapsulating an antigen. (B) Overlay of flow cytometry histogram plots of AF488-BSA loaded liposomes with “empty” liposomes over time. Gray corresponds to empty liposomes while green corresponds to AF488-BSA liposomes after 30 days storage at 4°C. (C) Size distribution measured by Zetasizer of Ag85B-loaded liposomes following 30 day storage at 4°C.

We therefore hypothesized that the PS associated antigens will similarly be taken up by professional APCs resulting in their cross-presentation and amplification of the immune response. Here, we present the evidence for the utility of this vaccine delivery system by demonstration that liposomally encapsulated Mtb antigens can enhance BCG-afforded protection against tuberculosis infection in mice.

Materials and Methods

Generation of PS Liposomes

Briefly, the inner monolayer lipid was prepared by suspending phosphatidylserine (PS, Avanti Polar Lipids) in 1 ml of anhydrous dodecane at the concentration of 0.2 mg/ml, sonication for 30 min and overnight incubation. The following day, 10 μg of Ag85B, or ESAT-6 (Lionex Diagnostics and Therapeutics), or bovine serum albumin conjugated to Alexafluor488 (AF488-BSA), Alexafluor647 (AF647) (Molecular Probes) or ovalbumin conjugated to BODIPY® FL [500 μg/ml] (DQ-OVA), were added to inner monolayer lipid suspension and sonicated until a homogeneous solution was obtained. The inner monolayer lipid for empty control liposomes was prepared using the same buffer used to suspend the respective antigen. The outer lipid monolayer was prepared by suspending PS in 99:1 dodecane: silicone solution to get a lipid concentration of 0.05 mg/ml. Thereafter, 2 ml of outer monolayer lipid suspension was added to 3 ml of 0.9% NaCl solution. Finally, the inner monolayer lipid suspension was added to 2 ml lipid phase and the sample was centrifuged at 120 × g for 10 min. After the centrifugation, liposomes were collected in the aqueous phase using a 5 ml syringe with a 16-gauge stainless steel needle. Liposomes were quantified and characterized in terms of dimensions as described (19). To determine antigen recovery following encapsulation, liposomes were dialysed against a 100 kDa membrane (Float-A-Lyzer® G2, Spectrum Labs), according to manufacturer's instructions. Encapsulated antigen was then quantified by CBQCA Protein Quantitation Kit (C-6667 Molecular Probes) according to manufacturer's instructions by fluorimetric analysis (Thermofisher VARIOSKAN LUX). The schematic representation of liposomes with encapsulated antigen is shown in Figure 1A. For the final vaccine formulation, equal numbers of Ag85B and ESAT-6 encapsulating liposomes were combined to generate the Lipo-AE vaccine candidate.

Generation of Human DC

Human blood monocytes from healthy volunteers were separated from peripheral blood mononuclear cells (PBMCs), by using anti-CD14 monoclonal antibodies conjugated to magnetic microbeads (Miltenyi Biotec), according to manufacturer's instructions. To obtain immature dendritic cells (iDc), cells were suspended in complete medium (RPMI 1640 supplemented with 10% fetal bovine serum, 2 mM L-Glutamine and 5 μg/ml Gentamicin) and incubated for 5 days in 24-well plates at the concentration of 5 ×105 cells/well in the presence of 20 ng/mL GM-CSF (Sigma-Aldrich) and 20 ng/mL IL-4 (Miltenyi Biotec). To obtain mature dendritic cells (mDC), iDCs were further stimulated for 18 h with 100 ng/ml lipopolysaccharides (Sigma-Aldrich).

Flow Cytometry Analysis of Stability and Antigen Delivery by PS Liposomes

The stability of PS liposomes loaded with AF488-BSA was assessed in terms of fluorescence intensity immediately and at 30 days after their preparation by flow cytometry analysis. Antigen internalization was analyzed after incubation of immature (iDC) or mature DC (mDC) with PS liposomes loaded with bovine serum albumin conjugated to Alexafluor647 (BSA-AF647) (Molecular Probes), at the ratio liposome: cell of 5:1, for 1 h at 37°C. Antigen processing was evaluated in iDC after exposure to ovalbumin conjugated to BODIPY® FL (DQ-OVA), a self-quenched conjugate that exhibits bright green fluorescence upon proteolytic processing and red fluorescence upon accumulation of proteolysed fragments in endosomal compartments. The analyses were performed by a FACSCalibur flow cytometer (Becton Dickinson).

Confocal Microscopy Analysis of Antigen Processing in Dendritic Cells

Briefly, iDC were stained with the nucleic acid stain Hoechst (Molecular Probes) and the acidophilic dye Lysotraker Red (Molecular Probes) for 15 min at 37°C. Thereafter, cells were washed with PBS, and exposed to PS liposomes loaded with AF488-BSA at the ratio 5:1 (liposome:cell) for 90 min at 37°C. The analysis was performed by a confocal laser scanning microscope IX 81 and OLYMPUS FV1000 operating system.

Animals

All animals were used with approval from St. George's University of London Ethics Committee under an approved UK Home Office animal project license and used in accordance with the Animals (Scientific Procedures) Act 1986. 8–10 weeks old female C57BL/6 mice were used for this study and were obtained from Charles River, UK. Animal work was conducted at St. George's University of London Biological Research Facility in accordance with local guidelines, including approval from the St. George's University of London Research Ethics Committee and national legislation, the Animals in Scientific Procedures Act, 1986. All procedures were performed under the approved UK Home Office animal project license.

Recombinant Proteins

Ag85B and ESAT-6 antigens of Mtb were produced in E. coli by Lionex company (Braunschweig, Germany) using the standard cloning techniques and the IPTG-inducible expression vector pLEXWO481. Recombinant proteins were isolated from inclusion bodies after denaturation in 8 M urea using metal chelate chromatography (Ni-NTA Superflow, Qiagen) and subsequent refolding by dialysis. Purity was assessed by SDS-PAGE (>97% purity) and identity confirmed by Western blots specific for antigens. Endotoxin content was measured by LAL assay and determined to be <5 I.U./mg.

Immunizations

Mice were first immunized subcutaneously at the base of the tail with 5 ×105 CFU BCG Pasteur in 0.1 ml or a matched volume of phosphate saline solution (Sigma) as a control. Ten weeks later, mice received 0.1 ml of Lipo-AE formulation (containing ~106 liposomes, 1 μg of Ag85B and 0.2 μg ESAT-6) also by s.c. injection at the base of the tail and then 3 weeks later a further intranasal inoculation of 0.05 ml of the same formulation, while under light anesthesia. All Lipo-AE immunizations included 20 μg/per dose of poly(I:C) as the adjuvant. Further details of the dosing regimen are given in the corresponding figure legends.

Low-Dose Aerosol Mtb Infection and Bacterial Enumeration

Mice were infected 4 weeks after the final immunization by aerosol with Mtb (H37Rv strain) at a low dose of ~200 bacilli per animal. The dose was delivered by nose only exposure using the Biaera aerosol generator controlled by the AeroMP software (Biaera Technologies) and housed in a dedicated Containment Level 3 (CL3) laboratory at Biological Research facilities at St. George's. Mice were left infected for 4 weeks before culling and bacterial enumeration in the lungs and spleens. The organs were homogenized in 3 ml of 0.1% Triton x-100 using the Precellys equipment. Serial dilutions of the homogenate were prepared and plated on Middlebrook 7H11 plates supplemented by OADC (Becton Dickinson) and bacterial colonies counted 3 weeks later. The pathogenic Mtb in vitro work was performed in the CL3 TB suite at the Institute for Infection and Immunity at St. George's.

Mucosal Antibody Responses

IgG and IgA in bronchoalveolar lavage (BAL) specific for antigens was measured by ELISA. Antigens (Ag85B or ESAT-6, Lionex) at 2 μg/ml were used to coat the wells of an ELISA plate. After washing with PBS 0.05% v/v Tween-20 and blocking with PBS 1% w/v BSA, 0.05% v/v Tween-20, samples were added in 3-fold dilutions. Specific IgG and IgA were detected with alkaline phosphatase conjugated anti-mouse IgG (Jackson Immunoresearch) and anti-mouse IgA (Sigma), respectively, and the substrate SigmaFast p-nitrophenyl phosphate (Sigma). Triplicate assays were read at 450 nm on a Tecan200 plate reader and data plotted as relative antibody titers as described in Hart et al. (20).

T Cell Proliferation, Cytokine Production, and Lung Trm

T cell proliferation was assessed by measuring the incorporation of radio-labeled thymidine [3H] after stimulation of splenocytes with recall antigens. Erythrocyte-depleted splenocytes were seeded at 1.5 ×105/well in complete RPMI 1640 medium supplemented with 10% FBS and stimulated with 5 μg/ml antigen or 1 μg.ml ConA as the positive control. After 48 h incubation, 1 μiCi of 3H-thymidine (PerkinElmer, Wallac, UK) was added before a further 24 h incubation. Cells were harvested with the Harvester 96 (TomTec Life Sciences, Hamdem, USA) onto Printed Filtermat paper (PerkinElmer) prior to the addition of melted wax (MeltiLex TM A. PerkinElmer) onto each scintillation sheet. Radioactive counts per minute (cpm) were measured using the 1,450 Microbeta Plus-Liquid Scintillation Counter (PerkinElmer).

For phenotypic analysis of proliferating T cells, splenocytes were stimulated with 5 μg/mL Ag85B or 1 μg/mL α-CD3 (Biolegend) for 5 days, followed by surface staining with CD4-PerCP/Cy5.5, CD8-Brilliant Violet 510, CD44-FITC, CD62L-PE, and CD90.2-Brilliant Violet 421—all from Biolegend. Cells were then fixed and permeabilized using the eBioscience Foxp3/Transcription Factor Staining Buffer Set and stained with Ki67-APC. Example of gating strategy is shown in Supplemental Figure S1.

Culture supernatant cytokine levels were measured using the mouse LegendPlexTM kit (Biolegend) according to the manufacturer's instructions. Samples were acquired on a BD FACSCalibur, and data analyzed using the proprietary data analysis software (Biolegend).

For detection of lung resident memory T cells (Trm), lungs were perfused of blood by flushing PBS through the right ventricle. Tissue was then dissected into 1 mm pieces using a scalpel, followed by digestion in 1 mg/mL collagenase and 0.5 mg/mL DNase I (Roche). Cells were then passed through a 70 μm strainer (Becton Dickinson), contaminating erythrocytes were lysed, and mononuclear cells were stained for CD3-APC, CD4-PerCP/Cy5.5, CD8-Brilliant Violet 510, CD44-FITC, CD62L-PE, CD69-PE/Cy7, and CD103-Brilliant Violet 421—all from Biolegend. Gating strategy as in Hart et al. (20).

Sample Size, Data Presentation, and Statistical Analysis

For animal experiments, sample size calculations for Mtb challenge studies were based on anticipated magnitude of vaccine effect as 1 Log10 reduction of CFU, the intragroup variability of 0.5 Log10 and a confidence level of 95%. This necessitated 6 mice per group but due to protracted nature of experiments seven were used per group. For immunological evaluation three mice per group were used and data expressed as arithmetic means ± standard error. Two in vivo experiments were performed with similar outcomes with the dataset from one experiment shown in full in Figures 37, and only Mtb challenge data from the second experiment shown in the Supplemental Information. For all experiments based on multiple test groups, One-way ANOVA was performed followed by Dunnett's multiple comparison test. Further details of statistical analyses are described in the relevant figure legends. All analysis was performed using FlowJo v10, Microsoft Excel 2010 and GraphPad Prism 7.

Results

Biophysical Characterization and Uptake Analysis of PS Liposomes

Stability is an important issue to be addressed during the generation of novel liposome based vaccine formulations in order to ensure efficient antigen delivery (21). This issue has been addressed by monitoring the kinetics of the encapsulation of fluorescently labeled AF488-BSA, used as a model antigen. The analysis performed by flow cytometry and illustrated in Figure 1B shows that liposomes with encapsulated AF488-BSA remain stably fluorescent up to 30 days upon generation and storage at 4°C. Then, we encapsulated PS liposomes with mycobacterial antigens (Ag85B and ESAT-6) and further tested the physical properties of the novel liposome formulation in terms of size distribution by a Malverin Zetasizer. Results shown in Figure 1C indicate that the formulation was largely homogenous with an average size of the liposomes ~240 nm.

An antigen delivery system should ideally target APC and promote uptake and processing in dendritic cells (DC). Thus, we preliminarily determined whether PS liposome formulation, encapsulated with AF647-BSA, were efficiently internalized by immature and mature human DC. In order to avoid the contribution of free antigen, liposome formulations were dialyzed against a 100 kDa membrane to remove non-encapsulated antigen. Figure 2A shows that the majority of cells became fluorescent after exposure to the liposome formulation, suggesting that most of the cells have taken up the antigen. Moreover, in order to establish whether the antigen was efficiently processed by APC, iDC were exposed to PS liposomes loaded with AF488 BSA and analyzed by confocal microscopy after staining with the acidofilic dye lysotraker red. Results shown in Figure 2B show co-localization of liposomal AF488-BSA with acid compartments. Finally, as acidification of endosomal compartments is a prerequisite for protease activation and the final antigen degradation, we encapsulated PS liposomes with DQ-OVA, which is a fluorogenic substrate for proteases, and monitored fluorescence emission following liposome internalization in iDC. Figure 2C shows 75% of cells exhibiting green fluorescence, as a consequence of proteolytic processing of the protein, and about 23% of cells displaying green/red double fluorescence, indicating endosomal accumulation of the processed antigen. Altogether, these results show that PS/PS liposomes may efficiently deliver the antigen cargo to DC and favor subsequent antigen processing.

FIGURE 2
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Figure 2. Antigen internalization and processing in human DC after delivery by PS liposome. (A) Immature and mature DC cells were exposed to dialyzed PS liposomes loaded with AF647-BSA to a ratio of 5:1 for 1 h. Analysis was performed by flow cytometry. (B) Immature DC cells were stained with the nucleic acid stain Hoechst and the acidophilic dye Lysotraker Red and stimulated with PS liposomes loaded withAF647-BSA at the ratio 5:1 for 90 min. A representative image from over many taken by confocal microscopy, is shown. Sample analysis indicated majority of cells positively stained with ~23% strongly positive for both stains. (C) Immature DC cells were exposed to PS liposomes loaded with DQ-OVA or to empty liposomes at a ratio of 5:1 for 1 h. Red and green fluorescence was evaluated by flow cytometry. A representative experiment with cells from one, out of three, healthy donors is shown.

Lipo-AE Enhanced BCG Mediated Protection Against Mtb

In our Mtb infection experiment, BCG afforded ~8-fold reduction in the lung and spleen bacterial load (Figure 3), at 4 weeks after the aerosol challenge. Boosting BCG with Lipo-AE imparted additional statistically significant reduction of the bacterial load in both organs sets. The Mtb challenge experiment was performed twice and in both instances the Lipo-AE vaccine candidate conferred additional statistically significant protection over BCG alone, though in one of the experiments the non-immunized animals group showed greater than expected intragroup variability (Supplemental Figure S2).

FIGURE 3
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Figure 3. Reduced Mtb infection in Lipo-AE immunized mice. Four weeks after the final immunization, mice were challenged with aerosolised Mtb and then 4 weeks later culled and organs harvested for bacterial enumeration. Each point corresponds to log CFU value for the individual animals (n = 7). (A) Schematic depicting immunization and Mtb infection schedule. (B) CFU in the lungs and spleens. The horizontal bars represent the mean for each group ± SEM. Log transformed data were analyzed using a 1-way ANOVA and a Dunnett's multiple comparison test comparing all groups to the BCG control or comparing Lipo-AE with empty liposomes (Lipo); *P ≤ 0.05, **P ≤ 0.01, ****P ≤ 0.0001.

Lipo-AE Induced Mucosal Antibodies and T Resident Memory Cells (Trm) in Lungs

To measure mucosal responses induced by the vaccine, antibody levels post-immunization were assessed in bronchoalveolar lavage (BAL). BAL collected 3 weeks after final immunization from animals that received Lipo-AE showed similar levels of IgG but higher levels of IgA specific to Ag85B (Figure 4A), compared to BCG immunization alone. No detectable anti-ESAT-6 antibodies were present in either group (not shown).

FIGURE 4
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Figure 4. Mucosal antibody responses and lung Trm induced by Lipo-AE. (A) Levels of anti-Ag85B specific BAL IgG and IgA determined by antigen-specific ELISA. Each bar corresponds to the mean of triplicate samples from 3 animals from each group ± SEM. The set of bars represent 3-fold serial dilutions from the starting neat sample. Average end point titres are indicated above the bars. (B) Analysis of the lung resident memory T cell populations. Except for the PBS group, animals were vaccinated with BCG sc and then with Lipo-AE or empty liposomes, both containing PolyIC, as described in Methods. Cells isolated from the lungs of immunized animals were stained and analyzed by flow cytometry to determine the Trm populations. The gating strategy used was cells -> single cells -> live cells -> CD3+ -> CD4+/CD8+ -> CD44 high/CD62Llow and the CD69/CD103 double positive Trm presented. Data originated from n = 3 pooled animals and a representative plot is shown.

Upon observing mucosal antibody responses induced by Lipo-AE, we investigated for evidence of cellular immunity. We were particularly interested if there was evidence of T cell resident memory (Trm) in the lungs and used flow cytometry to quantify these cells in the lung homogenates. Prior to harvest, the lungs were perfused to reduce blood contamination. The harvested lungs were then treated and mechanically disrupted to isolate the cells, which were stained for Trm phenotype (Figure 4B). The top and bottom panels represent CD4 and CD8 compartments, respectively. As depicted in the flow plots the total numbers of Trm as defined by the phenotype CD44 high/CD62L low were very low for the BCG immunized animals, and this was true for both the CD4 and CD8 compartments. In stark contrast, there was a significant increase in Trm populations in the Lipo-AE group for both T cell compartments, increasing from 2.04 in the BCG group to 13.22 in the Lipo-AE groups for CD4+ and from 1.50 to 8.16 for CD8+ T cells, respectively (Figure 4B). Naïve animals showed only background levels of Trm. Although our analysis was restricted to total and not antigen-specific Trm in the lungs, together with the evidence of specific antibodies to Ag85B, it indicates the presence of a mucosal immune response in the lungs of immunized animals.

Splenic T Cell Proliferation and Polyfunctional T Cells

We then tested splenocyte proliferation in response to recall antigens as measured by incorporation of radiolabelled thymidine. As shown in Figure 5A, splenocytes from Lipo-AE immunized animals proliferated robustly in response to Ag85B, with a stimulation index of 22, but only modest level of proliferation was observed for ESAT-6, with a stimulation index of 4. Cells from the PBS and BCG groups did not proliferate in response to any of the stimuli. Since liposomes are thought to enhance cross priming and elicit CD8+ T cell responses, T cell proliferation in the CD8+ compartment was additionally investigated by the measurement of Ki67+ cells. Stimulation with Ag85B but not ESAT-6 induced high levels of proliferation in the CD8+ T cell population with most of the proliferating cells being of the CD62Llow/ CD44High phenotype (Figure 5B). Furthermore, since Lipo-AE induced T cell proliferation (Figure 5A), we speculated that T cell-associated cytokines were also being elicited. To test this, splenocyte culture supernatants were analyzed with a beads-based multiplex immunoassay. The analytes tested were IFN-y (Figure 5C), IL-10 (Figure 5D), IL-17 (Figure 5E), and IL-4 (Figure 5F). Stimulation with Ag85B as a recall antigen induced high levels of all cytokines, reflecting a mixed T cell response with the production of Th1 (IFN-y), Th2 (IL-4), and a Treg cytokines (IL-10 and IL-17), with the latter characteristic of Th17 responses. BCG vaccination resulted in minimal cytokine production in these assays.

FIGURE 5
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Figure 5. Cellular immune response induced by Lipo-AE. (A) Antigen specific splenocyte and T cell proliferation. Splenocytes harvested from immunized animals were stimulated with Ag85B (blue) o ESAT-6 (red) as the recall antigens and media alone as the negative control, and proliferative responses were then measured by radiolabelled thymidine incorporation. Vertical bars represent the stimulation indices (stimulation index = antigen specific radioactive counts per minute/background radioactive counts per minute). (B) CD8 T cell proliferation. Splenocytes were stimulated with the recall antigens and the CD8+ Ki67+ cells identified. The gating strategy used was cells -> single cells -> live cells -> CD90.2+ -> CD8+ -> KI67+ and CD44/CD62L cells. The bars represent the percent of CD8+ cells that are Ki67+ and are broken down based on memory marker phenotype. (D,E,F) Cytokine production following antigen recall assay. Splenocyte stimulation culture supernatants were collected and assayed for cytokine presence by. Legendplex: IFN-y (C), IL-10 (D), IL-17 (E), and IL-4 (F). Bars depict means pg/ml ± SEM, with *indicating statistically significant values above the background (P < 0.05).

Splenocytes from Lipo-AE immunized animals displayed low level ESAT-6 responses (not shown) but stimulation with Ag85B resulted in a significant number of cytokine producing CD4+ (1.77%) and CD8+ (0.45%) T cells (Figures 6A,F). In the CD4+ T cell compartment, 1.63% of those cells produced IFN-γ, 1.17% IL-2, and 1.76% TNF-α (Figure 6B). Lipo-AE also induced the highest number of polyfunctional T cells producing three or more of the measured cytokines simultaneously with 1.13% of cells in this category (Figure 6C). A large portion of these cells (1.13%) were triple producers, producing INF-γ, IL-2, and TNF-α simultaneously, with a further population (0.51%) double producers of IFN-γ and TNF-α (Figure 6D). Of the cytokine producing cells, most were triple producers (64%) with 31% producing two cytokines and 5% producing only one of the measured cytokines (Figure 6E).

FIGURE 6
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Figure 6. Polyfunctional T cell responses induced by Lipo-AE. Splenocytes isolated from immunized animals were stimulated with Ag85B and the production of IFN-γ, IL-2, IL-17A, and TNF-α measured by intracellular cytokine staining and flow cytometry. (A,F) Proportion of CD4 and CD8 positive cells producing cytokines. (B,G) Proportion of CD4 and CD8 cells expressing each individual cytokine. (C,H) Proportion of CD4 abd CD8 cells producing at least 3 or 4 cytokines. (D,I) Polyfunctional CD4 and CD8 T cells phenotype by cytokine combinations. (E,J) Frequency of single or multiple cytokine producing CD4 and CD8 T cells as a proportion of all antigen specific cells. Gating strategy was the same as in our recent report (20).

FIGURE 7
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Figure 7. Analysis of the lung resident memory T cell populations. Except for the PBS group, animals were vaccinated with BCG sc and then received one s.c. and one i.n. administration of Lipo-AE or empty PS/PS liposomes with PolyIC. Cells isolated from the lungs of immunized animals were stained and analyzed by flow cytometry to determine the Trm populations. The gating strategy used was cells -> single cells -> live cells -> CD3+ -> CD4+/CD8+ -> CD44 high / CD62Llow and the CD69/CD103 double positive Trm presented. Data originated from n = 3 pooled animals and a representative plot is shown.

A similar picture was observed in the CD8+ T cell compartment, where Lipo-AE group splenocytes had the highest number of cytokine producing cells, with 0.11% producing IFN-γ and 0.32% producing IL-17A. The highest number of polyfunctional cells producing 3 or more cytokines simultaneously was also found in the Lipo-AE group (0.036%).

Stimulation with Ag85B resulted in 0.04% of CD8+ T cells producing IFN-γ, IL-2, and IL-17A, with high levels of single cytokine producing cells for IFN-γ, 0.12%, and IL-17A, 0.30%. Of the cytokine producing cells the majority were single producers (92%) with a small proportion of triple producers (8%).

Discussion

Liposomes have been tested in the context of systemic immunizations but also as oral vaccine vehicles (22, 23). Despite their relative instability, liposomes were shown to be robust enough to survive oral delivery to the intestinal lumen and enhance the antigen presentation (24). Indeed, our own stability experiments showed that the liposomes used in this study are stable for at least 30 days. Subsequent Zetasizer analysis also demonstrated that the formulation was still homogeneous and the size of the liposomes remained unchanged at ~200 nm.

The mucosal delivery of liposomes in vivo has been tested extensively through the oral route (22, 25) and also through the intranasal route (26). A comparison between the two routes in terms of ability to induce long term local immune responses seemed to favor the intranasal route (24). Here we demonstrate the ability of a novel liposome formulation to protect against Mtb infection when delivered first subcutaneously and then intranasally. This vaccine strategy was explored as a heterologous immunization approach on a BCG background. In human population, boosting BCG would make use of the large number of already immunized individuals whilst taking advantage of protective properties of BCG against severe forms of childhood TB.

Immunization of mice with BCG reduced the burden of infection significantly in the lungs and spleens in comparison to unvaccinated animals in a low dose aerosol challenge model. This protection afforded by BCG was further increased by boosting with Lipo-AE and this added protection was found to be statistically significant in both the lungs and spleens. Upon observing enhancement of protection conferred by Lipo-AE the immunological profile induced by the vaccine was studied. Other pre-clinical studies demonstrated that liposomes promoted antibody and cell mediated immunity to a wide range of bacterial, protozoan, and viral antigens as well as tumor cell antigens, venoms and allergens and even live or attenuated microbial vaccines (6). With regards to cellular immunity, we observed that stimulation of splenocytes from vaccinated animals with a recall antigen induced high levels of IFN-y. IgG and IgA specific to Ag85B was also detected by ELISA in BAL indicating the vaccine had also successfully primed the B cells in the mucosa.

With the view of elucidating further what immune mechanisms could be behind the observed protection we further investigated the cellular profiles induced. A cell proliferation assay revealed that splenocytes isolated from Lipo-AE vaccinated animals in culture proliferated in response to Ag85B and to a lesser extent to ESAT-6. These cells produced high amounts of IFN-y in response to Ag85B stimulation. IFN-y is considered essential for resistance to tuberculosis infection (27, 28). However, despite IFN-y being required for protection a number of studies have suggested that other mechanisms may also be needed for protection (29) and the magnitude of IFN-y response alone is not a reliable correlate of protection (30, 31).

Splenocytes were also found to produce IL-10, which has an ambiguous role in TB, with some reports showing that it is undesirable (32) while other suggesting that it can convert human DCs into macrophage like cells that have increased antibacterial activity against Mtb (33). Intriguingly, high levels of IL-17A were also detected in response to Ag85B and to a lesser extent to ESAT-6 in splenocyte cultures from Lipo-AE vaccinate animals. Whilst the role of IL-17 in Mtb infection is not clearly defined it has been reported that its induction after vaccination could be beneficial. Thus, Khader et al. hypothesized that IL-17 producing CD4+ T cells occupy the lung after infection and elicit the production of chemokines that attract IFN-y secreting CD4+ T cells resulting in better control of infection (34).

Thus, the cytokine profile characterized by high IFN-y and IL-17A with low levels of IL-10 observed here could be the key to enhanced protection. IL-10 produced by vaccine-induced Tregs could limit collateral damage within the lung. It was suggested that granulomas depended on a balance of inflammatory and anti-inflammatory cytokines in order to effectively control bacteria (35). This concept was validated in the Rhesus macaque model, where sterile granulomas were associated with a balance of IFN-y/IL-17A and IL-10 in contrast to the non-sterile granulomas that featured a predominantly inflammatory response lacking IL-10 (36). Finally, evidence from T. gondii model of infection has shown that multifunctional IL-10-producing Th1 cells retain their ability to activate intracellular killing mechanisms in macrophages, and in fact are superior to conventional IL-10 negative Th1 cells at inducing macrophage nitrite (NO) production (37). Given that we observed modest IL-10 and even lower IL-4 production alongside potent Th1/Th17 responses, we therefore conclude that the vaccine induced a strong Th1-Th17 response with only modest Th2-Treg activity and this may have contributed to the protection observed.

The superior immunogenicity of Ag85B over ESAT-6 has also been observed in other studies where both antigens were used together (38, 39), Ag85B is known to be one of the most immunogenic TB antigens whilst ESAT-6 is weakly immunogenic. Nevertheless, both antigens have been previously shown to be protective, particularly when used in combination (38, 39).

Ichihashi et al showed that PS could deliver antigens to APCs resulting in the stimulation of helper and cytotoxic T cell responses in vivo (17). In keeping with those observations, a flow cytometry assay measuring Ki67 expression indicated that the CD8 T cells from the Lipo-AE group proliferated robustly in response to Ag85B antigen and had a CD62LLow/CD44High phenotype.

CD4+ T cell responses to aerosol Mtb challenge are characterized by a delayed recruitment of effector T cells in the lungs, potentially hampering the host's response to infection and permitting the bacteria to establish a persistent infection (40). The rationale behind the heterologous systemic prime mucosal boost strategy was to elicit a robust systemic response with a strong mucosal component to challenge the pathogen on entry. Recently, tissue-memory resident T (Trm) cells have become topical in the field. Thus, Perdomo et al demonstrated that mucosal but not subcutaneous, BCG immunization generates lung resident memory T cell populations that mediate protection against TB (41). We established that Lipo-AE given mucosally could generate Trm, characterized as CD69+CD103+ memory T cells in the lung parenchyma. These cells were found to belong to both CD4 and CD8 compartment and are likely to be antigen specific, though we have no formal evidence of their antigen specificity as we did not have appropriate MHC tetramers to confirm this.

In conclusion, boosting BCG with Lipo-AE mediated enhanced immunity and protection over that afforded by BCG alone. This vaccine delivery platform is well-suited for TB but the liposomal system can be adapted to suit other diseases and recently the first ever liposomes-adjuvanted vaccine was licensed indicated for malaria (42, 43), while a therapeutic vaccine candidate RUTI formulated in liposomes is currently in clinical trials (44). This underscores the potential of liposome technology as an attractive vaccine delivery system.

Data Availability

The datasets generated for this study are available on request to the corresponding author.

Ethics Statement

This study was carried out in accordance with the recommendations of UK Home office and St. George's Ethics committee, The protocol was approved by the St. George's University of London.

Author Contributions

GD, AC, and PH performed all immunization and Mtb infection experiments, as well as key immunological analyses. M-YK performed bronchoalveolar antibody analysis. AT performed statistical analysis. NP generated Lipo-AE and performed APC experiments. MP contributed to processing of tissues and setting up CFUs. MS provided antigens. MF conceived the potential use of liposomes as a vaccine delivery platform. GD, MF, and RR co-wrote the manuscript.

Funding

European Commisson. This work was supported by the European Community H2020 Grant No 643558.

Conflict of Interest Statement

MS was employed by company Lionex GmBH.

The remaining 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.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2019.01349/full#supplementary-material

References

1. Churchyard G, Kim P, Shah NS, Rustomjee R, Gandhi N, Mathema B, et al. What we know about tuberculosis transmission: an overview. J Infect Dis. (2017) 216:S629–35. doi: 10.1093/infdis/jix362

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Ottenhoff TH, Kaufmann SH. Vaccines against tuberculosis: where are we and where do we need to go? PLoS Pathog. (2012) 8:e1002607. doi: 10.1371/journal.ppat.1002607

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Rodrigues LC, Pereira SM, Cunha SS, Genser B, Ichihara MY, De Brito SC, et al. Effect of BCG revaccination on incidence of tuberculosis in school-aged children in Brazil: the BCG-REVAC cluster-randomised trial. Lancet. (2005) 366:1290–5. doi: 10.1016/S0140-6736(05)67145-0

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Roth AE, Benn CS, Ravn H, Rodrigues A, Lisse IM, Yazdanbakhsh M, et al. Effect of revaccination with BCG in early childhood on mortality: randomised trial in Guinea-Bissau. BMJ. (2010) 340:c671. doi: 10.1136/bmj.c671

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Ellens H, Morselt H, Scherphof G. In vivo fate of large unilamellar sphingomyelin-cholesterol liposomes after intraperitoneal and intravenous injection into rats. Biochim Biophys Acta. (1981) 674:10–8. doi: 10.1016/0304-4165(81)90341-X

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Gregoriadis G. Immunological adjuvants: a role for liposomes. Immunol Today. (1990) 11:89–97. doi: 10.1016/0167-5699(90)90034-7

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Wassef NM, Alving CR, Richards RL. Liposomes as carriers for vaccines. Immunomethods. (1994) 4:217–22. doi: 10.1006/immu.1994.1023

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Lachman LB, Ozpolat B, Rao XM. Cytokine-containing liposomes as vaccine adjuvants. Eur Cytokine Netw. (1996) 7:693–8.

PubMed Abstract | Google Scholar

9. Fulton SA, Cross JV, Toossi ZT, Boom WH. Regulation of interleukin-12 by interleukin-10, transforming growth factor-beta, tumor necrosis factor-alpha, and interferon-gamma in human monocytes infected with Mycobacterium tuberculosis H37Ra. J Infect Dis. (1998) 178:1105–14. doi: 10.1086/515698

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Ambrosch F, Wiedermann G, Jonas S, Althaus B, Finkel B, Gluck R, et al. Immunogenicity and protectivity of a new liposomal hepatitis A vaccine. Vaccine. (1997) 15:1209–13. doi: 10.1016/S0264-410X(97)00015-7

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Kwak LW, Pennington R, Boni L, Ochoa AC, Robb RJ, Popescu MC. Liposomal formulation of a self lymphoma antigen induces potent protective antitumor immunity. J Immunol. (1998) 160:3637–41.

PubMed Abstract | Google Scholar

12. Kovacsovics-Bankowski M, Rock KL. A phagosome-to-cytosol pathway for exogenous antigens presented on MHC class I molecules. Science. (1995) 267:243–6. doi: 10.1126/science.7809629

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Sigal LJ, Crotty S, Andino R, Rock KL. Cytotoxic T-cell immunity to virus-infected non-haematopoietic cells requires presentation of exogenous antigen. Nature. (1999) 398:77–80. doi: 10.1038/18038

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Fadok VA, Voelker DR, Campbell PA, Cohen JJ, Bratton DL, Henson PM. Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages. J Immunol. (1992) 148:2207–16.

PubMed Abstract | Google Scholar

15. Tanaka Y, Schroit AJ. Insertion of fluorescent phosphatidylserine into the plasma membrane of red blood cells. Recognition by autologous macrophages. J Biol Chem. (1983) 258:11335–43.

PubMed Abstract | Google Scholar

16. Schlegel RA, Williamson P. Phosphatidylserine, a death knell. Cell Death Differ. (2001) 8:551–63. doi: 10.1038/sj.cdd.4400817

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Ichihashi T, Satoh T, Sugimoto C, Kajino K. Emulsified phosphatidylserine, simple and effective peptide carrier for induction of potent epitope-specific T cell responses. PLoS ONE. (2013) 8:e60068. doi: 10.1371/journal.pone.0060068

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Miyanishi M, Tada K, Koike M, Uchiyama Y, Kitamura T, Nagata S. Identification of Tim4 as a phosphatidylserine receptor. Nature. (2007) 450:435–9. doi: 10.1038/nature06307

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Greco E, Quintiliani G, Santucci MB, Serafino A, Ciccaglione AR, Marcantonio C, et al. Janus-faced liposomes enhance antimicrobial innate immune response in Mycobacterium tuberculosis infection. Proc Natl Acad Sci USA. (2012) 109:E1360–8. doi: 10.1073/pnas.1200484109

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Hart P, Copland A, Diogo GR, Harris S, Spallek R, Oehlmann W, et al. Nanoparticle-fusion protein complexes protect against Mycobacterium tuberculosis infection. Mol Ther. (2018) 26:822–33. doi: 10.1016/j.ymthe.2017.12.016

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Nisini R, Poerio N, Mariotti S, De Santis F, Fraziano M. The multirole of liposomes in therapy and prevention of infectious diseases. Front Immunol. (2018) 9:155. doi: 10.3389/fimmu.2018.00155

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Jackson S, Mestecky J, Childers NK, Michalek SM. Liposomes containing anti-idiotypic antibodies: an oral vaccine to induce protective secretory immune responses specific for pathogens of mucosal surfaces. Infect Immun. (1990) 58:1932–6.

PubMed Abstract | Google Scholar

23. Michalek SM, Childers NK, Katz J, Dertzbaugh M, Zhang S, Russell MW, et al. Liposomes and conjugate vaccines for antigen delivery and induction of mucosal immune responses. Adv Exp Med Biol. (1992) 327:191–8. doi: 10.1007/978-1-4615-3410-5_21

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Elson CO, Beagley KW, Sharmanov AT, Fujihashi K, Kiyono H, Tennyson GS, et al. Hapten-induced model of murine inflammatory bowel disease: mucosa immune responses and protection by tolerance. J Immunol. (1996) 157:2174–85.

PubMed Abstract | Google Scholar

25. Childers NK, Michalek SM, Denys F, Mcghee JR. Characterization of liposomes for oral vaccines. Adv Exp Med Biol. (1987) 216B:1771–80.

PubMed Abstract | Google Scholar

26. Romero EL, Morilla MJ. Topical and mucosal liposomes for vaccine delivery. Wiley Interdiscip Rev Nanomed Nanobiotechnol. (2011) 3:356–75. doi: 10.1002/wnan.131

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Flynn JL, Chan J, Triebold KJ, Dalton DK, Stewart TA, Bloom BR. An essential role for interferon gamma in resistance to Mycobacterium tuberculosis infection. J Exp Med. (1993) 178:2249–54. doi: 10.1084/jem.178.6.2249

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Reljic R. IFN-gamma therapy of tuberculosis and related infections. J Interferon Cytokine Res. (2007) 27:353–64. doi: 10.1089/jir.2006.0103

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Gallegos AM, Van Heijst JW, Samstein M, Su X, Pamer EG, Glickman MS. A gamma interferon independent mechanism of CD4 T cell mediated control of M. tuberculosis infection in vivo. PLoS Pathog. (2011) 7:e1002052. doi: 10.1371/journal.ppat.1002052

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Mittrucker HW, Steinhoff U, Kohler A, Krause M, Lazar D, Mex P, et al. Poor correlation between BCG vaccination-induced T cell responses and protection against tuberculosis. Proc Natl Acad Sci USA. (2007) 104:12434–9. doi: 10.1073/pnas.0703510104

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Sakai S, Kauffman KD, Sallin MA, Sharpe AH, Young HA, Ganusov VV, et al. CD4 T cell-derived IFN-gamma plays a minimal role in control of pulmonary Mycobacterium tuberculosis infection and must be actively repressed by PD-1 to prevent lethal disease. PLoS Pathog. (2016) 12:e1005667. doi: 10.1371/journal.ppat.1005667

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Redford PS, Murray PJ, O'garra A. The role of IL-10 in immune regulation during M. tuberculosis infection. Mucosal Immunol. (2011) 4:261–70. doi: 10.1038/mi.2011.7

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Fortsch D, Rollinghoff M, Stenger S. IL-10 converts human dendritic cells into macrophage-like cells with increased antibacterial activity against virulent Mycobacterium tuberculosis. J Immunol. (2000) 165:978–87. doi: 10.4049/jimmunol.165.2.978

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Khader SA, Bell GK, Pearl JE, Fountain JJ, Rangel-Moreno J, Cilley GE, et al. IL-23 and IL-17 in the establishment of protective pulmonary CD4+ T cell responses after vaccination and during Mycobacterium tuberculosis challenge. Nat Immunol. (2007) 8:369–77. doi: 10.1038/ni1449

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Wigginton JE, Kirschner D. A model to predict cell-mediated immune regulatory mechanisms during human infection with Mycobacterium tuberculosis. J Immunol. (2001) 166:1951–67. doi: 10.4049/jimmunol.166.3.1951

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Gideon HP, Phuah J, Myers AJ, Bryson BD, Rodgers MA, Coleman MT, et al. Variability in tuberculosis granuloma T cell responses exists, but a balance of pro- and anti-inflammatory cytokines is associated with sterilization. PLoS Pathog. (2015) 11:e1004603. doi: 10.1371/journal.ppat.1004603

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Jankovic D, Trinchieri G. IL-10 or not IL-10: that is the question. Nat Immunol. (2007) 8:1281–3. doi: 10.1038/ni1207-1281

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Dietrich J, Andersen C, Rappuoli R, Doherty TM, Jensen CG, Andersen P. Mucosal administration of Ag85B-ESAT-6 protects against infection with Mycobacterium tuberculosis and boosts prior bacillus Calmette-Guerin immunity. J Immunol. (2006) 177:6353–60. doi: 10.4049/jimmunol.177.9.6353

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Van Dissel JT, Soonawala D, Joosten SA, Prins C, Arend SM, Bang P, et al. Ag85B-ESAT-6 adjuvanted with IC31(R) promotes strong and long-lived Mycobacterium tuberculosis specific T cell responses in volunteers with previous BCG vaccination or tuberculosis infection. Vaccine. (2011) 29:2100–9. doi: 10.1016/j.vaccine.2010.12.135

CrossRef Full Text | Google Scholar

40. Reiley WW, Calayag MD, Wittmer ST, Huntington JL, Pearl JE, Fountain JJ, et al. ESAT-6-specific CD4 T cell responses to aerosol Mycobacterium tuberculosis infection are initiated in the mediastinal lymph nodes. Proc Natl Acad Sci USA. (2008) 105:10961–6. doi: 10.1073/pnas.0801496105

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Perdomo C, Zedler U, Kuhl AA, Lozza L, Saikali P, Sander LE, et al. Mucosal BCG vaccination induces protective lung-resident memory T cell populations against tuberculosis. MBio. (2016) 7:e01686–16. doi: 10.1128/mBio.01686-16

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Hawkes N. European medicines agency approves first malaria vaccine. BMJ. (2015) 351:h4067. doi: 10.1136/bmj.h4067

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Morrison C. Landmark green light for Mosquirix malaria vaccine. Nat Biotechnol. (2015) 33:1015–6. doi: 10.1038/nbt1015-1015

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Cardona PJ. RUTI: a new chance to shorten the treatment of latent tuberculosis infection. Tuberculosis. (2006) 86:273–89. doi: 10.1016/j.tube.2006.01.024

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: liposomes, tuberculosis, vaccine, BCG, immunity

Citation: Diogo GR, Hart P, Copland A, Kim M-Y, Tran AC, Poerio N, Singh M, Paul MJ, Fraziano M and Reljic R (2019) Immunization With Mycobacterium tuberculosis Antigens Encapsulated in Phosphatidylserine Liposomes Improves Protection Afforded by BCG. Front. Immunol. 10:1349. doi: 10.3389/fimmu.2019.01349

Received: 12 February 2019; Accepted: 28 May 2019;
Published: 12 June 2019.

Edited by:

Nahid Ali, Indian Institute of Chemical Biology (CSIR), India

Reviewed by:

Sylvie Fournel, Université de Strasbourg, France
Julio Alonso Padilla, Instituto Salud Global Barcelona (ISGlobal), Spain

Copyright © 2019 Diogo, Hart, Copland, Kim, Tran, Poerio, Singh, Paul, Fraziano and Reljic. 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: Rajko Reljic, rreljic@sgul.ac.uk

These authors have contributed equally to this work