key: cord-0820413-dqvgng2s
authors: Ohtsuka, Junpei; Fukumura, Masayuki; Furuyama, Wakako; Wang, Shujie; Hara, Kenichiro; Maeda, Mitsuyo; Tsurudome, Masato; Miyamoto, Hiroko; Kaito, Aika; Tsuda, Nobuyuki; Kataoka, Yosky; Mizoguchi, Akira; Takada, Ayato; Nosaka, Tetsuya
title: A versatile platform technology for recombinant vaccines using non-propagative human parainfluenza virus type 2 vector
date: 2019-09-09
journal: Sci Rep
DOI: 10.1038/s41598-019-49579-y
sha: e8fa6ff57f5e18b27fa9d70df3d3c90f4633264d
doc_id: 820413
cord_uid: dqvgng2s

Ectopic protein with proper steric structure was efficiently loaded onto the envelope of the F gene-defective BC-PIV vector derived from human parainfluenza virus type 2 (hPIV2) by a reverse genetics method of recombinant virus production. Further, ectopic antigenic peptide was successfully loaded either outside, inside, or at both sides of the envelope of the vector. The BC-PIV vector harboring the Ebola virus GP gene was able to elicit neutralizing antibodies in mice. In addition, BC-PIV with antigenic epitopes of both melanoma gp100 and WT1 tumor antigen induced a CD8+ T-cell-mediated response in tumor-transplanted syngeneic mice. Considering the low pathogenicity and recurrent infections of parental hPIV2, BC-PIV can be used as a versatile vector with high safety for recombinant vaccine development, addressing unmet medical needs.

Generation of BC-PIV/EBOV-GP. First, we generated EBOV vaccine using the full-length EBOV GP gene.

It should be noted that, depending on the property of the ectopically expressed envelope protein, the ability to proliferate in the non-propagative recombinant vector can be regained in the absence of the cognate envelope protein. This is what happens with EBOV-GP 7, 8 . However, double mutations 9,10 in the GP gene (F88A/F535A) completely abrogated the GP-mediated proliferation of the recombinant BC-PIV in vitro (Figs 2 and 3b) while retaining the antigenicity. In addition, mutations within the GP1 region were introduced to prevent RNA editing 11 without affecting the amino acid sequence (Fig. 3a,b) . The resultant vaccine BC-PIV/EBOV-GP incorporated a large amount of GP protein on the viral particles, as shown in the Western blot analysis (Fig. 1c) .

Consistent with previous reports [6] [7] [8] 12 , transmembrane and cytoplasmic regions of the envelope protein of the cognate virus are not necessarily required for the efficient incorporation of exogenous protein onto the virions compared with that of an authentic form of the exogenous protein (Figs 1c and 3c,d) . The band at around 100 kDa is weaker in the authentic EBOV-GP than in the hybrid form (extracellular domain: EBOV-GP, transmembrane domain and cytoplasmic tail: hPIV2 F), while the upper smear bands are much stronger in the authentic form than in the hybrid form. These differences may be derived from different levels of glycosylation of incorporated EBOV GP 13 . www.nature.com/scientificreports www.nature.com/scientificreports/ Visualization of the ectopically expressed antigen on the vector particle. Immunoelectron microscopy using an anti-EBOV-GP neutralizing monoclonal antibody recognizing a conformational epitope 14 in its trimeric, pre-fusion form showed that the native form of the GP protein is abundantly present on the viral surface (Fig. 4a) . Each colloidal gold corresponds to each molecule (GP1-GP2 heterodimer) of the GP protein.

Coiled ribonucleocapsid complex of hPIV2 is clearly visible inside the virion.

Induction of neutralizing antibody against EBOV. The ability of the EBOV vaccine to induce efficient humoral immunity (IgG 1 and IgG 2a ) in mice was revealed by an enzyme-linked immunosorbent assay measuring the specific antibody titer of the sera (>100,000 × dilution, data not shown) and a pseudotype virus-based inhibition assay 15 measuring the neutralizing antibody titer of the sera (Fig. 5a,b) . These titers were comparable to those induced by Ebola VLPs in mice 16 , or by chimeric hPIV3 bearing the EBOV GP in guinea pigs 8 . Antibodies elicited by BC-PIV/EBOV-GP also induced antibody-dependent enhancement (ADE) 17 of pseudotyped EBOV infection (Fig. 5c ). The ADE activities induced by BC-PIV/EBOV GP were also comparable to those induced by Ebola VLPs in mice 16 and those of the sera from monkeys that survived challenge with EBOV 16 . A sufficient neutralizing activity of the sera indicates that the ADE effects were overcome by the inhibitory effects of the sera in virus infection. Replication-competent vesicular stomatitis virus (VSV)/EBOV-GP was previously reported to protect against lethal EBOV challenge in nonhuman primates 7, 18 , thereby CD4+ T cell-depleted animals succumbed to EBOV infection due to a lack of induction of specific antibodies while the CD8+ T cell-depleted ones survived 19 . These findings suggested that antibodies play an important role in VSV/EBOV-GP-mediated protection against EBOV challenge. Although BC-PIV/EBOV-GP would not propagate in vivo in contrast to VSV/EBOV-GP, toxicity and protection studies in primates will still be required in the future. www.nature.com/scientificreports www.nature.com/scientificreports/ Generation of BC-PIVs carrying antigenic peptides. We also generated vaccines against antigenic peptide via another strategy (Fig. 1b) . We made three types of recombinant vaccines against the ectodomain of matrix protein 2 (M2e) peptide of influenza A virus, designated as BC-PIV/M2e. In these vaccines, the M2e peptide 2-25 (SLLTEVETPIRNEWGCRCNDSSDP) was loaded either inside, outside, or at both sides of the viral envelope of BC-PIV by fusing the M2e peptide gene with the C-terminus of hPIV2 F gene or with that of the HN gene. For the construction of the inside version, the M2e peptide gene was fused with the F gene and stably transfected into Vero cells as packaging cells to produce the recombinant vectors. For the outside version, the M2e peptide gene was fused with the HN gene in the hPIV2 genome and used to produce the recombinant vectors in the Vero/ BC-F cells or genetically modified Vero cells expressing M2e-fused F protein. Since F and HN proteins are oppositely oriented across the viral membrane, these strategies work (Fig. 1b,d) . The M2e peptide was detected by a Western blot analysis in each case (Fig. 1d) . The bands of the inside peptide are more abundant than those of the outside peptide. This may have resulted from differences in the expression of these peptides: the inside peptide was derived from its abundant and stable expression in the packaging cells, while the outside peptide was derived from transcripts from the vector. However, the possibility of better incorporation or enhanced stability of the inside-peptide, compared with the outside peptide, cannot be excluded.

The inside-type M2e peptide-fused protein was shown to be localized within the viral particle by immunoelectron microscopy (Fig. 4b) . The inside type would be suitable for inducing cellular immunity after cross-presentation, escaping neutralization by antibodies.

Induction of CD8+ lymphocytes via BC-PIV carrying antigenic peptides against melanoma in a syngeneic mouse tumor model. Cytotoxic T lymphocyte (CTL) induction is another prerequisite as a vaccine vector. We made anti-cancer vaccines expressing CTL epitopes of melanoma gp100 and WT1 using the strategy shown in Fig. 1b , and tested the effects of these vaccines after inactivation with β-propiolactone 3 . Vaccination of the mice with gp100 (outside) and WT1 (inside) peptides loaded on the BC-PIV envelope suppressed melanoma growth with CD8+ tumor-infiltrating lymphocytes (Fig. 6) . a melanoma gp100-specific CTL epitope KVPRNQDWL fused with hPIV2 HN (the peptide is located outside the viral membrane, see Fig. 1b,d) and a WT1-specific CTL epitope RMFPNAPYL fused with hPIV2 F (the peptide is located inside the viral membrane). The anticancer drug dacarbazine was intraperitoneally injected (100 mg/kg) at the same timing as each vaccination in order to compare the effects. BC-PIV/gp100 & WT1 was treated with 0.01% β-propiolactone (BPL) to inactivate the viral genome before injection 3 . The 0.01% BPL treatment was confirmed to be sufficient to abolish the expression of the transgene in BC-PIV (data not shown). Five mice per group were used, and the means ± SD are shown. PBS-injected mice were euthanized at day 12. (c) Hematoxylin and Eosin staining of the transplanted tumors. Left, PBS-injected group at day 12; middle, dacarbazine-administered group at day 21. Tumor cells were diffusely dying; right, vaccinated group with BC-PIV/gp100 & WT1 at day 21.

It is noteworthy that mice are not permissive for hPIV2 transcription and replication 20 . The results showing the efficacy of the vaccine in mice in the present study suggest the applicative potential of hPIV2 vector in humans that allow much more efficient transcription of BC-PIV, in addition to its use as inactivated vaccine without transcription.

The platform technology we have developed is based on the non-propagative hPIV2, which has ideal properties for the efficient delivery of ectopically expressed vaccine antigens. To achieve high yields of the non-propagative vector, it is essential to establish a packaging cell line stably producing the deleted gene product. Using Vero/BC-F packaging cells, we were able to obtain a maximum titer of 6 × 10 8 TCID 50 (median tissue culture infectious dose)/mL of BC-PIV/EGFP 5 . In contrast to virosome technology, the system in the present study does not require complex processes of antigen incorporation into the vector. Our system utilizes self-assembly of viral components such as VLP by reverse genetics, which allows us to create a stable steric structure of the antigen. In addition, BC-PIV was shown to have an intrinsic adjuvant activity 3 and is capable of delivering the gene and protein through intranasal, transtracheal, subcutaneous, and intramuscular administrations.

Chimeric hPIV3 bearing the EBOV GP, named HPIV3/ΔF-HN/EboGP, was previously reported 8 . However, this virus is replication-competent, as in VSV/EBOV-GP 7 , and the stable packaging cell lines expressing deleted genes have not been established. Similarly, attenuated hPIV1 expressing EBOV GP 12 , a chimeric bovine/human PIV3 vector expressing respiratory syncytial virus F protein 21 , and PIV5-vectored vaccines against human and animal infectious diseases 22 were also reported. All of these PIV vectors are replication-competent. Although replication-competent recombinant vaccines are beneficial for the massive induction of an antigen unless adverse events occur, replication-defective vaccines are safer. Balancing the efficacy and likelihood of side effects with a vaccine is important.

Our platform technology may be useful for fast-track vaccine development in addressing various emerging infectious diseases and cancers. Immunoelectron microscopy. Immunoelectron microscopy using the silver-enhancement technique was performed as described previously 24 . In brief, vector-producing Vero/BC-F cells cultured in a chamber were fixed with 2% fresh formaldehyde and 2.5% glutaraldehyde in 0.15 M sodium cacodylate buffer/2 mM CaCl 2 (pH 7.4) at room temperature (RT) for 2 h, treated with 0.1 M phosphate buffer (PB) (pH 7.4) containing 4% Block Ace (DS Pharma Biomedical, Suita, Japan), protease inhibitor cocktail tablets (Roche Diagnostics, Mannheim, Germany), and 0.02% saponin (Nacalai USA, Inc., San Diego, CA, USA), and incubated at RT for 20 min. The samples were then incubated with an anti-EBOV GP (KZ52; Absolute Antibody Ltd, Oxford, UK) or the anti-M2e mAb at 4 °C for 2 h, followed by reaction with an anti-mouse IgG Ab coupled with 1.4 nm gold particles (Nanoprobes, Stony Brook, NY, USA) at RT for a further 2 h. The Abs were diluted in 0.1M PB (pH 7.5) containing 0.02% saponin, 1% Block Ace, and protease inhibitor cocktail. The sample-bound gold particles were silver-enhanced at 18 °C for 12 min using an HQ-silver kit (Nanoprobes). The samples were washed, postfixed, dehydrated, and embedded in epoxy resin. From this sample, 75-nm-thick ultrathin sections were cut, stained with uranyl acetate and lead citrate, and then observed with an electron microscope (JEM-1200EX, and JEM-1230; JEOL, Tokyo, Japan).

Zaire Ebola GP-pseudotyped replication-incompetent VSVs containing the GFP gene instead of VSV G were generated as described previously 15 . Pseudotyped viruses suspended in growth medium were mixed with an equal volume of heat-inactivated mouse serum diluted in the medium and incubated for 30 min at RT. The mixture was then inoculated to confluent Vero E6 cells grown in 96-well plates (1200-1500 infectious units (IUs)/well). Twenty hours later, the GFP-positive cells were counted. Virus infectivity was quantified by comparing the GFP-positive cell numbers, in which the relative percentage of infectivity in the absence of mouse serum was set as 100%. The IUs of replication-incompetent pseudotyped VSVs were determined using Vero E6 cells as described previously 15 .

The center was necrotic, and massive infiltration of lymphocytes was found at the tumor boundary. (d) The accumulation of CD8+ T-lymphocytes towards the tumor cells in the mice vaccinated with BC-PIV/gp100 & WT1. CD8 was stained with Cy3. Blue regions correspond to nuclei. IDs are the same as in c. CD8+ cells were not found in the PBS-injected group, and a few CD8+ cells were scattered in the dacarbazine-administered group. However, CD8+ cells accumulated at the tumor boundary in the vaccinated group.

Reverse genetics of mononegavirales

Recovery of infectious human parainfluenza type 2 virus from cDNA clones and properties of the defective virus without V-specific cysteine-rich domain

Human parainfluenza virus type 2 vector induces dendritic cell maturation without viral RNA replication/transcription

Parainfluenza viruses

Vero/BC-F: an efficient packaging cell line stably expressing F protein to generate single round-infectious human parainfluenza virus type 2 vector

Foreign glycoproteins expressed from recombinant vesicular stomatitis viruses are incorporated efficiently into virus particles

Single-dose attenuated Vesiculovax vaccines protect primates against Ebola Makona virus

Chimeric human parainfluenza virus bearing the Ebola virus glycoprotein as the sole surface protein is immunogenic and highly protective against Ebola virus challenge

Mutational analysis of the putative fusion domain of Ebola virus glycoprotein

A mutation in the Ebola virus envelope glycoprotein restricts viral entry in a host species-and cell-type-specific manner

A new Ebola virus nonstructural glycoprotein expressed through RNA editing

Attenuated human parainfluenza virus type 1 expressing Ebola virus glycoprotein GP administered intranasally is immunogenic in African green monkeys

The roles of ebolavirus glycoproteins in viral pathogenesis

Structure of the Ebola virus glycoprotein bound to an antibody from a human survivor

A system for functional analysis of Ebola virus glycoprotein

Epitopes required for antibody-dependent enhancement of Ebola virus infection

Antibody-dependent enhancement of Ebola virus infection

VSV-EBOV rapidly protects macaques against infection with the 2014/15 Ebola virus outbreak strain

Antibodies are necessary for rVSV/ZEBOV-GP-mediated protection against lethal Ebola virus challenge in nonhuman primates

Incomplete replication of human parainfluenza virus type 2 in mouse L929 cells

Packaging and prefusion stabilization separately and additively increase the quantity and quality of respiratory syncytial virus (RSV)-neutralizing antibodies induced by an RSV fusion protein expressed by a parainfluenza virus vector

Parainfluenza virus 5-vectored vaccines against human and animal infectious diseases

Isolation of monoclonal antibodies directed against the V protein of human parainfluenza virus type 2 and localization of the V protein in virus-infected cells

Localization of Rabphilin-3A on the synaptic vesicle

We thank Dr. Masaki Inagaki for providing helpful discussion, and Mr. Brian Quinn for editing the manuscript. This work was supported in part by Grants-in-Aid from the Ministry of Education, Culture, Sports, Science and Technology in Japan (17K19652), Japan Agency for Medical Research and Development (C-CAM project A16), Takeda Science Foundation, Mie Medical Research Foundation, and Mie University (for research institutes of excellence).

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