Patent Grant
12090196
This application is a U.S. National Stage Application under 35 U.S.C. § 371 which claims the benefit of priority to International Patent Application No. PCT/GB2020/050022, filed Jan. 7, 2020, which claims the benefit of priority to GB Patent Application No. 1900187.4 filed Jan. 7, 2019, each of which is hereby incorporated by reference in its entirety.
The invention relates to a trypanosomal vaccine, to pharmaceutical compositions comprising said vaccine and to their uses in vaccination to prevent trypanosomal infection in a mammal.
The livelihoods of millions of people living in Africa are at risk due to infectious diseases that affect the health of livestock animals that provide them with essential food, milk, clothing and draught power. One major livestock disease is animal African trypanosomiasis (AAT) which is caused by blood-dwelling Trypanosome parasites that affect many important farm animals including cattle, goats, sheep, horses, and pigs. AAT is endemic from the Southern edge of the Sahara to Zimbabwe/Mozambique and is estimated to cause annual productivity losses of over $1 billion, representing a major barrier for the socioeconomic advancement of many African countries. Such is the impact of this disease that the United Nations Food and Agricultural Organisation consider it to “lie at the heart of Africa's struggle against poverty”.
The disease is mainly caused by two species of trypanosome: T. congolense and T. vivax which are transmitted through the bite of an infected tsetse fly. T. vivax transmission does not require tsetse flies for transmission and can be transmitted by other biting insects; as a consequence, T. vivax is a problem in countries outside of Africa, primarily Brazil. The few drugs available for AAT are not satisfactory: they cause serious side effects, and parasite resistance to these drugs is increasing. Importantly, even if new effective drugs were developed, these trypanosome parasites are endemic in wild animals meaning there would be little chance of eradicating the disease, and so livestock animals would require constant monitoring and treatment. The best solution would be the deployment of an effective vaccine; however, vaccinating against trypanosome infections has long been considered unachievable because the surface of these parasites is immunologically protected by a highly abundant cell surface protein called the variable surface glycoprotein (VSG). VSGs comprise a large family of related but not identical proteins, and trypanosomes express a small number or even a single variant on their surface at any one time. Host antibodies to VSG alleles are able to kill parasites; however, individual parasites within a population of trypanosomes can switch between variants and those that have switched to an antigenically distinct variant are able to effectively evade the host immune response ensuring the survival of the population as a whole.
One commonly-used strategy in the development of vaccines is to use inactivated or attenuated parasites, however, these vaccines are difficult to manufacture and can sometimes cause outbreaks if not appropriately attenuated. Modern vaccines, therefore, are typically purified recombinant proteins that can elicit protective immune responses and are consequently chemically defined.
There is therefore a great need to provide an alternative and effective vaccine against trypanosomes such as T. vivax.
According to a first aspect of the invention, there is provided a trypanosomal vaccine comprising a protein which comprises the amino acid sequence as set forth in SEQ ID NO: 1, or a protein having at least 90% sequence identity to said amino acid sequence, or a fragment of said amino acid sequence thereof, or a nucleic acid molecule encoding said protein.
According to a further aspect of the invention, there is provided a pharmaceutical composition comprising a trypanosomal vaccine as defined herein.
According to a further aspect of the invention, there is provided a method of preventing trypanosomal infection in a mammal which comprises administering to the mammal a therapeutically effective amount of the vaccine composition as defined herein.
According to a further aspect of the invention, there is provided a method of inducing an immune response in a mammal, wherein the method includes administering to the mammal, an effective amount of the vaccine composition as defined herein.
According to a further aspect of the invention, there is provided a kit of parts comprising a vaccine composition as defined herein, a medical instrument or other means for administering the vaccine composition and instructions for use.
According to a first aspect of the invention, there is provided a trypanosomal vaccine comprising a protein which comprises the amino acid sequence as set forth in SEQ ID NO: 1, or a protein having at least 90% sequence identity to said amino acid sequence, or a fragment of said amino acid sequence thereof, or a nucleic acid molecule encoding said protein.
The present invention relates to the identification of non-variant cell surface T. vivax proteins, which, when used in the context of a vaccine can elicit protective immune responses. Using the genome sequence to identify potential candidates, a vaccine target antigen has been identified which, when produced as a purified recombinant protein and administered with an appropriate immunostimulatory adjuvant, confers protection to T. vivax infections in mice. The results presented herein indicate that this non-variant parasite protein will be an important component of a vaccine to prevent AAT in livestock animals.
References herein to the amino acid sequence set forth in SEQ ID NO: 1 refer to:
The amino acid sequence of SEQ ID NO: 1 corresponds to the ectodomain of a cell surface T. vivax protein known as TvY486_0003730.
The full length amino acid sequence of TvY486_0003730 is shown below:
IRVLIAKTARDAGALRQQRAAFFEAWSNAVSLRNLKNVAKKVKKATEAV
DWATQCEGVMFMTLQTIIRALNTMRGHVSDKDGTAPSDCGLEPHQGRAA
DRNMTYVEVIEHIKSTERRLQELSMFAEESVRTFYGNYVNGVGLLNDTN
NYFAAAEAARRALREADEAMKDASDRKELNEKRVQLGCEVEKGLFFMRE
IFLTLHSVSERVISRERALKAKVGELDEGPGACGMAHTMFRSTAYANLR
ASSAKDESSLAVVELSEFMGIKGHSTLHHELEYDDDFKISLTNCRDSEL
EQSLVFRFARGEENDNIYDFDRWRAAADELWNKVESHTHIISEKCTKVS
GVDCSEAVGAVTMLIGRLRQLEGDLERGLGAAIRALKTVEDGIATSQDA
MRKCQHGGAVNEHHTEAKEPQTTSGRREANTDSAPAKEQLDAASKLEGG
SRLEEEVDGNEKEEQQEAPANGPQGALGVRQEETSYEGDAGRGSVDTGH
DEFATYLASRSACSTAGDGIESSSTAGDAAAVEARSKKKYLALMSVLCF
wherein the underlined portion represents the ectodomain region of TvY486_0003730.
TvY486_0003730 is also referred to herein as V31. Data is presented herein which surprisingly shows that V31 elicited a longer delay to the ascending phase of parasitaemia. In a repeat study, V31 further reduced the rate of parasite multiplication (see Study 2 and
In one embodiment, the trypanosomal vaccine as defined herein comprises a protein which comprises the amino acid sequence as set forth in SEQ ID NO: 1, or a protein having at least 90% sequence identity to said amino acid sequence, or a fragment of said amino acid sequence thereof.
It will be appreciated that references herein to “identity” are to be understood as meaning the percentage identity between two protein sequences, e.g.: SEQ ID NO: X and SEQ ID NO: 1, which is the sum of the common amino acids between aligned sequences SEQ ID NO: X and SEQ ID NO: 1, divided by the shorter length of either SEQ ID NO: X or SEQ ID NO: 1, expressed as a percentage.
In one embodiment, the protein of the invention has greater than 90% sequence identity with the ectodomain region of TvY486_0003730 (SEQ ID NO: 1), such as at least 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity with the ectodomain region of TvY486_0003730 (SEQ ID NO: 1).
References herein to ‘fragment’ include, for example, functional fragments with a C-terminal truncation, or with an N-terminal truncation. Fragments are suitably greater than 10 amino acids in length, for example greater than 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, 200, 210, 220, 230, 240, 250, 260, 270, 280, 290, 300, 310, 320, 330, 340, 350, 360, 370, 380, 390, 400, 410, 420, 430, 440, 450, 460, 470, 480, 490 or 500 amino acids in length.
In a further embodiment, the protein of the invention consists of the amino acid sequence as set forth in SEQ ID NO: 1.
In an alternative embodiment, the vaccine comprises a nucleic acid molecule encoding said protein of the invention. References herein to “nucleic acid molecule” typically refers to DNA or RNA. In a further embodiment, the nucleic acid molecule comprises an oligonucleotide encoding said protein.
References herein to “trypanosomal” refer to a genus of kinetoplastids (class Kinetoplastida), a monophyletic group of unicellular parasitic flagellate protozoa. The name is derived from the Greek trypano-(borer) and soma (body) because of their corkscrew-like motion. Most trypanosomes are heteroxenous (requiring more than one obligatory host to complete life cycle) and most are transmitted via a vector. The majority of species are transmitted by blood-feeding invertebrates, but there are different mechanisms among the varying species. Some, such as Trypanosoma equiperdum, are spread by direct contact. In an invertebrate host they are generally found in the intestine, but normally occupy the bloodstream or an intracellular environment in the mammalian host.
Examples of trypanosomal species include: T. ambystomae, T. antiquus, T. avium, T. boissoni, T. brucei, T. cruzi, T. congolense, T. equinum, T. equiperdum, T. evansi, T. everetti, T. hosei, T. irwini, T. lewisi, T. melophagium, T. paddae, T. parroti, T. percae, T. rangeli, T. rotatorium, T. rugosae, T. sergenti, T. simiae, T. sinipercae, T. suis, T. theileri, T. triglae, T. tungarae and T. vivax.
In one embodiment, the trypanosomal vaccine is a T. congolense or T. vivax vaccine. In a further embodiment, the trypanosomal vaccine is a T. vivax vaccine.
According to a further aspect of the invention, there is provided a pharmaceutical composition comprising a trypanosomal vaccine as defined herein.
In one embodiment, the vaccine composition additionally comprises one or more adjuvants. References herein to the term “adjuvant” refer to a compound that, when used in combination with a specific immunogen in a formulation, will augment or otherwise alter or modify the resultant immune response. Modification of the immune response can include intensification or broadening the specificity of either or both antibody and cellular immune responses. Modification of the immune response can also mean decreasing or suppressing certain antigen-specific immune responses.
In a further embodiment, at least about 1 μg and up to about 20 μg adjuvant is present within the vaccine composition. Examples of suitable adjuvants include: alum; aluminum hydroxide; aluminum phosphate; calcium phosphate hydroxide; paraffin oil; killed bacteria such as Bordetella pertussis, Mycobacterium bovis and toxoids; squalene, detergents; plant saponins from quillaja, soybean, polygala senega; cytokines such as IL-1, IL-2, IL-12; Freund's complete adjuvant; and Freund's incomplete adjuvant.
In a yet further embodiment, said adjuvant comprises aluminium hydroxide, such as a wet gel suspension of aluminium hydroxide, in particular Alhydrogel®, more particularly Alhydrogel® 2%. In one particular embodiment, said adjuvant comprises Montanide® ISA 201 VG. This adjuvant is a water-in-oil-in-water adjuvant and full details of this adjuvant may be found: https://www.seppic.com/montanide-isa-w-o-w. In an alternative embodiment, said adjuvant comprises Quil-A®. Quil-A® adjuvant is a saponin adjuvant which is used in a wide variety of veterinary vaccines. Full details of Quil-A® may be found: https://www.invivogen.com/quila.
In one embodiment, the vaccine composition additionally comprises a pharmaceutically acceptable carrier, diluent, excipient, or combination thereof, in which the immunogen (i.e. the proteins as defined herein) is/are suspended or dissolved.
Pharmaceutically acceptable carriers are known, and include but are not limited to, water for injection, saline solution, buffered saline, dextrose, water, glycerol, sterile isotonic aqueous buffer, and combinations thereof. For parenteral administration, such as subcutaneous injection, the carrier may include water, saline, alcohol, a fat, a wax, a buffer or combinations thereof. Pharmaceutically acceptable carriers, diluents, and other excipients are described in detail in Remington's Pharmaceutical Sciences (Mack Pub. Co. N.J. current edition). The formulation should suit the mode of administration. In a preferred embodiment, the formulation is suitable for administration to humans, preferably is sterile, non-particulate and/or non-pyrogenic.
In other embodiments, the vaccine composition can include one or more diluents, preservatives, solubilizers and/or emulsifiers. For example, the vaccine composition can include minor amounts of wetting or emulsifying agents, or pH buffering agents to improve vaccine efficacy. The composition can be a solid form, such as a lyophilized powder suitable for reconstitution, a liquid solution, suspension, emulsion, tablet, pill, capsule, sustained release formulation, or powder. Oral formulation can include standard carriers such as pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate, etc.
It may also be desirable to include other components in a vaccine composition, such as delivery vehicles including but not limited to aluminum salts, water-in-oil emulsions, biodegradable oil vehicles, oil-in-water emulsions, biodegradable microcapsules, and liposomes. In other embodiments, the vaccine composition can include antibacterial agents such as benzyl alcohol or methyl paraben; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediaminetetraacetic acid; buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose.
Administration of the vaccine composition can be systemic or local. Methods of administering a vaccine composition include, but are not limited to, parenteral administration (e.g., intradermal, intramuscular, intravenous and subcutaneous), epidural, and mucosal (e.g., intranasal and oral or pulmonary routes or by suppositories). In a specific embodiment, compositions described herein are administered intramuscularly, intravenously, subcutaneously, transdermally or intradermally. The compositions may be administered by any convenient route, for example by infusion or bolus injection, by absorption through epithelial or mucocutaneous linings (e.g., oral mucous, colon, conjunctiva, nasopharynx, oropharynx, vagina, urethra, urinary bladder and intestinal mucosa, etc.) and may be administered together with other biologically active agents. In some embodiments, intranasal or other mucosal routes of administration of a composition may induce an antibody or other immune response that is substantially higher than other routes of administration. In another embodiment, intranasal or other mucosal routes of administration of a composition described herein may induce an antibody or other immune response at the site of immunization.
In one embodiment, the vaccine composition has a volume of between about 50 μl and about 500 μl.
According to a further aspect of the invention, there is provided a method of preventing trypanosomal infection in a mammal which comprises administering to the mammal a therapeutically effective amount of the vaccine composition as defined herein.
References herein to “trypanosomal infection” refer to infection by a trypanosome as defined herein, such as T. congolense or T. vivax, in particular T. vivax. Thus, in one embodiment, the trypanosomal infection is an infection mediated by Trypanosoma vivax.
In one embodiment, the trypanosomal infection is animal African trypanosomiasis (AAT). References herein to “effective amount” refer to a dose which is sufficient or most likely to elicit antibodies such that the immunized subject has reduced severity of infection.
According to a further aspect of the invention, there is provided a method of inducing an immune response in a mammal, wherein the method includes administering to the mammal, an effective amount of the vaccine composition as defined herein.
Examples of suitable mammals include ungulates, such as those selected from cattle, goats, sheep, horses, pigs and camels.
In one embodiment, the vaccine composition is administered in a single dose regimen. In another embodiment, the vaccine composition is administered in a two dose regimen that includes a first and a second dose. In one embodiment, the second dose is administered at least about 1 week, 2 weeks, 3 weeks, 1 month or 1 year after the first dose. In another embodiment, the vaccine composition is administered in a three dose regimen.
According to a further aspect of the invention, there is provided a kit of parts comprising a vaccine composition as defined herein, a medical instrument or other means for administering the vaccine composition and instructions for use.
In one embodiment, the vaccine composition is packaged in a hermetically sealed container such as an ampoule or sachette indicating the quantity of composition. In one embodiment, the composition is supplied as a liquid. In another embodiment, the composition is supplied as a dry sterilized lyophilized powder or water free concentrate in a hermetically sealed container, wherein the composition can be reconstituted, for example, with water or saline, to obtain an appropriate concentration for administration to a subject.
When the vaccine composition is systemically administered, for example, by subcutaneous or intramuscular injection, a needle and syringe, or a needle-less injection device can be used. The vaccine formulation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic.
The following studies illustrate the invention:
Study 1
Design, Synthesis and Purification of T. vivax TvY486_0003730
The region corresponding to the entire extracellular domains of TvY486_0003730 was determined by using transmembrane (TMHMMv2.0 (Sonnhammer et al. (1998) Proceedings International Conference on Intelligent Systems for Molecular Biology 6, 175-182) and signal peptide prediction software (SignalP v4.0 (Petersen et al. (2011) Nature methods 8, 785-786)). Sequences encoding the entire extracellular domains of these proteins from the Y486 strain of Trypanosoma vivax, with the exception of their signal peptide, were made by gene synthesis (GeneartAG, Germany and Twist Bioscience, USA). All sequences were codon-optimized for expression in human cells. The coding sequences were flanked by unique NotI and AscI sites and cloned into a derivative of the pTT3 expression vector between the leader sequence of the mouse variable light chain 7-33 (Crosnier et al. (2013) Molecular & cellular proteomics: MCP 12, 3976-3986). The ectodomain was expressed as a soluble recombinant protein in HEK293 cells as described (Crosnier et al. (2013), supra). Protein was purified by Ni2+ immobilised metal ion affinity chromatography using HisTRAP columns (GEHealthcare, UK), eluted in 400 mM imidazole as described (Bartholdson et al. (2012) PLoS pathogens 8, e1003031), dialysed into HBS, aliquoted and snap-frozen prior to immunisation.
Animals, Immunisations, Challenge and Bioluminescence Measurement
All animal experiments were performed in accordance with UK Home office legislation and according to local ethical review board approval. Six to eight-week old female BALB/c mice were bred and housed at the Research Support Facility of the Wellcome Trust Sanger Institute. Recombinant proteins were adsorbed to Alhydrogel® adjuvant 2% (Brenntag Biosector, Denmark) as an adjuvant using a final volume ratio of 1:1. Animals were immunised intraperitoneally with an initial priming dose of 100 micrograms followed by two further booster immunisations of 100 micrograms given at two week intervals.
Vaccinated animals were rested for 4 weeks after the final immunisation to mitigate any possible non-specific protective effects elicited by residual adjuvant. Animal challenges were performed using a transgenic form of the T. vivax Y486 strain genetically engineered to ubiquitously express the firefly luciferase enzyme as described (Chamond et al. (2010) PLoS neglected tropical diseases 4, e792). Parasites were maintained by weekly passage in wild type BALB/c mice. For infection challenges, bloodstream forms of T. vivax parasites were obtained from the blood of an infected donor mouse at the peak of parasitaemia and between 100 to 1000 parasites were used to infect mice by intravenous injection.
From day three post-infection, animals were injected intraperitoneally with luciferase substrate, D-luciferin (D-Luciferin potassium salt, Source BioScience, Nottingham, UK) at a dose of 200 mg/kg, 10 mins before bioluminescence acquisitions. The mice were anaesthetized with 3% isoflurane and placed in the imaging chamber for analysis. Emitted photons were acquired by a charge coupled device (CCD) camera (IVIS Spectrum Imaging System, Perkin Elmer). Total photons emitted from the image of each mouse were quantified using Living Image software (Xenogen Corporation, Almeda, California), and results were expressed as number of photons/sec/ROI. Seven days post-challenge, thin-film parasitemia quantification was conducted where blood parasite counts were established under a light microscope and expressed as the number of parasites per milliliter of blood as an independent measurement of parasite load.
Results
To discover potential subunit vaccine candidates for T. vivax, we analysed the genome sequence to identify proteins that fulfilled the following criteria: 1) were predicted to encode cell surface proteins that would be accessible to vaccine-elicited host antibodies; 2) did not belong to a paralogous group of parasite proteins that might indicate functional redundancy; 3) contained more than 300 amino acids and so are likely to project beyond the VSG coat on the parasite membrane. A protein that met these criteria was TvY486_0003730.
To increase the chances that the extracellular regions of the protein were expressed in a correctly folded conformation and therefore elicit antibodies that would bind to the native parasite protein, we expressed the protein using a mammalian expression system to promote the formation of structurally-critical disulphide bonds. The entire ectodomain region was identified and the gene constructed by gene synthesis using codons optimised for expression in human cells. This gene construct was cloned into a mammalian protein expression plasmid. Human embryonic kidney (HEK)293 cells were transfected with this plasmid and the protein secreted into the tissue culture medium. The protein was purified from the tissue culture supernatant by immobilised metal ion chromatography (IMAC) and resolved as a series of glycoforms by SDS-PAGE (
Groups of five mice were immunised intraperitoneally using a prime followed by two boost regime with the protein adjuvanted with Alhydrogel; control animals were immunised with adjuvant only. Vaccinated animals were challenged with T. vivax parasites delivered intravenously from the blood of an infected donor animal. Animals immunised with TvY486_0003730 exhibited significant delays in parasitaemia relative to adjuvant-only control mice (
Study 2
Mouse Strains and Ethical Approvals
All animal experiments were performed under UK Home Office governmental regulations (project license number PD3DA8D1F) and European directive 2010/63/EU. Research was ethically approved by the Sanger Institute Animal Welfare and Ethical Review Board. Mice were obtained from the Research Support Facility, Wellcome Sanger Institute.
Trypanosoma vivax Parasite Strain and Maintenance
A transgenic form of Trypanosoma vivax genetically engineered to ubiquitously express the firefly luciferase enzyme was kindly provided by the Institut Pasteur, Paris. The parental strain of this parasite is the IL1392 line derived from the Y486 strain used for genome sequencing (Jackson et al. 2012, Proc. Natl. Acad. Sci. U.S.A. 109, 3416-3421) and is fully documented by Chamond et al. (Chamond et al. 2010, PLoS Negl. Trop. Dis. 4, e792). Parasites were initially recovered from a frozen sample by intraperitoneal administration into two mice and transferred to naïve mice when parasites became patent in the blood. Parasites were maintained by weekly serial blood passage in wild type female BALB/C mice by taking a blood biopsy, quantifying living parasites in PBS/10 mM D-glucose by microscopy and infecting four naïve mice by intravenous infection. During the course of the project, two further aliquots of frozen parasites were thawed and then used for infection challenges, no significant differences in the kinetics of infection between the batches of parasites were observed.
Quantification of Trypanosoma vivax Infections by Bioluminescent In Vivo Imaging
To quantify T. vivax infections by bioluminescent in vivo imaging, infected animals were intraperitoneally administered with the luciferase substrate, luciferin. D-luciferin (potassium salt, Source BioScience, UK) was reconstituted to 30 mg mL−1 in Dulbecco's PBS without Ca2+ and Mg2+ (Hyclone), filter-sterilised (0.22 μm) and stored in aliquots at −20° C. Aliquots were thawed and administered to animals at a dose of 200 mg/kg, by intraperitoneal injection ten minutes before bioluminescence acquisitions. The mice were given three minutes of free movement before being anaesthetized with 3% isoflurane and placed in the imaging chamber where anaesthesia was maintained for acquisition. To determine the long-term persistence of the parasites in different organs of infected mice, animals were administered with luciferin, imaged, and then euthanised with an overdose of anaesthetic. Mice were then perfused with PBS until the perfusion fluid ran clear, the organs dissected, arranged on a petri dish, and bathed in PBS containing 10 mM glucose and luciferin for imaging. Emitted photons were acquired by a charge coupled device (CCD) camera (IVIS Spectrum Imaging System, Perkin Elmer). Total photons emitted from the image of each mouse were quantified using Living Image software (Xenogen Corporation, Almeda, California), and the results were expressed as bioluminescence: number of photons/sec/ROI.
Vaccine Target Identification and Expression
The T. vivax genome was searched for proteins encoding predicted type I, GPI-anchored and secreted proteins using protein feature searching in TryTrypDB (Aslett et al. 2010, Nucleic Acids Res. 38, D457-D462). The regions corresponding to the entire extracellular domains of T. vivax cell-surface and secreted proteins from the Y486 strain were determined by using transmembrane (Sonnhammer et al. 1998, Proc. Int. Conf. Intell. Syst. Mol. Biol. 6, 175-182) and GPI-anchor (Eisenhaber et al. 1999, J. Mol. Biol. 292, 741-758) or signal peptide (Bendtsen et al. 2004, J. Mol. Biol. 340, 783-795) prediction software. Protein sequences encoding the extracellular domain and lacking their signal peptide, were codon-optimized for expression in human cells and made by gene synthesis (GeneartAG, Germany and Twist Bioscience, USA). The sequences were flanked by unique NotI and AscI restriction enzyme sites and cloned into a pTT3-based mammalian expression vector (Durocher et al. 2002, Nucleic Acids Res. 30, E9) between an N-terminal signal peptide to direct protein secretion and a C-terminal tag that included a protein sequence that could be enzymatically biotinylated by the BirA protein-biotin ligase (Bushell et al. 2008, Genome Res. 18, 622-630) and a 6-his tag for purification (Sun et al. 2012, Anal. Biochem. 424, 45-53). The ectodomain was expressed as a soluble recombinant protein in HEK293 cells which were obtained from Yves Durocher (NRC, Montreal) as described (Crosnier et al. 2013, Mol. Cell. Proteomics 12, 3976-3986; Kerr and Wright 2012, J. Vis. Exp. e3881). Cell lines were regularly tested (every six months, Surrey Diagnostics, UK) for mycoplasma contamination and found to be negative. To prepare purified proteins for immunisation, between 50 and 1.2 L (depending on the level at which the protein was expressed) of spent culture media containing the secreted ectodomain was harvested from transfected cells, filtered and purified by Ni2+ immobilised metal ion affinity chromatography using HisTRAP columns using an AKTAPure instrument (GEHealthcare, UK). Proteins were eluted in 400 mM imidazole as described (Bartholdson et al. 2012, PLoS Pathog. 8, e1003031), and extensively dialysed into HBS before quantified by spectrophotometry at 280 nm. Protein purity was determined by resolving approximately one microgram of purified protein by SDS-PAGE using NuPAGE 4-12% Bis Tris precast gels (ThermoFisher) for 50 minutes at 200V. Where reducing conditions were required NuPAGE reducing agent and anti-oxidant (Invitrogen) were added to the sample and the running buffer, respectively. The gels were stained with SYPRO Orange (ThermoFisher), destained in 7.5% acetic acid and imaged using a Typhoon 9400 phosphoimager (GE Healthcare). Purified proteins were aliquoted and stored frozen at −20° C. until use. Where enzymatically monobiotinylated proteins were required to determine antibody titres by ELISA, proteins were co-transfected with a secreted version of the protein biotin ligase (BirA) as described (Kerr and Wright 2012, supra), and extensively dialysed against HEPES-buffered saline and their level of expression determined by ELISA.
Vaccine Formulation and Administration
For the initial screening of antigens, aliquots of purified protein for immunisation were thawed, diluted in PBS and mixed 50% v/v with Alhydrogel adjuvant 2% (InvivoGen) for two hours at room temperature. For each antigen, groups of five six to eight-week old female BALB/C mice were immunised intraperitoneally initially with 100 μg protein followed by two additional fortnightly immunisations using 20 μg protein. Where the quantity of purified antigen was insufficient to achieve these levels, lower doses of proteins were administered.
Trypanosoma vivax Vaccine Testing
For infection challenges, bloodstream forms of T. vivax parasites were obtained from the blood of an infected donor mouse at the peak of parasitaemia, diluted in PBS/10 mM D-glucose, quantified by microscopy, and between 100 to 1000 parasites were used to infect mice by intravenous injection. While establishing the infection model in our facility, we observed that the T. vivax parasite was labile and gradually lost virulence once removed from living mice. To reduce the possibility of any artefactual protective effects being due to the loss of parasite virulence during the challenge procedure, we screened the protective effects of antigens in a cohort design. Each cohort contained six cages of five animals: four cages contained mice immunised with a different query subunit vaccine candidate, and the other two cages contained control mice immunised with adjuvant alone. During the infection procedure, the mice in the control cages were challenged first and last and the data from the cohort only used if the infections in the control mice from the two cages were not statistically different. During the infection procedures, parasites were outside of a living mouse for no more than 30 minutes. Eight to ten days after the final immunisation, blood biopsies were collected from the tail of each animal and clotted for two hours at room temperature. Cells were removed by centrifugation and sera collected, sodium azide added to a final concentration of 2 mM and stored at −20° C. Vaccinated animals were rested for four weeks after the final immunisation to mitigate any possible non-specific protective effects elicited by residual adjuvant.
Mice were normally challenged by intravenous delivery of 102 to 103 parasites for the initial screening and passive transfer protection experiments, but were also challenged intraperitoneally during the establishment of the model and subcutaneously when investigating the duration of protection. For retesting antigens, two groups of 15 animals were each housed in three cages containing five mice. The animals were not randomised between cages and the operator was not blinded to the group condition. Groups were compared using bioluminescence quantification as a proxy for parasitaemia and groups were compared using one-way ANOVA. No readings were excluded from the analysis.
Results
Investigation of V31 Immunity to T. vivax
The gene sequence encoding the entire extracellular region of V31 was synthesised and cloned into a mammalian protein expression plasmid containing a secretion peptide and purification tags. V31 was expressed as a soluble recombinant protein in mammalian HEK293 cells to increase the chances that structurally-critical posttranslational modifications were added and therefore elicit host antibodies that recognize native antigens displayed by the parasite. V31 yielded sufficient protein after purification for the vaccination trials. For vaccination, we selected a prime and two boost regime using alum as an adjuvant to bias host responses towards humoral immunity. To reduce any systemic adjuvant-elicited effects on disease progression, vaccinated animals were rested for four weeks following the final boost before parasite challenge. In preliminary experiments, we observed that T. vivax lost virulence once removed from donor animals, and so to avoid confounding effects due to loss of parasite viability during the infection procedure, we ensured that infections were comparable in control animals challenged before and after animals vaccinated with the V31 antigen.
We observed that V31 exhibited a longer delay to the ascending phase of parasitaemia (
Discussion
Animal African trypanosomiasis continues to be a significant impediment in the successful raising of livestock animals in sub-Saharan Africa and previous attempts to vaccinate against the trypanosome parasites that cause this disease have been unsuccessful. Here we have shown that vaccinating with a recombinant protein comprising the entire ectodomain of a conserved T. vivax cell surface protein TvY486_0003730 confers protection in a mouse model of infection suggesting that this protein could be an effective subunit vaccine. We note that the disease is acute in the BALB/c mice used in our infection trials since control mice develop rapid uncontrolled parasitaemia whereas in livestock animals such as goats and cattle the infection is typically a chronic disease with lower parasitaemia suggesting the mouse infection model provides a stringent test of our vaccine candidates. We envisage that a vaccine containing TvY486_0003730 in whole or in part and in the context of an appropriate adjuvant will constitute a vaccine to treat this disease in livestock animals.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1900187 | Jan 2019 | GB | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/GB2020/050022 | 1/7/2020 | WO |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2020/144464 | 7/16/2020 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 20170296637 | Pleguezuelos Mateo et al. | Oct 2017 | A1 |
| 20180185461 | Vincendeau et al. | Jul 2018 | A1 |
| 20190351035 | Baeremaecker | Nov 2019 | A1 |
| Number | Date | Country |
|---|---|---|
| WO 2016185135 | Nov 2016 | WO |
| WO 2017187179 | Nov 2017 | WO |
| WO 2020144464 | Jul 2020 | WO |
| WO 2020144465 | Jul 2020 | WO |
| Entry |
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| Number | Date | Country | |
|---|---|---|---|
| 20220096613 A1 | Mar 2022 | US |
