Patent Application
20210236619
A Sequence Listing associated with this application is being submitted electronically via EFS-Web in text format and is hereby incorporated by reference in its entirety into the specification. The name of the text file containing the Sequence Listing is 104545-0032-WO1-SequenceListing.txt. The text file, created on May 2, 2019, is 882,663 bytes in size.
Poxviruses (members of the Poxviridae family) are double-stranded DNA viruses that can infect both humans and animals. Poxviruses are divided into two subfamilies based on host range. The Chordopoxviridae subfamily, which infects vertebrate hosts, consists of eight genera, of which four genera (Orthopoxvirus, Parapoxvirus, Molluscipoxvirus, and Yatapoxvirus) are known to infect humans. Smallpox is caused by infection with variola virus (VARV), a member of the genus Orthopoxvirus (OPV). The OPV genus comprises a number of genetically related and morphologically identical viruses, including camelpox virus (CMLV), cowpox virus (CPXV), ectromelia virus (ECTV, “mousepox agent”), horsepox virus (HPXV), monkeypox virus (MPXV), rabbitpox virus (RPXV), raccoonpox virus, skunkpox virus, Taterapox virus, Uasin Gishu disease virus, vaccinia virus (VACV), variola virus (VARV) and volepox virus (VPV). Other than VARV, at least three other OPVs, including VACV, MPXV and CPXV, are known to infect humans.
In the ongoing search for therapeutics that are capable of eliminating or reducing tumor cells, oncolytic viruses have shown great potential in preclinical studies. These viruses are typically genetically engineered or have a natural tropism for tumor cells, so as to only replicate in and kill neoplastic cells. Among therapeutic viruses, oncolytic Vaccinia virus is one of the most promising candidates for cancer therapy. As an example, JX-594 is a Vaccinia virus with TK gene deletion and GM-CSF (a cytokine able to stimulate the immune system to kill tumor cells) gene insertion and is currently undergoing phase III trials (Park S H et al. Phase 1b trial of biweekly intravenous Pexa-Vec (JX-594), an oncolytic and immunotherapeutic vaccinia virus in colorectal cancer. Mol Ther (2015); 23(9):1532-40).
To improve delivery of viral therapeutics and circumvent antiviral immunity, a number of studies have explored the possibility of using infected cells as delivery vehicles for oncolytic viruses (Garcia-Castro, J., et al., Treatment of metastatic neuroblastoma with systemic oncolytic virotherapy delivered by autologous mesenchymal stem cells: an exploratory study. Cancer Gene Ther, 2010. 17(7): 476-83; Coukos, G., et al., Use of carrier cells to deliver a replication-selective herpes simplex virus-1 mutant for the intraperitoneal therapy of epithelial ovarian cancer. Clin Cancer Res, 1999. 5(6): 1523-37; Komarova, S., et al., Mesenchymal progenitor cells as cellular vehicles for delivery of oncolytic adenoviruses. Mol Cancer Ther, 2006. 5(3): 755-66). Mesenchymal stem cells have shown great promise in this respect.
Although promising, these studies have been limited by their inability to explore the therapeutic efficacy of mesenchymal stem cells loaded with oncolytic viruses. Additionally, cell therapies, such as administration of stem cells, have been associated with formation of malignant cancers in subjects receiving stem cell therapies. While the potential of cellular therapy in the treatment of diseases, disorders and injury is significant, the formation of tumors, such as teratomas, as a result of such treatment is an unacceptable outcome.
Accordingly, there exists a need for methods of delivering oncolytic viruses and safely administering cellular compositions that reduce the risk of tumor formation in subjects receiving cellular therapy.
The present invention, in one aspect, provides stem cells comprising a synthetic chimeric poxvirus (scPV), which can be used for the treatment of cancer or other infectious diseases. Because chemical genome synthesis is not dependent on a natural template, a plethora of structural and functional modifications of the viral genome are possible. Chemical genome synthesis is particularly useful when a natural template is not available for genetic replication or modification by conventional molecular biology methods.
Therefore, in one aspect, the invention relates to an isolated stem cell or population thereof comprising a synthetic chimeric poxvirus (scPV), wherein the virus is replicated and reactivated from DNA derived from synthetic DNA, the viral genome of said virus differing from a wild type genome of said virus in that it is characterized by one or more modifications.
In another aspect, the invention relates to a pharmaceutical composition comprising the isolated stem cells of the invention, and a pharmaceutically acceptable carrier.
In another aspect, the invention relates to a method for delivering the scPV of the invention to a subject, comprising infecting the stem cells of the invention and administering the scPV-infected stem cells into the subject.
In another aspect, the invention relates to a method of treating or preventing cancer in a subject, comprising administering the stem cells of the invention or the pharmaceutical composition of the invention to the subject, to thereby contact the cancer cells of the subject with the scPV.
In another aspect, the invention relates to a method of treating a variola virus infection, comprising administering to a subject in need thereof the stem cells of the invention or the pharmaceutical composition of the invention.
This patent application contains at least one drawing executed in color. Copies of this patent application with color drawings will be provided by the Office upon request and payment of the necessary fee.
The foregoing summary, as well as the following detailed description of the disclosure, will be better understood when read in conjunction with the appended drawings. For the purpose of illustrating various aspects of the invention there are shown in the drawings embodiment(s) which are presently preferred. It should be understood, however, that the invention is not limited to the precise arrangements and instrumentalities shown.
Unless otherwise defined herein, scientific and technical terms used in this application shall have the meanings that are commonly understood by those of ordinary skill in the art. Generally, nomenclature used in connection with, and techniques of, pharmacology, cell and tissue culture, molecular biology, cell and cancer biology, neurobiology, neurochemistry, virology, immunology, microbiology, genetics and protein and nucleic acid chemistry, described herein, are those well-known and commonly used in the art. In case of conflict, the present specification, including definitions, will control.
The practice of various aspects of the present invention will employ, unless otherwise indicated, conventional techniques of molecular biology (including recombinant techniques), microbiology, cell biology, biochemistry and immunology, which are within the skill of the art. Such techniques are explained fully in the literature, such as Molecular Cloning: A Laboratory Manual, second edition (Sambrook et al., 1989) Cold Spring Harbor Press; Oligonucleotide Synthesis (M. J. Gait, ed., 1984); Methods in Molecular Biology, Humana Press; Cell Biology: A Laboratory Notebook (J. E. Cellis, ed., 1998) Academic Press; Animal Cell Culture (R. I. Freshney, ed., 1987); Introduction to Cell and Tissue Culture (J. P. Mather and P. E. Roberts, 1998) Plenum Press; Cell and Tissue Culture: Laboratory Procedures (A. Doyle, J. B. Griffiths, and D. G. Newell, eds., 1993-1998) J. Wiley and Sons; Methods in Enzymology (Academic Press, Inc.); Gene Transfer Vectors for Mammalian Cells (J. M. Miller and M. P. Calos, eds., 1987); Current Protocols in Molecular Biology (F. M. Ausubel et al., eds., 1987); PCR: The Polymerase Chain Reaction, (Mullis et al., eds., 1994); Sambrook and Russell, Molecular Cloning: A Laboratory Manual, 3rd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (2001); Ausubel et al., Current Protocols in Molecular Biology, John Wiley & Sons, N Y (2002); Harlow and Lane Using Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1998); Coligan et al., Short Protocols in Protein Science, John Wiley & Sons, N Y (2003); Short Protocols in Molecular Biology (Wiley and Sons, 1999).
Enzymatic reactions and purification techniques are performed according to manufacturer's specifications, as commonly accomplished in the art or as described herein. The nomenclatures used in connection with, and the laboratory procedures and techniques of, analytical chemistry, biochemistry, immunology, molecular biology, synthetic organic chemistry, and medicinal and pharmaceutical chemistry described herein are those well-known and commonly used in the art. Standard techniques are used for chemical syntheses, and chemical analyses.
Throughout this specification and embodiments, the word “comprise,” or variations such as “comprises” or “comprising,” will be understood to imply the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers.
It is understood that wherever embodiments are described herein with the language “comprising,” otherwise analogous embodiments described in terms of “consisting of” and/or “consisting essentially of” are also provided.
The term “including” is used to mean “including but not limited to.” “Including” and “including but not limited to” are used interchangeably.
Any example(s) following the term “e.g.” or “for example” is not meant to be exhaustive or limiting.
Unless otherwise required by context, singular terms shall include pluralities and plural terms shall include the singular.
The articles “a”, “an” and “the” are used herein to refer to one or to more than one (i.e., to at least one) of the grammatical object of the article. By way of example, “an element” means one element or more than one element. Reference to “about” a value or parameter herein includes (and describes) embodiments that are directed to that value or parameter per se. For example, description referring to “about X” includes description of “X.” Numeric ranges are inclusive of the numbers defining the range.
Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the application are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements. Moreover, all ranges disclosed herein are to be understood to encompass any and all subranges subsumed therein. For example, a stated range of “1 to 10” should be considered to include any and all subranges between (and inclusive of) the minimum value of 1 and the maximum value of 10; that is, all subranges beginning with a minimum value of 1 or more, e.g., 1 to 6.1, and ending with a maximum value of 10 or less, e.g., 5.5 to 10.
Exemplary methods and materials are described herein, although methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present invention. The materials, methods, and examples are illustrative only and not intended to be limiting.
The following terms, unless otherwise indicated, shall be understood to have the following meanings:
As used herein, the terms “wild type virus”, “wild type genome”, “wild type protein,” or “wild type nucleic acid” refer to a sequence of amino or nucleic acids that occurs naturally within a certain population (e.g., a particular viral species, etc.).
The terms “chimeric” or “engineered” or “modified” (e.g., chimeric poxvirus, engineered polypeptide, modified polypeptide, engineered nucleic acid, modified nucleic acid) or grammatical variations thereof are used interchangeably herein to refer to a non-native sequence that has been manipulated to have one or more changes relative a native sequence.
As used herein, “synthetic virus” refers to a virus initially derived from synthetic DNA (e.g., chemically synthesized DNA, PCR amplified DNA, engineered DNA, polynucleotides comprising nucleoside analogs, etc., or combinations thereof) and includes its progeny, and the progeny may not necessarily be completely identical (in morphology or in genomic DNA complement) to the original parent synthetic virus due to natural, accidental, or deliberate mutation. In some embodiments, the synthetic virus refers to a virus where substantially all of the viral genome is initially derived from synthetic DNA (e.g., chemically synthesized DNA, PCR amplified DNA, engineered DNA, polynucleotides comprising nucleoside analogs, etc., or combinations thereof). In a preferred embodiment, the synthetic virus is derived from chemically synthesized DNA.
As outlined elsewhere herein, certain positions of the viral genome can be altered. By “position” as used herein is meant a location in the genome sequence. Corresponding positions are generally determined through alignment with other parent sequences.
As used herein, the term “residue” in the context of a polypeptide refers to an amino-acid unit in the linear polypeptide chain. It is what remains of each amino acid, i.e —NH—CHR—C—, after water is removed in the formation of the polypeptide from α-amino-acids, i.e. NH2-CHR—COOH.
As known in the art, “polynucleotide,” or “nucleic acid,” as used interchangeably herein, refer to chains of nucleotides of any length, and include DNA and RNA. The nucleotides can be deoxyribonucleotides, ribonucleotides, modified nucleotides or bases, and/or their analogs, or any substrate that can be incorporated into a chain by DNA or RNA polymerase. A polynucleotide may comprise modified nucleotides, such as methylated nucleotides and their analogs. If present, modification to the nucleotide structure may be imparted before or after assembly of the chain. The sequence of nucleotides may be interrupted by non-nucleotide components. A polynucleotide may be further modified after polymerization, such as by conjugation with a labeling component. Other types of modifications include, for example, “caps”, substitution of one or more of the naturally occurring nucleotides with an analog; internucleotide modifications such as, for example, those with uncharged linkages (e.g., methyl phosphonates, phosphotriesters, phosphoamidates, carbamates, etc.) and with charged linkages (e.g., phosphorothioates, phosphorodithioates, etc.); those containing pendant moieties, such as, for example, proteins (e.g., nucleases, toxins, antibodies, signal peptides, poly-L-lysine, etc.); those with intercalators (e.g., acridine, psoralen, etc.); those containing chelators (e.g., metals, radioactive metals, boron, oxidative metals, etc.); those containing alkylators; those with modified linkages (e.g., alpha anomeric nucleic acids, etc.); as well as unmodified forms of the polynucleotide(s). Further, any of the hydroxyl groups ordinarily present in the sugars may be replaced, for example, by phosphonate groups, phosphate groups, protected by standard protecting groups, or activated to prepare additional linkages to additional nucleotides, or may be conjugated to solid supports. The 5′ and 3′ terminal OH can be phosphorylated or substituted with amines or organic capping group moieties of from 1 to 20 carbon atoms. Other hydroxyls may also be derivatized to standard protecting groups. Polynucleotides can also contain analogous forms of ribose or deoxyribose sugars that are generally known in the art, including, for example, 2′-O-methyl-, 2′-O-allyl, 2′-fluoro- or 2′-azido-ribose, carbocyclic sugar analogs, alpha- or beta-anomeric sugars, epimeric sugars such as arabinose, xyloses or lyxoses, pyranose sugars, furanose sugars, sedoheptuloses, acyclic analogs and abasic nucleoside analogs such as methyl riboside. One or more phosphodiester linkages may be replaced by alternative linking groups. These alternative linking groups include, but are not limited to, embodiments wherein phosphate is replaced by P(O)S (“thioate”), P(S)S (“dithioate”), (O)NR2 (“amidate”), P(O)R, P(O)OR′, CO or CH2 (“formacetal”), in which each R or R′ is independently H or substituted or unsubstituted alkyl (1-20 C) optionally containing an ether (—O—) linkage, aryl, alkenyl, cycloalkyl, cycloalkenyl or araldyl. Not all linkages in a polynucleotide need be identical. The preceding description applies to all polynucleotides referred to herein, including RNA and DNA.
The terms “polypeptide”, “oligopeptide”, “peptide” and “protein” are used interchangeably herein to refer to chains of amino acids of any length. The chain may be linear or branched, it may comprise modified amino acids, and/or may be interrupted by non-amino acids. The terms also encompass an amino acid chain that has been modified naturally or by intervention; for example, disulfide bond formation, glycosylation, lipidation, acetylation, phosphorylation, or any other manipulation or modification, such as conjugation with a labeling component. Also included within the definition are, for example, polypeptides containing one or more analogs of an amino acid (including, for example, unnatural amino acids, etc.), as well as other modifications known in the art. It is understood that the polypeptides can occur as single chains or associated chains.
“Homologous,” in all its grammatical forms and spelling variations, refers to the relationship between two proteins that possess a “common evolutionary origin,” including proteins from superfamilies in the same species of organism, as well as homologous proteins from different species of organism. Such proteins (and their encoding nucleic acids) have sequence homology, as reflected by their sequence similarity, whether in terms of percent identity or by the presence of specific residues or motifs and conserved positions. “Homologous” may also refer to a nucleic acid which is native to the virus.
However, in common usage and in the instant application, the term “homologous,” when modified with an adverb such as “highly,” may refer to sequence similarity and may or may not relate to a common evolutionary origin.
“Heterologous,” in all its grammatical forms and spelling variations, may refer to a DNA which is non-native to the virus. It means derived from a different species or a different strain than the DNA of the organism to which the DNA is described as heterologous relative to. In a non-limiting example, the viral genome of the scPV comprises heterologous terminal hairpin loops. Said heterologous terminal hairpin loops can be derived from a different virus species or from a different virus strain.
The term “sequence similarity,” in all its grammatical forms, refers to the degree of identity or correspondence between nucleic acid or amino acid sequences that may or may not share a common evolutionary origin.
“Percent (%) sequence identity” or “sequence % identical to” with respect to a reference polypeptide (or nucleotide) sequence is defined as the percentage of amino acid residues (or nucleic acids) in a candidate sequence that are identical with the amino acid residues (or nucleic acids) in the reference polypeptide (nucleotide) sequence, after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent sequence identity, and not considering any conservative substitutions as part of the sequence identity. Alignment for purposes of determining percent amino acid sequence identity can be achieved in various ways that are within the skill in the art, for instance, using publicly available computer software such as BLAST, BLAST-2, ALIGN or Megalign (DNASTAR) software. Those skilled in the art can determine appropriate parameters for aligning sequences, including any algorithms needed to achieve maximal alignment over the full length of the sequences being compared.
As used herein, a “host cell” includes an individual cell or cell culture that can be or has been a recipient for vector(s) for incorporation of polynucleotide inserts. Host cells include progeny of a single host cell, and the progeny may not necessarily be completely identical (in morphology or in genomic DNA complement) to the original parent cell due to natural, accidental, or deliberate mutation. A host cell includes cells transfected and/or transformed in vivo with a nucleic acid of this disclosure.
As used herein, “vector” means a construct, which is capable of delivering, and, preferably, expressing, one or more gene(s) or sequence(s) of interest in a host cell. Examples of vectors include, but are not limited to, viral vectors, naked DNA or RNA expression vectors, plasmid, cosmid or phage vectors, DNA or RNA expression vectors associated with cationic condensing agents, DNA or RNA expression vectors encapsulated in liposomes, and certain eukaryotic cells, such as producer cells.
As used herein, “isolated molecule” (where the molecule is, for example, a polypeptide, a polynucleotide, or fragment thereof) is a molecule that by virtue of its origin or source of derivation (1) is not associated with one or more naturally associated components that accompany it in its native state, (2) is substantially free of one or more other molecules from the same species (3) is expressed by a cell from a different species, or (4) does not occur in nature. Thus, a molecule that is chemically synthesized, or expressed in a cellular system different from the cell from which it naturally originates, will be “isolated” from one or many of its naturally associated components. A molecule also may be rendered substantially free of from one or many of naturally associated components by isolation, using purification techniques well known in the art. Molecule purity or homogeneity may be assayed by a number of means well known in the art. For example, the purity of a polypeptide sample may be assayed using polyacrylamide gel electrophoresis and staining of the gel to visualize the polypeptide using techniques well known in the art. For certain purposes, higher resolution may be provided by using HPLC or other means well known in the art for purification.
As used herein, the term “isolated”, in the context of viruses, refers to a virus that is derived from a single parental virus. A virus can be isolated using routine methods known to one of skill in the art including, but not limited to, those based on plaque purification and limiting dilution.
As used herein, the phrase “multiplicity of infection” or “MO” is the average number of viruses per infected cell. The MOI is determined by dividing the number of virus added (ml added×plaque forming units (PFU)) by the number of cells added (ml added×cells/ml).
As used herein, “purify,” and grammatical variations thereof, refers to the removal, whether completely or partially, of at least one impurity from a mixture containing the polypeptide and one or more impurities, which thereby improves the level of purity of the polypeptide in the composition (i.e., by decreasing the amount (ppm) of impurity(ies) in the composition). As used herein “purified” in the context of viruses refers to a virus which is substantially free of cellular material and culture media from the cell or tissue source from which the virus is derived. The language “substantially free of cellular material” includes preparations of virus in which the virus is separated from cellular components of the cells from which it is isolated or recombinantly produced. Thus, virus that is substantially free of cellular material includes preparations of protein having less than about 30%, 20%, 10%, or 5% (by dry weight) of cellular protein (also referred to herein as a “contaminating protein”). The virus is also substantially free of culture medium, i.e., culture medium represents less than about 20%, 10%, or 5% of the volume of the virus preparation. A virus can be purified using routine methods known to one of skill in the art including, but not limited to, chromatography and centrifugation.
As used herein, “substantially pure” refers to material which is at least 50% pure (i.e., free from contaminants), more preferably, at least 90% pure, more preferably, at least 95% pure, yet more preferably, at least 98% pure, and most preferably, at least 99% pure.
The terms “patient”, “subject”, or “individual” are used interchangeably herein and refer to either a human or a non-human animal. These terms include mammals, such as humans, primates, livestock animals (including bovines, porcines, camels, etc.), companion animals (e.g., canines, felines, etc.) and rodents (e.g., mice and rats).
As used herein, the terms “prevent”, “preventing” and “prevention” refer to the delay of the recurrence or onset of disease, or a reduction in one or more symptoms of a disease (e.g., a poxviral infection) in a subject as a result of the administration of a therapy (e.g., a prophylactic or therapeutic agent). For example, in the context of the administration of a therapy to a subject for an infection, “prevent”, “preventing” and “prevention” refer to the inhibition or a reduction in the development or onset of an infection (e.g., a poxviral infection or a condition associated therewith), or the prevention of the recurrence, onset, or development of one or more symptoms of an infection (e.g., a poxviral infection or a condition associated therewith), in a subject resulting from the administration of a therapy (e.g., a prophylactic or therapeutic agent), or the administration of a combination of therapies (e.g., a combination of prophylactic or therapeutic agents).
As used herein, the terms “treat”, “treating” or “treatment” refer to treating a condition or patient and refers to taking steps to obtain beneficial or desired results, including clinical results. With respect to infections (e.g., a poxviral infection or a variola virus infection), treatment refers to the eradication or control of the replication of an infectious agent (e.g., the poxvirus or the variola virus), the reduction in the numbers of an infectious agent (e.g., the reduction in the titer of the virus), the reduction or amelioration of the progression, severity, and/or duration of an infection (e.g., a poxviral/variola infection or a condition or symptoms associated therewith), or the amelioration of one or more symptoms resulting from the administration of one or more therapies (including, but not limited to, the administration of one or more prophylactic or therapeutic agents). With respect to cancer, treatment refers to the eradication, removal, modification, or control of primary, regional, or metastatic cancer tissue that results from the administration of one or more therapeutic agents of the disclosure. In certain embodiments, such terms refer to minimizing or delaying the spread of cancer resulting from the administration of one or more therapeutic agents of the invention to a subject with such a disease. In other embodiments, such terms refer to elimination of disease-causing cells.
“Administering” or “administration of” a substance, a compound or an agent to a subject can be carried out using one of a variety of methods known to those skilled in the art. For example, a compound or an agent can be administered sublingually or intranasally, by inhalation into the lung or rectally. Administering can also be performed, for example, once, a plurality of times, and/or over one or more extended periods. In some aspects, the administration includes both direct administration, including self-administration, and indirect administration, including the act of prescribing a drug. For example, as used herein, a physician who instructs a patient to self-administer a drug, or to have the drug administered by another and/or who provides a patient with a prescription for a drug is administering the drug to the patient.
Each embodiment described herein may be used individually or in combination with any other embodiment described herein.
Poxviruses are large (˜200 kbp) DNA viruses that replicate in the cytoplasm of infected cells. The Orthopoxvirus (OPV) genus comprises a number of poxviruses that vary greatly in their ability to infect different hosts. Vaccinia virus (VACV), for example, can infect a broad group of hosts, whereas variola virus (VARV), the causative agent of smallpox, only infects humans. A feature common to many, if not all poxviruses, is their ability to non-genetically “reactivate” within a host. Non-genetic reactivation refers to a process wherein cells infected by one poxvirus can promote the recovery of a second “dead” virus (for example one inactivated by heat) that would be non-infectious on its own.
Purified poxvirus DNA is not infectious because the virus life cycle requires transcription of early genes via the virus-encoded RNA polymerases that are packaged in virions. However, this deficiency can be overcome if virus DNA is transfected into cells previously infected with a helper poxvirus, providing the necessary factors needed to transcribe, replicate, and package the transfected genome in trans (Sam C K, Dumbell K R. Expression of poxvirus DNA in coinfected cells and marker rescue of thermosensitive mutants by subgenomic fragments of DNA. Ann Virol (Inst Past). 1981; 132:135-50). Although this produces mixed viral progeny, the problem can be overcome by performing the reactivation reaction in a cell line that supports the propagation of both viruses, and then eliminating the helper virus by plating the mixture of viruses on cells that do not support the helper virus' growth (Scheiflinger F, Dorner F, Falkner F G. Construction of chimeric vaccinia viruses by molecular cloning and packaging. Proceedings of the National Academy of Sciences of the United States of America. 1992; 89(21):9977-81).
Previously, Yao and Evans described a method in which the high-frequency recombination and replication reactions catalyzed by a Leporipoxvirus, Shope fibroma virus (SFV), can be coupled with an SFV-catalyzed reactivation reaction, to rapidly assemble recombinant vaccinia strains using multiple overlapping fragments of viral DNA (Yao X D, Evans D H. High-frequency genetic recombination and reactivation of orthopoxviruses from DNA fragments transfected into leporipoxvirus-infected cells. Journal of Virology. 2003; 77(13):7281-90).
One aspect of the invention provides stem cells comprising a synthetic chimeric poxvirus (scPV), which can be used for the treatment of cancer and infectious diseases. The functional synthetic chimeric poxvirus (scPV) comprised within the stem cells, is initially replicated and assembled from chemically synthesized DNA. The scPV can be any poxvirus whose genome has been sequenced or can be sequenced in large part or for which a natural isolate is available. The viruses that may be produced in accordance with various embodiments of the methods of the invention can be any poxvirus whose genome has been sequenced in large part or for which a natural isolate is available. In some aspects, an scPV of the invention may be based on the genome sequences of naturally occurring strains, variants or mutants, mutagenized viruses or genetically engineered viruses. In some aspects, the viral genome of an scPV of the invention comprises one or more modifications relative to the wild type genome or base genome sequence of said virus. The modifications may include, for example, one or more deletions, insertions, substitutions, or combinations thereof. It is understood that the modifications may be introduced in any number of ways commonly known in the art.
As used herein, a “stem cell” is any totipotent, pluripotent or multipotent cell that has the ability to differentiate into multiple different types of cells (e.g., terminally differentiated cells). The term “stem cell”, as used herein, refers to a subset of progenitors that have the capacity or potential, under particular circumstances, to differentiate to a more specialized or differentiated phenotype, and which retains the capacity, under certain circumstances, to proliferate without substantially differentiating. In one embodiment, the term stem cell refers generally to a naturally occurring mother cell whose descendants (progeny) specialize, often in different directions, by differentiation, e.g., by acquiring completely individual characters, as occurs in progressive diversification of embryonic cells and tissues. Cellular differentiation is a complex process typically occurring through many cell divisions. A differentiated cell may derive from a multipotent cell which itself is derived from a multipotent cell, and so on. While each of these multipotent cells may be considered stem cells, the range of cell types each can give rise to may vary considerably. Some differentiated cells also have the capacity to give rise to cells of greater developmental potential. Such capacity may be natural or may be induced artificially upon treatment with various factors. In many biological instances, stem cells are also “multipotent” because they can produce progeny of more than one distinct cell type, but this is not required for “stem-ness.” Self-renewal is the other classical part of the stem cell definition, and it is essential as used in this invention. In theory, self-renewal can occur by either of two major mechanisms. Stem cells may divide asymmetrically, with one daughter retaining the stem state and the other daughter expressing some distinct other specific function and phenotype. Alternatively, some of the stem cells in a population can divide symmetrically into two stems, thus maintaining some stem cells in the population as a whole, while other cells in the population give rise to differentiated progeny only. Formally, it is possible that cells that begin as stem cells might proceed toward a differentiated phenotype, but then “reverse” and re-express the stem cell phenotype, a term often referred to as “dedifferentiation” or “reprogramming” or “retrodifferentiation”.
Any stem cell type can be used in the various aspects of the present invention. Stem cells include any type of stem cell, including embryonic stem cells (ES) cells, post-natal stem cells (e.g. from the umbilical cord and placenta), fetal stem cells and adult stem cells (i.e., somatic stem cells). Other types, such as induced pluripotent stem cells (iPSCs), are produced in the lab by reprogramming adult cells to express ES characteristics. In one embodiment, the adult stem cells are mesenchymal stem cells. In one embodiment, the adult stem cells are tissue or organ specific stem cells such as neuronal stem cells, vascular stem cells, or epidermal stem cells. In a preferred embodiment, the adult stem cells are mesenchymal stem cells (MSC).
Mesenchymal stem cells can be obtained from a variety of sources such as bone marrow, umbilical cord blood, and adipose tissue (adipose-tissue derived stem cells). Common sources of stem cells are human umbilical vein endothelial cells (HUVEC), and primary human cutaneous microvascular endothelial cells (HCMEC). Analogous non-human stem cells can be obtained from similar non-human sources as well. Stem cells for use in one aspect of the invention may be primary cells or cells that have been maintained in cell culture for an extended period. The stem cells may be obtained from any animal type, including human. In a preferred embodiment, the stem cell is a human cell.
As used herein, “embryonic stem cells” are stem cells obtained from an embryo that is typically six weeks old or less. Totipotent human embryonic stem cells (hESC) generally can be obtained from embryos that are 5 to 7 days old. Pluripotent human primordial germ cells (hEG) typically can be obtained from embryos that are six weeks old or less. As use herein, “fetal stem cells” refer to any stem cell that is obtained prenatally from a fetus that is typically greater that 6 weeks old. As used herein, “adult stem cells” refers to any stem cell that is obtained from a post-natal subject. Typically, the subject is a full grown adult. Exemplary adult stem cells include, but are not limited to, cells harvested from organs such as fat, muscle or bone marrow.
In one embodiment, the stem cells are autologous, i.e., the cells are obtained or derived from the subject's own stem cells. In one embodiment, the stem cells of the invention are obtained or derived from a subject who is in need of therapeutic treatment for a cell proliferative disorder (tumor or cancer). The subject may already have the cell proliferative disorder or be at risk for the disorder.
In another embodiment, the stem cells are allogeneic, i.e., the cells are obtained or derived from a donor whose human leukocyte antigens (HLA) are acceptable matches to the subject's.
In one aspect, the invention relates to an isolated stem cell or population thereof comprising a synthetic chimeric poxvirus (scPV), wherein the virus is replicated and reactivated from DNA derived from synthetic DNA, the viral genome of said virus differing from a wild type genome of said virus in that it is characterized by one or more modifications.
In another aspect, the invention relates to an isolated stem cell or population thereof comprising a synthetic chimeric orthopoxvirus, wherein the virus is replicated and reactivated from DNA derived from synthetic DNA, the viral genome of said virus differing from a wild type genome of said virus in that it is characterized by one or more modifications.
In another aspect, the invention relates to an isolated stem cell or population thereof comprising a synthetic chimeric vaccinia virus, wherein the virus is replicated and reactivated from DNA derived from synthetic DNA, the viral genome of said virus differing from a wild type genome of said virus in that it is characterized by one or more modifications.
In one aspect, the invention relates to an isolated stem cell or population thereof comprising a synthetic chimeric horsepox virus, wherein the virus is replicated and reactivated from DNA derived from synthetic DNA, the viral genome of said virus differing from a wild type genome of said virus in that it is characterized by one or more modifications.
In one embodiment, the stem cell of the invention is a non-cancer stem cell.
Chemical genome synthesis is particularly useful when a natural template is not available for genetic modification, amplification, or replication by conventional molecular biology methods. For example, a natural isolate of horsepox virus (HPXV) is not readily available to obtain template DNA but the genome sequence for HPXV (strain MNR-76) has been described. The HPXV genome sequence, however, is incomplete. The sequence of the terminal hairpin loops was not determined. Therefore, a functional synthetic chimeric HPXV (scHPXV) can be generated by using terminal hairpin loops based on VACV telomeres in lieu of HPXV terminal hairpin loop sequences. Similarly, the genome sequence for wtVACV (strain NYCBH, clone ACAM2000) has been described and published, though it is not complete. The sequence of the terminal hairpin loops was not determined, only four 54 bp repeat sequences were identified. Therefore, a functional synthetic chimeric VACV ACAM2000 can be generated by using terminal hairpin loops based on a different strain of VACV (such as WR strain) in lieu of VACV ACAM2000 terminal hairpin loop sequences. In other embodiments, the terminal hairpin loops are based on the VACV ACAM2000 terminal hairpin loop sequences.
In some embodiments, the poxvirus belongs to the Chordopoxvirinae subfamily. In some embodiments, the poxvirus belongs to a genus of Chordopoxvirinae subfamily selected from Avipoxvirus, Capripoxvirus, Cervidpoxvirus, Crocodylipoxvirus, Leporipoxvirus, Molluscipoxvirus, Orthopoxvirus, Parapoxvirus, Suipoxvirus, or Yatapoxvirus. In some embodiments, the poxvirus is an Orthopoxvirus. In some embodiments, the Orthopoxvirus is selected from camelpox virus (CMLV), cowpox virus (CPXV), ectromelia virus (ECTV, “mousepox agent”), HPXV, monkeypox virus (MPXV), rabbitpox virus (RPXV), raccoonpox virus, skunkpox virus, Taterapox virus, Uasin Gishu disease virus, vaccinia virus (VACV), variola virus (VARV) and volepox virus (VPV). In a preferred embodiment, the poxvirus is an HPXV. In another preferred embodiment, the poxvirus is a VACV. In some embodiments, the poxvirus is a Parapoxvirus. In some embodiments, the Parapoxvirus is selected from orf virus (ORFV), pseudocowpox virus (PCPV), bovine popular stomatitis virus (BPSV), squirrel parapoxvirus (SPPV), red deer parapoxvirus, Ausdyk virus, Chamois contagious ecythema virus, reindeer parapoxvirus, or sealpox virus. In some embodiments, the poxvirus is a Molluscipoxvirus. In some embodiments, the Molluscipoxvirus is molluscum contagiousum virus (MCV). In some embodiments, the poxvirus is a Yatapoxvirus. In some embodiments, the Yatapoxvirus is selected from Tanapox virus or Yaba monkey tumor virus (YMTV). In some embodiments, the poxvirus is a Capripoxvirus. In some embodiments, the Capripoxvirus is selected from sheepox, goatpox, or lumpy skin disease virus. In some embodiments, the poxvirus is a Suipoxvirus. In some embodiments, the Suipoxvirus is swinepox virus. In some embodiments, the poxvirus is a Leporipoxvirus. In some embodiments, the Leporipoxvirus is selected from myxoma virus, Shope fibroma virus (SFV), squirrel fibroma virus, or hare fibroma virus. New poxviruses (e.g., Orthopoxviruses) are still being constantly discovered. It is understood that an scPV of the various aspects of the invention may be based on such a newly discovered poxvirus.
In some aspects, the scPV is a CMLV whose genome is based on a published genome sequence (e.g., strain CMS (Genbank Accession AY009089.1)). In some aspects, the scPV is a CPXV whose genome is based on a published genome sequence (e.g., strain Brighton Red (Genbank Accession AF482758), strain GRI-90 (Genbank Accession X94355)). In some aspects, the scPV is a ECTV whose genome is based on a published genome sequence (e.g. strain Moscow (Genbank Accession NC_004105)). In some aspects, the scPV is a MPXV whose genome is based on a published genome sequence (e.g., strain Zaire-96-1-16 (Genbank Accession AF380138)). In some aspects, the scPV is a RPXV whose genome is based on a published genome sequence (e.g. strain Utrecht (Genbank Accession AY484669)). In some aspects, the scPV is a Taterapox virus whose genome is based on a published genome sequence (e.g., strain Dahomey 1968 (Genbank Accession NC_008291)).
Chemical viral genome synthesis also opens up the possibility of introducing a large number of useful modifications to the resulting genome or to specific parts of it. The modifications may improve ease of cloning to generate the virus, provide sites for introduction of recombinant gene products, improve ease of identifying reactivated viral clones and/or confer a plethora of other useful features (e.g., introducing a desired antigen, producing an oncolytic virus, etc.). In some embodiments, the modifications may include the attenuation or deletion of one or more virulence factors. In some embodiments, the modifications may include the addition or insertion of one or more virulence regulatory genes or gene-encoding regulatory factors.
In one aspect, the invention provides polynucleotides for producing a synthetic chimeric horsepox virus (scHPXV). In a specific embodiment, the scHPXV genome may be based on the genome sequence described for HPXV strain MNR-76 (SEQ ID NO: 49) (Tulman E R, Delhon G, Afonso C L, Lu Z, Zsak L, Sandybaev N T, et al. Genome of horsepox virus. Journal of Virology. 2006; 80(18):9244-58). This genome sequence is incomplete and appears not to include the sequence of the terminal hairpin loops. It is shown here that terminal hairpin loops from vaccinia virus (VACV) can be ligated onto the ends of the HPXV genome to produce functional scHPXV particles using the methods of the invention. The HPXV genome may be divided into 10 overlapping fragments as described in the working examples of the disclosure and shown in Table 1. In some embodiments, the genome may be divided into 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or 15 overlapping fragments. In some embodiments, the entire genome may be provided as one fragment. The genomic locations of the exemplary overlapping fragments and fragment sizes are shown in Table 1. Table 2 shows some of the modifications that may be made in these fragments relative to the base sequence. The polynucleotides of one aspect of the invention comprise nucleic acids sequences that are at least 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to SEQ ID NOs: 1-10. In some embodiments, an isolated polynucleotide of the invention comprises a variant of these sequences, wherein such variants can include missense mutations, nonsense mutations, duplications, deletions, and/or additions. SEQ ID NO: 11 and SEQ ID NO: 12 depict the nucleotide sequences of VACV (WR strain) terminal hairpin loops. In some embodiments, the terminal hairpin loops comprise nucleic acid sequences that are at least 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to SEQ ID NO: 11 or SEQ ID NO: 12.
In another aspect, the invention provides polynucleotides for producing a synthetic chimeric vaccinia virus (scVACV). In a specific embodiment, the scVACV genome may be based on the published genome sequence described for VACV strain NYCBH clone ACAM2000 (GenBank accession AY313847; Osborne J D et al. Vaccine. 2007; 25(52):8807-32). This genome sequence is incomplete and appears not to include the sequence of the terminal hairpin loops and only four 54 bp repeat sequences were identified. It is shown in the present application that terminal hairpin loops from vaccinia virus (VACV) strain WR can be ligated onto the ends of the VACV genome strain NYCBH clone ACAM2000 to produce functional scVACV particles using the methods of the disclosure. In some embodiments, the terminal hairpin loops from vaccinia virus (VACV) strain ACAM2000 can be ligated onto the ends of the VACV genome strain NYCBH clone ACAM2000 to produce functional scVACV particles using the methods of the disclosure. The scVACV genome may be divided into 9 overlapping fragments as described in the working examples of the disclosure and shown in Table 4. In some embodiments, the VACV genome may be divided into 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or 15 overlapping fragments. In some embodiments, the entire genome may be provided as one fragment. The fragment sizes are shown in Table 4. The polynucleotides of one aspect of the invention comprise nucleic acids sequences that are at least 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to SEQ ID NOs: 54-62. In some embodiments, an isolated polynucleotide of the invention comprises a variant of these sequences, wherein such variants can include missense mutations, nonsense mutations, duplications, deletions, and/or additions. SEQ ID NO: 11 and SEQ ID NO: 12 depict the nucleotide sequences of VACV (WR strain) terminal hairpin loops. SEQ ID NO: 117 and SEQ ID NO: 118 depict the nucleotide sequences of VACV (ACAM2000 strain) terminal hairpin loops. In some embodiments, the terminal hairpin loops comprise nucleic acid sequences that are at least 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to SEQ ID NO: 11 or to SEQ ID NO: 12. In some embodiments, the terminal hairpin loops comprise nucleic acid sequences that are at least 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identical to SEQ ID NO: 117 or to SEQ ID NO: 118.
Traditionally, the terminal hairpins of poxviruses have been difficult to clone and sequence, hence, it is not surprising that some of the published genome sequences (e.g., VACV, ACAM 2000 and HPXV MNR-76) are incomplete. The published sequence of the HPXV genome is likewise incomplete, probably missing ˜60 bp from the terminal ends. Thus, the HPXV hairpins cannot be precisely replicated. In an exemplary embodiment, 129 nt ssDNA fragments were chemically synthesized using the published sequence of the VACV terminal hairpins as a guide and ligated onto dsDNA fragments comprising left and right ends of the HPXV genome. Likewise, the genome sequence for wtVACV, strain NYCBH, clone ACAM2000, has been described and published, though it is not complete. The sequence of the terminal hairpin loops was not determined, only four 54 bp repeat sequences were identified. Since the published sequence of the wtVACV strain NYCBH, clone ACAM2000 genome is incomplete, the hairpins cannot be precisely replicated. In an exemplary embodiment, ssDNA fragments were chemically synthesized using the published sequence of the wtVACV WR strain terminal hairpin loops as a guide and ligated onto dsDNA fragments comprising left and right ends of the VACV strain NYCBH.
In another embodiment, the viral genome of the scPV of the present disclosure comprises homologous or heterologous terminal hairpin loops and the tandem repeat regions (the 70 bp, the 125 bp and the 54 bp tandem repeats) located downstream of the hairpin loops, wherein the tandem repeat regions comprise a different number of repeats than the wtVACV (i.e. the virus present in nature). The number of repeats of the 70 bp, the 125 bp and the 54 bp tandem repeats found in the VACV virus, strain WR were 22, 2 and 8, respectively. In another embodiment, the number of tandem repeat regions are variable in the different poxviruses, in the different vaccinia viruses or in the different vaccinia virus strains. The term “homologous terminal hairpin loops” means that said terminal hairpin loops are coming from the same virus species/the same strain, while the term “heterologous terminal hairpin loops” means that said terminal hairpin loops are coming from a different virus species/different strain.
In some embodiments, the terminal hairpins of an scPV of the invention are derived from VACV. In some embodiments, the terminal hairpins are derived from CMLV, CPXV, ECTV, HPXV, MPXV, RPXV, raccoonpox virus, skunkpox virus, Taterapox virus, Uasin Gishu disease virus or VPV. In some embodiments, the terminal hairpin loops are based on a strain selected from the group of: Western Reserve, Clone 3, Tian Tian, Tian Tian clone TP5, Tian Tian clone TP3, NYCBH, NYCBH clone Acambis 2000, Wyeth, Copenhagen, Lister, Lister 107, Lister-LO, Lister GL-ONC1, Lister GL-ONC2, Lister GL-ONC3, Lister GL-ONC4, Lister CTC1, Lister IMG2 (Turbo FP635), IHD-W, LC16m18, Lederle, Tashkent clone TKT3, Tashkent clone TKT4, USSR, Evans, Praha, L-IVP, V-VET1 or LIVP 6.1.1, Ikeda, EM-63, Malbran, Duke, 3737, CV-1, Connaught Laboratories, Serro 2, CM-01, NYCBH Dryvax clone DPP13, NYCBH Dryvax clone DPP15, NYCBH Dryvax clone DPP20, NYCBH Dryvax clone DPP17, NYCBH Dryvax clone DPP21, VACV-IOC, Chorioallantois Vaccinia virus Ankara (CVA), Modified vaccinia Ankara (MVA), and MVA-BN. In one embodiment, the terminal hairpin loops are based on the Western Reserve strain (WR strain) of VACV. In another embodiment, the terminal hairpin loops are based on the ACAM2000 strain. New VACV strains are still being constantly discovered. It is understood that an scPV of the various aspects of the invention may be based on such a newly discovered poxviruses or newly discovered strains.
In some embodiments, the modifications may include the deletion of one or more restriction sites. In some embodiments, the modifications may include the introduction of one or more restriction sites. In some embodiments, the restriction sites to be deleted from the genome or added to the genome may be selected from one or more of restriction sites such as but not limited to AanI, AarI, AasI, AatI, AatII, AbaSI, AbsI, Acc65I, AccI, AccI, AccIII, Aci, AcII, AcuI, AfeI, AflII, AfIHI, AgeI, AhdI, AeI, AluI, AwI, ALwNI, ApaI, ApaLI, ApeKI, ApoI, AscI, AseI, AsiSI, AvaI, AvaII, AvrII, BaeGI, BaeI, BamHI BanI, BanI, BbsI, BbvCI, BbvI, BccI, BceAI, BcgI, BciVI, BcI, BcoDI, BfaI, BfuAI, BfuCI, BglI, BglII, BlpI, BmgBI, BmrI, BmtI, BpmI, Bpu10I, BpuEI, BsaAI, BsaBI, BsaHI, BsaI, BsaJI, BsaWI, BsaXI, BseRI, BseYI, BsgI, BsiEI, BsiHKAI, BsiWI, BsI, BsmAI, BsmBI, BsmFI, BsmI, BsoBI, Bsp1286I, BspCNI, BspDI, BspEI, BspHI, BspMI, BspQI, BsrBI, BsrDI, BsrFa, BsrGI, BsrI, BssHII, BssSa, BstAPI, BstBI, BstEII, BstNI, BstUI, BstX, BstYI, BstZ17I, Bsu36I, BtgI, BtgZI, Btsa, BtsCI, BtsIMutI, Cac8I, ClaI, CspCI, CviAII, CviKI-1, CviQI, DdeI, DpnI, DpnII, DraI, DrdI, EaeI, EagI, EarI, EciI, Eco53kI, EcoNI, EcoO109I, EcoPI5I, EcoRI, EcoRV, FatI, FauI, Fnu4HI, FokI, FseI, FspEI, FspI, HaeII, HaeIII, HgaI, HhaI, HincI, Hindll, Hinfl, HinPl, HpaI, HpaII, HphI, Hpy166II, Hpy188I, Hpy188III, Hpy99I, HpyAV, HpyCH4III, HpyCH4IV, HpyCH4V, I-CeuI, I-SceI, KasI, KpnI, LpnPI, MboI, MboII, MfeI, MuCI, MZuI, MyI, MmeI, MnlI, MscI, MseI, MsI, MspA, MspI, MspJI, MwoI, NaeI, NarI, NciI, NcoI, NdeI, NgoMIV, NheI, NaIII, NaIV, NmeAIII, NotI, NruI, NsiI, NspI, PacI, PaeR7I, PciI, PflFI, PflMI, PleI, PluTI, PmeI, PmI, PpuMI, PshAI, PsiI, PspGI, PspOMI, PspXI, PstI, PvuI, PvuII, RsaI, RsrII, SacI, SacI, SaI, SapI, Sau3AI, Sau96I, Sbfl, ScrFI, SexAI, SfaNI, SfcI, SfiI, SfoI, SgrAI, SmaI, SmlI, SnaBI, SpeI, SphI, SrfI, SspI, StuI, StyD4I, StyI, SwaI, Taqa, TfI, TseI, Tsp45I, TspMI, TspRI, Tth111I, XbaI, XcmI, XhoI, XmaI, XmnI, or ZraI. It is understood that any desired restriction site(s) or combination of restriction sites may be inserted into the genome or mutated and/or eliminated from the genome. In some embodiments, one or more AarI sites are deleted from the viral genome. In some embodiments, one or more BsaI sites are deleted from the viral genome. In some embodiments, one or more restriction sites are completely eliminated from the genome (e.g., all the AarI sites in the viral genome may be eliminated). In some embodiments, one or more AvaI restriction sites are introduced into the viral genome. In some embodiments, one or more Stu sites are introduced into the viral genome. In some embodiments, the one or more modifications may include the incorporation of recombineering targets including, but not limited to, loxP or FRT sites.
In some embodiments, the modifications may include the introduction of fluorescence markers such as, but not limited to, green fluorescent protein (GFP), enhanced GFP, yellow fluorescent protein (YFP), cyan/blue fluorescent protein (BFP), red fluorescent protein (RFP), or variants thereof, etc.; selectable markers such as but not limited to drug resistance markers (e.g., E. coli xanthine-guanine phosphoribosyl transferase gene (gpt), Streptomyces alboniger puromycin acetyltransferase gene (pac), neomycin phosphotransferase I gene (nptI), neomycin phosphotransferase gene II (nptII), hygromycin phosphotransferase (hpt), sh ble gene, etc.; protein or peptide tags such as but not limited to MBP (maltose-binding protein), CBD (cellulose-binding domain), GST (glutathione-S-transferase), poly(His), FLAG, V5, c-Myc, HA (hemagglutinin), NE-tag, CAT (chloramphenicol acetyl transferase), DHFR (dihydrofolate reductase), HSV (Herpes simplex virus), VSV-G (Vesicular stomatitis virus glycoprotein), luciferase, protein A, protein G, streptavidin, T7, thioredoxin, Yeast 2-hybrid tags such as B42, GAL4, LexA, or VP16; localization tags such as an NLS-tag, SNAP-tag, Myr-tag, etc. It is understood that other selectable markers and/or tags known in the art may be used. In some embodiments, the modifications include one or more selectable markers to aid in the selection of reactivated clones (e.g., a fluorescence marker such as YFP, a drug selection marker such as gpt, etc.) to aid in the selection of reactivated viral clones. In some embodiments, the one or more selectable markers are deleted from the reactivated clones after the selection step.
The invention provides, in some aspects, systems and methods for synthesizing, reactivating and isolating functional synthetic chimeric poxviruses (scPVs) from chemically synthesized overlapping double-stranded DNA fragments of the viral genome. Recombination of overlapping DNA fragments of the viral genome and reactivation of the functional scPV are carried out in cells previously infected with a helper virus. Briefly, overlapping DNA fragments that encompass all or substantially all of the viral genome of the scPV are chemically synthesized and transfected into helper virus-infected cells. The transfected cells are cultured to produce mixed viral progeny comprising the helper virus and reactivated scPV. Next, the mixed viral progeny are plated on host cells that do not support the growth of the helper virus but allow the synthetic chimeric poxvirus to grow, in order to eliminate the helper virus and recover the synthetic chimeric poxvirus. In some embodiments, the helper virus does not infect the host cells. In some embodiments, the helper virus can infect the host cells but grows poorly in the host cells. In some embodiments, the helper virus grows more slowly in the host cells compared to the scPV.
In some embodiments, substantially all of the synthetic chimeric poxvirus genome is derived from chemically synthesized DNA. In some embodiments, about 40%, about 50%, about 60%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, about 96%, about 97%, about 98%, about 99%, over 99%, or 100% of the synthetic chimeric vaccinia virus genome is derived from chemically synthesized DNA. In some embodiments, the poxvirus genome is derived from a combination of chemically synthesized DNA and naturally occurring DNA. In some embodiments, all of the fragments encompassing the vaccinia virus genome are chemically synthesized. In some embodiments, one or more of the fragments are chemically synthesized and one or more of the fragments are derived from naturally occurring DNA (e.g., by PCR amplification or by well-established recombinant DNA techniques).
The number of overlapping DNA fragments used in the various embodiments of the methods of the invention will depend on the size of the poxvirus genome, such as horsepox virus or vaccinia virus. Practical considerations such as reduction in recombination efficiency as the number of fragments increases on the one hand, and difficulties in synthesizing very large DNA fragments as the number of fragments decreases on the other hand, will also inform the number of overlapping fragments used in the methods of the invention. In some embodiments, the synthetic chimeric vaccinia virus genome may be synthesized as a single fragment. In some embodiments, the synthetic chimeric vaccinia virus genome is assembled from 2-14 overlapping DNA fragments. In some embodiments, the synthetic chimeric vaccinia virus genome is assembled from 4-12 overlapping DNA fragments. In some embodiments, the synthetic chimeric vaccinia virus genome is assembled from 6-12 overlapping DNA fragments. In some embodiments, the synthetic chimeric vaccinia virus genome is assembled from 8-11 overlapping DNA fragments. In some embodiments, the synthetic chimeric vaccinia virus genome is assembled from 8-10, 10-12, or 10-14 overlapping DNA fragments. In some embodiments, the synthetic chimeric vaccinia virus genome is assembled from 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or 15 overlapping DNA fragments. In an exemplary embodiment, the synthetic chimeric vaccinia virus genome is assembled from 9 overlapping DNA fragments. In some embodiments, the synthetic chimeric horsepox virus genome is assembled from 2-14 overlapping DNA fragments. In some embodiments, the synthetic chimeric horsepox virus genome is assembled from 4-12 overlapping DNA fragments. In some embodiments, the synthetic chimeric horsepox virus genome is assembled from 6-12 overlapping DNA fragments. In some embodiments, the synthetic chimeric horsepox virus genome is assembled from 8-11 overlapping DNA fragments. In some embodiments, the synthetic chimeric horsepox virus genome is assembled from 8-10, 10-12, or 10-14 overlapping DNA fragments. In some embodiments, the synthetic chimeric horsepox virus genome is assembled from 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or 15 overlapping DNA fragments. In an exemplary embodiment of the disclosure, a synthetic vaccinia virus (scVACV) is reactivated from 9 chemically synthesized overlapping double-stranded DNA fragments. In another exemplary embodiment of the disclosure, a synthetic chimeric horsepox virus (scHPXV) is reactivated from 10 chemically synthesized overlapping double-stranded DNA fragments. In some embodiments, terminal hairpin loops are synthesized separately and ligated onto the fragments comprising the left and right ends of the vaccinia virus genome. In some embodiments, terminal hairpin loops may be derived from a naturally occurring template. In some embodiments, the terminal hairpins of an scPV of the disclosure are derived from VACV. In some embodiments, the terminal hairpins are derived from CMLV, CPXV, ECTV, HPXV, MPXV, RPXV, raccoonpox virus, skunkpox virus, Taterapox virus, Uasin Gishu disease virus or VPV. In other embodiments, the terminal hairpins of an scVACV of the invention are derived from wtVACV. In some embodiments, the terminal hairpins are derived from wtVACV terminal hairpins of a different strain in lieu of the VACV own terminal hairpin loop sequences. In some embodiments, the terminal hairpins are based on the terminal hairpins of any wtVACV whose genome has been completely sequenced or a natural isolate of which is available for genome sequencing. In a preferred embodiment, the terminal hairpins are derived from VACV.
The size of the overlapping fragments used in the various embodiments of the methods of the invention will depend on the size of the poxvirus genome. It is understood that there can be wide variations in fragment sizes and various practical considerations, such as the ability to chemically synthesize very large DNA fragments, will inform the choice of fragment sizes. In some embodiments, the fragments range in size from about 2,000 bp to about 50,000 bp. In some embodiments, the fragments range in size from about 3,000 bp to about 45,000 bp. In some embodiments, the fragments range in size from about 4,000 bp to 40,000 bp. In some embodiments, the fragments range in size from about 5,000 bp to 35,000 bp. In some embodiments, the largest fragments are about 18,000 bp, 20,000 bp, 21,000 bp, 22,000 bp, 23,000 bp, 24,000 bp, 25,000 bp, 26,000 bp, 27,000 bp, 28,000 bp, 29,000 bp, 30,000 bp, 31,000 bp, 32,000 bp, 33,000 bp, 34,000 bp, 35,000 bp, 36,000 bp, 37,000 bp, 38,000 bp, 39,000 bp, 40,000 bp, 41,000 bp, 42,000 bp, 43,000 bp, 44,000 bp, 45,000 bp, 46,000 bp, 47,000 bp, 48,000 bp, 49,000 bp, or 50,000 bp. In an exemplary embodiment of the disclosure, an scVACV is reactivated from 9 chemically synthesized overlapping double-stranded DNA fragments ranging in size from about 10,000 bp to about 32,000 bp (Table 4). In an exemplary embodiment of the disclosure, an scHPXV is reactivated from 9 chemically synthesized overlapping double-stranded DNA fragments ranging in size from about 10,000 bp to about 32,000 bp (Table 1).
The helper virus may be any poxvirus that can provide the trans-acting enzymatic machinery needed to reactivate a poxvirus from transfected DNA. The helper virus may have a different or narrower host cell range than an scPV to be produced (e.g., Shope fibroma virus (SFV) has a very narrow host range compared to Orthopoxviruses such as vaccinia virus (VACV) or HPXV). The helper virus may have a different plaque phenotype compared to the scPV to be produced. In some embodiments, the helper virus is a Leporipoxvirus. In some embodiments, the Leporipoxvirus is an SFV, hare fibroma virus, rabbit fibroma virus, squirrel fibroma virus, or myxoma virus. In a preferred embodiment, the helper virus is an SFV. In some embodiments, the helper virus is an Orthopoxvirus. In some embodiments, the Orthopoxvirus is a camelpox virus (CMLV), cowpox virus (CPXV), ectromelia virus (ECTV, “mousepox agent”), HPXV, monkeypox virus (MPXV), rabbitpox virus (RPXV), raccoonpox virus, skunkpox virus, Taterapox virus, Uasin Gishu disease virus, VACV and volepox virus (VPV). In some embodiments, the helper virus is an Avipoxvirus, Capripoxvirus, Cervidpoxvirus, Crocodylipoxvirus, Molluscipoxvirus, Parapoxvirus, Suipoxvirus, or Yatapoxvirus. In some embodiments, the helper virus is a fowlpox virus. In some embodiments, the helper virus is an Alphaentomopoxvirus, Betaentomopoxvirus, or Gammaentomopoxvirus. In some embodiments, the helper virus is a psoralen-inactivated helper virus. In an exemplary embodiment of the disclosure, an scPV is reactivated from overlapping DNA fragments transfected into SFV-infected BGMK cells. The SFV is then eliminated by plating the mixed viral progeny on BSC-40 cells.
The skilled worker will understand that appropriate host cells to be used for the reactivation of the scPV and the selection and/or isolation of the scPV will depend on the particular combination of helper virus and chimeric poxvirus being produced by the methods of the invention. Any host cell that supports the growth of both the helper virus and the scPV may be used for the reactivation step and any host cell that does not support the growth of the helper virus may be used to eliminate the helper virus and select and/or isolate the scPV. In some embodiments, the helper virus is a Leporipoxvirus and the host cells used for the reactivation step may be selected from rabbit kidney cells (e.g., LLC-RK1, RK13, etc.), rabbit lung cells (e.g., R9ab), rabbit skin cells (e.g., SF1Ep, DRS, RAB-9), rabbit cornea cells (e.g., SIRC), rabbit carcinoma cells (e.g., Oc4T/cc), rabbit skin/carcinoma cells (e.g., CTPS), monkey cells (e.g., Vero, BGMK, etc.) or hamster cells (e.g., BHK-21, etc.). In some embodiments, the helper virus is SFV.
In various aspects, the scPVs of the present invention can be propagated in any substrate that allows the virus to grow to titers that permit the uses of the scPVs described herein. In one embodiment, the substrate allows the scPVs to grow to titers comparable to those determined for the corresponding wild-type viruses. In some embodiments, the scPVs may be grown in cells (e.g., avian cells, bat cells, bovine cells, camel cells, canary cells, cat cells, deer cells, equine cells, fowl cells, gerbil cells, goat cells, human cells, monkey cells, pig cells, rabbit cells, raccoon cells, seal cells, sheep cells, skunk cells, vole cells, etc.) that are susceptible to infection by the poxviruses. Such methods are well-known to those skilled in the art. Representative mammalian cells include, but are not limited to BHK, BGMK, BRL3A, BSC-40, CEF, CEK, CHO, COS, CVI, HaCaT, HEL, HeLa cells, HEK293, human bone osteosarcoma cell line 143B, MDCK, NIH/3T3, Vero cells, etc.). For virus isolation, the scPV is removed from cell culture and separated from cellular components, typically by well-known clarification procedures, e.g., such as gradient centrifugation and column chromatography, and may be further purified as desired using procedures well known to those skilled in the art, e.g., plaque assays.
In one aspect, the invention relates to a pharmaceutical composition comprising the isolated stem cell or population thereof of the invention and a pharmaceutically acceptable carrier.
The term “pharmaceutically acceptable” means approved by a regulatory agency of the Federal or a state government or listed in the U.S. Pharmacopeia or other generally recognized pharmacopeia for use in animals, and more particularly in humans. The term “carrier” refers to a diluent, adjuvant, excipient, or vehicle with which the pharmaceutical composition (e.g., immunogenic or vaccine formulation) is administered. Saline solutions and aqueous dextrose and glycerol solutions can also be employed as liquid carriers, particularly for injectable solutions. Suitable excipients include starch, glucose, lactose, sucrose, gelatin, malt, rice, flour, chalk, silica gel, sodium stearate, glycerol monostearate, talc, sodium chloride, dried skim milk, glycerol, propylene, glycol, water, ethanol and the like. Examples of suitable pharmaceutical carriers are described in “Remington's Pharmaceutical Sciences” by E. W. Martin. The formulation should suit the mode of administration.
In some embodiments, the pharmaceutical composition of the invention may be administered by standard routes of administration. Many methods may be used to introduce the formulations into a subject, these include, but are not limited to, intranasal, intratracheal, oral, intradermal, intramuscular, intraperitoneal, intravenous, conjunctival and subcutaneous routes.
Method for Delivering the scPV by the Stem Cells of the Disclosure
In one aspect, the invention relates to a method for delivery of a synthetic chimeric poxvirus (scPV) into a subject, the method comprising infecting the stem cells of the invention with a synthetic chimeric poxvirus and administering the scPV-infected stem cells into the subject.
Methods to infect the stem cells of the invention with a synthetic chimeric poxvirus are known in the art. Those skilled in the art can determine appropriate parameters, such as number of stem cells and multiplicity of infection.
In one embodiment, the stem cells are autologous and the invention relates to a method for delivery of a scPV into a subject, the method comprising (a) obtaining the stem cells from said subject; (b) infecting the stem cells with the oncolytic scPV and (c) administer the scPV infected stem cells back into the subject. In another embodiment, the stem cells are mesenchymal stem cells (MSC). In another embodiment, the MSC derive from the subject's adipose tissue.
In another embodiment, the stem cells are allogeneic and the invention relates to a method for delivery of a scPV into a subject, the method comprising (a) obtaining the stem cells from a subject; (b) infecting the stem cells with the oncolytic scPV and (c) administer the scPV infected stem cells back into the subject.
In some embodiments, the stem cells of the invention are administered in a single administration or in multiple administrations.
The stem cells can be implanted locally at the site of cell damage or dysfunction, or systemically. Exemplary routes of administration of the stem cell compositions include, but are not limited to, intravenous, intramuscular, intradermal, intraperitonal, intracoronary, intramyocardial, transendocardial, trans-epicardial, intraspinal, intra-arterial, intra-striatum, intratumoral, topical, transdermal, rectal or sub-epidermal routes. The most suitable route for administration will vary depending upon the disorder or condition to be treated, such as the location of cell damage or dysfunction. For example, stem cells can be administered intraarterially or intra-spinally at the site of injury for the treatment of spinal cord injury. In other examples, stem cell compositions can be administered by an intracoronary, intramyocardial, transendocardial or trans-epicardial route for the treatment of cardiovascular disease. In a preferred embodiment, the administration is intravenously.
In one embodiment, the amount of scPV used for the stem cells infection is 1×105 or about 1×105 plaque forming units (PFU), 5×105 or about 5×105 PFU, at least 1×106 or about 1×106 PFU, 5×106 or about 5×106 PFU, 1×107 or about 1×107 PFU, 5×107 or about 5×107 PFU, 1×108 or about 1×108 PFU, 5×108 or about 5×108 PFU, 1×109 or about 1×109 PFU, 5×109 or about 5×109 PFU, 1×1010 or about 1×1010 PFU or 5×1010 or about 5×1010 PFU.
In one embodiment, the multiplicity of infection of scPV used for the stem cells infection is about 0.5 PFU/cell, or about 1 PFU/cell, or about 2 PFU/cell, or about 3 PFU/cell, or about 4 PFU/cell, or about 5 PFU/cell, or about 6 PFU/cell, or about 7 PFU/cell, or about 8 PFU/cell, or about 9 PFU/cell or about 10 PFU/cell.
Conditions amenable to stem cell therapy include any in which one or more cell populations are defective or have been depleted or destroyed. Such conditions include degenerative disorders or conditions and acute or chronic injuries. Once the stem cells are implanted or engrafted into the patient, such as at the location of cell or tissue damage or dysfunction, the stem cells can differentiate into the desired cell or tissue type based on the physical and chemical signals in the local extracellular microenvironment, thereby replacing the destroyed or defective cells with functional healthy cells. Exemplary conditions include, but are not limited to, cancer, cardiovascular disease, diabetes, spinal cord injury, neurodegenerative disease, traumatic brain injury, Alzheimer's disease, Parkinson's disease, multiple sclerosis (MS), Amyotrophic lateral sclerosis (ALS), Duchenne Muscular Dystrophy, muscle damage or dystrophy, stroke, burns, lung disease, retinal disease, kidney disease, osteoarthritis, and rheumatoid arthritis.
As used herein, a method for treating or preventing cancer means that any of the symptoms, such as the tumor, metastasis thereof, the vascularization of the tumors or other parameters by which the disease is characterized are reduced, ameliorated, prevented, placed in a state of remission, or maintained in a state of remission. It also means that the indications of cancer and metastasis can be eliminated, reduced or prevented by the treatment. Non-limiting examples of the indications include uncontrolled degradation of the basement membrane and proximal extracellular matrix, migration, division, and organization of the endothelial cells into new functioning capillaries, and the persistence of such functioning capillaries.
The synthetic chimeric poxviruses (scPVs) of the various aspects of the invention can be used as oncolytic agents that selectively replicate in and kill cancer cells. Cells that are dividing rapidly, such as cancer cells, are generally more permissive for poxviral infection than non-dividing cells. Many features of poxviruses, such as safety in humans, ease of production of high-titer stocks, stability of viral preparations, and capacity to induce antitumor immunity following replication in tumor cells make poxviruses desirable oncolytic agents. The scPVs produced according to the methods of the invention may comprise one or modifications that render them suitable for the treatment of cancer. Accordingly, in one aspect, the disclosure provides a method of inducing death in cancer cells, the method comprising contacting the cancer cells with an isolated scPV or pharmaceutical composition comprising an scPV of the invention or the stem cells of the invention. In one aspect, the disclosure provides a method of treating cancer, the method comprising administering to a patient in need thereof, a therapeutically effective amount of the stem cells of the invention or the pharmaceutical composition of the invention. Another aspect includes the use of the stem cells of the invention or the pharmaceutical composition described herein to induce death in a neoplastic disorder cell such as a cancer cell or to treat a neoplastic disorder such as cancer. In some embodiments, the poxvirus oncolytic therapy is administered in combination with one or more conventional cancer therapies (e.g., surgery, chemotherapy, radiotherapy, thermotherapy, and biological/immunological therapy). In specific embodiments, the oncolytic virus is a synthetic chimeric VACV (scVACV) of this invention. In some embodiments, the oncolytic virus is a synthetic chimeric myxoma virus of this invention. In some embodiments, the oncolytic virus is a synthetic chimeric HPXV (scHIPXV) of this invention. In some embodiments, the oncolytic virus is a synthetic chimeric raccoonpox virus of this invention. In some embodiments, the oncolytic virus is a synthetic chimeric yaba-like disease virus of this invention.
In various aspects, using the method of treatment of cancer of this invention, one or more desirable genes can be easily introduced, and one or more undesirable genes can be easily deleted from the synthetic chimeric poxviral genome. In some embodiments, the scPVs of the invention for use as oncolytic agents are designed to express transgenes to enhance their immunoreactivity, antitumor targeting and/or potency, cell-to-cell spread and/or cancer specificity. In some embodiments, an scPV of the invention is designed or engineered to express an immunomodulatory gene (e.g., GM-CSF, or a viral gene that blocks TNF function). In some embodiments, an scPV of the disclosure is designed to include a gene that expresses a factor that attenuates virulence. In some embodiments, an scPV of the invention is designed or engineered to express a therapeutic agent (e.g., hEPO, BMP-4, antibodies to specific tumor antigens or portions thereof, etc.). In some embodiments, the scPVs of the invention have been modified for attenuation. In some embodiments, the scPV of the invention is designed or engineered to lack the viral TK gene. In some embodiments, an scVACV of the invention is designed or engineered to lack vaccinia growth factor gene. In some embodiments, an scVACV of the invention is designed or engineered to lack the hemagglutinin gene.
The stem cells of the various embodiments of the invention are useful for treating a variety of neoplastic disorders and/or cancers. In some embodiments, the type of cancer includes but is not limited to bone cancer, breast cancer, bladder cancer, cervical cancer, colorectal cancer, esophageal cancer, gliomas, gastric cancer, gastrointestinal cancer, head and neck cancer, hepatic cancer such as hepatocellular carcinoma, leukemia, lung cancer, lymphomas, ovarian cancer, pancreatic cancer, prostate cancer, renal cancer, skin cancer such as melanoma, testicular cancer, etc. or any other tumors or pre-neoplastic lesions that may be treated.
In another embodiment, the method further comprises detecting the presence of the administered scPV, in the neoplastic disorder or cancer cell and/or in a sample from a subject administered an isolated or recombinant virus or composition described herein. For example, the subject can be tested prior to administration and/or following administration of the scPV or composition described herein to assess for example the progression of the infection. In some embodiments, an scPV of the disclosure comprises a detection cassette and detecting the presence of the administered chimeric poxvirus comprises detecting the detection cassette encoded protein. For example, wherein the detection cassette encodes a fluorescent protein, the subject or sample is imaged using a method for visualizing fluorescence.
In some embodiments, the stem cells of the various embodiments of the invention are administered in a single administration or in multiple administrations.
In other embodiments, the stem cells of the invention can be implanted locally at the site of cell damage or dysfunction, or systemically in order to be used in a method to treat cancer. Exemplary routes of administration of the stem cell compositions include, but are not limited to, intravenous, intramuscular, intradermal, intraperitonal, intracoronary, intramyocardial, transendocardial, trans-epicardial, intraspinal, intra-arterial, intra-striatum, intratumoral, topical, transdermal, rectal or sub-epidermal routes. The most suitable route for administration will vary depending upon the disorder or condition to be treated, such as the location of cell damage or dysfunction. For example, stem cells can be administered intraarterially or intra-spinally at the site of injury for the treatment of spinal cord injury. In other examples, stem cell compositions can be administered by an intracoronary, intramyocardial, transendocardial or trans-epicardial route for the treatment of cardiovascular disease. In a preferred embodiment, the administration is intravenously.
The scPV for use in a method of treatment of cancer can encode a therapeutic gene product. In some examples, the therapeutic gene product is an anti-cancer agent or anti-angiogenic agent. In one embodiment, the therapeutic gene product can be selected from among a cytokine, a chemokine, an immunomodulatory molecule, an antigen, an antibody or fragment thereof, an antisense RNA, a prodrug converting enzyme, an siRNA, an angiogenesis inhibitor, a toxin, an antitumor oligopeptide, a mitosis inhibitor protein, an antimitotic oligopeptide, an anti-cancer polypeptide antibiotic, a transporter protein, and a tissue factor.
The method for treatment of cancer including the stem cells of the invention can also include administering an anticancer agent. Exemplary anticancer agents include, but are not limited to, a cytokine, a chemokine, a growth factor, a photosensitizing agent, a toxin, an anti-cancer antibiotic, a chemotherapeutic compound, a radionuclide, an angiogenesis inhibitor, a signaling modulator, an antimetabolite, an anti-cancer vaccine, an anti-cancer oligopeptide, a mitosis inhibitor protein, an antimitotic oligopeptide, an anti-cancer antibody, an anti-cancer antibiotic, an immunotherapeutic agent, hyperthermia or hyperthermia therapy, a bacterium, radiation therapy and a combination of such agents. In some examples, the anticancer agent is cisplatin, carboplatin, gemcitabine, irinotecan, an anti-EGFR antibody, or an anti-VEGF antibody. In some examples, the anticancer agent is administered simultaneously, sequentially, or intermittently with the virus.
In methods provided herein for administering the oncolytic virus to a subject, the method can also include administering an anti-viral agent to attenuate replication of or eliminate the virus from the subject during or following therapy. Exemplary antiviral agents include, but are not limited to, cidofovir, alkoxyalkyl esters of cidofovir, Gleevec, gancyclovir, acyclovir and ST-26.
In one aspect of the method for treatment of cancer, the scPV contains a gene deletion. A gene deletion is understood to be the loss or absence of a DNA sequence of a gene, or a deficiency in that gene or a deletion mutation, in which part of a chromosome or a sequence of DNA is lost during DNA replication. In one embodiment, the deleted gene is selected from a gene encoding a protein or fragment thereof, a gene segment that regulates transcription, a gene segment that regulates viral replication, a gene segment that affects cellular mitosis, a gene segment that affects cellular metabolism, a gene segment that encodes an antisense RNA, a gene segment that encodes an siRNA, a gene segment that regulates angiogenesis, a gene segment that regulates one or more transporter proteins, or a gene segment that regulates one or more tissue factors. In another embodiment, the gene deletion potentiates the anti-cancer or the anti-angiogenic effect of the virus. The term “potentiates the effect”, as used herein, means that the anti-cancer or the anti-angiogenic compounds are more effective or more active after the gene deletion, which means that the activity of the compounds is augmented after the gene deletion was performed on the scPV.
The stem cells of the various aspects of the invention can be used to treat a variola virus infection. With respect to infections (e.g., a poxviral infection or a variola virus infection), treatment refers to the eradication or control of the replication of an infectious agent (e.g., the poxvirus or the variola virus), the reduction in the numbers of an infectious agent (e.g., the reduction in the titer of the virus), the reduction or amelioration of the progression, severity, and/or duration of an infection (e.g., a poxviral/variola infection or a condition or symptoms associated therewith), or the amelioration of one or more symptoms resulting from the administration of one or more therapies (including, but not limited to, the administration of one or more prophylactic or therapeutic agents).
In some embodiments, the stem cells of the invention are administered in a single administration or in multiple administrations for the treatment of a variola infection.
Exemplary routes of administration of the stem cell compositions include, but are not limited to, intravenous, intramuscular, intradermal, intraperitonal, intracoronary, intramyocardial, transendocardial, trans-epicardial, intraspinal, intra-arterial, intra-striatum, intratumoral, topical, transdermal, rectal or sub-epidermal routes.
Design of the scHPXV genome was based on the previously described genome sequence for HPXV (strain MNR-76;
Each fragment was chemically synthesized and subcloned into a plasmid using terminal SfiI restriction sites on each fragment. To assist with sub-cloning these fragments, AarI and BsaI restriction sites were silently mutated in all the fragments, except for the two ITR-encoding fragments (Table 2). The BsaI restriction sites in the two ITR-encoding fragments were not mutated, in case these regions contained nucleotide sequence-specific recognition sites that were important for efficient DNA replication and concatemer resolution.
A yfp/gpt cassette under the control of a poxvirus early late promoter was introduced into the HPXVO95/J2R locus within GA_Fragment_3) so that reactivation of HPXV (scHPXV YFP-gpt::095) was easy to visualize under a fluorescence microscope. The gpt locus also provided a potential tool for selecting reactivated viruses using drug selection. HPXV095 encodes the HPXV homolog of the non-essential VACV J2R gene and by co-transfecting Fragment_3 and other HPXV clones into SFV-infected BGMK cells, along with VACV DNA, a variety of hybrid viruses were recovered, validating the selection strategy (
8505-24,761
The Slow (S) and Fast (F) forms of the terminal hairpin loops from VACV (strain WR) were synthesized as 157 nt ssDNA fragments (Integrated DNA Technologies;
Digestion and Purification of scHPXV YFP-Gpt::095 Fragments
Synthetic HPXV fragments were digested with SfiI overnight at 50° C. The scHPXV ITR fragments were individually digested with SapI (ThermoFisher Scientific) for 1 h, inactivated at 65° C. for 10 minutes, before digestion with SfiI overnight at 50° C. Approximately 1 U of FastAP alkaline phosphatase was added to the scHPXV YFP-gpt::095 ITR digestions and incubated at 37° C. for an additional 1 h. All scHPXV YFP-gpt::095 fragments were subsequently purified using a QiaexII DNA cleanup kit (Qiagen). All scHPXV YFP-gpt::095 fragments were eluted from the QiaexII suspension in 10 mM Tris-HCl. DNA concentrations were estimated using a NanoDrop (ThermoFisher Scientific).
Poxviruses catalyze very high-frequency homologous recombination reactions that are inextricably linked to the process of virus replication. Herein, it is demonstrated that large fragments of chemically synthesized HPXV duplex DNA can be joined to form a functional scHPXV genome using virus-catalyzed recombination and replication reactions.
Using the published sequence of the HPXV genome (strain WNR-76), the 212,633 bp genome was divided into 10-overlapping fragments (
While the reaction efficiency may be affected by the number of transfected fragments, greater than or less than 10 overlapping fragments may be used in the methods of the disclosure. Without being bound by theory, ˜15 fragments may represent a practical upper limit without further optimization of the reactivation reaction. The ideal lower limit would be a single genome fragment, but in practice the telomeres are most easily manipulated as more modest-sized fragments (e.g., ˜10 kb).
Ligation of VACV F- and S-Terminal Hairpin Loops onto scHPXV YFP-Gpt::095 Left and Right ITR Fragments
Approximately one microgram of each of the terminal VACV hairpin loops was incubated at 95° C. for 5 minutes followed by a “snap” cool on ice to form the hairpin structure. The hairpin loops were subsequently phosphorylated at their 5′ end before ligation. Briefly, separate 20 μl reactions containing 1 μg of either VACV F-hairpin or VACV S-hairpin, 2 μl of 10×T4 polynucleotide kinase buffer (ThermoFisher Scientific), 1 mM ATP, and 10 units of T4 polynucleotide kinase (ThermoFisher Scientific) were incubated at 37° C. for 1 h. The reaction was terminated by heat inactivation at 75° C.
Approximately one microgram of either left ITR or right ITR was incubated separately with a 20-fold molar excess of each terminal hairpin in the presence of 5% PEG-4000, and 5 units of T4 DNA ligase overnight at 16° C. Each ligation reaction was heat-inactivated at 65° C. for 10 minutes followed by incubation on ice until ready to transfect into cells.
Orthopoxviruses encode linear dsDNA genomes bearing variable length inverted terminal repeats (ITR) at each end of the genome. The two strands of the duplex genome are connected by hairpin loops to form a covalently continuous polynucleotide chain. The loops are A+T-rich, cannot form a completely base-paired structure, and exist in two forms that are inverted and complementary in sequence (Baroudy B M, Venkatesan S, Moss B). Incompletely base-paired flip-flop terminal loops link the two DNA strands of the vaccinia virus genome into one uninterrupted polynucleotide chain. Cell. 1982; 28(2):315-24) (
Sequences derived from VACV were used based upon data suggesting a close common ancestry between HPXV and VACV. It may be possible to use other terminal hairpins from other poxviruses since there are sequence features that are commonly conserved between the hairpin ends of different Chordopoxviruses. For example, the resolution sites in the hairpin ends are highly conserved in both sequence and functionality (they resemble late promoters).
These single-stranded oligonucleotides were heated to 95° C. and then quickly chilled on ice to form the incompletely base-paired terminal hairpin (
To confirm that a hairpin-terminated structure was added to both ITR fragments, restriction digestion of the ITR fragments with PvuII was performed. Since it was impossible to visualize the addition of a ˜70 bp terminal hairpin onto the terminus of a ˜10 kb ITR by gel electrophoresis, a small amount of each ligation was digested with PvuII. If no terminal hairpin was ligated to the ITR, then digestion with PvuII resulted in a 1472 bp product (
Reactivation of scHPXV YFP-Gpt:: 095 from Chemically Synthesized dsDNA Fragments
SFV strain Kasza and BSC-40 were originally obtained from the American Type Culture Collection. Buffalo green monkey kidney (BGMK) cells were obtained from G. McFadden (University of Florida). BSC-40 and BGMK cells are propagated at 37° C. in 5% CO2 in minimal essential medium (MEM) supplemented with L-glutamine, nonessential amino acids, sodium pyruvate, antibiotics and antimycotics, and 5% fetal calf serum (FCS; ThermoFisher Scientific).
Buffalo green monkey kidney (BGMK) cells were grown in MEM containing 60 mm tissue-culture dishes until they reached approximately 80% confluency. Cells were infected with Shope Fibroma Virus (SFV) in serum-free MEM at a MOI of 0.5 for 1 h at 37° C. The inoculum was replaced with 3 ml of warmed MEM containing 5% FCS and returned to the incubator for an additional hour. Meanwhile, transfection reactions were set up as follows. Lipofectamine complexes were prepared by mixing approximately 5 μg total synthetic HPXV DNA fragments in 1 ml Opti-MEM with Lipofectamine2000 diluted in 1 ml Opti-MEM at a ratio of 3:1 (Lipofectamine2000 to total DNA). The complexes were incubated at room temperature for 10 minutes and then added dropwise to the BGMK cells previously infected with SFV. Approximately 16 h post infection, the media was replaced with fresh MEM containing 5% FCS. The cells were cultured for an additional 4 d (total of 5 d) at 37° C. Virus particles were recovered by scraping the infected cells into the cell culture medium and performing three cycles of freezing and thawing. The crude extract was diluted 102 in serum-free MEM and 4 ml of the inoculum was plated on 9-16 150 mm tissue culture plates of BSC-40 cells to recover reactivated scHPXV YFP-gpt::095. One hour post infection, the inoculum was replaced with MEM containing 5% FCS and 0.9% Noble Agar. Yellow fluorescent plaques were visualized under an inverted microscope and individual plaques were picked for further analysis. ScHPXV YFP-gpt::095 plaques were plaque purified three times with yellow fluorescence selection.
SFV-catalyzed recombination and reactivation of Orthopoxvirus DNA to assemble recombinant vaccinia viruses had previously been described (Yao X D, Evans D H. High-frequency genetic recombination and reactivation of orthopoxviruses from DNA fragments transfected into leporipoxvirus-infected cells. Journal of Virology. 2003; 77(13):7281-90). Construction of recombinant vaccinia viruses using leporipoxvirus-catalyzed recombination and reactivation of orthopoxvirus DNA. Methods Mol Biol. 2004; 269:51-64). Several biological features make this an attractive model system. First, SFV has a narrow host range, productively infecting rabbit cells and certain monkey cell lines, like BGMK. It can infect, but grows very poorly on cells like BSC-40. Second, it grows more slowly compared to Orthopoxviruses, taking approximately 4-5 days to form transformed “foci” in monolayers of cells, a characteristic that is very different from Orthopoxviruses, which produce plaques within 1-2 days in culture. This difference in growth between Leporipoxviruses and Orthopoxviruses allows one to differentiate these viruses by performing the reactivation assays in BGMK cells and plating the progeny on BSC-40 cells. In some embodiments, other helper viruses (such as but not limited to fowlpox virus) may be used. In some embodiments, different cell combinations may be used.
BGMK cells were infected with SFV at a MOI of 0.5 and then transfected with 5 μg of digested GA_HPXV fragments 2 h later. Five days post transfection all of the infectious particles were recovered by cell lysis and re-plated on BSC-40 cells, which only efficiently supported growth of HPXV (or other Orthopoxviruses). The resulting reactivated scHPXV YFP-gpt::095 plaques were visualized under a fluorescence microscope. The visualization was enabled by the yfp/gpt selectable marker in the HPXV095/J2R locus within Frag_3 (
Confirmation of scHPXV YFP-Gpt::095 Genome Sequence by PCR and Restriction Fragment Analysis
PCR and Restriction Digestion Analysis of scHPXV
To rapidly confirm the presence of scHPXV YFP-gpt::095 in reactivated plaque picks, PCR primers were designed to flank individual BsaI sites that were mutated in the scHPXV (Table 5). Genomic scHPXV YFP-gpt::095 DNA was isolated from BSC-40 cells infected with scHPXV YFP-gpt::095 and used as a template. Genomic DNA from VACV-infected BSC-40 cells was used as a control to confirm the presence of BsaI sites within each PCR product. Following PCR amplification, reactions were subsequently digested with BsaI for 1 h at 37° C. PCR reactions were separated on a 1% agarose gel containing SYBR® safe stain to visualize DNA bands.
Further analysis of scHPXV YFP-gpt::095 genomes by restriction digestion followed by pulse-field gel electrophoresis (PFGE) was carried out on genomic DNA isolated using sucrose gradient purification (Yao X D, Evans D H. Construction of recombinant vaccinia viruses using leporipoxvirus-catalyzed recombination and reactivation of orthopoxvirus DNA. Methods Mol Biol. 2004; 269:51-64). Briefly, 100 ng of purified viral genomic DNA was digested with 5 U of BsaI or HindIII for 2 h at 37° C. Digested DNA was run on a 1% Seakem Gold agarose gel cast and run in 0.5× tris-borate-EDTA electrophoresis (TBE) buffer [110 mM tris; 90 mM borate; 2.5 mM EDTA]. The DNA was resolved on a CHEF DR-III apparatus (BioRad) at 5.7V/cm for 9.5 h at 14° C., using a switching time gradient of 1 to 10 s, a linear ramping factor, and a 1200 angle. This program allows resolution of DNA species from 1 kbp to >200 kbp. To resolve fragments from 75 bp to 5 kbp, electrophoresis on 1.5% agarose gel cast and run in 1.0×TBE at 115V for 2 h at room temperature was carried out. The DNA was visualized with SYBR® gold stain. The size of digested scHPXV YFP-gpt::095 DNA fragments was compared to control VACV genomic DNA.
The genome sequence of virus isolated from plaques grown from the reactivation assay was confirmed by PCR, restriction digestion, and whole genome sequencing. The PCR analysis was based on the mutated BsaI sites within all but the ITR HPXV fragments. Primer sets were designed to flank each BsaI site in scHPXV YFP-gpt::095 (Table 5). It was confirmed that these primer sets would also amplify a similar region within VACV WR. After PCR amplification of an approximate 1 kb region surrounding these mutated BsaI sites within scHPXV YFP-gpt::095, each reaction was digested with BsaI and the resulting DNA fragments were analyzed by gel electrophoresis. Since no BsaI sites were mutated in VACV (wt), enzymatic digestion successfully digested each PCR product, resulting in a smaller DNA fragment. The PCR products generated from scHPXV YFP-gpt::095 genomic DNA were resistant to BsaI digestion, suggesting that the BsaI recognition site was successfully mutated in these genomes. The primer products for primer set 7C did not result in any amplification of DNA in the scHPXV YFP-gpt::095 PP1 and PP3 samples. To confirm whether this primer set was non-functional or if this area of Fragment 7 did not get assembled into the resulting scHPXV YFP-gpt::095 genome, PCR was performed on the original GA_Frag_7 plasmid DNA and this reaction was also unsuccessful in amplifying a product.
Genomic DNA was next isolated from sucrose-gradient purified scHPXV YFP-gpt::095 genomes, digested with BsaI or HindIII, and separated by agarose gel electrophoresis to confirm that the majority of the BsaI sites in scHPXV YFP-gpt::095 are successfully mutated. Interestingly, undigested genomic DNA from 3 different scHPXV YFP-gpt::095 clones run noticeably slower on a gel compared to VACV, confirming that the genome of scHPXV YFP-gpt::095 (213,305 bp) is larger than VACV-WR (194,711 bp) (
Since HPXV095 encodes the HPXV homolog of the non-essential VACV J2R gene, by co-transfecting Fragment_3 and other HPXV clones into SFV-infected BGMK cells, along with VACV DNA, a variety of hybrid viruses were recovered, validating the selection strategy (
Confirmation of scHPXV YFP-Gt:: 095 Genome Sequence by Whole Genome Sequence Analysis
Stocks of HPXV YFP-gpt::095 clones (plaque pick [PP] 1.1, PP 2.1, and PP 3.1]) were prepared and purified over sucrose gradients. Viral DNAs were extracted from each purified virus preparation using proteinase K digestion followed by phenol-chloroform extraction. The amount of dsDNA was determined using a Qubit dsDNA HS assay kit (ThermoFisher Scientific). Each viral genome was sequenced at the Molecular Biology Facility (MBSU) at the University of Alberta. Sequencing libraries were generated using the Nextera Tagmentation system (Epicentre Biotechnologies). Approximately 50 ng of each sample was sheared and library prepped for paired end sequencing (2×300 bp) using an Illumina MiSeq platform with an average read depth of 3,100 reads·nt−1 across the genome and ˜190 reads·nt−1 in the F- and S-hairpins.
Raw sequencing reads were trimmed of low-quality sequence scores and initially mapped to the HPXV reference sequence [GenBank Accession DQ792504] using CLC Genomics Workbench 8.5 software. All nucleotide insertions, deletions, and substitutions within the scHPXV YFP-gpt::095 sequence were verified against the HPXV reference sequence. The Genome Annotation Transfer Utility (GATU) (Tcherepanov V, Ehlers A, Upton C. Genome Annotation Transfer Utility (GATU): rapid annotation of viral genomes using a closely related reference genome. BMC Genomics. 2006; 7:150. Epub 2006/06/15) was used to transfer the reference annotation to the scHPXV genome sequences.
Purified scHPXV YFP-gpt::095 genomes were sequenced using a multiplex approach and an Illumina MiSeq sequencer. The sequence reads were mapped onto the wild-type HPXV (DQ792504) and scHPXV YFP-gpt::095 reference sequences to confirm the presence of specific modifications in the scHPXV YFP-gpt::095 genome. To confirm that the VACV terminal repeat sequences were correctly ligated onto the terminal end of the left ITR, sequencing reads in this area of the genome were analyzed. A string of Cs was added to the beginning of the scHPXV YFP-gpt::095 genome reference sequence to capture all of the sequence reads that mapped in this region. This was done because the program used to assemble the sequence reads will otherwise truncate the display of sequences at the point where the scHPXV YFP-gpt::095 genome reference sequence ends.
It was clear from the mapped reads that although the SapI recognition site was present in the scHPXV YFP-gpt::095 reference genome, all of the sequencing reads lacked this sequence. This confirmed that the approach described herein produces an authentic HPXV sequence at the site where the synthetic hairpin was ligated to the ends of the ITRs. The complete sequence of the VACV WR terminal hairpin loop was also successfully obtained, which proved to be identical to the sequence of the synthetic ssDNA that was ligated onto the TIR ends. Overall, these data suggested that the VACV-WR terminal hairpin loops were successfully ligated onto the HPXV ITR sequences and recovered in the infectious viruses. Moreover, the 1:1 distribution of F- and S-read in each of five viruses suggested that both ends were required to produce a virus.
Next, it was verified that each nucleotide substitution to silently mutate the BsaI sites had correctly been incorporated into the scHPXV YFP-gpt::095 genome. Sequencing reads were mapped to the HPXV (DQ792504) reference sequence. The overall Illumina sequencing read coverage in scHPXV YFP-gpt::095 from region 96,050 to 96,500 is shown in
Finally, it was determined that the nucleotide substitutions in HPXV044, designed to create unique restriction sites in GA_Frag_2, were also incorporated into the scHPXV YFP-gpt::095 genome. The sequencing reads that map to HPXV044 (region 44,400 to 45,100) showed that within this region there were two regions where the sequencing reads conflicted with that of the sequence in the HPXV YFP-gpt::095 reference sequence. Upon magnification of these regions, it was clear that two T to G substitutions were introduced into the non-coding strand of HPXV044 at positions 44,512 and 45,061, thus creating AvaI and StuI restriction sites in Frag_2. Overall, the sequencing data corroborated the in vitro genomic analysis data and confirmed that scHPXV YFP-gpt::095 was successfully reactivated in SFV-infected cells.
scHPXV YFP-Gpt:: 095 Replicates More Slowly in HeLa Cells Compared to Other Poxviruses
BSC-40, HeLa, and HEL fibroblasts were originally obtained from the American Type Culture Collection. BSC-40 cells are propagated at 37° C. in 5% CO2 in minimal essential medium (MEM) supplemented with L-glutamine, nonessential amino acids, sodium pyruvate, antibiotics and antimycotics, and 5% fetal calf serum (FCS; ThermoFisher Scientific). HeLa and HEL cells were propagated at 37° C. in 5% CO2 in Dulbecco's modified Eagle's medium supplemented with L-glutamine, antibiotics and antimycotics, and 10% FCS.
Multi-step growth curves and plaque size measurements were used to evaluate whether scHPXV YFP-gpt::095 replicated and spread in vitro similar to other Orthopoxviruses. Since a natural HPXV isolate was unavailable, the growth of scHPXV YFP-gpt::095 was compared to the prototypic poxvirus, VACV (strain WR), Cowpox virus (CPX), a poxvirus that was closely related to HPXV and a clone of Dryvax virus, DPP15. Monkey kidney epithelial cells (BSC-40), Vero cells, a human carcinoma cell line (HeLa), and primary human fibroblasts cells (HEL) were infected with VACV WR, CPX, DPP15, or scHPXV YFP-gpt::095 at a low MOI and infected cells were harvested over a 72 h time course. In BSC-40 cells, the rate of virus replication and spread was comparable among all viruses tested (
Next, the plaque size of scHPXV YFP-gpt::095 grown in BSC-40 cells was measured. A statistically significant decrease in plaque size of scHPXV YFP-gpt::095 compared to VACV WR and even cowpox virus (
Following reactivation of the scHPXV YFP-gpt::095, the yfp/gpt selection marker in the HPXV095 locus was removed. To do this, a 1349 bp region of sequence corresponding to nucleotide positions 91573 to 92921 in HPXV (DQ792504) was synthesized (ThermoFisher Scientific) (SEQ ID NO: 51). This fragment included approximately 400 bp of homology flanking either side of the wt HPXVO95/J2R gene. This sequence of DNA was cloned into a commercial vector provided by GeneArt. To replace the yfp/gpt cassette with the HPXV095 gene sequence, BSC-40 cells were infected with scHPXV YFP-gpt::095 at a MOI of 0.5 and then transfected, 2 h later, with 2 μg of linearized plasmid containing the wtHPXV095 sequence using Lipofectamine 2000 (ThermoFisher Scientific). The virus recombinants were harvested 48 h post infection and recombinant viruses (scHPXV (wt)) were isolated using three rounds of non-fluorescent plaque purification under agar. PCR was used to confirm the identity of the scHPXV (wt) using primers that flanked the HPXV095 gene locus. The primers used to confirm the correct replacement of the HPXV095 gene are HPXV095_check-FWD 5′-CCTATTAGATACATAGATCCTCGTCG-3′ (SEQ ID NO: 52) and HPXV095_check-REV 5′-CGGTTTATCTAACGACACAACATC-3′ (SEQ ID NO: 53).
Growth Properties of scHPXV (Wt) Versus scHPXV YFP-Gpt::095
In experiments performed as described above, scHPXV(wt) shows growth properties not significantly different from scHPXV YFP-gpt::095 in vitro (
Determination of the Virulence of scHPXV (Wt) in a Murine Intranasal Model
The toxicity effects of scHPXV (wt) were determined in this study. For this experiment, 6 groups of Balb/c mice were administered 3 different doses of scHPXV (ΔHPXV_095/J2R) or scHPXV (wt) described in the Examples and compared to a PBS control group as well as a VACV (WR) control group and a VACV (Dryvax strain DPP15) control group (9 treatment groups in total). There were 3 additional mice included in this experiment that did not receive any treatment for the duration of the study. All mice were sampled for blood at predetermined points throughout the experiment and the additional mice served as a baseline for serum analysis.
Prior to inoculation of Balb/c mice, all virus strains were grown in BSC-40 cells (African green monkey kidney), harvested by trypsinization, washed in PBS, extracted from cells by dounce homogenization, purified through a 36% sucrose cushion by ultracentrifugation, resuspended in PBS, and titered such that the final concentrations were: 1) VACV (WR)—5×105 PFU/ml; 2) VACV (DPP15)—109 PFU/ml; 3) scHPXV (ΔHPXV_095/J2R)—107 PFU/ml, 108 PFU/ml, and 109 PFU/ml and 4) scHPXV (wt)—107 PFU/ml, 108 PFU/ml, and 109 PFU/ml.
The scHPXV doses chosen for this study (105 PFU/dose, 106 PFU/dose, and 107 PFU/dose) were based on previous studies using known vaccine strains of VACV, including Dryvax and IOC (Medaglia M L, Moussatche N, Nitsche A, Dabrowski P W, Li Y, Damon I K, et al. Genomic Analysis, Phenotype, and Virulence of the Historical Brazilian Smallpox Vaccine Strain IOC: Implications for the Origins and Evolutionary Relationships of Vaccinia Virus. Journal of Virology. 2015; 89(23):11909-25; Qin L, Favis N, Famulski J, Evans D H. Evolution of and evolutionary relationships between extant vaccinia virus strains. Journal of Virology. 2015; 89(3):1809-24).
Since weight loss was used as a measurement of virulence in mice, VACV (strain WR) was administered intranasally at a dose of 5×103 PFU, which led to approximately 20-30% weight loss. The VACV Dryvax clone, DPP15, was also administered intranasally at 107 PFU/dose, so that the virulence of this well-known Smallpox vaccine could be directly compared to scHPXV (wt). Mice were purchased from Charles River Laboratories and once received, were acclimatized to their environment for at least one week prior to virus administration.
Each mouse received a single dose of virus (˜10 ul) administered via the intranasal injection while under anesthesia. Mice were monitored for signs of infection, such as swelling, discharge, or other abnormalities every day for a period of 30 days. Each mouse was specifically monitored for weight loss every day after virus administration. Mice that lose more than 25% of their body weight in addition to other morbidity factors were subjected to euthanasia in accordance with our animal health care facility protocols at the University of Alberta.
Even at the highest doses of scHPXV tested, there may be no overt signs of illness in Balb/c mice. The VACV strains most closely related to scHPXV, old South American viruses, in some cases produced no disease at 107 PFU (Medaglia M L, Moussatche N, Nitsche A, Dabrowski P W, Li Y, Damon I K, et al. Genomic Analysis, Phenotype, and Virulence of the Historical Brazilian Smallpox Vaccine Strain IOC: Implications for the Origins and Evolutionary Relationships of Vaccinia Virus. Journal of Virology. 2015; 89(23):11909-25). It was impractical to test much higher doses than this due to the difficulty of making purified stocks with titers in excess of 109 PFU/mL.
Determination of Whether scHPXV Confers Immune Protection Against a Lethal VACV-WR Challenge
Mice that appeared to have been unaffected by the initial virus administration described in the Example continued to gain weight normally throughout the experiment. Thirty days post virus inoculation, mice were subsequently challenged with a lethal dose of VACV-WR (106 PFU/dose) via intranasal inoculation. Mice were closely monitored for signs of infection as described above. Mice were weighed daily and mice that lost greater than 25% of their body weight in addition to other morbidity factors were subjected to euthanasia. We expected that mice inoculated with PBS prior to administration of a lethal dose of VACV-WR showed signs of significant weight loss and other morbidity factors within 7-10 days post inoculation. Approximately 14 days post lethal challenge with VACV-WR, all mice were euthanized and blood was collected to confirm the presence of VACV-specific neutralizing antibodies in the serum by standard plaque reduction assays.
Synthetic Chimeric VACV ACAM2000 Containing VACV WR Strain Hairpin and Duplex Sequence (scVACVACAM2000-WR DUP/HP)
The design of the scVACV genome was based on the previously described genome sequence for VACV ACAM2000 [GenBank accession AY313847] (Osborne J D et al. Vaccine. 2007; 25(52):8807-32). The genome was divided into 9 overlapping fragments (
To assist with sub-cloning of these fragments, AarI and BsaI restriction sites were silently mutated in all the fragments, except for the two ITR-encoding fragments. The BsaI restriction sites in the two ITR-encoding fragments were not mutated, in case these regions contain nucleotide sequence-specific recognition sites that are important for efficient DNA replication and concatamer resolution.
A YFP/gpt cassette under the control of a poxvirus early late promoter was introduced into the thymidine kinase locus, so that reactivation of VACV ACAM2000 (VACV ACAM2000 YFP-gpt::105) was easy to visualize under a fluorescence microscope. The gpt locus also provided a potential tool for selecting reactivated viruses using drug selection.
Traditionally, the terminal hairpins have been difficult to clone and sequence, hence, it is not surprising that the published sequence of the VACV ACAM2000 genome is not complete. Upon inspection of the very terminal region of the published VACV ACAM2000 strain, there appeared to be some differences between ACAM2000 and the very well characterized VACV WR strain (Genbank Accession #AY243312) (
Synthetic Chimeric VACV ACAM2000 Containing VACV ACAM2000 Strain Hairpin and Duplex Sequence (scVACVACAM2000-ACAM2000 DUP/HP)
The design of the scVACV genome was based on the previously described genome sequence for VACV ACAM2000 [GenBank accession AY313847] (Osborne J D et al. Vaccine. 2007; 25(52):8807-32). The genome was divided into 9 overlapping fragments (
To assist with sub-cloning of these fragments, AarI and BsaI restriction sites were silently mutated in all the fragments, except for the two ITR-encoding fragments. The BsaI restriction sites in the two ITR-encoding fragments were not mutated, in case these regions contain nucleotide sequence-specific recognition sites that are important for efficient DNA replication and concatemer resolution.
A YFP/gpt cassette under the control of a poxvirus early late promoter was introduced into the thymidine kinase locus, so that reactivation of VACV ACAM2000 (VACV ACAM2000 YFP-gpt::105) was easy to visualize under a fluorescence microscope. The gpt locus also provided a potential tool for selecting reactivated viruses using drug selection.
The F and S terminal hairpin loop sequences of the wtVACV ACAM2000 are shown in SEQ ID NO: 118 and 117, respectively.
Ligation of the VACV WR F and S Terminal Hairpin Loops onto the VACV ACAM2000 Right and Left ITR Fragments
A 70 bp repeat fragment that was identical to the VACV WR strain was synthesized (
This terminal hairpin/duplex/70 bp tandem repeat fragment was subsequently ligated onto the 70 bp ACAM2000 left or right ITR fragment that had been previously modified at their terminal ends to include the NheI restriction site. When this fragment was digested, a 5′-CTAG overhang was left at their 5′ termini. At the 3′ terminus of the 70 bp tandem repeat fragment, the NheI site is used to directly ligate this fragment to the LITR and RITR regions of the VACV ACAM2000 DNA fragments. Following digestion of the VACV ACAM2000 left and right ITR fragments, the S terminal hairpin/duplex/70 bp tandem repeat fragment or the F terminal hairpin/duplex/70 bp tandem repeat fragment were separately ligated to either the left or right ITR fragment using DNA ligase at a 1:1 molar ratio overnight at 16° C. The DNA ligase was subsequently heat inactivated at 65° C. prior to being transfected into Shope Fibroma virus (SFV)-infected BGMK cells.
Ligation of the VACV ACAM2000 F and S Terminal Hairpin Loops onto the VACV ACAM2000 Right and Left ITR Fragments
A 70 bp repeat fragment that was identical to the VACV ACAM2000 strain was synthesized. SapI and NheI restriction sites were included at the 5′ and 3′ terminus of the 70 bp tandem repeat fragment to facilitate the ligation onto the VACV ACAM2000 hairpin sequence and the VACV ACAM2000 right and left ITR fragments, respectively. Before the VACV ACAM2000 terminal hairpin loops could be ligated onto the 70 bp tandem repeat fragment, the loop had to be extended an additional 58 bp using a duplex sequence synthesized by IDT Technologies. This was due to the extra sequence being immediately downstream of the concatemer resolution site, prior to the first 70 bp repeat sequence found in VACV strain ACAM2000. The duplex sequence was produced by synthesizing two single-stranded DNA molecules that, when annealed together, would produce a duplex DNA molecule with a 5′-TGT overhang at the 5′ end and a 5′-GGT overhang at the 3′ end (SEQ ID NO: 119 and SEQ ID NO: 120). Since the VACV ACAM2000 F and S terminal hairpin loops generate a 3′-ACA overhang at their terminal loops, the 58 bp duplex was ligated to the hairpins to generate an ˜130 bp terminal hairpin loop. This hairpin/duplex fragment was gel purified and then subsequently ligated onto the SapI digested end of the 70 bp repeat fragment. Digesting the 70 bp tandem repeat fragment with SapI created a three-base overhang (5′-CCA), complementary to the 5′GGT overhang in the terminal hairpin/duplex structure. The 70 bp tandem repeat was mixed with either an F terminal hairpin/duplex structure or a S terminal hairpin/duplex structure at a ˜5-fold molar excess relative to the 70 bp tandem repeat fragment in the presence of DNA ligase. This produced an upward shift in the DNA electrophoresis gel compared to the 70 bp only reaction, indicating that the terminal hairpin/duplex was successfully ligated onto the 70 bp tandem repeat fragment.
This terminal hairpin/duplex/70 bp tandem repeat fragment was subsequently ligated onto the ACAM2000 left or right ITR fragment that had been previously modified at their terminal ends to include the NheI restriction site. When this left or right ITR fragment was digested, a 5′-CTAG overhang was left at their 5′ termini. At the 3′ terminus of the 70 bp tandem repeat fragment, the NheI site is used to directly ligate this fragment to the LITR and RITR regions of the VACV ACAM2000 DNA fragments. Following digestion of the VACV ACAM2000 left and right ITR fragments, the S terminal hairpin/duplex/70 bp tandem repeat fragment or the F terminal hairpin/duplex/70 bp tandem repeat fragment were separately ligated to either the left or right ITR fragment using DNA ligase at a 1:1 molar ratio overnight at 16° C. The DNA ligase was subsequently heat inactivated at 65° C. prior to being transfected into Shope Fibroma virus (SFV)-infected BGMK cells.
Each of the VACV ACAM2000 overlapping DNA fragments in Table 4 were cloned into a plasmid provided from GeneArt using the restriction enzyme I-SceI. Prior to transfection of these synthetic DNA fragments into BGMK cells, the plasmids were digested with I-SceI and the products were run on a gel to confirm that the DNA fragments were successfully linearized. Following digestion at 37° C. for 2 h, the reactions were subsequently heat-inactivated at 65° C. Samples were stored on ice or at 4° C. until the terminal hairpin/duplex/70 bp tandem repeat/ITR fragments were created (as described above).
Reactivation of scVACV ACAM2000-WR DUP/HP or scVACV ACAM2000-ACAM2000 DUP/HP in Shope Fibroma Virus-Infected Cells
SFV strain Kasza and BSC-40 were originally obtained from the American Type Culture Collection. Buffalo green monkey kidney (BGMK) cells were obtained from G. McFadden (University of Florida). BSC-40 and BGMK cells are propagated at 37° C. in 5% CO2 in minimal essential medium (MEM) supplemented with L-glutamine, nonessential amino acids, sodium pyruvate, antibiotics and antimycotics, and 5% fetal calf serum (FCS; ThermoFisher Scientific).
Buffalo green monkey kidney (BGMK) cells were grown in MEM containing 60 mm tissue-culture dishes until they reached approximately 80% confluency. Cells were infected with Shope Fibroma Virus (SFV) in serum-free MEM at a MOI of 0.5 for 1 h at 37° C. The inoculum was replaced with 3 ml of warmed MEM containing 5% FCS and returned to the incubator for an additional hour. Meanwhile, transfection reactions were set up as follows. After approximately 2 h at 37° C., the linearized VACV ACAM2000 fragments were transfected (using Lipofectamine 2000) into the SFV-infected BGMK cells at molar equivalents based on the length of each fragment that comprised the VACV ACAM2000 genome. Different amounts of total DNA were tried and 5, 6, and 7.5 μg of DNA were able to successfully reactivate ACAM2000 from these overlapping DNA fragments. The complexes were incubated at room temperature for 10 minutes and then added dropwise to the BGMK cells previously infected with SFV. Approximately 24 h post infection, the media was replaced with fresh MEM containing 5% FCS. The cells were cultured for an additional 4 days (total of 5 days) at 37° C.
Virus particles were recovered by scraping the infected cells into the cell culture medium and performing three cycles of freezing and thawing. The crude extract was diluted 102 in serum-free MEM and 4 ml of the inoculum is plated on 9-16 150 mm tissue culture plates of BSC-40 cells to recover reactivated scVACV ACAM2000 YFP-gpt::105. One hour post infection, the inoculum was replaced with MEM containing 5% FCS and 0.9% Noble Agar. Yellow fluorescent plaques were visualized under an inverted microscope and individual plaques were picked for further analysis. scVACV ACAM2000 YFP-gpt::105 plaques were plaque purified three times with yellow fluorescence selection.
After 4 days, the infected plates containing both SFV and VACV ACAM2000 clones were harvested, followed by three freeze thaw cycles to release virus, and then serially diluted and plated onto BSC-40 cells, which preferentially promote growth of the VACV ACAM2000 viruses compared to the SFV viruses. Three rounds of plaque purification were performed followed by a bulkup of the virus stocks in 10-150 mm tissue culture plates. The virus was subsequently lysed from these cells and separated on a 36% sucrose cushion, followed by further purification on a 24%-40% sucrose density gradient. Genomic DNA was isolated from these purified genomes and next generation Illumina sequencing was performed to confirm the sequence of the synthetic virus genomes.
In vitro multi-step growth curves of the isolated synthetic chimeric VACV ACAM2000-WR DUP/HP, scVACV ACAM2000-ACAM2000 DUP/HP and the wild type VACV ACAM2000 virus were performed in monkey kidney epithelial (BSC-40) cells. The cells were infected at a multiplicity of infection 0.03, the virus was harvested at the indicated times (3 h, 6 h, 12 h, 21 h, 48 h and 72 h), and the virus was titrated on BSC-40 cells. The data shown on
A comparison between the growth curves of scVACV ACAM2000-WR DUP/HP (YFP-gpt marker), scVACV ACAM2000-ACAM2000 DUP/HP (YFP-gpt marker), scVACV ACAM2000-WR DUP/HP (no marker) (YFP-gpt marker replaced with J2R gene sequence), scVACV ACAM2000-ACAM2000 DUP/HP (no marker) (YFP-gpt marker replaced with J2R gene sequence) and wtVACV ACAM2000, shows that there is statistically no difference in the growth properties of these viruses as compared to the wtACAM2000 VACV (
Confirmation of scVACV ACAM2000-WR DUP/HP YFP-Gpt::105 Genome Sequence by PCR and Restriction Fragment Analysis
Further analysis of scVACV ACAM2000 YFP-gpt::105 genomes by restriction digestion followed by pulse-field gel electrophoresis (PFGE) was carried out on genomic DNA isolated using sucrose gradient purification (Yao X D, Evans D H. Methods Mol Biol. 2004; 269:51-64). Two independent scVACV ACAM2000-WR DUP/HP clones plus a VACV_WRAJ2R control where the J2R gene sequence has been replaced with a YFP-gpt marker, and a wtVACV ACAM2000 control (VAC_ACAM2000) were purified and then left either undigested, digested with BsaI, HindIII, or Not and PvuI. The isolated genomic DNA from both scVACV ACAM2000-WR DUP/HP and wtVACV ACAM2000 were digested with BsaI and HindIII. Since most of the BsaI sites in the scVACV ACAM2000 genome had been silently mutated, a mostly intact ˜200 kbp fragment was observed following BsaI digestion (FIG. 17, lanes 8 and 9). This is unlike the wtVACV ACAM2000 and wtVACV WR control (VAC_WRAJ2R) genomes, which had been extensively digested when treated with BsaI (
In the wtVACV WR control (VAC_WRAJ2R) sample, a band at about 3.6 kbp (marked with asterisks) was detected, which encompasses all of the 70 bp tandem repeats in the WR strain of VAC. Given that the VACV WR strain used as a template to design the synthesis of the ITR repeat elements, it was expected that some bands were detected in the NotI/PvuI treated scVACV ACAM2000-WR DUP/HP clones at close to the same size as what was seen in strain WR. When the two scVACV ACAM2000-WR DUP/HP clones were compared differences in the size of this region were observed, suggesting that not all of the 70 bp repeats were incorporated into each reconstructed genome (
Overall, in vitro analysis of the scVACV-WR DUP/HP ACAM2000 YFP-gpt::105 genome suggested that reactivation of VACV-WR DUP/HP ACAM2000 from chemically synthesized DNA fragments was successful and that scVACV-WR DUP/HP ACAM2000 virus behaved in vitro like the wtVACV ACAM2000 virus.
Confirmation of scVACV ACAM2000 YFP-Gpt::105 Genome Sequence by Whole Genome Sequence Analysis
Two clones of scVACV ACAM2000-WR DUP/HP and two clones of scVACV ACAM2000-ACAM2000 DUP/HP were sequenced. The Illumina reads were de novo assembled using CLC Genomics Workstation (version 11) with a word size of 35 or 61. Assembled contigs were then imported into Snapgene software and aligned onto a reference sequence of the expected scACAM2000 sequence based on the synthetic fragments that were provided by GeneArt.
For clone 1 of scVACV ACAM2000-WR DUP/HP, contig 1 was 16,317 bp, and corresponded to most of the ITR region (except for the tandem repeat sequences. Contig 2 was 167,020 bp, and aligned with the central conserved region of the genome (nucleotide positions 19,467 to 186,486). For clone 2 of scVACV ACAM2000-WR DUP/HP, contig 3 was 16,322 bp, and corresponded to most of the ITR region (except for the tandem repeat sequences. Contig 1 was 167,020 bp, and aligned with the central conserved region of the genome (nucleotide positions 19,467 to 186,486). There was a single nucleotide substitution (C to A) at nucleotide position 136791 of the contig of clone 2. This corresponded to nucleotide position 156,256 in the scACAM2000 genome sequence and resulted in an amino acid change from an Asp to Tyr in VAC_ACAM2000_177 (A41L).
For clone 1 of scVACV ACAM2000-ACAM2000 DUP/HP, contig 1 was 167,020 bp, and aligned with the central conserved region of the genome (nucleotide positions 19,469 to 186,488). Contig 2 was 16,150 bp, and corresponded to most of the ITR region (except for tandem repeat sequences). When this contig was mapped to the reference genome in Snapgene, gaps in the sequence were observed at positions 2633 to 3417 and nucleotide positions 15,175 to 15220. The first gap region corresponds to the 54 bp repeat region and it is most likely due to the inability to accurately assemble these regions using de novo assembly tools. Mapping of the raw Illumina reads directly to the reference genome did not result in any gaps within either region. For clone 2 of scVACV ACAM2000-ACAM2000DUP/HP, contig 1 was 16,075 bp, and corresponded to most of the ITR region (except the tandem repeat sequences). Contig 2 was 167,078 bp and aligned with the central conserved region of the genome (nucleotide positions 19,469 to 186,546). There was a gap observed in contig 2 from nucleotide position 15,176 to 15,220. Mapping of the raw Illumina reads directly to the reference genome did not result in any gaps within this region, however. Neither sequenced clone of scVACV ACAM2000-ACAM2000 DUP/HP displayed any other nucleotide mutations at any position within the genome.
The Illumina reads were also mapped to a reference map in CLC Genomics. The Illumina reads covered the full length of the reference sequence with an average coverage of 1925 and 2533, for clone 1 and 2 of scVACV ACAM2000-WR DUP/HP, respectively, and an average coverage of 2195 and 1602 for clone 1 and 2 of scVACV ACAM2000-ACAM2000 DUP/HP, respectively.
Overall, the sequencing data corroborates the in vitro genomic analysis data and confirms that scVACV ACAM20000-WR DUP/HP and scVACV ACAM2000-ACAM2000 DUP/HP were successfully reactivated in SFV-infected cells.
Following reactivation of the scVACV ACAM2000 YFP-gpt::105, the yfp/gpt selection marker in the thymidine kinase locus can be removed.
Primary human MSCs are isolated from bone marrow of healthy donors, cultured, and characterized as described in Apel A et al. Exp Cell Res 2009; 315:498-507.
Human MSC are infected with the synthetic chimeric poxvirus, such as scHPXV, scVACV ACAM2000-WR DUP/HP or scVACV ACAM2000-ACAM2000 DUP/HP. Cells are infected in serum-free media 2 hours at 37° C. while in constant rotation to prevent cells from settling. Cells are infected at multiplicity of infection (MOI) of 2 or 4. After incubation, MSC are gently pelleted and supernatant removed. Cells are plated and allowed to incubate at 37° C. for 48 hours. The percent of infected cells is determined by flow cytometry.
The oncolytic activity of MSCs loaded with the synthetic chimeric poxvirus is determined by using a specific highly or intermediately proliferating cell line or in vivo.
Adipose tissue is an ideal source of mesenchymal stem cells. Human adipose tissues are obtained from healthy donors as fat biopsies in an outpatient clinic. 2 cubic cm of subcutaneous fat is excised prior to incision of the fascia. The fat tissues are minced with surgical scalpels and incubated in 0.075% collagenase type I (Worthington Biochemical, Lakewood, N.J.) for 90 min at 37° C. Digested tissue is centrifuged at 400 g for 5 min with the pellet washed in PBS, passed through a 70 m cell strainer (BD Biosciences, San Jose, Calif.), and incubated in red blood cell lysis buffer (154 mM NH4Cl, 10 mM KHCO3, 0.1 mM EDTA). Cells are grown in T-175 cm2 flasks at a concentration of 1.0-2.5×103 cells/cm2 in Advanced MEM with 5% PLTmax (Mill Creek Life Sciences, Rochester, Minn.), 100 U/ml penicillin, 100 g/ml streptomycin, and 2 mM L-glutamine (Invitrogen, Carlsbad, Calif., USA) in a 37° C. 5% CO2 incubator for 3-4 days. When cells are 60-80% confluent, they are passaged using TrypLE (Trypsin Like Enzyme, Invitrogen).
Cells are frozen in aliquots in liquid nitrogen and stored until use.
ADSCs are infected with the synthetic chimeric poxvirus, such as scHPXV, scVACV ACAM2000-WR DUP/HP or scVACV ACAM2000-ACAM2000 DUP/HP. Cells are infected in serum-free media 2 hours at 37° C. while in constant rotation to prevent cells from settling. Cells are infected at multiplicity of infection (MOI) of 2 or 4. After incubation, ADSCs are gently pelleted and supernatant removed. Cells are plated and allowed to incubate at 37° C. for 48 hours. The percent of infected cells is determined by flow cytometry.
The oncolytic activity of ADSCs loaded with the synthetic chimeric poxvirus is determined by using a specific highly or intermediately proliferating cell line or in vivo.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2019/030488 | 5/2/2019 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62666013 | May 2018 | US |
