Patent Application
20090162321
The present invention relates generally to negative-strand RNA viruses. In particular, the invention relates to methods and compositions for producing attenuated Vesicular stomatitis virus (VSV) in a cell culture.
Vesicular stomatitis virus (VSV) is a member of the Rhabdoviridae family, and as such is an enveloped virus that contains a non-segmented, negative-strand RNA genome. Its relatively simple genome consists of 5 gene regions arranged sequentially 3′-N-P-M-G-L-5′ (FIG. 1) (Rose and Whitt, Rhabdoviridae: The Viruses and Their Replication. In “Fields Virology”, 4th Edition, Vol.1. Lippincott and Williams and Wilkins, 1221-1244, 2001).
The N gene encodes the nucleocapsid protein responsible for encapsidating the genome while the P (phosphoprotein) and L (large) coding sequences specify subunits of the RNA-dependent RNA polymerase. The matrix protein (M) promotes virion maturation and lines the inner surface of the virus particle. VSV encodes a single envelope glycoprotein (G), which serves as the cell attachment protein, mediates membrane fusion, and is the target of neutralizing antibodies.
VSV has been subjected to increasingly intensive research and development efforts because numerous properties make it an attractive candidate as a vector in immunogenic compositions for human use (Bukreyev, et al. J. Virol. 80:10293-306, 2006; Clarke, et al. Springer Semin Immunopathol. 28: 239-253, 2006). These properties include: 1) VSV is not a human pathogen; 2) there is little pre-existing immunity that might impede its use in humans; 3) VSV readily infects many cell types; 4) it propagates efficiently in cell lines suitable for manufacturing immunogenic compositions; 5) it is genetically stable; 6) methods exist by which recombinant virus can be produced; 7) VSV can accept one or more foreign gene inserts and direct high levels of expression upon infection; and 8) VSV infection is an efficient inducer of both cellular and humoral immunity. Once reverse-genetics methods (Lawson, et al. Proc Natl Acad Sci USA 92:4477-81, 1995; Schnell, et al. EMBO J 13:4195-203, 1994) were developed, that made it possible to engineer recombinant VSV (rVSV), the first vectors were designed with foreign coding sequence inserted between the G and L genes (
Encouraging preclinical performance by prototype viruses has led to the development of rVSV vectors for use in humans (Clarke, et al. Springer Semin Immunopathol 28:239-253, 2006). Investigation of highly attenuated vectors is receiving considerable attention because they should offer enhanced safety profiles. This is particularly relevant since many immunogenic compositions under consideration might be used in patients with compromised immune systems (i.e. HIV-infected subjects).
The desire to develop highly attenuated vectors has focused some attention on propagation-defective rVSV vectors. Ideally, propagation-defective vectors are engineered with genetic defects that block virus propagation and spread after infection, but minimally disturb the gene expression apparatus allowing for adequate antigen synthesis to induce protective immune responses. With this objective in mind, propagation-defective rVSV vectors have been produced through manipulation of the VSV G, which is the viral attachment protein (G;
Although the ΔG and Gstem vectors are promising, the development of scaleable propagation methods that are compliant with regulations governing manufacture of immunogenic compositions for administration to humans remains a hurdle that must be addressed before clinical evaluation can be justified. A viable production method must provide sufficient quantities of functional G protein in trans to stimulate morphogenesis or “packaging” of infectious virus particles. Achieving satisfactory levels of G protein expression is complicated by the fact that G is toxic to cell lines, in part because it mediates membrane fusion (Rose and Whitt, Rhabdoviridae: The Viruses and Their Replication. In “Fields Virology”, 4th Edition, Vol. 1. Lippincott Williams and Wilkins, 1221-1244, 2001).
Transient production of G protein in transfected BHK (Majid, et al. J Virol 80:6993-7008, 2006) or 293T (Takada, et al. Proc Natl Acad Sci USA 94:14764-9, 1997) cells or electroporated Vero cells (Witko, et al. J Virol Methods 135:91-101, 2006) has been used to propagate propagation-defective VSV as well. These methods were proven adequate to produce relatively small-scale quantities of rVSV-ΔG and rVSV-Gstem vectors needed for preclinical studies, but are presently inadequate for clinical development because the published procedures routinely rely on cell lines that are not qualified for production for use in humans (i.e. BHK) or the protocols have not been adapted and optimized for large-scale manufacture. Furthermore, observed yields of viral particles with these transient expression complementation methods generally are less than 1×107 IUs per ml (data not shown), and given that a single human dose is expected to be at least 1×107 IUs per ml, manufacturing of a VSV vector will be practical only if greater than 107 IUs are produced per ml of culture medium.
Stable cell lines that supply genetic complementation are powerful tools for development of propagation-defective viral vectors. This is illustrated best by the large number of E1-region-deficient adenovirus vectors that have been developed with the aid of the 293 cell line (Graham, et al. J Gen Virol 36:59-74, 1977; Hitt and Graham, Adv Virus Res 55:479-505, 2000; Jones and Shenk, Cell 17:683-9, 1979). In general, complementing cell lines also offer a key manufacturing advantage when compared to transient expression complementation methods. For example, propagation-defective viral vectors can be propagated in stable cell lines without the manipulations inherent to electroporation or transfection, which can be difficult to manage when conducted with the large number and volume of cells needed to manufacture an immunogenic composition.
Although an attractive approach by which to produce propagation-defective vectors, stable complementing cell lines can be difficult to produce and maintain, particularly when the complementing gene product is toxic, like VSV G. This toxicity prevents development of complementing cell lines that constitutively express the viral glycoprotein. Similarly, development of stable cell lines that express G protein from an inducible promoter is problematic because leaky expression frequently results in toxicity, and levels achieved after induction often are insufficient to promote efficient packaging particularly on a scale needed for commercial manufacturing. One inducible cell line has been described (Schnell, et al. Cell 90:849-57, 1997), but it often loses its ability to express G protein after several passages and is derived from BHK cells, which are not a cell type presently qualified for production of immunogenic compositions for human administration. Attempts to produce Vero cells expressing G protein under the control of tetracycline-responsive systems (Corbel and Rossi, Curr Opin Biotechnol 13:448-52, 2002) have also failed.
Therefore, there is a need in the art for methods of producing attenuated VSV particles, wherein the yields of attenuated VSV particles recovered are sufficient to be of use in manufacture of immunogenic compositions. Also, such methods would employ cells qualified for production for administration to humans. Moreover, such cells would express G protein under the control of an inducible system.
The present invention provides a method of producing attenuated Vesicular Stomatitis Virus (VSV) in a cell culture. The method includes providing a cell that comprises an optimized VSV G gene, wherein expression of VSV G protein from said optimized VSV G gene is inducible; inducing the cell to express VSV G protein from said optimized VSV G gene; infecting the induced cell with an attenuated VSV; growing the infected cells in culture; and recovering attenuated VSV from the culture. In certain preferred embodiments, the attenuated VSV is a propagation-defective VSV.
The present invention provides a further method of producing attenuated Vesicular Stomatitis Virus (VSV) in a cell culture. This method includes: providing a cell that comprises an optimized VSV G gene, wherein expression of VSV G protein from said optimized VSV G gene is inducible; transfecting the cell that comprises an optimized VSV G gene with: a viral cDNA expression vector comprising a polynucleotide encoding a genome or antigenome of the attenuated VSV; one or more support plasmids encoding N, P, L and G proteins of VSV; and a plasmid encoding a DNA-dependent RNA polymerase. The method further includes inducing the transfected cell to express VSV G protein from said optimized VSV G gene; growing the induced cells in culture; and recovering attenuated VSV from the culture. In some embodiments of this method, the cell is further transfected with a support plasmid encoding an M protein of VSV. The attenuated VSV is preferably a propagation-defective VSV.
In some embodiments, viral genome-length RNA is transcribed from the polynucleotide encoding the genome or antigenome of the attenuated VSV. In some preferred embodiments, the DNA-dependent RNA polymerase is T7 RNA polymerase and the viral cDNA expression vector and the support plasmids are under the control of a T7 promoter. In certain embodiments, the VSV G protein encoded by the support plasmid is encoded by a non-optimized VSV G gene.
Also provided is a method of improving the packaging of a propagation-defective Vesicular Stomatitis Virus (VSV). This method includes: providing a cell that comprises an optimized VSV G gene, wherein expression of VSV G protein from said optimized VSV G gene is inducible; inducing the cell to express VSV G protein from said optimized VSV G gene; introducing a propagation-defective VSV into the cell; growing the cells in culture; and recovering the packaged VSV from the culture.
In preferred embodiments, the methods of the present invention employ cells that are qualified production cells. In some embodiments, the qualified production cells are Vero cells.
In some embodiments, the inducible cell employed in the instant methods includes a nucleic acid having a heat shock-inducible transcriptional control sequence to control VSV G protein expression. In one embodiment, the heat shock-inducible transcriptional control sequence comprises a hybrid promoter that includes multiple copies of a heat shock element located 5′ of a minimal hCMV promoter. In another embodiment, the heat shock-inducible transcriptional control sequence modulates a transcription unit that is recognized by RNA polymerase II and produces functional mRNA upon heat induction. In some embodiments, the heatshock-inducible transcriptional control sequence is represented by SEQ ID NO: 6.
In some embodiments of the present invention, the heat shock element is 5′-GAAnnTTC-3′ (SEQ ID NO: 7). In some particular embodiments, such a heat shock element may be selected from the following: 5′-GAACGTTC-3′ (SEQ ID NO: 8), 5′-GAAGCTTC-3′ (SEQ ID NO: 9), 5′-GAAATTTC-3′ (SEQ ID NO: 10), 5′-GAATATTC-3′ (SEQ ID NO: 11) and combinations thereof.
As described above, the heat shock elements are located 5′ of a minimal hCMV promoter. In certain embodiments, the minimal hCMV promoter is represented by SEQ ID NO: 12.
In some embodiments of the methods of the invention, the expression of VSV G protein from the optimized VSV G gene is under the control of a cytomegalovirus-derived RNA polymerase II promoter. In some further embodiments of the instant methods, the expression of VSV G protein from the optimized VSV G gene is under the control of a transcriptional unit recognized by RNA polymerase II producing a functional mRNA.
In certain embodiments, the optimized VSV G gene employed in the methods of the present invention is derived from an Indiana VSV serotype or New Jersey VSV serotype. In some embodiments, the optimized VSV G gene employed in the methods of the invention is selected from the following: SEQ ID NO: 3, SEQ ID NO: 4 and SEQ ID NO: 5.
In some embodiments, the attenuated VSV produced by the methods of this invention encodes a heterologous antigen. The heterologous antigen may be from a pathogen, for example. In some embodiments, the pathogen may be selected from, but is not limited to, the following: measles virus, subgroup A and subgroup B respiratory syncytial viruses, human parainfluenza viruses, mumps virus, human papilloma viruses of type 1 or type 2, human immunodeficiency viruses, herpes simplex viruses, cytomegalovirus, rabies virus, human metapneumovirus, Epstein Barr virus, filoviruses, bunyaviruses, flaviviruses, alphaviruses, influenza viruses, hepatitis C virus and C. trachomatis.
In some embodiments of the instant methods, the attenuated VSV further encodes a non-viral molecule selected from a cytokine, a T-helper epitope, a restriction site marker, or a protein of a microbial pathogen or parasite capable of eliciting an immune response in a mammalian host.
In one embodiment of the methods of the present invention, the attenuated VSV lacks a VSV G protein (VSV-ΔG). In certain embodiments, the yield of VSV-ΔG using the methods of the present invention is greater than about 1×106 IU per ml of culture.
In some other embodiments of the methods of this invention, the attenuated VSV expresses a G protein having a truncated extracellular domain (VSV-Gstem). In certain embodiments, the yield of VSV-Gstem using the methods of this invention is greater than about 1×106 IU per ml of culture.
In some further embodiments of the instant methods, the attenuated VSV expresses a G protein having a truncated cytoplasmic tail (CT) region. In certain embodiments, the attenuated VSV expresses a G protein having a cytoplasmic tail region truncated to one amino acid (G-CT1). In other particular embodiments, the attenuated VSV expresses a G protein having a cytoplasmic tail region truncated to nine amino acids (G-CT9).
In further embodiments of the instant methods, the attenuated VSV includes the VSV N gene that has been translocated downstream from its wild-type position in the viral genome, thereby resulting in a reduction in VSV N protein expression. In still further embodiments of the methods of this invention, the attenuated VSV contains noncytopathic M gene mutations (Mncp), said mutations reducing the expression of two overlapping in-frame polypeptides that are expressed from the M protein mRNA by initiation of protein synthesis at internal AUGs, affecting IFN induction, affecting nuclear transport, or combinations thereof.
The present invention also provides an immunogenic composition comprising an immunogenically effective amount of attenuated VSV produced according to any of the instant methods in a pharmaceutically acceptable carrier. In some embodiments, the attenuated VSV encodes a heterologous antigen.
This invention further provides an isolated cell comprising a nucleic acid that comprises an optimized VSV G gene. In certain embodiments, the optimized VSV G gene may be selected from SEQ ID NO: 3, SEQ ID NO: 4 or SEQ ID NO: 5.
In some embodiments, the optimized VSV G gene in the cell is operatively linked to a heat-shock inducible transcriptional control sequence. For example, the cell may express VSV G protein when exposed to an increase in temperature. In certain embodiments, the cell expresses the VSV G protein when exposed to a temperature of about 39° C. to about 45° C. In certain other embodiments, the cell expresses the VSV G protein when exposed to said temperature increase for a period of time of from about 30 minutes to about 6 hours.
In one embodiment, the transcriptional control sequence operatively linked to the optimized VSV G gene in the cell includes a hybrid heat shock element (HSE)/CMV promoter. In another embodiment, the hybrid promoter includes multiple copies of a heat shock element located 5′ of a minimal hCMV promoter.
In particular embodiments of the cell, the minimal hCMV promoter is represented by SEQ ID NO: 12. In other particular embodiments, the transcriptional control sequence is represented by SEQ ID NO: 6. In some further embodiments of the cell, the heat shock element may be represented by the following sequence: 5′-GAAnnTTC-3′ (SEQ ID NO: 7). For example, the heat shock element may be selected from the following: 5′-GAACGTTC-3′ (SEQ ID NO: 8), 5′-GAAGCTTC-3′ (SEQ ID NO: 9), 5′-GAAATTTC-3′ (SEQ ID NO: 10), 5′-GAATATTC-3′ (SEQ ID NO: 11) and combinations thereof.
The present invention further provides a transcriptional control sequence represented by SEQ ID NO: 6.
SEQ ID NO: 1 is a coding sequence for native VSV G protein (Indiana serotype);
SEQ ID NO: 2 is a coding sequence for native VSV G protein (New Jersey serotype);
SEQ ID NO: 3 is a codon optimized VSV G protein coding sequence (opt1; Indiana serotype);
SEQ ID NO: 4 is an RNA optimized VSV G protein coding sequence (RNAopt; Indiana serotype);
SEQ ID NO: 5 is an RNA optimized VSV G protein coding sequence (RNAopt; New Jersey serotype);
SEQ ID NO: 6 is an embodiment of a heat shock-inducible transcriptional control sequence for use in the cells of the present invention;
SEQ ID NO: 7 is a sequence of a suitable heat shock element for use in the cells of the present invention;
SEQ ID NO: 8 is one embodiment of a heat shock element for use in the cells of the present invention;
SEQ ID NO: 9 is another embodiment of a heat shock element for use in the cells of the present invention;
SEQ ID NO: 10 is a further embodiment of a heat shock element for use in the cells of the present invention;
SEQ ID NO: 11 is a still further embodiment of a heat shock element for use in the cells of the present invention;
SEQ ID NO: 12 is one embodiment of a minimal hCMV promoter for use in cells of the present invention; and
SEQ ID NO: 13 is a cytoplasmic domain of wild-type VSV G protein.
As used in the specification and claims, the singular form “a”, “an” and “the” include plural references unless the context clearly dictates otherwise. For example, the term “a cell” includes a plurality of cells, including mixtures thereof.
As used herein, the term “comprising” is intended to mean that the compositions and methods include the recited elements, but do not exclude other elements.
The term “attenuated virus” and the like as used herein refers to a virus that is limited in its ability to grow or replicate in vitro or in vivo.
The term “viral vector”, and the like refers to a recombinantly produced virus or viral particle that includes a polynucleotide to be delivered into a host cell, either in vivo, ex vivo or in vitro.
The term “polynucleotide,” as used herein, means a single or double-stranded polymer of deoxyribonucleotide or ribonucleotide bases and includes DNA and corresponding RNA molecules, including HnRNA and mRNA molecules, both sense and anti-sense strands, and comprehends cDNA, genomic DNA and recombinant DNA, as well as wholly or partially synthesized polynucleotides. An HnRNA molecule contains introns and corresponds to a DNA molecule in a generally one-to-one manner. An mRNA molecule corresponds to an HnRNA and/or DNA molecule from which the introns have been excised. A polynucleotide may consist of an entire gene, or any portion thereof. Operable anti-sense polynucleotides may comprise a fragment of the corresponding polynucleotide, and the definition of “polynucleotide” therefore includes all such operable anti-sense fragments. Anti-sense polynucleotides and techniques involving anti-sense polynucleotides are well known in the art and are described, for example, in Robinson-Benion et al. “Antisense techniques,” Methods in Enzymol. 254:363-375, 1995; and Kawasaki et al. Artific. Organs 20:836-848, 1996.
As used herein, “expression” refers to a process by which polynucleotides are transcribed into mRNA and translated into peptides, polypeptides, or proteins. If the polynucleotide is derived from genomic DNA, expression may include splicing of the mRNA, if an appropriate eukaryotic host is selected.
The terms “transient expression”, “transiently expressed” and the like is intended to mean the introduction of a cloned gene into cells such that it is taken up by the cells for the purpose of expressing a protein or RNA species, wherein the expression decays with time and is not inherited. Transfection is one approach to introduce cloned DNA into cells. Transfection agents useful for introducing DNA into cells include, for example, calcium phosphate, liposomes, DEAE dextrans, and electroporation.
The terms “constitutive expression”, “constitutively expressed” and the like means constant expression of a gene product.
The term “inducible expression” means expression of a gene product from an inducible promoter. For example, an inducible promoter may respond to a chemical inducer or heat to promote expression of the gene product.
The term “inducible” as applied to a promoter is well understood by those skilled in the art. In essence, expression under the control of an inducible promoter is “switched on” or increased in response to an applied stimulus. The nature of the stimulus varies between promoters. Some inducible promoters cause little or undetectable levels of expression (or no expression) in the absence of the appropriate stimulus. Other inducible promoters cause detectable constitutive expression in the absence of the stimulus. Whatever the level of expression is in the absence of the stimulus, expression from any inducible promoter is increased in the presence of the correct stimulus. The preferable situation is where the level of expression increases upon application of the relevant stimulus by an amount effective to alter a phenotypic characteristic. Thus an inducible (or “switchable”) promoter may be used which causes a basic level of expression in the absence of an applied stimulus, which basic expression level is too low to bring about a desired phenotype (and may in fact be zero). Upon application of the stimulus, the promoter is induced and expression is increased (or switched on) to a level that brings about the desired phenotype.
The term “promoter” as used herein refers to a regulatory region a short distance from the 5′ end of a gene that acts as the binding site for RNA polymerase.
The term “enhancer” as used herein refers to a cis-regulatory sequence that can elevate levels of transcription from an adjacent promoter.
The term “operatively linked” refers to an arrangement of elements wherein the components so described are configured so as to perform their usual function. In some instances, the term “operatively linked” refers to the association of two or more nucleic acid fragments on a single nucleic acid fragment so that the function of one is affected by the other. For example, a promoter is operatively linked with a coding sequence when it is capable of affecting the expression of that coding sequence when the regulatory proteins and proper enzymes are present. In some instances, certain control elements need not be contiguous with the coding sequence, so long as they function to direct the expression thereof. For example, intervening untranslated, yet transcribed sequences can be present between the promoter sequence and the coding sequence and the promoter can still be considered to be “operatively linked” to the coding sequence. Thus, a coding sequence is “operatively linked” to a transcriptional and translational control sequence in a cell when RNA polymerase transcribes the coding sequence into mRNA, which is then trans-RNA spliced and translated into the protein encoded by the coding sequence. As another example, a polynucleotide may be operatively linked with transcription terminator sequences when transcription of the polynucleotide is capable of being terminated by the transcription terminator sequences. As yet another example, a polynucleotide may be operatively linked with a ribozyme sequence when transcription of the polynucleotide affects cleavage at the ribozyme sequence.
The term “antigen” refers to a compound, composition, or immunogenic substance that can stimulate the production of antibodies or a T-cell response, or both, in an animal, including compositions that are injected or absorbed into an animal. The immune response may be generated to the whole molecule, or to a portion of the molecule (e.g., an epitope or hapten). The term may be used to refer to an individual macromolecule or to a homogeneous or heterogeneous population of antigenic macromolecules. An antigen reacts with the products of specific humoral and/or cellular immunity. The term “antigen” broadly encompasses moieties including proteins, polypeptides, antigenic protein fragments, nucleic acids, oligosaccharides, polysaccharides, organic or inorganic chemicals or compositions, and the like. The term “antigen” includes all related antigenic epitopes. Epitopes of a given antigen can be identified using any number of epitope mapping techniques, well known in the art. See, e.g., Epitope Mapping Protocols in Methods in Molecular Biology, Vol. 66 (Glenn E. Morris, Ed., 1996) Humana Press, Totowa, N.J. For example, linear epitopes may be determined by e.g., concurrently synthesizing large numbers of peptides on solid supports, the peptides corresponding to portions of the protein molecule, and reacting the peptides with antibodies while the peptides are still attached to the supports. Such techniques are known in the art and described in, e.g., U.S. Pat. No. 4,708,871; Geysen et al. (1984) Proc. Natl. Acad. Sci. USA 81:3998-4002; Geysen et al. (1986) Molec. Immunol. 23:709-715, all incorporated herein by reference in their entireties. Similarly, conformational epitopes are identified by determining spatial conformation of amino acids such as by, e.g., x-ray crystallography and 2-dimensional nuclear magnetic resonance. See, e.g., Epitope Mapping Protocols, supra. Furthermore, for purposes of the present invention, an “antigen” refers to a protein that includes modifications, such as deletions, additions and substitutions (generally conservative in nature, but they may be non-conservative), to the native sequence, so long as the protein maintains the ability to elicit an immunological response. These modifications may be deliberate, as through site-directed mutagenesis, or through particular synthetic procedures, or through a genetic engineering approach, or may be accidental, such as through mutations of hosts, which produce the antigens. Furthermore, the antigen can be derived or obtained from any virus, bacterium, parasite, protozoan, or fungus, and can be a whole organism. Similarly, an oligonucleotide or polynucleotide, which expresses an antigen, such as in nucleic acid immunization applications, is also included in the definition. Synthetic antigens are also included, for example, polyepitopes, flanking epitopes, and other recombinant or synthetically derived antigens (Bergmann et al. (1993) Eur. J. Immunol. 23:2777 2781; Bergmann et al. (1996) J. Immunol. 157:3242 3249; Suhrbier, A. (1997) Immunol. and Cell Biol. 75:402 408; Gardner et al. (1998) 12th World AIDS Conference, Geneva, Switzerland, Jun. 28 Jul. 3, 1998).
The term “heterologous antigen” as used herein is an antigen encoded in a nucleic acid sequence, wherein the antigen is either not from the organism, or is not encoded in its normal position or its native form.
The terms “optimized VSV G gene”, “optimized VSV G coding sequence”, and the like as used herein refers to a modified VSV G protein coding sequence, wherein the modified VSV G protein coding sequence results in expression of VSV G protein in increased amounts relative to the native G protein open reading frame.
The term “G protein complementation” as used herein refers to a method wherein a virus is complemented by complementing cell lines, helper virus, transfection or some other means to provide lost G function.
The term “growing” as used herein refers to the in vitro propagation of cells on or in media of various kinds. The maintenance and growing of cells in the laboratory involves recreating an environment that supports life and avoids damaging influences, such as microbial contamination and mechanical stress. Cells are normally grown in a growth medium within culture vessels (such as flasks or dishes for adherent cells or constantly moving bottles or flasks for cells in suspension) and maintained in cell incubators with constant temperature, humidity and gas composition. However, culture conditions can vary depending on the cell type and can be altered to induce changes in the cells. “Expansion”, and the like as used herein, is intended to mean a proliferation or division of cells.
The terms “cell”, “host cell” and the like as used herein is intended to include any individual cell or cell culture which can be or have been recipients for vectors or the incorporation of exogenous nucleic acid molecules, polynucleotides and/or proteins. It is also intended to include progeny of a single cell. However, the progeny may not necessarily be completely identical (in morphology or in genomic or total DNA complement) to the original parent cell due to natural, accidental, or deliberate mutation. The cells may be prokaryotic or eukaryotic, and include, but are not limited to, bacterial cells, yeast cells, animal cells, and mammalian cells (e.g., murine, rat, simian or human).
The term “qualified production cells” as used herein means that the cells have been qualified successfully and used to produce immunogenic compositions or gene therapy vectors for human use. Examples of such cells include, for example, Vero cells, WI-38, PERC.6, 293-ORF6, CHO, FRhL or MRC-5 cells.
The term “cytopathic effect” or “CPE” is defined as any detectable changes in the host cell due to viral infection. Cytopathic effects may consist of cell rounding, disorientation, swelling or shrinking, death, detachment from a surface, etc.
The term “multiplicity of infection” or “MOI” is the ratio of infectious agents (e.g., virus) to infection targets (e.g., cell).
By “infectious clone” or “infectious cDNA” of a VSV, it is meant cDNA or its product, synthetic or otherwise, as well as RNA capable of being directly incorporated into infectious virions which can be transcribed into genomic or antigenomic viral RNA capable of serving as a template to produce the genome of infectious viral or subviral particles.
As described above, VSV has many characteristics, which make it an appealing vector for immunogenic compositions. For example, VSV is not considered a human pathogen. Also, VSV is able to replicate robustly in cell culture and is unable to either integrate into host cell DNA or undergo genetic recombination. Moreover, multiple serotypes of VSV exist, allowing the possibility for prime-boost immunization strategies. Furthermore, foreign genes of interest can be inserted into the VSV genome and expressed abundantly by the viral transcriptase. Moreover, pre-existing immunity to VSV in the human population is infrequent.
The present invention provides methods of producing attenuated Vesicular Stomatitis Virus (VSV) in a cell culture. The methods of the present invention provide G protein complementation to an attenuated VSV. In some embodiments, the G protein complementation provides G function to an attenuated VSV that lacks a G protein or expresses a non-functional G protein. Such vectors must be “packaged” in cells that express G protein.
The methods of the present invention are based on achieving higher levels of transient G protein expression. The methodology has been applied to the production of Gstem vectors producing over 1×107 IUs per ml.
The instant methods are scaleable for manufacturing. In some embodiments, the methods of the present invention employ Vero cells, which are a well-characterized substrate for production of immunogenic compositions and have been used to produce a licensed rotavirus vaccine (Merck, RotaTeq (Rotavirus Vaccine, Live, Oral, Pentavalent) FDA. Online, 2006 posting date; Sheets, R. (History and characterization of the Vero cell line) FDA. Online, 2000 posting date).
The present invention provides a packaging procedure for attenuated VSVs. The methods of the present invention may be applied to the packaging of propagation-defective recombinant VSVs, such as VSV-ΔG and VSV-Gstem. VSV-ΔG is a vector in which the G gene has been deleted completely (Roberts, et al. J Virol 73: 3723-32, 1999), whereas VSV-Gstem is a vector in which the G gene has been truncated to encode a G protein lacking most of the extracellular domain (VSV-Gstem; Robison and Whitt J Virol 74: 2239-46, 2000). In such instances, a vector packaging procedure based on providing sufficient quantities of functional G protein as a means to compensate for lost G function will support further clinical development of VSV vector candidates, provided several criteria are met.
Among these criteria are that all materials and procedures should be compliant with regulations governing production of immunogenic compositions for human administration. Moreover, the method used to provide functional G protein should be efficient and scaleable to accommodate manufacturing. Furthermore, G protein expression should be sufficient to promote efficient packaging of the Gstem or ΔG vector. Also, virus particle yields should preferably routinely achieve or exceed 1×106 IUs per ml. More preferably, virus particle yields should routinely achieve or exceed 1×107 IUs per ml in most instances. The compositions and methods of the present invention meet these criteria.
The present invention provides a scaleable method that reproducibly yields 1×107 IU per ml. With respect to clinical development of candidate VSV vectors, complementation methods that rely on stable cell lines provide a key manufacturing advantage over transient expression complementation methods from plasmids. In particular, propagation-defective viral vectors can be propagated in stable cell lines without the manipulations inherent to electroporation or transfection, which can be difficult to manage when conducted with the large number and volume of cells needed to manufacture such vectors.
It has been surprisingly discovered that significant quantities of VSV G protein were capable of being produced by a heat-shock induced cell line comprising an optimized VSV gene. Moreover, the heat-shock inducible cell line was found to be useful for production of propagation-defective VSV Gstem. In particular, genetic complementation with the heat-shock inducible cell line was capable of producing over 1×107 IU per ml when packaging Gstem vectors encoding HIV gag. The fact that yields of more than 1×107 IU per ml were observed for the Gstem vector with the packaging method of the present invention, and that this was achieved with Vero cells, indicates that it is possible to produce attenuated VSV vectors, such as propagation-defective Gstem, on a manufacturing-scale.
The methods of VSV G complementation according to the present invention were applied to the production of VSV Gstem vector, although the present invention is not limited to this embodiment. For example, the methods of the present invention can be applied to the production of other attenuated VSVs. Examples of various recombinant VSV vectors are provided herein.
Moreover, other propagation-defective paramyxovirus or rhabdovirus vectors (i.e. Sendai virus, measles virus, mumps virus, parainfluenza virus, or vesiculoviruses) lacking their native attachment proteins may be packaged with VSV G protein on their surface using the complementation systems described herein. In fact, VSV G protein has been shown to function as an attachment protein for replication-competent recombinant measles viruses (Spielhofer, et al. J Virol 72:2150-9, 1998) indicating that it should function similarly in the context of propagation-defective morbillivirus vectors. VSV G protein also is widely used to ‘pseudotype’ retrovirus particles, thereby providing an attachment protein that can mediate infection of a broad spectrum of cell types (Cronin, et al. Curr Gene Ther 5:387-98, 2005; Yee, et al. Methods Cell Biol 43 Pt A:99-112, 1994). The packaging methods described above should be adaptable to retrovirus particle production, and might significantly simplify the production and improve yields of virus particles containing VSV G protein.
The complementation method of the present invention has been developed for VSV G protein expression in Vero cells, but the technology should be readily applicable to other viruses, cell types, and complementing proteins. It particularly is worth noting that the use of a heat-shock inducible stable cell line described herein circumvented the toxic nature of VSV G, allowing for efficient packaging of propagation-defective VSV vectors. This suggests that this method would be adaptable to other complementation systems that require controlled expression of a toxic protein in trans.
General procedures for recovery of non-segmented negative-stranded RNA viruses according to the invention can be summarized as follows. A cloned DNA equivalent (which is positive-strand, message sense) of the desired viral genome is placed between a suitable DNA-dependent RNA polymerase promoter (e.g., a T7, T3 or SP6 RNA polymerase promoter) and a self-cleaving ribozyme sequence (e.g., the hepatitis delta ribozyme) which is inserted into a suitable transcription vector (e.g. a propagatable bacterial plasmid). This transcription vector provides the readily manipulable DNA template from which the RNA polymerase (e.g., T7 RNA polymerase) can faithfully transcribe a single-stranded RNA copy of the viral antigenome (or genome) with the precise, or nearly precise, 5′ and 3′ termini. The orientation of the viral DNA copy of the genome and the flanking promoter and ribozyme sequences determine whether antigenome or genome RNA equivalents are transcribed.
Also required for rescue of new virus progeny according to the invention are virus-specific trans-acting support proteins needed to encapsidate the naked, single-stranded viral antigenome or genome RNA transcripts into functional nucleocapsid templates. These generally include the viral nucleocapsid (N) protein, the polymerase-associated phosphoprotein (P) and the polymerase (L) protein.
Functional nucleocapsid serves as a template for genome replication, transcription of all viral mRNAs, and accumulation of viral proteins, triggering ensuing events in the viral replication cycle including virus assembly and budding. The mature virus particles contain the viral RNA polymerase necessary for further propagation in susceptible cells.
The present invention is directed to the recovery of attenuated VSV. Certain attenuated viruses selected for rescue require the addition of support proteins, such as G and M for virus assembly and budding. For example, the attenuated VSV may be a propagation-defective VSV vector comprising a deletion of sequence encoding either all of the G protein (ΔG) or most of the G protein ectodomain (Gstem). Both ΔG and Gstem are unable to spread beyond primary infected cells in vivo. This results in a virus that can propagate only in the presence of transcomplementing G protein. In the present invention, a stable cell line provides this transcomplementing G protein when it is induced by an applied stimulus (e.g., heat-shock).
Typically, although not necessarily exclusively, rescue of non-segmented negative-stranded RNA viruses also requires an RNA polymerase to be expressed in host cells carrying the viral cDNA, to drive transcription of the cDNA-containing transcription vector and of the vectors encoding the support proteins.
Within the present invention, rescue of attenuated VSV in a cell typically involves providing a cell that includes an optimized VSV G gene, wherein expression of VSV G protein from the optimized VSV G gene is inducible. The method further includes transfecting the cell that includes the optimized VSV G gene (e.g., by electroporation) with: a viral cDNA expression vector comprising a polynucleotide encoding a genome or antigenome of the attenuated VSV; one or more support plasmids encoding N, P, L and optionally G proteins of VSV; and a plasmid encoding a DNA-dependent RNA polymerase. The transfected cells are induced (by an applied stimulus) to express VSV G protein from the optimized VSV G gene. The induced cells are grown in culture; and attenuated VSV is recovered from the culture. Although the host cells used for viral rescue express a VSV G protein upon being induced by an applied stimulus, such as heat shock, the present inventors have found that the yield of attenuated VSV may be enhanced by use of a G plasmid in transient transfection.
The rescued material may be used to infect plaque expansion cells for further viral expansion, as described in further detail below. These plaque expansion cells may be of the same type as the cells used for virus rescue, if desired.
The host cells used for viral rescue are often impaired in their ability to support further viral expansion. Therefore, the method of producing attenuated VSV in a cell culture typically further includes infecting plaque expansion cells with the rescued, attenuated VSV. In some embodiments of the present invention, cells expressing VSV G protein encoded by an optimized VSV G gene are infected with the rescued attenuated VSV; the infected cells are grown; and the attenuated VSV is recovered from the culture of infected cells.
In some embodiments of viral rescue, the polynucleotide encoding the genome or antigenome of the attenuated VSV is introduced into the cell in the form of a viral cDNA expression vector that includes the polynucleotide operatively linked to an expression control sequence to direct synthesis of RNA transcripts from the cDNA expression vector. In some embodiments, the expression control sequence is a suitable DNA-dependent RNA polymerase promoter (e.g., a T7, T3 or SP6 RNA polymerase promoter).
In some embodiments, the support plasmids, as well as the viral cDNA expression vector used during viral rescue are under the control of a promoter of the DNA-dependent RNA polymerase. For example, in embodiments where the RNA polymerase is T7 RNA polymerase, the support plasmids and the viral cDNA expression vector would preferably be under the control of a T7 promoter.
In some other embodiments, the expression of the DNA-dependent RNA polymerase is under the control of a cytomegalovirus-derived RNA polymerase II promoter. The immediate-early human cytomegalovirus [hCMV] promoter and enhancer is described, for e.g., in U.S. Pat. No. 5,168,062, incorporated herein by reference.
In some embodiments, the method for recovering attenuated VSV from cDNA involves introducing a viral cDNA expression vector encoding a genome or antigenome of the subject virus into a host cell, and coordinately introducing: a polymerase expression vector encoding and directing expression of an RNA polymerase. Useful RNA polymerases in this context include, but are not limited to, a T7, T3, or SP6 phage polymerase. The host cells also express, before, during, or after coordinate introduction of the viral cDNA expression vector, the polymerase expression vector and the N, P, L, M and G support proteins necessary for production of mature attenuated VSV particles in the host cell.
Typically, the viral cDNA expression vector and polymerase expression vector will be coordinately transfected into the host cell with one or more additional expression vector(s) that encode(s) and direct(s) expression of the support proteins. The support proteins may be wild-type or mutant proteins of the virus being rescued, or may be selected from corresponding support protein(s) of a heterologous non-segmented negative-stranded RNA virus. In alternate embodiments, additional viral proteins may be co-expressed in the host cell, for example a polymerase elongation factor (such as M2-1 for RSV) or other viral proteins that may enable or enhance recovery or provide other desired results within the subject methods and compositions. In other embodiments, one or more of the support protein(s) may be expressed in the host cell by constitutively expressing the protein(s) in the host cell, or by co-infection of the host cell with a helper virus encoding the support protein(s).
In more detailed aspects of the invention, the viral cDNA expression vector comprises a polynucleotide encoding a genome or antigenome of VSV operably linked to an expression control sequence to direct synthesis of viral RNA transcripts from the cDNA expression vector. The viral cDNA vector is introduced into a host cell transiently expressing an RNA polymerase and the following VSV support proteins: an N protein, a P protein, an L protein, an M protein and a G protein. Each of the RNA polymerase and the N, P, L, M and G proteins may be expressed from one or more transfected expression vector(s). Often, each of the RNA polymerase and the support proteins will be expressed from separate expression vectors, commonly from transient expression plasmids. Following a sufficient time and under suitable conditions, an assembled infectious, attenuated VSV is rescued from the host cells.
To produce infectious, attenuated VSV particles from a cDNA-expressed genome or antigenome, the genome or antigenome is coexpressed with those viral proteins necessary to produce a nucleocapsid capable of RNA replication, and render progeny nucleocapsids competent for both RNA replication and transcription. Such viral proteins include the N, P and L proteins. In the instant invention, attenuated VSV vectors with lost G function also require the addition of the G viral protein. Moreover, an M protein may also be added for a productive infection. The G and M viral proteins can be supplied by coexpression. In some embodiments, the VSV G support plasmid employed during viral rescue contains a non-optimized VSV G gene. However, in other embodiments, as described below, the VSV G support plasmid employed during viral rescue contains an optimized VSV G gene.
In certain embodiments of the invention, complementing sequences encoding proteins necessary to generate a transcribing, replicating viral nucleocapsid (i.e., L, P and N), as well as the M and G proteins are provided by one or more helper viruses. Such helper viruses can be wild type or mutant. In certain embodiments, the helper virus can be distinguished phenotypically from the virus encoded by the recombinant viral cDNA. For example, it may be desirable to provide monoclonal antibodies that react immunologically with the helper virus but not the virus encoded by the recombinant viral cDNA. Such antibodies can be neutralizing antibodies. In some embodiments, the antibodies can be used in affinity chromatography to separate the helper virus from the recombinant virus. To aid the procurement of such antibodies, mutations can be introduced into the viral cDNA to provide antigenic diversity from the helper virus, such as in a glycoprotein gene.
A recombinant viral genome or antigenome may be constructed for use in the present invention by, e.g., assembling cloned cDNA segments, representing in aggregate the complete genome or antigenome, by polymerase chain reaction or the like (PCR; described in, e.g., U.S. Pat. Nos. 4,683,195 and 4,683,202, and PCR Protocols: A Guide to Methods and Applications, Innis et al., eds., Academic Press, San Diego, 1990) of reverse-transcribed copies of viral mRNA or genome RNA. For example, a first construct may be generated which comprises cDNAs containing the left hand end of the antigenome, spanning from an appropriate promoter (e.g., T7, T3, or SP6 RNA polymerase promoter) and assembled in an appropriate expression vector (such as a plasmid, cosmid, phage, or DNA virus vector). The vector may be modified by mutagenesis and/or insertion of a synthetic polylinker containing unique restriction sites designed to facilitate assembly. The right hand end of the antigenome plasmid may contain additional sequences as desired, such as a flanking ribozyme and single or tandem T7 transcriptional terminators. The ribozyme can be hammerhead type, which would yield a 3′ end containing a single nonviral nucleotide, or can be any of the other suitable ribozymes such as that of hepatitis delta virus (Perrotta et al., Nature 350:434-436, 1991) that would yield a 3′ end free of non-viral nucleotides.
Alternative means to construct cDNA encoding the viral genome or antigenome include reverse transcription-PCR using improved PCR conditions (e.g., as described in Cheng et al., Proc. Natl. Acad. Sci. USA 91:5695-5699, 1994, incorporated herein by reference) to reduce the number of subunit cDNA components to as few as one or two pieces. In other embodiments different promoters can be used (e.g., T3 or SPQ). Different DNA vectors (e.g., cosmids) can be used for propagation to better accommodate the larger size genome or antigenome.
As noted above, defined mutations can be introduced into an infectious viral clone by a variety of conventional techniques (e.g., site-directed mutagenesis) into a cDNA copy of the genome or antigenome. The use of genomic or antigenomic cDNA subfragments to assemble a complete genome or antigenome cDNA as described herein has the advantage that each region can be manipulated separately, where small cDNA constructs provide for better ease of manipulation than large cDNA constructs, and then readily assembled into a complete cDNA.
Certain of the attenuated viruses of the invention will be constructed or modified to limit the growth potential, replication competence, or infectivity of the recombinant virus. Such attenuated viruses and subviral particles are useful as vectors and immunogens, but do not pose certain risks that would otherwise attend administration of a fully infectious (i.e., having approximately a wild-type level of growth and/or replication competence) virus to a host. By attenuated, it is meant a virus or subviral particle that is limited in its ability to grow or replicate in a host cell or a mammalian subject, or is otherwise defective in its ability to infect and/or propagate in or between cells. By way of example, ΔG and G stem are attenuated viruses that are propagation-defective, but replication competent. Often, attenuated viruses and subviral particles will be employed as “vectors”, as described in detail herein below.
Thus, various methods and compositions are provided for producing attenuated VSV particles. In more detailed embodiments, the attenuated virus will exhibit growth, replication and/or infectivity characteristics that are substantially impaired in comparison to growth, replication and/or infectivity of a corresponding wild-type or parental virus. In this context, growth, replication, and/or infectivity may be impaired in vitro and/or in vivo by at least approximately 10-20%, 20-50%, 50-75% and up to 95% or greater compared to wild-type or parental growth, replication and/or infectivity levels.
In some embodiments, viruses with varying degrees of growth or replication defects may be rescued using a combined heat shock/T7-plasmid rescue system described in detail below. Exemplary strains include highly attenuated strains of VSV that incorporate modifications as described below (e.g., a C-terminal G protein truncation, or translocated genes) (see, e.g., Johnson et al., J. Virol. 71:5060-5078, 1997, Schnell et al., Proc. Natl. Acad. Sci. USA 93:11359-11365, 1996; Schnell et al., Cell 90:849-857, 1997; Roberts et al., J. Virol. 72:4704-4711, 1998; and Rose et al., Cell 106:539-549, 2001, each incorporated herein by reference).
Further examples of attenuated viruses are described in further detail below. The attenuated viruses are useful as “vectors”, e.g., by incorporation of a heterologous antigenic determinant into a recombinant vector genome or antigenome. In specific examples, a measles virus (MV) or human immunodeficiency virus (HIV) glycoprotein, glycoprotein domain, or one or more antigenic determinant(s) is incorporated into a VSV vector or “backbone”.
For ease of preparation the N, P, L, M and G viral proteins can be assembled in one or more separate vectors. Many suitable expression vectors are known in the art which are useful for incorporating and directing expression of polynucleotides encoding the RNA polymerase and support proteins, including for example plasmid, cosmid, or phage vectors, defective viral vectors, so-called “replicons” (e.g. sindbis or Venezuelan equine encephalitis replicons) and other vectors useful for directing transient and/or constitutive expression. Transient expression of the RNA polymerase and, where applicable, the N, P, L, M and G proteins, is directed by a transient expression control element operably integrated with the polymerase and/or support vector(s). In one exemplary embodiment, the transient expression control element for the RNA polymerase is an RNA polymerase II regulatory region, as exemplified by the immediate-early human cytomegalovirus [hCMV] promoter and enhancer (see, e.g., U.S. Pat. No. 5,168,062). In other exemplary embodiments, the transient expression control elements for one or more of the N, P, L, M and G proteins is a DNA-dependent RNA polymerase promoter, such as the T7 promoter.
The vectors encoding the viral cDNA, the transiently-expressed RNA polymerase, and the N, P, L, M and G proteins may be introduced into appropriate host cells by any of a variety of methods known in the art, including transfection, electroporation, mechanical insertion, transduction or the like. In some preferred embodiments, the subject vectors are introduced into the cells by electroporation. In other embodiments, the subject vectors are introduced into cultured cells by calcium phosphate-mediated transfection (Wigler et al., Cell 14:725, 1978; Corsaro et al., Somatic Cell Genetics 7:603, 1981; Graham et al., Virology 52:456, 1973), electroporation (Neumann et al., EMBO J. 1:841-845, 1982), DEAE-dextran mediated transfection (Ausubel et al., (ed.) Current Protocols in Molecular Biology, John Wiley and Sons, Inc., NY, 1987), or cationic lipid-mediated transfection (Hawley-Nelson et al., Focus 15:73-79, 1993). In alternate embodiments, a transfection facilitating reagent is added to increase DNA uptake by cells. Many of these reagents are known in the art. LIPOFECTACE® (Life Technologies, Gaithersburg, Md.) and EFFECTENE® (Qiagen, Valencia, Calif.) are common examples. These reagents are cationic lipids that coat DNA and enhance DNA uptake by cells. LIPOFECTACE® forms a liposome that surrounds the DNA while EFFECTINE® coats the DNA but does not form a liposome. Another useful commercial reagent to facilitate DNA uptake is LIPOFECTAMINE-2000® (Invitrogen, Carlsbad, Calif.).
Suitable host cells for use within the invention are capable of supporting a productive infection of the subject attenuated VSV, and are capable of being induced by heat or some other applied stimulus to permit expression of the requisite vectors and their encoded products necessary to support viral production. Examples of host cells for use in the methods of the present invention are described in further detail below.
Within the methods and compositions provided herein, coordinate introduction of the RNA polymerase vector, viral cDNA clone, and support vector(s) (e.g., plasmid(s) encoding N, P, L, M and G proteins) into a host cell will be simultaneous. For example, all of the subject DNAs may be combined in a single DNA transfection (e.g., electroporation) mixture and added to a host cell culture simultaneously to achieve coordinate transfection. In alternate embodiments separate transfections may be performed for any two or more of the subject polymerase and support vectors and the viral cDNA vector. Typically, separate transfections will be conducted in close temporal sequence to coordinately introduce the polymerase and support vectors and viral cDNA vector in an effective cotransfection procedure. In one such coordinate transfection protocol, the viral cDNA and/or N, P, L, M and G support plasmid(s) is/are introduced into the host cell prior to transfection of the RNA polymerase plasmid. In other embodiments, the viral cDNA and/or the N, P, L, M and P support plasmid(s) is/are introduced into the host cell simultaneous with or following transfection of the RNA polymerase plasmid into the cell, but before substantial expression of the RNA polymerase begins (e.g., before detectable levels of a T7 polymerase have accumulated, or before levels of T7 sufficient to activate expression of plasmids driven by a T7 promoter have accumulated) in the host cell.
In some embodiments, the method for producing the infectious, attenuated RNA virus involves a heat shock treatment of the host cell to increase recovery of the recombinant virus. After one or more of the viral cDNA expression vectors and the one or more transient expression vectors encoding the RNA polymerase, N protein, P protein, L protein, M protein and G protein are introduced into the host cell, the host cell may be exposed to an effective heat shock stimulus that increases recovery of the recombinant virus.
In one such method, the host cell is exposed to an effective heat shock temperature for a time period sufficient to effectuate heat shock of the cells, which in turn stimulates enhanced viral recovery. An effective heat shock temperature is a temperature above the accepted, recommended or optimal temperature considered in the art for performing rescue of the subject virus. In many instances, an effective heat shock temperature is above 37° C. When a rescue method of the invention is carried out at an effective heat shock temperature, there results an increase in recovery of the desired recombinant virus over the level of recovery of recombinant virus when rescue is performed in the absence of the increase in temperature. The effective heat shock temperature and exposure time may vary based upon the rescue system used. Such temperature and time variances can result from differences in the virus selected or host cell type.
Although the temperature may vary, an effective heat shock temperature can be readily ascertained by conducting several test rescue procedures with a particular recombinant virus, and establishing a rate percentage of recovery of the desired recombinant virus as temperature and time of exposure are varied. Certainly, the upper end of any temperature range for performing rescue is the temperature at which the components of the transfection are destroyed or their ability to function in the transfection is depleted or diminished. Exemplary effective heat shock temperature ranges for use within this aspect of the invention are: from about 37° C. to about 50° C., from about 38°C. to about 50° C., from about 39° C. to about 49° C., from about 39° C. to about 48° C., from about 40° C. to about 47° C., from about 41° C. to about 47° C., from about 41° C. to about 46° C. Often, the selected effective heat shock temperature range will be from about 42° C. to about 46° C. In more specific embodiments, effective heat shock temperatures of about 43° C., 44° C., 45° C. or 46° C. are employed.
In conducting the tests to establish a selected effective heat shock temperature or temperature range, one can also select an effective time period for conducting the heat shock procedure. A sufficient time for applying the effective heat shock temperature is a time over which there is a detectable increase in recovery of the desired recombinant virus over the level of recovery of recombinant virus when rescue is performed in the absence of an increase in temperature as noted above. The effective heat shock period may vary based upon the rescue system, including the selected virus and host cell. Although the time may vary, the amount of time for applying an effective heat shock temperature can be readily ascertained by conducting several test rescue procedures with a particular recombinant virus, and establishing a rate or percentage of recovery of the desired recombinant virus as temperature and time are varied. The upper limit for any time variable used in performing rescue is the amount of time at which the components of the transfection are destroyed or their ability to function in the transfection is depleted or diminished. The amount of time for the heat shock procedure may vary from several minutes to several hours, as long as the desired increase in recovery of recombinant virus is obtained. Exemplary effective heat shock periods for use within this aspect of the invention, in minutes, are: from about 5 to about 500 minutes, from about 5 to about 200 minutes, from about 15 to about 300, from about 15 to about 240, from about 20 to about 200, from about 20 to about 150. Often, the effective heat shock period will be from about 30 minutes to about 150 minutes.
Numerous means can be employed to determine the level of improved recovery of a recombinant, attenuated VSV through exposure of host cells to effective heat shock. For example, a chloramphenicol acetyl transferase (CAT) reporter gene can be used to monitor rescue of the recombinant virus according to known methods. The corresponding activity of the reporter gene establishes the baseline and improved level of expression of the recombinant virus. Other methods include detecting the number of plaques of recombinant virus obtained and verifying production of the rescued virus by sequencing. One exemplary method for determining improved recovery involves preparing a number of identically transfected cell cultures and exposing them to different conditions of heat shock (time and temperature variable), and then comparing recovery values for these cultures to corresponding values for control cells (e.g., cells transfected and maintained at a constant temperature of 37° C.). After 72 hours post-transfection, the transfected cells are transferred to a 10 cm plate containing a monolayer of about 75% confluent Vero cells (or cell type of choice for determining plaque formation of the recombinant virus) and continuing incubation until plaques are visible. Thereafter, the plaques are counted and compared with the values obtained from control cells. Optimal heat shock conditions should maximize the number of plaques.
According to these embodiments of the invention, improved viral recovery will be at least about 10% or 25%, and often at least about 40%. In certain embodiments, the increase in the recombinant virus recovered attributed to effective heat shock exposure is reflected by a 2-fold, 5-fold, and up to 10-fold or greater increase in the amount of recombinant virus observed or recovered.
In some embodiments of the invention, the host cell in which the viral cDNA, RNA polymerase vector and one or more vector(s) encoding support proteins, have been introduced is subjected to a “plaque expansion” step. This procedure is typically conducted after a period of time (e.g., post-transfection) sufficient to permit expression of the viral cDNA expression vector and one or more expression vectors that encode(s) and direct(s) transient expression of the RNA polymerase, N protein, P protein, L protein, M protein and G protein. To achieve plaque expansion, the host cell, which often has become impaired in its ability to support further viral expansion, is co-cultured with a plaque expansion cell of the same or different cell type. The co-culture step allows spread of rescued virus to the plaque expansion cell, which is more amenable to vigorous expansion of the virus. Typically, a culture of host cells is transferred onto one or more layer(s) of plaque expansion cells. For example, a culture of host cells can be spread onto a monolayer of plaque expansion cells and the attenuated VSV will thereafter infect the plaque expansion cells and expand further therein. In some embodiments, the host cell is of the same, or different, cell type as the plaque expansion cell.
In certain embodiments, both the host cells used for viral rescue, as well as the plaque expansion cells of are of the same type and may be induced (by an applied stimulus, such as heat) to express a VSV G protein from an optimized VSV G gene. In other embodiments, the host cells used for viral rescue may express a functional, but non-optimized G coding sequence (e.g., a native G coding sequence), provided that the plaque expansion cells, which are to be infected with the rescued virus, may be induced to express the VSV G protein from an optimized VSV G gene.
The plaque expansion methods and compositions of the invention provide improved rescue methods for producing attenuated VSV, such as including, but not limited to, propagation-defective VSV. Typically, the viral rescue method entails providing a host cell that comprises an optimized VSV G gene, wherein expression of VSV G protein from the optimized VSV G gene is inducible. The method also includes introducing into the host cell a transcription vector comprising an isolated nucleic acid molecule encoding a genome or antigenome of an attenuated VSV and a transient expression vector encoding and directing transient expression of an RNA polymerase, along with one or more other support expression vectors which comprise at least one isolated nucleic acid molecule encoding trans-acting proteins necessary for encapsidation, transcription and replication (i.e., N, P, and L VSV proteins). The viral rescue method may further include introducing into the cells a support vector encoding an M protein of VSV for a productive infection. The vectors are introduced into the host cell under conditions sufficient to permit co-expression of said vectors and production of the attenuated, mature virus particles.
The attenuated VSV is rescued and the rescued material is then preferably co-cultured with plaque expansion cells. This allows spread of the rescued virus to the plaque expansion cell via infection. The plaque expansion cell is more amenable to vigorous expansion of the virus. The attenuated VSV may then be recovered from the co-culture. In some embodiments, the viral rescue cells are transferred onto at least one layer of plaque expansion cells that have been induced to express VSV G protein from an optimized VSV G gene.
In order to achieve plaque expansion, the transfected viral rescue cells are typically transferred to co-culture containers of plaque expansion cells. Any of the various plates or containers known in the art can be employed for the plaque expansion step. In certain embodiments, the viral rescue cells are transferred onto a monolayer of plaque expansion cells that is at least about 50% confluent. Alternatively, the plaque expansion cells are at least about 60% confluent, or even at least about 75% confluent. In certain embodiments, the surface area of the plaque expansion cells is greater than the surface area used for preparing the transfected virus. An enhanced surface area ratio of from 2:1 to 100:1 can be employed as desired. An enhanced surface area of at least 10:1 is often desired.
Propagation-defective viruses offer clear safety advantages for use in humans. These vectors are restricted to a single round of replication and are unable to spread beyond primary infected cells. One such vector, which is described in detail below, has the entire G gene deleted (ΔG), and therefore requires G protein transcomplementation for propagation of infectious virus particles in vitro. Another vector, which is described in detail below, has most of the G protein ectodomain deleted (Gstem), retaining the cytoplasmic tail (CT) region, transmembrane domain, and 42 amino acids of the membrane proximal ectodomain. This vector is also propagation-defective, requiring G protein in trans for production of infectious particles in vitro.
Although propagation-defective viruses have been known to offer safety advantages, prior to the present invention, there were difficulties in providing adequate quantities of complementing G protein to allow efficient vector amplification during industrial scale manufacture. As detailed in the Examples, extensive studies were conducted to identify conditions that support maximal G protein expression. Two methods of coding sequence optimization were analyzed to determine if they might improve transient expression of VSV G protein. One method, described as RNA optimization (RNAopt), and used synonymous nucleotide substitutions to increase GC content and disrupt sequence motifs that inhibit nuclear export, decrease translation, or destabilize mRNAs (Schneider, et al. J Virol 71:4892-903, 1997); Schwartz, et al. J Virol 66:7176-82, 1992; Schwartz, et al. J Virol 66:150-9, 1992). VSV G (RNA optimized) coding sequences for Indiana and New Jersey serotypes are shown, for example, in
As described in further detail in the Examples, it was discovered that electroporation of plasmids containing optimized G protein coding sequences produced higher levels of G protein expression in Vero cells as compared to the native Gin open reading frame. Thereafter, studies were conducted to determine whether the increased abundance of G enhanced packaging yields of propagation-defective vectors. As described in further detail in the Examples and in
In some embodiments, an optimized VSV G gene is selected from the following: SEQ ID NO: 3, SEQ ID NO: 4, and SEQ ID NO: 5.
Host cells used for viral rescue can be selected from a prokaryotic cell or a eukaryotic cell. Suitable cells include insect cells such as Sf9 and Sf21, bacterial cells with an appropriate promoter such as E. coli, and yeast cells such as S. cerevisiae. Host cells are typically chosen from vertebrate, e.g., primate, cells. Typically, a cell line is employed that yields a detectable cytopathic effect in order that rescue of viable virus may be easily detected. Often, the host cells are derived from a human cell, such as a human embryonic kidney (HEK) cell. Vero cells (African green monkey kidney cells), as well as many other types of cells can also be used as host cells. In some exemplary embodiments, Vero cells are used as host cells. In the case of VSV, the transfected cells are grown on Vero cells because the virus spreads rapidly on Vero cells and makes easily detectable plaques. Moreover, Vero cells are qualified for production for human administration. The following are examples of other suitable host cells: (1) Human Diploid Primary Cell Lines: e.g. WI-38 and MRC-5 cells; (2) Monkey Diploid Cell Line: e.g. Cos, Fetal Rhesus Lung (FRhL) cells; (3) Quasi-Primary Continuous Cell Line: e.g. AGMK—African green monkey kidney cells.; (4) Human 293 cells (qualified) and (5) rodent (e.g., CHO, BHK), canine e.g., Madin-Darby Canine Kidney (MDCK), and primary chick embryo fibroblasts. Exemplary specific cell lines that are useful within the methods and compositions of the invention include HEp-2, HeLa, HEK (e.g., HEK 293), BHK, FRhL-DBS2, LLC-MK2, MRC-5, and Vero cells.
In the present invention, the viral rescue cells are preferably cells of the types described above, wherein the cells contain an optimized VSV G gene and may be induced by an applied stimulus (e.g., heat shock treatment) to express VSV G protein from the optimized gene.
As described in further detail herein, a method of producing attenuated VSV particles according to the present invention may include growing the host cells used in the rescue of the viral particles with plaque expansion cells. This permits the spread of recovered attenuated VSV particles to the plaque expansion cells. In some embodiments, the plaque expansion cells are of a same or different cell type as the host cells used for viral rescue.
The plaque expansion cells are selected based on the successful growth of the native or recombinant virus in such cells. Often, the host cell employed in conducting the transfection is not an optimal host for growth of the desired recombinant, attenuated virus. The recovery of recombinant, attenuated virus from the transfected cells can therefore be enhanced by selecting a plaque expansion cell in which the native virus or the recombinant virus exhibits enhanced growth. Various plaque expansion cells can be selected for use within this aspect of the invention, in accordance with the foregoing description. Exemplary specific plaque expansion cells that can be used to support recovery and expansion of recombinant, attenuated VSVs of the invention are selected from HEp-2, HeLa, HEK, BHK, FRhL-DBS2, LLC-MK2, MRC-5, and Vero cells. In the present invention, the plaque expansion cells are preferably cells of these types, wherein the cells contain an optimized VSV G gene and may be induced by an applied stimulus (e.g., heat shock treatment) to express VSV G protein from the optimized gene. Additional details concerning heat shock and plaque expansion methods for use within the invention are provided in PCT publication WO 99/63064, incorporated herein by reference.
In some embodiments of the methods of the present invention, the plaque expansion cells are induced to express VSV G protein encoded in the cell by an optimized VSV G gene. Thereafter, the plaque expansion cells are used to establish a coculture with the viral rescue cells. The rescued, attenuated virus infects the plaque expansion cells during the coculture step, and the virus expands further therein.
In certain embodiments, an attenuated VSV for use in the present invention expresses a G protein having a truncated cytoplasmic tail (CT) region. For example, it is known in the art that G gene mutations which truncate the carboxy-terminus of the cytoplasmic domain influence VSV budding and attenuate virus production (Schnell, et al. The EMBO Journal 17(5):1289-1296, 1998; Roberts, et al. J Virol, 73:3723-3732, 1999). The cytoplasmic domain of wild-type VSV G protein comprises twenty-nine amino acids (RVGIHLCIKLKHTKKRQIYTDIEMNRLGK-COOH; SEQ ID NO: 13).
In some embodiments, an attenuated VSV expresses a G protein having a cytoplasmic tail region truncated to one amino acid (G-CT1). For example, the attenuated VSV may express a G protein in which the last twenty-eight amino acid residues of the cytoplasmic domain are deleted (retaining only arginine from the twenty-nine amino acid wild-type cytoplasmic domain of SEQ ID NO: 13).
In some other embodiments, an attenuated VSV expresses a G protein having a cytoplasmic tail region truncated to nine amino acids (G-CT-9). For example, the attenuated VSV may express a G protein in which the last twenty carboxy-terminal amino acids of the cytoplasmic domain are deleted (relative to the twenty-nine amino acid wild-type cytoplasmic domain of SEQ ID NO: 13).
In some embodiments, an attenuated VSV lacks a VSV G protein (VSV-ΔG). For example, an attenuated VSV of the invention may be a virus in which a VSV G gene) is deleted from the genome. In this regard, Roberts, et al. described a VSV vector in which the entire gene encoding the G protein was deleted (ΔG) and substituted with influenza haemagglutinin (HA) protein, wherein the VSV vector (ΔG-HA) demonstrated attenuated pathogenesis (Roberts, et al. Journal of Virology, 73:3723-3732, 1999).
In some other embodiments, an attenuated VSV expresses a G protein having a truncated extracellular domain (VSV-Gstem). For example, an attenuated VSV of the invention may include a mutation in the G gene, wherein the encoded G protein has a mutation in the membrane-proximal stem region of the G protein ectodomain, referred to as G-stem protein. The G-stem region comprises amino acid residues 421-462 of the G protein. Prior studies have demonstrated the attenuation of VSV via insertion and/or deletion (e.g., truncation) mutations in the G-stem of the G protein (Robison and Whitt, J Virol 74 (5):2239-2246, 2000; Jeetendra, et al., J Virol 76(23):12300-11, 2002; Jeetendra, et al., J Virol 77 (23):12807-18, 2003).
In some embodiments, the attenuated VSV is one in which the G coding sequence is replaced with a modified version that encodes only 18 amino-terminal residues of the signal sequence fused to the C-terminal 91 amino acids of G of which approximately 42 residues from a truncated extracellular domain (G-stem). This type of G gene modification may be constructed using the method of Robison and Whitt, J Virol 74 (5):2239-2246, 2000.
In certain embodiments, an attenuated VSV of the invention comprises a gene shuffling mutation in its genome. As defined herein, the terms “gene shuffling”, “shuffled gene”, “shuffled”, “shuffling”, “gene rearrangement” and “gene translocation” may be used interchangeably and refer to a change (mutation) in the order of the wild-type VSV genome. As defined herein, a wild-type VSV genome has the following gene order, which is depicted in
It is known in the art, that the position of a VSV gene relative to the 3′ promoter determines the level of expression and virus attenuation (U.S. Pat. No. 6,596,529 to Wertz, et al. and Wertz et al., Proc. Natl. Acad. Sci USA 95:3501-6, 1998, each specifically incorporated herein by reference). There is a gradient of expression, with genes proximal to the 3′ promoter expressed more abundantly than genes distal to the 3′ promoter. The nucleotide sequences encoding VSV G, M, N, P and L proteins are known in the art (Rose and Gallione, J Virol 39:519-528, 1981; Gallione et al., J Virol 39:529-535, 1981). For example, U.S. Pat. No. 6,596,529 describes gene shuffling mutations in which the gene for the N protein is translocated (shuffled) from its wild-type promoter-proximal first position to successively more distal positions on the genome, in order to successively reduce N protein expression (e.g., 3′-PNMGL-5′, 3′-PMNGL-5′, 3′-PMGNL-5′, referred to as N2, N3 and N4, respectively). Positionally-shifted VSV mutants are also described in, for e.g., U.S. Pat. No. 6,136,585 to Ball, et al.
Thus, in certain embodiments, an attenuated VSV comprises a gene shuffling mutation in its genome. A gene shuffling mutation may comprise a translocation of the N gene (e.g., 3′-PNMGL-5′ or 3′-PMNGL-5′). For example, in some embodiments, the attenuated VSV comprises the N gene, which has been translocated downstream from its wild-type position in the viral genome, thereby resulting in a reduction in N protein expression.
It should be noted herein, that the insertion of a foreign nucleic acid sequence (e.g., HIV gag) into the VSV genome 3′ to any of the N, P, M, G or L genes, effectively results in a “gene shuffling mutation” as defined above. For example, when the HIV gag gene is inserted into the VSV genome at position one (e.g., 3′-gag1-NPMGL-5′), the N, P, M, G and L genes are each moved from their wild-type positions to more distal positions on the genome. Thus, in certain embodiments of the invention, a gene shuffling mutation includes the insertion of a foreign nucleic acid sequence into the VSV genome 3′ to any of the N, P, M, G or L genes (e.g., 3′-gag1-NPMGL-5′, 3′-N-gag2-PMGL-5′, 3′-NP-gag3-MGL-5′, etc.).
In certain other embodiments, an attenuated VSV of the invention includes a non-cytopathic mutation (Mncp) in the M gene. The VSV (Indiana serotype) M gene encodes a 229 amino acid M (matrix) protein.
It is known in the art that the M mRNA further encodes two additional proteins, referred to as M2 and M3 (Jayakar and Whitt, J Virol 76(16):8011-8018 2002). The M2 and M3 proteins are synthesized from downstream methionines in the same reading frame that encodes the 229 amino acid M protein (referred to as M1), and lack the first thirty-two (M2 protein) or fifty (M3 protein) amino acids of the M1 protein. It has been observed that cells infected with a recombinant VSV that expresses the M protein, but not M2 and M3, exhibit a delayed onset of cytopathic effect (in certain cell types), yet produce a normal virus yield.
Thus, in certain embodiments, an attenuated VSV of the invention includes a non-cytopathic mutation in the M gene, wherein the M gene mutation reduces the expression of two overlapping in-frame polypeptides that are expressed from the M protein mRNA by initiation of protein synthesis at internal AUGs. Such an M gene mutation results in a virus that does not express the M2 or M3 protein. These mutations also affect IFN induction, nuclear transport, and other functions. See, for example, Jayakar and Whitt, J Virol 76(16):8011-8018, 2002.
In some embodiments, the attenuated VSV expresses a heterologous antigen, so that the VSV serves as a vector. For example, in certain embodiments, the attenuated VSV may include a foreign RNA sequence as a separate transcriptional unit inserted into or replacing a site of the genome nonessential for replication, wherein the foreign RNA sequence (which is in the negative sense) directs the production of a protein capable of being expressed in a host cell infected by VSV. This recombinant genome is originally produced by insertion of foreign DNA encoding the protein into the VSV cDNA. In certain embodiments, any DNA sequence which encodes an immunogenic antigen, which produces prophylactic or therapeutic immunity against a disease or disorder, when expressed as a fusion or non-fusion protein in an attenuated VSV of the invention, alone or in combination with other antigens expressed by the same or a different VSV, is isolated and incorporated in the VSV vector for use in the immunogenic compositions of the present invention.
In certain embodiments, expression of an antigen by an attenuated recombinant VSV induces an immune response against a pathogenic microorganism. For example, an antigen may display the immunogenicity or antigenicity of an antigen found on bacteria, parasites, viruses, or fungi which are causative agents of diseases or disorders. In one embodiment, antigens displaying the antigenicity or immunogenicity of an antigen of a human pathogen or other antigens of interest are used.
In some embodiments, the heterologous antigen encoded by the attenuated VSV is selected from one or more of the following: measles virus, subgroup A and subgroup B respiratory syncytial viruses, human parainfluenza viruses, mumps virus, human papilloma viruses of type 1 or type 2, human immunodeficiency viruses, herpes simplex viruses, cytomegalovirus, rabies virus, human metapneumovirus, Epstein Barr virus, filoviruses, bunyaviruses, flaviviruses, alphaviruses, influenza viruses, hepatitis C virus and C. trachomatis.
To determine immunogenicity or antigenicity by detecting binding to antibody, various immunoassays known in the art are used, including but not limited to, competitive and non-competitive assay systems using techniques such as radioimmunoassays, ELISA (enzyme linked immunosorbent assay), “sandwich” immunoassays, immunoradiometric assays, gel diffusion precipitin reactions, immunodiffusion assays, in situ immunoassays (using colloidal gold, enzyme or radioisotope labels, for example), western blots, immunoprecipitation reactions, agglutination assays (e.g., gel agglutination assays, hemagglutination assays), complement fixation assays, immunofluorescence assays, protein A assays, and immunoelectrophoresis assays, neutralization assays, etc. In one embodiment, antibody binding is measured by detecting a label on the primary antibody. In another embodiment, the primary antibody is detected by measuring binding of a secondary antibody or reagent to the primary antibody. In a further embodiment, the secondary antibody is labeled. Many means are known in the art for detecting binding in an immunoassay. In one embodiment for detecting immunogenicity, T cell-mediated responses are assayed by standard methods, e.g., in vitro or in vivo cytotoxicity assays, tetramer assays, elispot assays or in vivo delayed-type hypersensitivity assays.
Parasites and bacteria expressing epitopes (antigenic determinants) that are expressed by an attenuated VSV (wherein the foreign RNA directs the production of an antigen of the parasite or bacteria or a derivative thereof containing an epitope thereof) include but are not limited to those listed in Table 2.
Plasmodium spp.
Eimeria spp.
nematodes
Schistosoma spp.
Leishmania spp.
Vibrio cholerae
Streptococcus pneumoniae
Streptococcus pyogenes
Streptococcus agalactiae
Neisseria meningitidis
Neisseria gonorrhoeae
Staphylococcus aureus
Staphylococcus epidermidis
Corynebacterium diphtheriae
Clostridium tetani
Bordetella pertussis
Haemophilus spp. (e.g., influenzae)
Chlamydia spp.
Helicobacter pylori
mycobacteria
In another embodiment, the antigen comprises an epitope of an antigen of a nematode, to protect against disorders caused by such worms. In another embodiment, any DNA sequence which encodes a Plasmodium epitope, which when expressed by a recombinant VSV, is immunogenic in a vertebrate host, is isolated for insertion into VSV (−) DNA according to the present invention. The species of Plasmodium which serve as DNA sources include, but are not limited to, the human malaria parasites P. falciparum, P. malariae, P. ovale, P. vivax, and the animal malaria parasites P. berghei, P. yoelii, P. knowlesi, and P. cynomolgi. In yet another embodiment, the antigen comprises a peptide of the β-subunit of Cholera toxin.
Viruses expressing epitopes that are expressed by an attenuated VSV (wherein the foreign RNA directs the production of an antigen of the virus or a derivative thereof comprising an epitope thereof) include, but are not limited to, those listed in Table 3, which lists such viruses by family for purposes of convenience and not limitation.
In specific embodiments, the antigen encoded by the foreign sequences that is expressed upon infection of a host by the attenuated VSV, displays the antigenicity or immunogenicity of an influenza virus hemagglutinin; human respiratory syncytial virus G glycoprotein (G); measles virus hemagglutinin or herpes simplex virus type-2 glycoprotein gD.
Other antigens that are expressed by attenuated VSV include, but are not limited to, those displaying the antigenicity or immunogenicity of the following antigens: Poliovirus I VP1; envelope glycoproteins of HIV I; Hepatitis B surface antigen; Diphtheria toxin; streptococcus 24M epitope, SpeA, SpeB, SpeC or C5a peptidase; and gonococcal pilin.
In other embodiments, the antigen expressed by the attenuated VSV displays the antigenicity or immunogenicity of pseudorabies virus g50 (gpD), pseudorabies virus II (gpB), pseudorabies virus gIII (gpC), pseudorabies virus glycoprotein H, pseudorabies virus glycoprotein E, transmissible gastroenteritis glycoprotein 195, transmissible gastroenteritis matrix protein, swine rotavirus glycoprotein 38, swine parvovirus capsid protein, Serpulina hydodysenteriae protective antigen, Bovine Viral Diarrhea glycoprotein 55, Newcastle Disease Virus hemagglutinin-neuraminidase, swine flu hemagglutinin, or swine flu neuraminidase.
In certain embodiments, an antigen expressed by the attenuated VSV displays the antigenicity or immunogenicity of an antigen derived from a canine or feline pathogen, including, but not limited to, feline leukemia virus, canine distemper virus, canine adenovirus, canine parvovirus and the like.
In certain other embodiments, the antigen expressed by the attenuated VSV displays the antigenicity or immunogenicity of an antigen derived from Serpulina hyodysenteriae, Foot and Mouth Disease Virus, Hog Cholera Virus, swine influenza virus, African Swine Fever Virus, Mycoplasma hyopneumoniae, infectious bovine rhinotracheitis virus (e.g., infectious bovine rhinotracheitis virus glycoprotein E or glycoprotein G), or infectious laryngotracheitis virus (e.g., infectious laryngotracheitis virus glycoprotein G or glycoprotein I).
In another embodiment, the antigen displays the antigenicity or immunogenicity of a glycoprotein of La Crosse Virus, Neonatal Calf Diarrhea Virus, Venezuelan Equine Encephalomyelitis Virus, Punta Toro Virus, Murine Leukemia Virus or Mouse Mammary Tumor Virus.
In other embodiments, the antigen displays the antigenicity or immunogenicity of an antigen of a human pathogen, including but not limited to human herpesvirus, herpes simplex virus-1, herpes simplex virus-2, human cytomegalovirus, Epstein-Barr virus, Varicella-Zoster virus, human herpesvirus-6, human herpesvirus-7, human influenza virus, human immunodeficiency virus (type 1 and/or type 2), rabies virus, measles virus, hepatitis B virus, hepatitis C virus, Plasmodium falciparum, and Bordetella pertussis.
Potentially useful antigens or derivatives thereof for use as antigens expressed by attenuated VSV are identified by various criteria, such as the antigen's involvement in neutralization of a pathogen's infectivity, type or group specificity, recognition by patients' antisera or immune cells, and/or the demonstration of protective effects of antisera or immune cells specific for the antigen.
In another embodiment, foreign RNA of the attenuated VSV directs the production of an antigen comprising an epitope, which when the attenuated VSV is introduced into a desired host, induces an immune response that protects against a condition or disorder caused by an entity containing the epitope. For example, the antigen can be a tumor specific antigen or tumor-associated antigen, for induction of a protective immune response against a tumor (e.g., a malignant tumor). Such tumor-specific or tumor-associated antigens include, but are not limited to, KS 1/4 pan-carcinoma antigen; ovarian carcinoma antigen (CA125); prostatic acid phosphate; prostate specific antigen; melanoma-associated antigen p97; melanoma antigen gp75; high molecular weight melanoma antigen and prostate specific membrane antigen.
The foreign DNA encoding the antigen, that is inserted into a non-essential site of the attenuated VSV DNA, optionally further comprises a foreign DNA sequence encoding a cytokine capable of being expressed and stimulating an immune response in a host infected by the attenuated VSV. For example, such cytokines include but are not limited to interleukins 1α, 1β, 2, 4, 5, 6, 7, 8, 10, 12, 13, 14, 15, 16, 17 and 18, interferon-α, interferon-β, interferon-γ, granulocyte colony stimulating factor, granulocyte macrophage colony stimulating factor and the tumor necrosis factors α, and β.
In certain embodiments, the invention is directed to an immunogenic composition comprising an immunogenically effective amount of attenuated VSV particles produced according to the methods of the present invention in a pharmaceutically acceptable carrier. In some embodiments, at least one foreign RNA sequence is inserted into or replaces a region of the VSV genome non-essential for replication.
The attenuated VSV particles of the invention are formulated for administration to a mammalian subject (e.g., a human). Such compositions typically comprise the VSV vector and a pharmaceutically acceptable carrier. As used hereinafter the language “pharmaceutically acceptable carrier” is intended to include any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like, compatible with pharmaceutical administration. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the VSV vector, such media are used in the immunogenic compositions of the invention. Supplementary active compounds may also be incorporated into the compositions.
Thus, a VSV immunogenic composition of the invention is formulated to be compatible with its intended route of administration. Examples of routes of administration include parenteral (e.g., intravenous, intradermal, subcutaneous, intramuscular, intraperitoneal) and mucosal (e.g., oral, rectal, intranasal, buccal, vaginal, respiratory). Solutions or suspensions used for parenteral, intradermal, or subcutaneous application include the following components: a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediaminetetraacetic acid; buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose. The pH is adjusted with acids or bases, such as hydrochloric acid or sodium hydroxide. The parenteral preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic.
Pharmaceutical compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion. For intravenous administration, suitable carriers include physiological saline, bacteriostatic water, Cremophor EL™ (BASF, Parsippany, N.J.) or phosphate buffered saline (PBS). In all cases, the composition must be sterile and should be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi. The carrier is a solvent or dispersion medium containing, for example, water, ethanol, polyol (e.g., glycerol, propylene glycol, and liquid polyetheylene glycol, and the like), and suitable mixtures thereof. The proper fluidity is maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Prevention of the action of microorganisms is achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, and the like. In many cases, it is preferable to include isotonic agents, for example, sugars, polyalcohols such as mannitol, sorbitol, sodium chloride in the composition. Prolonged absorption of the injectable compositions is brought about by including in the composition an agent which delays absorption, for example, aluminum monostearate and gelatin.
Sterile injectable solutions are prepared by incorporating the VSV vector in the required amount (or dose) in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the active compound into a sterile vehicle which contains a basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and freeze-drying which yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.
For administration by inhalation, the compounds are delivered in the form of an aerosol spray from pressured container or dispenser which contains a suitable propellant (e.g., a gas such as carbon dioxide, or a nebulizer). Systemic administration can also be by mucosal or transdermal means. For mucosal or transdermal administration, penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art, and include, for example, for mucosal administration, detergents, bile salts, and fusidic acid derivatives. Mucosal administration is accomplished through the use of nasal sprays or suppositories. The compounds are also prepared in the form of suppositories (e.g., with conventional suppository bases such as cocoa butter and other glycerides) or retention enemas for rectal delivery.
In certain embodiments, it is advantageous to formulate oral or parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used hereinafter refers to physically discrete units suited as unitary dosages for the subject to be treated; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. The specification for the dosage unit forms of the invention are dictated by and directly dependent on the unique characteristics of the active compound and the particular therapeutic effect to be achieved, and the limitations inherent in the art of compounding such an active compound for the treatment of individuals.
All patents and publications cited herein are hereby incorporated by reference.
A plasmid vector encoding T7 RNAP (pCMV-T7) was prepared by cloning the polymerase open reading frame (ORF) into pCl-neo (Promega) 3′ of the hCMV immediate-early promoter/enhancer region. Before insertion of the T7 RNAP ORF, pCl-neo was modified to remove the T7 promoter located 5′ of the multiple cloning site, generating vector pCl-neo-Bcl. The T7 RNAP gene was inserted into pCl-Neo-BCl using EcoR I and Xba I restriction sites incorporated into PCR primers used to amplify the T7 RNAP coding sequence. A Kozak (Kozak, J Cell Biol 108, 229-241, 1989) consensus sequence was included 5′ of the initiator ATG to provide an optimal sequence context for translation.
Plasmids encoding VSV N, P, L, M and G polypeptides were prepared by inserting the appropriate ORFs 3′ of the T7 bacteriophage promoter and encephalomyocarditis virus internal ribosome entry site (IRES) (Jang et al., J Virol 62, 2636-2643, 1988; Pelletier and Sonenberg, Nature 334, 320-325, 1988) in plasmid vector pT7 as described by Parks, et al. (Parks, et al. Virus Res 83, 131-147, 2002). The inserted coding sequences are flanked at the 3′ end by a plasmid-encoded poly-A sequence and a T7 RNAP terminator. Plasmids encoding VSV N, P, L, M, and glycoprotein (G) were derived from the Indiana serotype genomic cDNA clone (Lawson, et al., Proc Natl Acad Sci USA 92, 4477-4481, 1995) or the New Jersey serotype clone (Rose, et al. J Virol 74, 10903-10910, 2000).
Expression plasmids encoding VSV native G or VSV optimized G coding sequences controlled by the hCMV promoter/enhancer (pCMV-G or pCMV-Opt1; pCMV-RNAopt, respectively) are described below in Example 2. These plasmids were used to provide the glycoprotein in trans while propagating VSVΔG or VSV-Gstem vectors. The G protein coding sequences were cloned into the modified pCl-neo vector described above in the present example. The G coding sequence was inserted into the modified pCl-neo vector using Xho I (5′) and Xba I (3′) restriction sites incorporated into PCR primers used to amplify the G coding sequence.
Recombinant VSV genomic clones were prepared using standard cloning procedures (Ausubel, et al., Current Protocols in Molecular Biology. Greene Publishing Associates and Wiley Interscience, New York, 1987) and the Indiana serotype pVSV-XN2 genomic cDNA clone as starting material (Lawson, et al., Proc Natl Acad Sci USA 92, 4477-4481, 1995). Genomic clones lacking the G gene (ΔG) were similar to those described by Roberts, et al. (Roberts, et al. J Virol 73, 3723-3732, 1999). A second type of G gene modification was constructed using the approach of Robison and Whitt (Robison and Whitt, J Virol 74, 2239-2246, 2000) in which the G coding sequence was replaced with a modified version that encodes only 18 amino-terminal (N-terminal) residues of the signal sequence fused to the C-terminal 91 amino acids of which approximately 42 residues forms a truncated extracellular domain (Gstem). In some recombinant VSV constructs, the G protein gene was replaced with the equivalent gene from the New Jersey Serotype (Rose, et al. J Virol 74, 10903-10910, 2000).
Studies were conducted to identify conditions that supported maximal G protein expression from plasmid DNA. Empirical research performed earlier identified electroporation as a method that promoted reproducible and efficient introduction of plasmid DNA into Vero cells (Parks, et al., 2006, Method for the recovery of non-segmented, negative-stranded RNA viruses from cDNA, published United States patent application 20060153870; Witko, et al. J Virol Methods 135:91-101) and subsequent method refinement relied on this finding, because electroporation is a scalable technology (Fratantoni, et al. Cytotherapy 5:208-10, 2003), and because Vero cells are a well characterized cell substrate that has been used for production of a live rotavirus vaccine (Merck, RotaTeq (Rotavirus Vaccine, Live, Oral, Pentavalent) FDA. Online, 2006 posting date; Sheets, R. (History and characterization of the Vero cell line) FDA. Online, 2000 posting date).
To improve on this finding, two methods of coding sequence optimization were analyzed to determine if they might improve transient expression of VSV G (Indiana serotype; Gin). One method, described as RNA optimization (RNAopt), uses synonymous nucleotide substitutions to increase GC content and disrupt sequence motifs that inhibit nuclear export, decrease translation, or destabilize mRNAs (Schneider, et al. J Virol 71:4892-903, 1997; Schwartz, et al. J Virol 66:7176-82, 1992; Schwartz, et al. J Virol 66:150-9). The second method of optimization is a codon optimization method detailed in Table 1 (Opt-1). The modified coding sequences, as well as the native Gin open reading frame, were then cloned 3′ of the human cytomegalovirus (hCMV) promoter and enhancer from immediate early region 1 (Boshart, et al. Cell 41: 521-30, 1985; Meier and Stinski, Intervirology 39: 331-42, 1996) to produce three vectors (Top
After finding that electroporation of plasmids containing optimized genes produced high levels of G protein expression in Vero cells, studies were conducted to determine whether the increased abundance of G enhanced vector packaging. Important as well in this experiment, a comparison of packaging yields was conducted with ΔG and Gstem vectors (
To lessen the effects of anti-vector immunity directed against G protein, live replicating VSV vectors can be produced that encode G proteins derived from different serotypes (Rose, et al. J Virol 74:10903-10, 2000). Similarly, ΔG and Gstem vectors can be packaged with G proteins from different serotypes. To determine if the transient expression packaging method would work readily with a glycoprotein derived from a different strain, plasmid vectors encoding VSV G protein from the New Jersey serotype (Gnj) were constructed with either the native coding sequence or a sequence that was subjected to RNA optimization. The Gnj plasmid vectors were tested first by evaluating transient protein expression after electroporation.
The present example describes the preparation of a stable cell line that was used to supply genetic complementation for development of propagation-defective viral vectors. Although an attractive approach by which to produce propagation-defective vectors, stable complementing cell lines can be difficult to produce and maintain, particularly when the complementing gene product is toxic like VSV G. Previous attempts to produce Vero cells expressing G under control of tetracycline-responsive systems (Corbel and Rossi Curr Opin Biotechnol 13: 448-52, 2002) failed, prompting the present investigation of additional approaches (data not shown).
The stable cell line developed by Applicants employs the heat shock response as an attractive alternative to chemical inducers. Promoters controlling expression of heat shock proteins (HSPs) have been used before to control expression of a foreign gene (Rome et al. Methods 35: 188-98, 2005), and it is known that Vero cells readily withstand relatively severe heat shock treatments that might be required for maximal induction (Witko, et al. J Virol Methods 135:91-101, 2006). Moreover, induction by heat shock alleviates the need to use chemical inducers that are frequently necessary when using other controllable expression systems. Although it was appealing to make use of heat shock response, it is known that promoters controlling expression of the HSPs do exhibit significant basal activity (Rome, et al. Methods 35: 188-98, 2005) that might be sufficient to cause toxicity when controlling expression of VSV G protein. Therefore, a modified strategy was investigated by Applicants to minimize basal promoter activity.
A heat shock-inducible transcriptional control region was constructed by starting with a minimal promoter that was expected to exhibit very low levels of basal activity. The minimal promoter (
Cell lines were established by introducing linearized plasmid DNA into Vero cells by electroporation and applying G418 selection 24 hours later. Drug resistant cell colonies were isolated and tested for G expression by Western blotting (data not shown), and the cell line herein designated VeroHS4-Gin was selected for further evaluation.
Inducible expression of Gin protein by VeroHS4-Gin is illustrated in
The present example demonstrates that Gstem vector was capable of being successfully propagated in VeroHS4-Gin cells with yields of 1×107 IUs in two experiments. These results indicate that cell lines like VeroHS4-Gin are effective substrates for manufacture of VSV vectors.
It is noteworthy as well that the VeroHS4-Gin cell line has proven to be stable, and inducible expression of G protein has been maintained for more than 20 cell passages. The hybrid HSE/minimal CMV promoter likely was a key element of cell line stability because it exhibited a low level of basal activity that minimized G protein expression and toxicity. Although the basal activity was low, induced expression levels were substantial and supported vigorous propagation of VSV-Gstem-gag1. The high levels of inducible expression probably were due to a combination of factors the most influential of which were 1) potent transcriptional activation directed by 9 HSEs, and 2) the optimized G protein coding sequence that contributed to efficient protein synthesis.
For each electroporation, the following plasmid DNAs were combined in a microfuge tube: 25-50 μg plasmid expressing T7 (pCl-Neo-Bcl-T7) “hCMV-T7 expression plasmid”, 10 μg VSV Full Length plasmid, 8 μg N plasmid, 4 μg P plasmid, 1 μg L plasmid; 1 μg M plasmid and 1 μg G plasmid. While working in a biosafety hood, the DNA volume was adjusted to 250 μl with sterile, nuclease-free water. Next, 50 μl of 3M Sodium Acetate (pH 5) was added, and the tube contents were mixed. Subsequently, 750 μl of 100% Ethanol was added and the tube contents were mixed. This was followed by incubation of the tube at −20° C. for 1 hour to overnight. Thereafter, the DNA was pelleted in a microfuge at 14,000 rpm, 4° C. for 20 minutes. While working in a biosafety hood, the supernatant was discarded without disturbing the DNA pellet. Residual ethanol was removed from the tube, and the DNA pellet was then allowed to air dry in a biosafety hood for 5-10 minutes. The dried DNA pellet was resuspended with 50 μl of sterile, nuclease-free water.
The following solutions were employed during cell culture and virus rescue: Trypsin/EDTA, Hank's buffered saline, 1 mg per ml soybean trypsin inhibitor prepared in PBS, and the media shown below in Table 4.
Vero cells were maintained in Complete DMEM composed of Dulbecco's Modified Eagle's minimum essential medium (DMEM; Invitrogen or Cellgro) supplemented with 10% heat-inactivated fetal bovine serum (Cellgro), 1% sodium pyruvate (Invitrogen), 1% Nonessential amino acids, 220 μM 2-mercaptoethanol, 50 μg/ml gentamicin (Invitrogen) and 1 mg/ml geneticin. This corresponded to Medium 4. Cells were subcultured the day prior to conducting electroporation and incubated at 37° C. in 5% CO2.
Virus rescue was initiated after introduction of plasmid DNA into Vero cells by electroporation. Optimal conditions for electroporation were determined empirically beginning from conditions recommended for Vero cells by David Pasco in online Protocol 0368 available at www.btxonline.com (BTX Molecular Delivery Systems).
For a single electroporation, Vero cells from a near-confluent monolayer (T150 flask) were washed 1× with approximately 5 ml of Hank's Buffered Saline Solution. Then, the cells were detached from the flask in 4 ml of trypsin-EDTA (0.05% porcine trypsin, 0.02% EDTA; Invitrogen). In particular, after addition of the trypsin/EDTA solution to the monolayer, the flask was rocked to evenly distribute the solution, followed by incubation at room temperature for 3-5 minutes. The trypsin/EDTA solution was then aspirated, and the sides of the flask were tapped to dislodge cells. Medium 1 (10 ml) was then used to collect cells from the flask and the cells were transferred to a 50 ml conical tube. Subsequently, 1 ml of trypsin inhibitor (1 mg/ml) was added to the tube containing the cells and the contents were mixed gently. The cells were collected from the suspension by centrifugation at 300×g for 5 minutes at room temperature after which the supernatant was aspirated and the pellet was resuspended in 10 ml of Medium 2. Next, 1 ml of trypsin inhibitor (1 mg/ml) was added to the cell suspension and the suspension was gently mixed. Subsequently, the cells were collected from the suspension by centrifugation at 300×g for 5 minutes at room temperature. The supernatant was aspirated and the cell pellet was resuspended in a final volume of 0.70 ml of Medium 2.
A 50 μl DNA solution prepared as described above in nuclease-free water, which contained 25-50 μg plasmid expressing T7 (pCl-Neo-Bcl-T7) “hCMV-T7 expression plasmid”, 10 μg VSV Full Length plasmid, 8 μg N plasmid, 4 μg P plasmid, and 1 μg each of L, M and G plasmids, was combined with the 0.7 ml of cell suspension. The cells and DNA were gently mixed and the mixture was transferred to an electroporation cuvette (4 mm gap; VWR or BTX). A BTX Square-Wave Electoporator (BTX ECM 820 or 830; BTX Molecular Delivery Systems) was used to pulse the cells (four times, 140-145 V, 70 ms) after which they were incubated at room temperature for approximately 5 min before 1 ml of Medium 1 was added and the cuvette contents were transferred to a sterile 15 ml centrifuge tube containing 10 ml of Medium 1 followed by gentle mixing. Electroporated cells were then collected by centrifugation at 300×g for 5 min at room temperature and resuspended in 10 ml of Medium 1 before transfer to a T150 flask containing 25 ml of Medium 1. The cells in the flask were heat shocked at 43° C. (3-5% CO2) for 6 hours. Thereafter, the flask was incubated overnight at 37° C., 5% CO2. The following day, the medium was replaced with 15-30 ml of Medium 4. Incubation was continued at 37° C., 5% CO2 with periodic medium changes until cytopathic effect (CPE) was evident. VSV replication was typically evident as early as 3-4 days, but in some instances could take as long as 6 days. Also, in some instances, a coculture step was required before CPE was evident.
Coculture was initiated approximately 48-72 h after electroporation by aspirating all but 10 ml of medium from the flask after which the cells were detached by scraping. The detached cells were pipeted multiple times to minimize the sized of the cell aggregates and transferred to a flask containing an established 50%-confluent monolayer of Vero cells that express an optimized G protein.
For example, a suitable coculture method employed for rescue of propagation-defective rVSV lacking a functional G protein (ΔG and Gstem viruses) employed a coculture monolayer of HS-optG cells described above. The Hs-optG cells are maintained in Medium 4. The coculture monolayer was prepared from a confluent or near-confluent (e.g., about 80% confluent) T150 flask. It is noted that, in order to prepare a large viral stock, multiple flasks (e.g., 20 or more T150 flasks) may each be employed as a coculture monolayer. Prior to heat shock treatment, the medium was removed from each flask and replaced with 20 ml of Medium 1. The cells in the flask were then heat shocked at 43° C. (3-5% CO2) for 6 hours to allow for expression of VSV G protein from the optimized VSV G gene. These cells are referred to herein as “plaque expansion cells”, and may be used as a monolayer to establish coculture with the virus rescue cells described in the preceding paragraph.
The monolayer of plaque expansion cells are infected with virus (e.g., Gstem) at a multiplicity of infection (MOI) between 0.1 and 0.01 during the coculturing step. The coculture was incubated at 32-37° C., 5% CO2 until CPE was evident, which generally took about 24 to 48 hours. The virus was thereafter purified by centrifugation through a sucrose cushion using methods well known in the art.
The rescue procedure employed in the present example was the same as described in Example 4 except that the VSV full length plasmid employed in the electroporation contains RSV-F gene either in position one (Fa1) or position three (Fa3) of the genome, as shown in
Cell culture and rescue conditions were performed as explained in Example 4. Stable cell lines expressing optimized VSV G protein were infected with the recombinant viruses at MOI 0.01 and a final harvest was done at 48 hours post infection. Data on virus titers obtained from two separate experiments is shown in Table 5 below. The constructs employed for rescue were derived from the Indiana serotype of VSV, but the same procedure is applicable to the New Jersey serotype of VSV, as well. In addition, the procedure is applicable to other serotypes of VSV as well depending upon the construction of complementing cell line for that particular serotype.
Respiratory syncytial virus (RSV) is a significant cause of serious lower respiratory tract (LRT) disease, particularly in infant and elderly populations; there is currently no vaccine available against RSV. Candidate RSV vaccines were generated using a recombinant vesicular stomatitis virus (rVSV) replicon in which the attachment and fusion domains of the VSV glycoprotein (G) were deleted (rVSV-Gstem), rendering the virus propagation-defective except on cells in which complementing VSV G was provided in trans. The purpose of the study was to compare the immune responses of Gstem-F1 vs. F3 vectors rescued according to the method of Example 5; and to determine the efficacy of Gstem-F vectors following RSV challenge. In the case of Gstem-F1, the RSV F gene was inserted at position 1 in the replicon genome relative to the VSV genomic promoter, whereas for Gstem-F3, the RSV F gene was inserted at position 3.
Six animal groups were employed in these studies, as shown in Table 6 below. Groups 2-6 received intramuscular injection at week 0; Groups 3-6 received a boost at week 4; and all groups (Groups 1-6) were challenged with RSV at 1.5×106 pfu RSV (A2 strain) at week 8. Animals were evaluated at day 4 post-challenge. In addition, a prime-boost regimen was compared in which the boosting replicon was complemented with either a homologous VSV G or a heterologous G, derived from a different serotype of VSV, as compared to the priming replicon.
Mice immunized intramuscularly with rVSV-Gstem replicons encoding the RSV (A2 strain) F protein generated anti-F antibodies, as measured by ELISA. These results are shown below.
Table 7 below shows total IgG values (Log10 titer) for the replicons at week 4 and week 8 following intramuscular injection, where the limit of detection was a titer of 2.0 log10.
Moreover, mice immunized intramuscularly with rVSV-Gstem replicons encoding the RSV (A2 strain) F protein had balanced TH1-TH2 responses, as shown in Table 8 below where IgG2a/IgG1 log10 anti-F titer ratios are indicated for the replicons at weeks 4 and 8. The limit of detection was a titer of 2.0 log10.
Anti-F ELISA log10 titer results for serum IgA are provided in Table 9 below for week 8. The limit of detection was 1.0 log10 titer.
Mice immunized intramuscularly with rVSV-Gstem replicons encoding the RSV (A2 strain) F protein also generated anti-RSV neutralizing titers, as measured by ELISA. These results are shown below in Table 10, where anti-RSV neutralizing titers (Log10 titer) are indicated for the replicons at weeks 4 and 8 following intramuscular injection. The data in Table 10 are presented as (−) GPC Complement or (+) GPC Complement. The neutralizing titer was the dilution of antibody that caused 60% RSV plaque reduction. The limit of detection was a titer of 1.3 log10.
Moreover, mice immunized intramuscularly with rVSV-Gstem replicons encoding the RSV (A2 strain) F protein also generated F-specific interferon-gamma (IFN-γ) producing cells. F-specific IFN-γ producing lymphocytes were observed in mice primed and boosted with the rVSV-Gstem-RSV-F replicon, but not in mice primed with RSV A2 (data not shown).
Furthermore, mice immunized intramuscularly with rVSV-Gstem replicons encoding the RSV (A2 strain) F protein were completely protected from both upper and lower respiratory tract infections following intranasal challenge with RSV A2. As shown in
The results described above indicate that the rVSV-Gstem-RSVFa vectors rescued according to the methods of the present invention were immunogenic. Furthermore, equivalent immune responses were generated when the RSV F gene was inserted at either the first or third gene position in the replicon genome relative to the VSV genomic promoter. Moreover, with respect to the prime-boost regimen, while immune responses were slightly higher following the heterologous boost, mice boosted with a homologous glycoprotein were equally protected from LRT infection following RSV A2 challenge, indicating the feasibility of a homologous replicon for multiple doses. It was also observed that a single dose of the Gstem-RSV-F replicon protected mice from RSV A2 challenge (data not shown). Finally, the safety of the Gstem-RSV-F replicon was assessed by evaluating its ability to propagate in culture in the absence of added VSV G. The data showed that Gstem-RSV-F vectors (Fa1 and Fa3) were not capable of propagating in the absence of added VSV G protein (data not shown).
Any articles or references referred to in the specification, including patents and patent applications, are incorporated herein in their entirety for all purposes.
This application claims the benefit of U.S. provisional application No. 61/015,353, filed Dec. 20, 2007, the entire contents of which are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 61015353 | Dec 2007 | US |
