WO2000073480A1

WO2000073480A1 - Compositions and methods for production of recombinant virus using a carrier vector derived from a nonmammalian virus

Info

Publication number: WO2000073480A1
Application number: PCT/US2000/014481
Authority: WO
Inventors: Siyamak Rasty; Matthew A. Gonda; Haifeng Chen
Original assignee: Genovo, Incorporated
Priority date: 1999-05-27
Filing date: 2000-05-25
Publication date: 2000-12-07
Also published as: AU783672B2; AU5164700A; EP1180158A1; JP2003501042A; CA2375119A1

Abstract

This invention relates to nonmammalian carrier vectors and viruses useful in the production of high titers of recombinant viruses which may contain foreign DNA inserts or which may be point-mutated or deleted viruses, and methods of producing those viruses. The nonmammalian carrier vector ('carrier vector') is a chimeric vector which includes those portions of a nonmammalian virus backbone which allow replication in a nonmammalian host cell. The carrier vector includes various nucleic acid cassettes, which may include an embedded recombinant viral genome containing a desired transgene, components necessary for production of a replication-defective recombinant virus containing the transgene, and domains that permit the carrier vector to bind to mammalian cells. The invention also provides methods of producing high concentrations of recombinant virus as a substantially homogeneous preparation, compositions to produce the recombinant virus, and recombinant viruses.

Description

WO 00/73480 PCT/USOO/l4481

COMPOSITIONS AND METHODS FOR PRODUCTION OF RECOMBINANT VIRUS USING A CARRIER VECTOR DERIVED FROM A NONMAMMALIAN VIRUS

TECHNICAL FIELD OF THE INVENTION

This invention relates to novel nonmammalian carrier vectors and 5 viruses useful in the production of high titers of recombinant viruses which may

contain foreign DNA inserts or which may be point-mutated or deleted viruses, and

methods of producing those viruses. The nonmammalian carrier vector ("carrier

vector") is a chimeric vector which includes those portions of a nonmammalian

virus backbone which allow replication in a nonmammalian host cell. The carrier

0 vector includes various nucleic acid cassettes, which may include an embedded

recombinant viral genome containing a desired transgene, components necessary for

production of a replication-defective recombinant virus containing the transgene,

and domains that permit the carrier vector to bind to mammalian cells. The invention also provides methods of producing high concentrations of recombinant

5 virus as a substantially homogeneous preparation, compositions to produce the

recombinant virus, and novel recombinant viruses. BACKGROUND OF THE INVENTION

A recombinant virus carrying a foreign DNA insert may be used to

deliver genes to cells, where the gene may be expressed, if desired, to permit

production of recombinant proteins in vitro or in vivo, vaccination of human and

non-human mammals, or treatment or amelioration of diseases or genetic defects in

humans or non-human mammals. One may treat or ameliorate diseases or genetic

defects by providing normal gene products, increased levels of gene products or by blocking endogenous production of a gene, whose expression would be deleterious

to the cell or organism.

Methods for delivering an exogenous gene to a mammalian cell

include the use of mammalian viral vectors, such as those which are derived from

retroviruses, adenoviruses, herpes viruses, vaccinia viruses, polio viruses, adeno-

associated viruses, hybrid viruses (e.g., hybrid adenovirus-AAV, see U.S. Pat. No.

5,856, 152) and the like. Other methods include direct injection of DNA, biolistic

administration of DNA, electroporation, calcium phosphate precipitation, as well as

methods of administration which utilize ligand-DNA conjugates, liposome

conjugates of DNA, polycation-DNA complexes or adenovirus-ligand-DNA

conjugates.

A transgene is a nucleic acid encoding a protein of interest; it may be a gene to allow for genetic or drug selection, e.g., a gene conferring resistance to

antibiotics, or a reporter gene allowing detection, e.g., by color in the case of the use of green fluorescent protein. Alternatively, the transgene may be one that is

useful for corrective applications. For instance, a transgene may be a normal gene that replaces or augments the function of a patient's defective gene The transgene

may be one that counteracts the effects of a disease, such as introduction and

expression of a gene that is distinct from the one that it replaces or augments, but

which has the same function or compensates for the defective gene's function. The

transgene may be a gene which blocks or represses the expression of a

malfunctioning, mutated, or viral gene in the patient, thereby giving rise to a corrective effect A transgene may also be used for immunization against various

agents, by provoking an immunogenic response in an animal. Delivery of

therapeutic transgenes to a patient thus effects a correction of a defect or

prevention of disease. The transgene also may be one which is useful for production of proteins in vitro, such as for large-scale production of therapeutic

proteins

Appropriate genes for expression in the cell include, without

limitation, those genes which are normally expressed in cells but whose products are

produced in insufficient amounts. Alternatively, the appropriate gene for expression

is one which expresses a normal gene product which replaces a defective gene

product, encodes ribozymes or antisense molecules which repair or destroy mutant

cellular RNAs expressed from mutated genes, or modifies or destroys viral RNAs

Transgenes used for production of proteins in vitro include proteins such as secreted factors, including hormones, growth factors and enzymes.

Many gene therapy methods involve supplying an exogenous gene to

overcome a deficiency in the expression of a gene in a patient. Some of these

deficiencies are congenital and are due to a mutation in a particular gene in all the cells of the patient For instance, in cystic fibrosis, there are one or more mutations

in the gene encoding the cystic fibrosis transmembrane conductance regulator

(CFTR) which prevents the CFTR protein from functioning properly In other

cases, a deficiency in gene expression is due to an accident or disease that occurs

during the patient's life For instance, in Type I diabetes mellitus, the β pancreatic

islet cells, which produce insulin, are destroyed, such that patients with this disease

can no longer synthesize insulin In other cases, the endogenous gene may be

structurally normal but is not produced in high enough quantities due to disease, medical treatment or other environmental conditions, or mutations in the regulatory

elements of the endogenous gene. For example, there are a number of blood

disorders, such as anemia, in which there is insufficient production of red blood

cells, which may be treated with erythropoietin (EPO) or with a transgene encoding

EPO Transgenes may also be used for genetic immunization, i.e., to elicit an

immune response to a pathogen in an animal, including humans. For instance, a

transgene may include a sequence from a viral, bacterial or fungal pathogen, such as

influenza virus, human immunodeficiency virus (HIV), or mycobacterium

tuberculosis.

Certain methods are amenable to targeted delivery of the exogenous gene to specific tissues, such as liver tissue. One method of delivering genes to specific cells relies upon the function of a cell-specific receptor. The

asialoglycoprotein receptor (ASGP-R), which is present on the surface of

hepatocytes (Spiess et al., 1990, Biochem. 29: 10009-10018), is a lectin which has

affinity for the terminal galactose residues of glycoproteins, and has been used to target gene delivery to liver hepatocytes. For example, a DNA complex is bound to

a ASGP-R on the cell surface, allowing subsequent endoyctosis by the liver

hepatocyte

Viruses that are commonly used in gene delivery applications are

modified by replacing viral nucleic acid with a desired transgene Frequently, DNA

removed from the virus encodes proteins necessary for viral replication or

encapsidation, in which case the recombinant virus containing a transgene is

replication-deficient and will not replicate or encapsidate in the host To permit

replication and encapsidation, current methods recognize that those portions of

D A which have been deleted must be supplied by wild-type or modified viruses or

by plasmids containing DNA encoding the required gene products Supplying wild-

type or modified virus may result in recombinant virus stocks contaminated with wild-type or modified virus Supplying plasmids encoding the required gene

products through cotransfection results in low efficiency of recombinant virus

production, as well as recombination events which yield wild-type virus

contaminants.

A number of different viruses have been used to deliver a transgene

to mammalian cells These viruses include retrovirus, hepatitis B virus (HBV),

adenovirus, adeno-associated virus (AAV) and herpesvirus. AAV possesses unique

features that make it attractive as a vector for delivering foreign DNA (i.e , a transgene) to cells, and various groups have studied the potential use of AAV in the treatment of disease states. AAV is a parvovirus, the genome of which is about 4.7 kb in length,

including 145 nucleotide inverted terminal repeats (ITRs). The AAV genome

encodes two genes, rep and cap, each of which expresses a family of related

proteins from separate open reading frames and produced as a result of alternative

mRNA splicing. Rep polypeptides (repl , rep68, rep52, and rep40) are involved in

replication, rescue and integration of the AAV genome. Cap proteins (VP1, VP2,

and VP3) form the virion capsid. Flanking the rep and cap open reading frames at

the 5' and 3' ends of the AAV genome are the 145 bp ITRs, the first 125 bp of

which are capable of forming Y- or T- shaped duplex structures. The entire nucleic

acid encoding rep and cap can be excised and replaced with a transgene [B. J.

Carter, in "Handbook of Parvoviruses", ed. , P. Tijsser, CRC Press, pp.155-168

( 1990)] . The ITRs represent the minimal sequence required for replication, rescue,

packaging, and integration of the AAV genome.

When this nonpathogenic human virus infects a human cell, the viral

genome integrates into chromosome 19 resulting in latent infection of the cell.

Production of infectious virus and replication of the virus does not occur unless the

cell is coinfected with a lytic helper virus, such as adenovirus (Ad) or herpesvirus.

Upon infection with a helper virus, the AAV provirus is rescued and amplified, and

both AAV and helper virus are produced. The infecting parental ssDNA is

converted to duplex replicating form (RF) DNAs in a rep dependent manner. The

rescued AAV genomes are packaged into preformed protein capsids (icosahedral symmetry approximately 20 nm in diameter) and released as infectious virions that

have packaged either + or - ss DNA genomes following cell lysis. However, progress towards establishing AAV as a transducing vector for the delivery of DNA

in the form of a desired transgene has been slow for a variety of reasons.

Replacing the rep and cap sequences with a desired transgene yields

a recombinant virus capable of delivering the transgene to target host cells.

However, because AAV requires a particular genome packaging size, addition of a

transgene results in deletion of necessary gene functions for rep and cap. In current

methods, necessary gene functions replaced by the transgene are supplied by viruses

or additional plasmids. Furthermore, the requirement by AAV for helper virus

functions also requires the use of helper viruses (either wildtype or crippled viruses)

or plasmids containing the helper virus functions.

One method that has been used to produce recombinant AAV

(rAAV) vectors comprises co-transfecting eukaryotic cells with a plasmid

containing rAAV (the cis plasmid) and a plasmid containing rep and cap (the trans

plasmid), and infecting the cells with a helper virus (e.g., adenovirus or herpes

virus). See U.S. Pat. No. 5,753,500. The disadvantage of this method is that the rAAV vector stock is contaminated with helper virus, which is labor-intensive and

difficult to separate from the helper virus, and co-transfection of two plasmids along

with infection by a helper virus is inefficient and cannot be easily scaled up for industrial production of rAAV.

A second method that has been used to produced rAAV involves a triple plasmid transfection of eukaryotic cells. In this method, one plasmid carries

the transgene and ITRs (the cis plasmid), a second plasmid encodes the rep and cap

genes (the trans plasmid), and the third plasmid encodes the helper virus functions, i e adenoviral genes such as El a, El b, E2a and E4 (the helper plasmid) The

disadvantage of this method is that a triple transfection is also inefficient and is

difficult to scale up

A third method involves the use of a packaging cell line such as one

including AAV functions rep and cap. See U S Pat No 5,658,785 and U S Serial

No PCT US98/19463 The packaging cell line may be transfected with a cis

plasmid comprising the transgene and ITRs, and infected by wild-type adenovirus (Ad) helper See U S Pat No 5,658,785 Alternatively, the packaging cell line

may be co-infected by a hybrid Ad/ AAV, in which a hybrid Ad vector caries the cis

plasmid in the El locus (see U S Pat. No. 5,856,152), and by a wild-type or mutant

Ad that supplies El The disadvantage of this method is that wild-type Ad may be

produced, which must be separated from the rAAV vector before use in a patient

Thus, current methods of producing recombinant AAV are incapable of yielding the high amounts of essentially homogeneous virus for pharmaceutical

compositions needed for the treatment of a large number of patients in a easily

scaled industrial production.

Nonmammalian viruses have been used to transiently express particular individual exogenous proteins in either mammalian or non-mammalian

cells For example, viruses of the family Baculoviridae, or "baculoviruses", which

normally infect members of the order Lepidoptera, have been used to express

exogenous genes in insect cells Baculoviruses have also been reported to enter mammalian cells, and baculoviral DNA has been detected in nuclear extracts of

mammalian cells (Volkman et al, 1983, Appl. Environ. Microbiol. 45' 1085-1093) While one report of baculovirus-mediated gene expression in mammalian cells has

appeared, the authors later attributed the apparent reporter gene activity to the

reporter gene product being carried into the cell after a prolonged incubation of the

cell with the virus (Carbonell et al , 1987, Appl Environ Microbiol 53 1412-

1417) These authors reported that, when the exogenous gene gains access to the

cell as part of the baculovirus genome, the exogenous gene is not expressed de

nova Subsequent studies have demonstrated baculovirus-mediated gene expression

of particular proteins in mammalian cells (Boyce et al , 1996, Proc Natl Acad Sci

USA, 93 2348-2352)

While baculovirus has been used for expressing particular proteins in

a mammalian cell, see U S Pat No 5,731,182, baculovirus has not been used to

produce pharmaceutical compositions of replication-deficient recombinant virus

using an easily scaled industrial process As disclosed in U S Pat No 5,731,182,

the genome of the baculovirus may be modified by insertion of ligand DNA, which

comprises a gene encoding a mammalian receptor specific protein that allows the

baculovirus to bind and enter mammalian cells The nonmammalian virus infecting

the mammalian cells allows only for transient expression of the transgene within the

mammalian cell In addition, the methods disclosed in U S Pat No 5,731,182 do

not result in production of an altogether distinct, essentially homogeneous recombinant virus, at high titers

The problem of generating recombinant replication-deficient virus

that is produced in the absence of helper viruses and by an efficient method that is

applicable to large-scale industrial production has not been solved until the present invention. Current viral production methods include costly and time consuming purification and concentration steps, and are incapable of producing sufficient

recombinant virus for pharmaceutic applications. In the case of AAV, for example,

current methods produce at most on the order of 10⁴-10⁵ genomic copies (gc) of

recombinant virus per producer cell. Similarly, current methods are suitable for

producing recombinant adenovirus in amounts on the order of IO⁴ particles per

producer cell, and retroviruses in amounts on the order of 10²-10⁴ colony forming

units (cfu) per producer cell. Current production methods result in contaminating

helper virus which must be inactivated and/or removed from the final products prior to pharmaceutical application. Thus, there exists an unfulfilled need for a method of manufacturing recombinant mammalian virus at high titers free of other

contaminating virus in order to produce recombinant viruses capable of delivering a

desired transgene to mammalian cells, or immunizing cells against viral or bacterial

infection by the use of such recombinant viruses, in a stable fashion.

SUMMARY OF THE INVENTION

The invention exploits the properties of nonmammalian and

mammalian viruses to create novel chimeric vectors and viruses for the manufacture of an essentially homogeneous recombinant virus preparation in the absence of

contaminating helper virus using a process that may be easily scaled for industrial production. The essentially homogeneous recombinant virus may be used for

various purposes, including delivering a desired transgene to mammalian cells for

pharmaceutic applications including immunization and correction of genetic defects; transient and stable gene transfer in vivo, in vitro and ex vivo; production of

proteins in vivo or in vitro, and other methods in which high levels of gene

transduction into a cell are required, e.g , in the production of expression libraries

for screening compounds or for introducing genes into cells that are not easily

transfected

The carrier vector of the invention is a chimeric vector backbone

derived from the nucleic acid of a nonmammalian virus, and includes one or more of

the following elements 1) an embedded recombinant viral genome, 2) nucleic acid sequences which encode proteins required for replication and encapsidation of the recombinant virus genome, 3) nucleic acid sequences encoding helper functions (if

the recombinant virus to be produced is helper-dependent, e.g., AAV), 4) nucleic

acid sequences encoding a ligand that can interact with a mammalian cell, and 5)

regulatory control sequences that regulate nucleic acid sequences in the

nonmammalian virus backbone or in a replication-deficient portion or modification

thereof. The carrier vector may also include any other nucleic acid sequences that

are required to produce a replication-deficient recombinant virus.

In one embodiment of the invention, one or more carrier vectors may

comprise all of the elements required to produce a replication-deficient recombinant vector in a particular host cell or cell line. The number and type of elements that

are required will depend upon the particular host cell used and the type of

recombinant vector produced. For instance, if a recombinant AAV vector is desired and the host cell line is one which has rep and cap stably integrated in its genome,

the carrier vector or vectors would comprise 1) an embedded recombinant viral genome comprising the AAV ITRs and the transgene and 2) separate helper functions, which may include any nucleic acid sequence required for replication and

encapsidation of the rAAV For instance, these helper functions may include any

one or a combination of El, E2a, E4ORF6 and VAI from adenovirus (Ad) If a

recombinant AAV vector is to be produced in a host cell line that does not express

/ ep and cap, then the carrier vector or vectors may also include the DNA sequences

encoding / ep and cap

Alternatively, if a recombinant retrovirus is desired, the carrier

vector or vectors would comprise 1) an embedded recombinant viral genome

comprising the retroviral LTRs and the transgene of interest driven from the

retroviral LTRs or from a heterologous promoter, and 2) DNA sequences encoding anv one or a combination oϊ gag, pol and env for the functions of replication and

encapsidation of the retrovirus not supplied in the host cell In a preferred

embodiment, all of the required elements to produce a recombinant virus in a

particular host cell are contained on a single carrier vector because the use of a

single carrier vector having all functions not supplied by a host cell increases the efficiency of transduction, and can be more easily scaled for industrial production of the embedded recombinant virus

In an alternative embodiment, the earner vector comprises an

embedded recombinant viral genome, and any required replication, encapsidation and/or helper functions are provided by a helper virus or a plasmid

The embedded recombinant viral genome may comprise a transgene and DNA elements required for replication of a mammalian virus The transgene comprises the gene of interest, regulatory elements to regulate its expression, and

an optional DNA spacer. The transgene is flanked by the DNA elements required

for replication of a mammalian virus, such as the ITRs of AAV, the LTRs of

retrovirus, or the ITRs of adenovirus. The recombinant viral genome is embedded

within the nonmammalian virus backbone, optionally along with one or more of the

other DNA sequences listed above, resulting in a chimeric carrier vector of the

present invention.

In an alternative embodiment, the embedded recombinant viral

genome does not contain a transgene but the recombinant viral genome itself contains point mutations or deletions. In this embodiment, the point mutations or

deletions function to attenuate the replication of the subsequently-produced

recombinant virus. The attenuated recombinant virus may be any virus which could

be useful for vaccination, including, without limitation, picornaviruses such as

poliovirus; hepatitis viruses such as hepatitis B and hepatitis C; cold-adapted

respiratory syncytial virus (RSV); cold-adapted influenza virus; parainfluenza virus types 1, 2 and 3; and rotavirus.

The carrier vector is replication-proficient in its native host cells.

For example, employing a baculovirus backbone results in a chimeric carrier vector

that is replication-proficient in insect cells. In contrast, the embedded recombinant viral genome, optionally containing a transgene, is unable to excise, replicate, and package into virions because its promoters are inactive in insect cells. However,

once the chimeric carrier vector infects a mammalian cell, the essential gene

products required for replication and packaging of the carrier vector in its permissive native cell are no longer expressed. Thus, the carrier vector does not

replicate in mammalian cells, and instead exists transiently within the mammalian

cell.

In contrast, once the carrier vector has infected a mammalian cell,

the mammalian regulatory sequences within the carrier vector controlling the

embedded recombinant viral genome and other mammalian DNA sequences are

activated, such that the recombinant viral genome is capable of being excised from

the carrier vector and replicated. The capsid proteins which form the capsid of the

recombinant virus are expressed such that the recombinant viral genome is

encapsidated, which yields an infectious recombinant virus. The recombinant virus

is essentially free of carrier vector because the carrier vector is not replicated in

mammalian cells.

In a preferred embodiment, the recombinant virus is replication-

deficient because there are no replication or helper functions present in the newly

formed virions; i.e., the recombinant virus lacks part or all of the coding regions of

the native virus genome. In embodiments of the invention in which the recombinant

virus is helper-dependent, such as rAAV, the recombinant virus lacks both

functional replication and encapsidation functions. In embodiments of the invention

in which the recombinant virus is not helper-dependent, the recombinant virus lacks

functional replication coding regions or other essential genes.

In cases where helper functions are required for recombinant virus production, recombinant virus may be produced without the need for coinfection

and subsequent production of helper virus if a carrier vector includes the necessary helper functions. Thus, the invention yields lysates of substantially pure and

essentially homogeneous preparations of the particular recombinant virus of interest

in the absence of helper virus.

This invention thus has many advantages over current methods for manufacturing recombinant viruses. These advantages include: (l) the

nonmammalian virus backbone permits insertion of large DNA sequences without

compromising the efficiency of recombinant virus production; (2) sequences

normally toxic to mammalian cells (e.g., AAV rep, VSV-G, retroviral envelope proteins, eukaryotic regulatory proteins, etc.) are not expressed in substantial

amounts from their mammalian regulatory sequences in the nonmammalian host cell

of the nonmammalian carrier vector and thus can be tolerated by the nonmammalian

carrier vector during the course of its replication in the nonmammalian host cell; (3)

nonmammalian viruses do not replicate in mammalian cells, precluding

contamination of the final eukaryotic vector stocks with the nonmammalian carrier

vector; (4) in some embodiments no helper viruses are necessary, with the result

that the final recombinant virus preparation is essentially free of helper virus; (5)

frequency of wildtype virus production due to homologous or non-homologous recombination is minimized; and (6) the methods of the present invention are

particularly suitable to large scale production of recombinant viruses which are

themselves replication-deficient. Additionally, nonmammalian viruses are not

normally pathogenic to mammalian cells, may be propagated in serum free media,

and may be grown to a high titer. Other features and advantages of the invention will be apparent from the following drawings, the description of the invention and

its preferred embodiments, and the examples described herein.

In one embodiment, the present invention includes nonmammalian

carrier vectors containing elements that are required to produce replication-deficient

recombinant viral vectors. In a preferred embodiment, the nonmammalian carrier

vector contains all the elements required to produce a replication-deficient recombinant viral vector. In an even more preferred embodiment, a single

nonmammalian carrier vector contains all the required elements to produce a

replication-deficient recombinant viral vector. In another preferred embodiment,

the nonmammalian carrier vector is a baculovirus.

In another embodiment, the invention includes a method of

producing replication-deficient recombinant viral vector lysates and stocks that are free of helper or other contaminating virus. In a preferred embodiment, the method

is one which is easily scaled for industrial production of recombinant viral vectors.

In another preferred embodiment, the method is one in which a high titer of

recombinant viral vector lysates and stocks is achieved.

In another embodiment, the invention includes attenuated,

replication-competent recombinant viruses and a method of producing such viruses

free of helper or other contaminating virus. In a preferred embodiment, these

attenuated, replication-competent viruses may be used for immunization. BRIEF DESCRIPTION OF THE DRAWINGS

Figure 1 is a schematic diagram of recombinant baculoviruses with

target genes inserted into the loci of either polyhedrin or plO genes

Figures 2A and 2B represent a genetic map of AAV type 2 Figure

2 A is a schematic representation of the viral genome rep encodes replication

proteins (Rep78, Rep68, Rep52, and Rep40) and cap encodes encapsidation

functions (VP1, VP2, and VP3) Right-angled arrows: the p5, pl9, and p40 viral

promoters, downward vertical arrow: common polyadenylation signal upstream of

the 3 '-ITR Figure 2B represents the transcripts derived from each of the three

promoters A,," polyadenylation.

Figure 3 is a schematic diagram of constructed plasmids used in this

invention

Figure 4 shows the steps involved in rAAV production by traditional

adenovirus infection/plasmid co-transfection method (Shenk et al., US patent

#5,436, 146)

Figure 5 shows the steps required for rAAV production through the

use of two recombinant baculoviruses (BV-EiOV-RC and BV-cisEFGFP).

Figure 6 shows the steps required for rAAV production through the

use of stable cell line 293-CG3 together with one recombinant baculovirus (BV- EiOV-RC)

Figure 7 shows the steps required for rAAV production through the

use of stable cell line expressing AAV rep and cap genes together with recombinant

baculovirus (BV-EiOV-cisEFGFP-El). DET AILED DESCRIPTION OF THE INVENTION

Definitions and General Techniques

Unless otherwise defined, all technical and scientific terms used

herein have the meaning as commonly understood by one of ordinary skill in the art

to which this invention belongs The practice of the present invention employs,

unless otherwise indicated, conventional techniques of chemistry, molecular

biology, microbiology, recombinant DNA, genetics, virology and immunology See, e g , Sambrook et al , 1989, Ausubel et al , 1992, Harlow et al 1989 (which

are incorporated herein by reference)

A "recombinant viral genome" comprises all or a part of a viral

genome, wherein the viral genome may be wild type or may contain point mutations

or deletions, and optionally comprises a transgene operably linked to expression

control sequences In one embodiment, the transgene is flanked by flanking

elements The recombinant viral genome of the invention is embedded in the

genome of the carrier vector, and is ultimately packaged into a recombinant virus

A "recombinant virus" is a virus derived from the recombinant viral

genome described above The recombinant virus may comprise a transgene, may be an attenuated, replication-competent virus without a transgene, may be a

replication-competent virus with one or more point mutation(s), or may be a replication-deficient virus with one or more point mutations or genomic deletions,

or combinations thereof The recombinant virus comprising a transgene is capable

of transducing mammalian cells and delivering the transgene thereto

A "flanking element" or "flanking nucleic acid" is a nucleic acid sequence generally derived from a mammalian virus which, when located in positions flanking a transgene, permits the packaging of the transgene into a

recombinant virus. Flanking elements may be the naturally-occurring flanking

elements from a mammalian virus which permit the packaging of the recombinant

virus, or may be artificial nucleic acid elements, e.g. mutated sequences of flanking

elements, that have the same or similar packaging function. Flanking elements

include, without limitation, the inverted terminal repeats (ITRs) of AAV or Ad, the long terminal repeats (LTRs) of retrovirus, the "α" or packaging sequence of herpes

simplex virus (HSV), as well as any other sequences that are required for packaging

from other viruses known in the art.

A "transgene" is a nucleic acid sequence that is to be delivered or

transferred to a mammalian cell. A transgene may encode a protein, peptide or polypeptide that is useful as a marker, reporter or therapeutic molecule. A

transgene may also encode a protein, polypeptide or peptide that is useful for

protein production, diagnostic assays or for any transient or stable gene transfer in

vitro or in vivo. Alternatively, a transgene may not encode a protein but rather be

used as an antisense molecule, ribozyme or other regulatory nucleic acid to inhibit

replication, transcription or translation of a nucleic acid to which it is

complementary or to target a complementary mRNA for degradation.

"Expression control sequences" are nucleic acid sequences that regulate the expression of a gene by being operably linked to the gene of interest.

"Operably linked" sequences include both expression control sequences that are

contiguous with the gene of interest and expression control sequences that act in trans or at a distance to control the gene of interest. Expression control sequences include appropriate transcription initiation, termination, promoter and enhancer

sequences; efficient RNA processing signals such as splicing and polyadenylation

signals; sequences that stabilize cytoplasmic mRNA; sequences that enhance

translation efficiency (i.e., Kozak consensus sequence); sequences that enhance

protein stability; and when desired, sequences that enhance protein secretion.

As used herein, a "carrier vector" means a nucleic acid molecule

comprising a nonmammalian viral nucleic acid backbone and nucleic acid sequences

derived from mammalian sources, mammalian viral sources, nonmammalian sources,

and nonmammalian viral sources. The nonmammalian viral nucleic acid backbone

may be selected from a wide variety of sources, see, for example Table 1 of U.S. Pat. No. 5,731,182, herein incorporated by reference. The nonmammalian viral

nucleic acid backbone, upon transfection of the carrier vector nucleic acid into non¬

mammalian cells, is sufficient to produce packaged carrier virus comprising the

nucleic acid sequences inserted into the carrier vector.

A "carrier virus" is an encapsidated carrier vector capable of binding

to a mammalian cell and delivering the carrier vector's genome to the cell's nucleus.

As used herein, "ligand nucleic acid" means a nucleic acid which

encodes a protein which allows the carrier virus of the invention to bind to and

enter a mammalian cell. The nucleic acid encoding the protein may be operably

linked to expression control sequences that regulate the expression of the nucleic acid encoding the ligand.

"Helper function nucleic acid" is one or more nucleic acid sequences that encode one or more proteins, peptides or polypeptides, or that is transcribed to

an RNA, wherein the one or more proteins, peptides, polypeptides or RNAs are

required by certain viruses for production of recombinant viruses. The sequences

may be naturally-occurring helper functions or may be sequences that have been

mutated or altered but which retain their respective helper functions. The sequences

may be derived from helper viruses or may be naturally-occurring or artificial

nucleic acid sequences that encode non-viral proteins that act as helper functions for

production of recombinant viruses. The nucleic acid sequences that are transcribed

to RNA or which encode the proteins, polypeptides or peptides may be operably linked to expression control sequences that regulate the expression of the nucleic

acid encoding the helper functions.

"Replication and/or encapsidation nucleic acid" is a nucleic acid

sequence or sequences which encode proteins or polypeptides that are required for replication and encapsidation of the recombinant virus. The sequences may be

naturally-occurring replication or encapsidation sequences or may be sequences that

have been mutated or altered but which retain their respective functions of

replication or encapsidation. The nucleic acid sequences encoding the proteins may

be operably linked to expression control sequences that regulate the expression of the nucleic acid encoding the replication and encapsidation sequences. A "replicon" is an episomal replication origin and those necessary

proteins (or DNA encoding these proteins) to initiate nucleic acid replication. The Carrier Vector

The carrier vector of the invention is a chimeric vector backbone

derived from the nucleic acid of a nonmammalian virus. The carrier vector

comprises sufficient vector sequences to be able to replicate and encapsidate within

the appropriate nonmammalian host cell. The carrier vector also includes one or

more of the following inserts' an embedded recombinant viral genome, a ligand

nucleic acid providing for expression of a protein which can interact with a mammalian cell, replication and/or encapsidation nucleic acid required to replicate

and encapsidate a recombinant virus; and helper virus functions nucleic acids.

In a preferred embodiment, the carrier vector comprises an

embedded recombinant viral genome within its nonmammalian virus genomic

backbone The recombinant viral genome may comprise a transgene with associated expression regulatory sequences, wherein the transgene and regulatory

sequences are bordered by flanking elements of a mammalian virus Alternatively,

the recombinant viral genome does not contain a transgene but rather contains

deletions or point mutations in its sequence such that it produces an attenuated,

replication-proficient recombinant virus, or other deletions or point mutations that

produce a replication-deficient recombinant virus.

In a more preferred embodiment, the carrier vector comprises the

embedded recombinant viral genome and either or both of 1) nucleic acid sequences

encoding replication and/or encapsidation and 2) nucleic acid sequences encoding helper functions In an even more preferred embodiment of this invention, the

carrier vector additionally comprises a ligand nucleic acid providing for expression of a protein which can interact with a mammalian cell In another preferred

embodiment, the ligand nucleic acid encodes a protein which can bind to a specific mammalian cell receptor

In the most preferred embodiment, the carrier vector comprises the

embedded recombinant viral genome and all of those nucleic acid inserts required

for production of a recombinant virus in a mammalian cell For instance, if the

carrier virus comprising the carrier vector is to be used to infect a cell line which expresses replication and encapsidation proteins for a recombinant AAV virus (e g ,

the A64 cell line described in U S Pat No 5,658,785 and the B50 cell line

described in PCT US98/19463), then the carrier vector would comprise the

embedded recombinant viral genome and the helper functions, and optionally the ligand nucleic acid Alternatively, if carrier virus is to be used to infect a cell line

which expresses a helper function for a recombinant AAV virus (e g , the 293 cell

line which expresses El), then the earner vector would comprise the embedded

recombinant viral genome, the replication and encapsidation nucleic acids for AAV

(/ ep and cap), and the helper functions required in addition to El (e g , E2a, E4ORF6 and VAI RNA), and optionally the ligand nucleic acid

If the earner virus is to be used to produce a recombinant retrovirus,

which does not require helper functions, the carrier vector would comprise the

embedded recombinant retroviral viral genome and the nucleic acids required for its replication and encapsidation (e g , gag, pol and env) and optionally, in cases where

the retrovirus is a lentivirus, one or more of the nucleic acids encoding regulatory or

auxilliary proteins (e g , tat, rev, ne vpr, vpu) If the earner virus is to be used to produce a recombinant retrovirus in a cell line that expresses gag, pol and env or

the other functions described above in the case of lentiviruses, then the carrier virus

would need only comprise the embedded recombinant retroviral genome and

optionally the ligand nucleic acid Similarly, if the carrier virus is to be used to

produce a recombinant adenovirus, the earner vector would comprise the embedded

recombinant adenoviral genome and the nucleic acid sequences required for its replication and encapsidation The type of nucleic acid sequences required for

replication and encapsidation of the recombinant adenoviral genome depends upon

which adenoviral genes are deleted from the recombinant adenoviral genome and

whether the mammalian cell line that the earner virus infects expresses any adenoviral genes (e g , 293 cells express El) Any carrier vector genome may

optionally comprise a ligand nucleic acid to increase infection by the carrier virus of

a mammalian cell

The embedded recombinant viral genome and other nucleic acid

inserts may be carried on separate carrier vectors, but in the most preferred embodiment, the embedded recombinant viral genome and all other desired nucleic

acid inserts are carried on a single carrier vector The advantage of a single carrier

vector is that only a single infection by the earner virus of the mammalian host cell

is required in order to produce a recombinant virus

In another embodiment of the invention, the inability of the carrier vector to replicate in mammalian cells is overcome by supplying a mammalian

rephcon to the carrier vector The provision of a replicon assures that mammalian

cells infected by the carrier vector maintain a sufficient copy number of the carrier vector extrachromosomally throughout a population of proliferating and dividing

mammalian cells

Based on this description, other embodiments of the carrier vector

will be readily apparent to those of ordinary skill in the art

Nonmammalian Virus Backbone

The chimeric carrier vector is constructed from a backbone of a

nonmammalian virus The backbone need not be the entire genome of the nonmammalian virus, but may be only that portion of the genome necessary for

replication in a nonmammalian host Preferably, the vector backbone is derived

from an invertebrate virus Table 1 of U S Pat No 5,731,182 lists several

examples of viruses that may be used to form the backbone of the chimeric vector,

the sequences of which are available from various sources, such as Genbank In a

preferred embodiment, the invertebrate DNA virus is a baculovirus In a more

preferred embodiment, the bacuolovirus is a Granulovirus or Nucleopolyhedrovirus

In an even more preferred embodiment, the nonmammalian viral backbone is

derived from the baculovirus Autographa californica nuclear polyhedrosis virus

(AcNPV) See, e g , GenBank Accession No L22858

In a preferred embodiment, the nonmammalian virus backbone must

be capable of replication in its ordinary host cell, but incapable of replication in a

mammalian cell For example, the baculovirus virus backbone exemplified herein replicates only in insect cells The Embedded Recombinant Viral Genome

The methods of the present invention allow for large scale

production of high titers of recombinant virus, i.e., one that has a transgene inserted

therein to be delivered to target mammalian cells, or one that does not have a

transgene but rather has a mutation or deletion in a viral gene and is to be used as a

vaccine, e.g., an attenuated and replication-proficient recombinant virus or a

replication-deficient mutant virus. The recombinant virus may be any virus of

interest for use to deliver transgenes to mammalian cells or for use as a vaccine.

Preferred recombinant viruses for delivery of a transgene include adenoviruses,

retroviruses, adeno-associated viruses, herpesvirus amplicons and hepatitis B

viruses.

In order to manufacture a recombinant virus containing a transgene,

the method of the present invention begins with a desired transgene, then associates

the transgene with appropriate expression regulatory sequences (ERS), e.g.,

promoter, enhancer, polyadenylation site, then inserts this ERS-transgene construct

between the packaging elements of the virus to be manufactured, in place of the

genes normally found therein. Where the length of the replacement is shorter than

that being replaced, and that shorter length would pose an obstacle to proper

packaging, an optional spacer or "stuffer" sequence may be inserted in order to

maintain the proper length for packaging. The entire construct of the ERS- transgene constructed bordered by the flanking elements is the genome of the

recombinant virus of the present invention, which is then embedded in the carrier vector's genome, at which point it subsists as an embedded recombinant viral genome. Each of these elements is described in detail below:

^'The Transgene

The composition of the transgene sequence depends upon the

intended use for the resulting recombinant virus. For example, one type of

transgene sequence comprises a reporter or marker sequence, which upon

expression produces a detectable signal. Such reporter or marker sequences

include, without limitation, DNA sequences encoding E. coli β-lactamase, β-

galactosidase (LacZ), alkaline phosphatase, HSV thymidine kinase, green

fluorescent protein (GFP), bacterial chloramphenicol acetyltransferase (CAT),

firefly luciferase, eukaryotic membrane bound proteins including, for example, CD2,

CD4, CD8, the influenza hemagglutinin protein, and others well known in the art, to

which high affinity antibodies directed to them exist or can be made routinely, and

fusion proteins comprising a membrane bound protein appropriately fused to an

antigen tag domain from, among others, hemagglutinin or myc.

These sequences, when associated with regulatory elements which

drive their expression, provide signals detectable by conventional means, including

enzymatic, radiographic, colorimetric, fluorescence or other spectroscopic assays,

fluorescent activated cell sorting assay and immunological assays, including ELISA, RIA and immunohistochemistry. For example, where the transgene is the LacZ

gene, the presence of a recombinant virus is detected by assays for β-galactosidase activity. Similarly, where the transgene is luciferase, the recombinant virus gene

expression may be measured by light production in a luminometer. However, desirably, the transgene is a non-marker gene which can

be delivered to a cell or an animal via the recombinant virus produced by this

method. The transgene may be selected from a wide variety of gene products useful

in biology and medicine, such as proteins, antisense nucleic acids (e.g., RNAs), or

catalytic RNAs. The invention may be used to correct or ameliorate gene

deficiencies, wherein normal genes are expressed but at less than normal levels, and

may also be used to correct or ameliorate genetic defects wherein a functional gene

product is not expressed. A preferred type of transgene sequence is a therapeutic gene which expresses a desired corrective gene product in a host cell. These

therapeutic nucleic acid sequences typically encode products which, upon

expression, are able to correct, complement or compensate an inherited or non-

inherited genetic defect, or treat an epigenetic disorder or disease. However, the

selected transgene may encode any product desirable for study. The selection of the transgene sequence is not a limitation of this invention. Choice of a transgene

sequence is within the skill of the artisan in accordance with the teachings of this

application.

The invention also includes methods of producing recombinant virus

and compositions thereof which can be used to correct or ameliorate a gene defect

caused by a multi-subunit protein. In certain situations, a different transgene may be used to encode each subunit of the protein. This may be desirable when the size

of the DNA encoding the protein subunit is large, e.g., for an immunoglobulin or

the platelet-derived growth factor receptor. In order for the cell to produce the multi-subunit protein, a cell would be infected with recombinant virus expressing each of the different subunits

Alternatively and more preferably, different subunits of a protein

may be encoded by the same transgene In this case, a single transgene would

include the DNA encoding each of the subunits, with the DNA for each subunit

separated by an internal ribosome entry site (IRES) The use of IRES permits the

creation of multigene or polycistronic mRNAs IRES elements are able to bypass

the nbosome scanning model of 5' methylated cap-dependent translation and begin

translation at internal sites (Pelletier and Sonenberg, 1988) IRES elements from two members of the picornavirus family (polio and encephalomyocarditis) have

been described (Pelletier and Sonenberg, 1988), as well an IRES from a mammalian

mRNA (Macejak and Sarnow, 1991) IRES elements can be linked to heterologous

open reading frames By virtue of the IRES element, each open reading frame is accessible to ribosomes for efficient translation Thus, multiple genes can be

efficiently expressed using a single promoter/enhancer to transcribe a single

message This is preferred when the size of the DNA encoding each of the subunits

is sufficiently small that the total of the DNA encoding the subunits and the IRES is

no greater than the maximum size of the DNA insert that the virus can encompass For instance, for rAAV, the insert size can be no greater than approximately 4 8

kilobases, however, for an adenovirus which lacks all of its helper functions, the

insert size is approximately 28 kilobases.

Useful gene products include hormones and growth and

differentiation factors including, without limitation, insulin, glucagon, growth

hormone (GH), parathyroid hormone (PTH), calcitonin, growth hormone releasing factor (GRF), thyroid stimulating hormone (TSH), adrenocorticotropic hormone

(ACTH), prolactin, melatonin, vasopressin, β-endorphin, met-enkephalin, leu-

enkephalin, prolactin-releasing factor, prolactin-inhibiting factor, corticotropin-

releasing hormone, thyrotropin-releasing hormone (TRH), follicle stimulating

hormone (FSH), luteinizing hormone (LH), chorionic gonadotropin (CG), vascular

endothelial growth factor (VEGF), angiopoietins, angiostatin, endostatin,

granulocyte colony stimulating factor (GCSF), erythropoietin (EPO), connective tissue growth factor (CTGF), basic fibroblast growth factor (bFGF), bFGF2, acidic

fibroblast growth factor (aFGF), epidermal growth factor (EGF), transforming

growth factor (TGFα), platelet-derived growth factor (PDGF), insulin-like

growth factors I and II (IGF-I and IGF-II), any one of the transforming growth

factor β (TGFβ) superfamily comprising TGFβ, activins, inhibins, or any of the

bone morphogenic proteins (BMP) BMPs 1-15, any one of the

heregulin/neuregulin ARIA/neu differentiation factor (NDF) family of growth

factors, nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), neurotrophins NT-3, NT-4/5 and NT-6, ciliary neurotrophic factor (CNTF), glial

cell line derived neurotrophic factor (GDNF), neurtuin, persephin, agrin, any one of

the family of semaphorins/collapsins, netrin-1 and netrin-2, hepatocyte growth

factor (HGF), ephrins, noggin, sonic hedgehog and tyrosine hydroxylase.

Other useful gene products include proteins that regulate the immune system including, without limitation, cytokines and lymphokines such as thrombopoietin (TPO), interleukins (IL) IL-lα, IL-lβ, TL-2, LL-3, IL-4, IL-5, IL-6,

IL-J IL-8, IL-9, IL-10, ΓL-11, IL-12, LL-13, IL-14, IL-15, IL-16, and IL-17, monocyte chemoattractant protein (MCP-1), leukemia inhibitory factor (LIF), granulocyte-macrophage colony stimulating factor (GM-CSF), granulocyte colony

stimulating factor (G-CSF), monocyte colony stimulating factor (M-CSF), Fas

ligand, tumor necrosis factors and β (TNFα and TNFβ), interferons (IFN) IFN- ,

IFN-β and IFN-γ, stem cell factor, fTk-2/flt3 ligand. Gene products produced by the immune system are also encompassed by this invention. These include, without

limitations, immunglobulins IgG, IgM, IgA, IgD and IgE, chimeric

immunoglobulins, humanized antibodies, single chain antibodies, T cell receptors,

chimeric T cell receptors, single chain T cell receptors, class I and class II MHC

molecules, as well as engineered MHC molecules including single chain MHC molecules. Useful gene products also include complement regulatory proteins such

as membrane cofactor protein (MCP), decay accelerating factor (DAF), CR1, CR2

and CD59.

Still other useful gene products include any one of the receptors for

the hormones, growth factors, cytokines, lymphokines, regulatory proteins and immune system proteins. Examples of such receptors include flt-1, flk-1, TIE-2,

the trb family of receptors such as TrkA, MuSK, Eph, PDGF receptor, EGF

receptor, HER2, insulin receptor, IGF-1 receptor, the FGF family of receptors, the

TGFβ receptors, the interleukin receptors, the interferon receptors, serotonin

receptors, α-adrenergic receptors, β-adrenergic receptors, the GDNF receptor, p75

neurotrophin receptor, among others. The invention encompasses receptors for

extracellular matrix proteins, such as integrins, counter-receptors for

transmembrane-bound proteins, such as intercellular adhesion molecules (ICAM-1, ICAM-2, ICAM-3 and ICAM-4), vascular cell adhesion molecules (VCAM), and

selectins E-selectin, P-selectin and L-selectin. The invention encompasses receptors

for cholesterol regulation, including the LDL receptor, HDL receptor, VLDL

receptor, and the scavenger receptor. The inventions encompasses the

apolipoprotein ligands for these receptors, including ApoAI, ApoAIV and ApoE.

The invention also encompasses gene products such as steroid hormone receptor

superfamily including glucocorticoid receptors and estrogen receptors, Vitamin D

receptors and other nuclear receptors. In addition, useful gene products include

antimicrobial peptides such as defensins and maginins, transcription factors such as juif f s, max, mad, serum response factor (SRF), AP-1, AP-2, myb, MRG1,

CREM, Alx4, FREAC1, NF-κB, members of the leucine zipper family, C2H4 zinc

finger proteins, including Zif268, EGR1, EGR2, C6 zinc finger proteins, including

the glucocorticoid and estrogen receptors, POU domain proteins, exemplified by

Pitl, homeodomain proteins, including HOX-1, basic helix-loop-helix proteins, including myc, MyoD and myogenin, ETS-box containing proteins, TFE3, E2F,

ATF1, ATF2, ATF3, ATF4, ZF5, NFAT, CREB, HNF-4, C/EBP, SPI, CCAAT-

box binding proteins, interferon regulation factor 1 (IRF-1), Wilms tumor protein,

ETS-binding protein, STAT, GATA-box binding proteins, e.g., GATA-3, and the forkhead family of winged helix proteins.

Other useful gene products include carbamoyl synthetase I, ornithine

transcarbamylase, arginosuccinate synthetase, arginosuccinate lyase, arginase,

fumarylacetoacetate hydrolase, phenylalanine hydroxylase, alpha- 1 antitrypsin,

glucose-6-phosphatase, porphobilinogen deaminase, factor VII, factor VIII, factor IX, factor II, factor V, factor X, factor XII, factor XI, von Willebrand factor,

superoxide dismutase, glutathione peroxidase and reductase, heme oxygenase, angiotensin converting enzyme, endothelin- 1 , atrial natriuetic peptide, pro-

urokinase, urokinase, plasminogen activator, heparin cofactor II, activated protein

C (Factor V Leiden), Protein C, antithrombin, cystathione beta-synthase, branched

chain ketoacid decarboxylase, albumin, isovaleryl-CoA dehydrogenase, propionyl CoA carboxylase, methyl malonyl CoA mutase, glutaryl CoA dehydrogenase,

insulin, beta-glucosidase, pyruvate carboxylase, hepatic phosphorylase,

phosphorylase kinase, glycine decarboxylase (also referred to as P-protein), H-

protein, T-protein, Menkes disease protein, tumor suppressors (e.g., p53), cystic

fibrosis transmembrane regulator (CFTR), the product of Wilson's disease gene

PWD, Cu/Zn superoxide dismutase, aromatic aminoacid decarboxylase, tyrosine hydroxylase, acetylcholine synthetase, prohormone convertases, protease inhibitors,

lactase, lipase, trypsin, gastrointestinal enzymes including chyromotrypsin, and

pepsin, adenosine deaminase, αl anti-trypsin, tissue inhibitor of metalloproteinases

(TIMP), GLUT-1, GLUT-2, trehalose phosphate synthase, hexokinases I, II and

III, glucokinase, any one or more of the individual chains or types of collagen, elastin, fibronectin, thrombospondin, vitronectin and tenascin, and suicide genes

such as thymidine kinase and cytosine deaminase.

Other useful transgenes include non-naturally occurring

polypeptides, such as chimeric or hybrid polypeptides or polypeptides having a non- naturally occurring amino acid sequence containing insertions, deletions or amino acid substitutions. For example, single-chain engineered immunoglobulins could be useful in certain immunocompromised patients Other useful proteins include

truncated receptors which lack their transmembrane and cytoplasmic domain

These truncated receptors can be used to antagonize the function of their respective

ligands by binding to them without concomitant signaling by the receptor Other

types of non-naturally occurring gene sequences include antisense molecules and

catalytic nucleic acids, such as ribozymes, which could be used to reduce

overexpression of a gene

Other useful transgenes include those that encode antigemc peptides

capable of generating an immune response Recombinant vectors comprising these

transgenes can be used for genetic immunization Useful transgenes include those

that encode peptides specific for Epstein Barr virus, HIV, simian immunodeficiency

virus (SIV), human T-cell leukemia viruses I and II (HTLV-I and HTLV-II),

hepatitis A, B, C, D and E, pseudorabies virus, rabies virus, cytomegalovirus,

respiratory syncytial virus, parainfluenza virus types 1-4, mumps virus, rubella virus,

polio virus, rubeola virus, influenza virus types A, B and C, rotavirus, herpes

simplex viruses types 1 and 2, varicella-zoster virus, human herpes virus type 6,

hantavirus, adenoviruses, chlamydia pneumoniae, chlamydia trachomatis,

mycoplasma pneumoniae, mycobacterium tuberculosis, atypical mycobacteria, feline

leukemia virus, feline immunodeficiency virus, bovine immunodeficiency virus,

equine infectious anemia virus, caprine arthritis encephalitis virus, visna virus, Staphlococcus species and Streptococcus species The transgenes may also be directed against peptides from tumor antigens to provide immunization for tumors

and cancers Expression Control Sequences

A great number of expression control sequences — native,

constitutive, inducible and/or tissue-specific — are known in the art and may be

utilized to drive expression of the transgene and the nucleic acid sequences

encoding the replication and encapsidation functions of the recombinant virus, the

helper functions and the ligand. The choice of expression control sequence depends

upon the type of expression desired. For eukaryotic cells, expression control

sequences typically include a promoter, an enhancer, such as one derived from an immunoglobulin gene, SV40, cytomegalovirus, etc., and a polyadenylation sequence which may include splice donor and acceptor sites. The polyadenylation sequence

generally is inserted following the transgene sequences and before the 3' flanking

sequence of the transgene. A transgene-carrying molecule useful in the present invention may also contain an intron, desirably located between the

promoter/enhancer sequence and the transgene. One possible intron sequence is

also derived from SV-40, and is referred to as the SV-40 T intron sequence.

Another vector element that may be used is an internal ribosome entry site (IRES),

as described above. An IRES sequence is used to produce more than one polypeptide from a single gene transcript. An IRES sequence can be used for the

transgene or for any of the other nucleic acid sequences encoding the replication

and encapsidation polypeptides, the helper functions or the ligand. Selection of

these and other common vector elements are conventional and many such

sequences are available [see, e.g., Sambrook et al, and references cited therein at,

for example, pages 3.18-3.26 and 16.17-16.27 and Ausubel et al., Current Protocols in Molecular Biology, John Wiley & Sons, New York, 1989]

In one embodiment, high-level constitutive expression will be desired Examples of such promoters include, without limitation, the retroviral Rous sarcoma virus (RSV) LTR promoter/enhancer, the cytomegalovirus (CMV)

immediate early promoter/enhancer [see, e g , Boshart et al, Cell, 41 521-530

(1 85)], the SV40 promoter, the dihydrofolate reductase promoter, the cytoplasmic

β-actin promoter and the phosphoglycerol kinase (PGK) promoter

In another embodiment, inducible promoters may be desired

Inducible promoters are those which are regulated by exogenously supplied

compounds, either in cis or in trans, including without limitation, the zinc-inducible

sheep metallothionine (MT) promoter; the dexamethasone (Dex)-inducible mouse

mammary tumor virus (MMTV) promoter; the T7 polymerase promoter system [WO 98/10088], the ecdysone insect promoter [No et al, Proc Natl Acad Sci

USA, 93 3346-3351 (1996)], the tetracycline-repressible system [Gossen et al,

Proc Natl Acad Sci USA. 89 5547-5551 ( 1992)] , the tetracycline-inducible

system [Gossen et al , Science, 268: 1766-1769 (1995); see also Harvey et al., Curr

Opin Chem Biol . 2.512-518 (1998)]; the RU486-inducible system [Wang et al.,

Nat Biotech . 15.239-243 (1997) and Wang et al , Gene Ther . 4.432-441 (1997)];

and the rapamycin-inducible system [Magari et al., J. Clin Invest . 100.2865-2872

(1997), Rivera et al . Nat Medicine. 2: 1028-1032 (1996)]. Other types of inducible

promoters which may be useful in this context are those which are regulated by a specific physiological state, e.g., temperature, acute phase, or in replicating cells

only In a preferred embodiment, the transgene is under the control of the native p5 promoter of AAV

In another embodiment, the native promoter for the transgene or

nucleic acid sequence of interest will be used The native promoter may be

preferred when it is desired that expression of the transgene or the nucleic acid

sequence should mimic the native expression The native promoter may be used

when expression of the transgene or other nucleic acid sequence must be regulated

temporally or developmentally, or in a tissue-specific manner, or in response to

specific transcπptional stimuli In a further embodiment, other native expression

control elements, such as enhancer elements, polyadenylation sites or Kozak

consensus sequences may also be used to mimic the native expression

In one embodiment, the recombinant viral genome comprises a

transgene operably linked to a tissue-specific promoter For instance, if expression

in skeletal muscle is desired, a promoter active in muscle may be used These

include the promoters from genes encoding skeletal α-actin, myosin light chain 2A,

dystrophin, muscle creatme kinase, as well as synthetic muscle promoters with

activities higher than naturally-occurring promoters [see Li et al , Nat Biotech .

17 241-245 (1999)] Examples of promoters that are tissue-specific are known for

liver [albumin, Miyatake et al J Virol , 71 5124-32 (1997), hepatitis B virus core

promoter, Sandig et al , Gene Ther , 3 1002-9 (1996), alpha-fetoprotein (AFP),

Arbuthnot et al , Hum Gene Ther . 7 1503-14 (1996)], bone [osteocalcm, Stein et al , Mol Biol Rep . 24 185-96 (1997), bone sialoprotein, Chen et al , J Bone Miner Res . 11 654-64 (1996)], lymphocytes [CD2, Hansal et al , J Immunol .

161 1063-8 (1998), lmmunoglobu n heavy chain, T cell receptor a chain], neuronal [neuron-specific enolase (NSE) promoter, Andersen et al. Cell Mol Neurobiol ,

13 503-15 (1993), neurofilament light-chain gene, Piccioli et al , Proc Natl Acad

Sci USA, 88 561 1-5 (1991), the neuron-specific vgf gene, Piccioli et al , Neuron,

15 373-84 (1995)], among others.

Of course, not all vectors and expression control sequences will

function equally well to express all of the transgenes or other nucleic acid sequences

of this invention However, one of skill in the art may make a selection among

these expression control sequences without departing from the scope of this

invention Suitable promoter/enhancer sequences which function in the appropriate

host cell of choice may be selected by one of skill in the art using the guidance

provided by this application. Such selection is a routine matter and is not a

limitation of the molecule or construct.

In one method of identifying a suitable expression control sequence

for a desired nucleic acid sequence, one may select one or more expression control

sequences and operably link the expression control sequence to the nucleic acid sequence to be regulated. Then, one may insert these operably linked sequences

comprising the expression control sequence and regulated sequence into the

genome of the carrier vector. In one embodiment, one may insert a recombinant viral genome comprising the expression control sequence and the transgene into a

nonmammalian vector of the instant invention After following one of the methods for producing and packaging the recombinant vector as taught in this specification

one may infect suitable cells in vitro or in vivo. The number of copies of the

transgene in the cell may be monitored by Southern blotting or quantitative PCR, the level of RNA expression may be monitored by Northern blotting or quantitative

RT-PCR, and the level of protein expression may be monitored by Western blotting,

immunohistochemistry, ELISA, RIA, tests of the transgene' s gene product's

biological activity, either in vitro or in vivo, or tests for correction or amelioration

of a genetic defect

In a similar fashion, one may select one or more expression control

sequences and operably link it to a nucleic acid sequence encoding replication and

encapsidation proteins, helper functions or a ligand, and insert the resultant desired

nucleic acid molecule into a vector of the instant invention. One may also select one or more vector replication sequences and insert them into a vector of the instant

invention After packaging and infecting nonmammalian cells, one may measure the

particular effects, e g , on expression of the ligand or on replication of the vector,

by one of the methods described above. One may also use a functional test to

determine if one or more particular expression control sequences operably linked to

a nucleic acid sequence encoding a ligand produces a carrier virus which is able to

infect mammalian cells efficiently. One may assay a number of different expression

control sequences to determine which one is most effective for mammalian cell

infection. The same may be done using a variety of vector replication sequences.

Furthermore, after infecting mammalian host cells and obtaining

recombinant virus, one may infect mammalian cells with the recombinant virus, then

measure the expression of the replication and encapsidation proteins and/or helper functions by one of the methods described above. One may also use a functional

test to determine if one or more particular expression control sequences operably linked to one or more helper functions or replication or encapsidation functions is

capable of supporting production of a infectious recombinant virus One may

determine which of many expression control sequences are most effective in

producing a high titer of infectious recombinant virus

Flanking Elements

Flanking elements are required for replication, excision and

packaging of many viruses, and each type of virus has its own type of flanking

elements In a wild-type virus, these elements flank the viral genes when the viral

DNA integrates into a host cell chromosome In the case of integrating viruses,

when the wild-type virus is rescued from the host chromosome, the flanking

elements excise along with the viral DNA and remain in flanking positions surrounding the rescued viral DNA, in a form suitable for packaging into virions

For non-integrating, extrachromosomal viruses (e g HSV), flanking sequences

serve functions in DNA replication and packaging In recombinant viruses, much or

all of the viral nucleic acid sequences between the flanking elements are removed

from the virus and are replaced with a transgene and its associated expression

regulatory sequences

In one embodiment of the invention, the recombinant virus is a

recombinant adenovirus, and comprises a selected transgene operably linked to

expression regulatory sequences and the adenoviral flanking elements Adenoviral flanking elements are ITRs and are 100-200 bp in length A large number of

adenoviral flanking elements are known, such as those from human adenoviruses types 1 -46, chimpanzee adenoviruses, canine adenoviruses, bovine adenoviruses [all

available from the American Type Culture Collection (ATCC), 10801 University

Boulevard, Manassas, VA 20110-2209]

In another embodiment, the recombinant virus is a recombinant

retrovirus, and comprises a selected transgene operably linked to expression

regulatory sequences and retroviral flanking elements The flanking elements are

long terminal repeat (LTR) sequences that are present at the 5' and 3' ends of the

retroviral genome These LTRs contain strong promoter and enhancer sequences

and are also required for integration in the host cell genome (Coffin, 1990) A large number of retroviral LTRs are known. See, for instance, U S Pat No 5,672,510

In yet another embodiment of the invention, the recombinant virus is

a recombinant AAV, and comprises a selected transgene operably linked to expression regulatory sequences and AAV flanking elements The naturally-

occurring AAV ITRs consist of approximately 145 bp at the 5' and 3' ends of the

AAV genome The AAV ITRs are required for replication, excision and encapsidation of both wild type and recombinant AAV virions

In another embodiment, the recombinant virus is either a herpesvirus

derivative containing one or more mutations or deletions of viral genes, or is a

herpesvirus amplicon In either case, the flanking elements would be the viral

terminal repeats (e g , the "α " sequence if the virus is HSV) HSV amplicons are defective HSV genomes containing the packaging sequence ( ), viral origin of DNA

replication (on) and the transgene cassette of interest operably linked to the desired

expression regulatory sequences In the presence of helper herpesvirus or substitute helper functions, the amplicon is replicated and packaged as head-to-tail

concatemers to form wild-type size genomes.

In another embodiment, the recombinant virus is a recombinant

defective hepatitis B virus (HBV) and comprises a selected transgene operably

linked to expression regulatory sequences and inserted into the HBV genome. In

vitro studies have shown that the recombinant hepatitis B virus retains the ability for

helper-dependent packaging and reverse transcription despite the deletion of up to

80% of its genome (Horwich et al., 1990). This suggests that large portions of the genome may be replaced with foreign genetic material. The hepatotropism and

persistence (integration) were particularly attractive properties for liver-directed

gene transfer.

Liuand DNA

Most nonmammalian viruses are not infectious to mammalian cells;

however, it has been reported that in some cases, nonmammalian viruses will infect

certain particularly infection-susceptible mammalian cell lines. [Barsoum et al.,

Human Gene Therapy 8:2011-2018 (Nov. 20, 1997)]. Where the host cell to be

used for manufacturing the recombinant virus is not susceptible to infection by the

nonmammalian virus, the nonmammalian virus may be modified by incorporating

ligand DNA in the nonmammalian backbone. The nonmammalian backbone may

also be modified by incorporation of ligand DNA to increase infection of mammalian host cell by the nonmammalian virus. The expression of the ligand

DNA by the subsequently produced nonmammalian virus will permit infection or mcrease infection of mammalian cells The backbone of the carrier vector of the

present invention is modified by addition of DNA encoding components needed to

produce a ligand which is recognized by a desired mammalian cell

The ligand DNA is selected from genes which, when expressed, yield

a gene product that will be present on the surface of the encapsidated carrier vector,

thus presenting the ligand to the mammalian cell target receptors and allowing the

carrier vector to bind to and enter mammalian cells [Barsoum et al , Human Gene

Therapy 8 201 1-2018 (Nov 20, 1997) ] The ligand DNA is placed under the

regulatory control of expression regulatory sequences that insure that the ligand

gene product is expressed coordinately with the replicated DNA of the carrier

vector to allow efficient chimeric carrier vector production in nonmammalian host

cells The nonmammalian expression regulatory sequence may be identical, similar,

or distinct from the backbone's native regulatory sequences, so long as it is capable

of regulatory functions in the nonmammalian host cell In a preferred embodiment,

the expression regulatory sequences comprise a promoter derived from the native

nonmammalian virus from which the nonmammalian vector backbone is derived In

a more preferred embodiment, the promoter is polyhedπn early promoter (polH)

and the nonmammalian vector backbone is derived from baculovirus

In general, if a ligand DNA is regulated by nonmammalian

expression regulatory sequences, the ligand DNA will not be expressed when the

chimeric vector infects the mammalian host cell The absence of expression of the

ligand encoded by the DNA may be useful to prevent incorporation of ligand mto

the recombinant virus coat encoded from the carrier nonmammalian vector, which could disrupt its structural integrity or cause adverse immunogemc reactions in an animal However, if ligand expression is desired in the mammalian host cell, then

alternative or additional expression regulatory sequences may be operably linked to

the sequences encoding the ligand to permits its expression in mammalian and

nonmammalian host cells Alternatively, there may be some instances in which the

ligand DNA is expressed because the nonmammalian expression regulatory

sequences are also activated in the mammalian cells

The ligand DNA can be essentially any nucleic acid that encodes a

protein, polypeptide or peptide that modifies the mature nonmammalian virus to

enable it to bind to and enter mammalian cells The ligand can be naturally- occurring protein, a fragment of a naturally-occurring protein that has a desired

binding capability, or an artificial or mutated polypeptide or peptide that has a

desired binding capability The ligand can be one of general specificity, which

would allow binding to a wide variety of mammalian cells (e g , vesicular stomatitis

virus glycoprotem G (VSV-G) gene, bovine syncytial virus (BSV) envelope

glycoprotem gene, or amphotropic envelope gene as illustrated below), or it may be

more specific, allowing binding to targeted specific cell types For instance, the

ligand may cause the virus to bind via electrostatic interactions or other general

mechanism of interacting the mammalian cell, or it may be a specific ligand-receptor interaction

Useful ligand nucleic acids may be any nucleic acid which encodes a ligand that permits the nonmammalian virus to interact with the mammalian cell

For instance, the ligand may be one which increases the electrostatic interaction between the virus and the mammalian cell for a receptor found on the mammalian

host cells that are to be infected by the carrier virus Other useful ligand nucleic

acids include, without limitation, nucleic acids encoding peptide hormones, growth

factors, or other normally secreted factors for which the mammalian host cell of

interest expresses a receptor The nucleic acids useful as a ligand include all those

secreted factors, peptide hormones and growth factors which have a normal cellular

receptor and which are disclosed above for transgenes For instance, the ligand

nucleic acid may encode PDGF, EGF, bFGF, aFGF, insulin, IGF-I, IGF-II, apoE,

apoAl, apoA4, EPO, PTH, GH or GRF The ligand nucleic acid may encode a

native or genetically engineered immunoglobulin (e g , ScFv, chimeric immunoglobulin, humanized immunoglobulin, etc ) or MHC molecule that

specifically binds to a particular cell surface protein on the mammalian cell Other

ligand nucleic acids of interest encode a member of the extracellular matrix such as

a collagen, elastin, thrombospondin, tenascin or vitronectin, which bind to integrins

and other cellular transmembrane receptors The nucleic acid sequence encoding a

ligand which is normally secreted may be modified by incorporating a nucleic acid

sequence encoding an "anchoring domain" at either the 5' or 3' end of the coding

sequence for the ligand The anchoring domain is a region that secures the ligand in

the viral coat In a preferred embodiment, the anchoring domain is at the 3' end of

the coding sequence for the ligand In a further preferred embodiment, the

anchoring domain is derived from a viral coat protein, such as HIV gp41 (which

anchors gpl20 coat protein to the viral envelope) Other examples include E protein of dengue virus or the 14 kDa protein of vaccinia virus The ligand nucleic acid also may encode a protein that is normally

anchored in the cell membrane of a mammalian cell which binds to a particular cell

surface protein or counter-receptor on a mammalian host cell Examples of this

type of ligand nucleic acid include a number of the CD antigens, such as the T cell

receptor (TCR), CTLA-4 receptor and B-7, integrins such as Mac-1, LFA-1, and

pi 50,95, intercellular adhesion molecules such as ICAM-1, ICAM-2, ICAM-3 and

ICAM-4, and selectins, such as E-selectin, P-selectin and L-selectin The ligand may also be an artificial or mutated counter-receptor, such as a cell-surface

anchored or hybrid immunoglobulin or TCR.

In one embodiment, the ligand is one that is normally present on a

virus and which mediates binding to a mammalian cell, for example, gpl20 of HIV

or HA from influenza In another embodiment, the ligand is one that is normally

present on a bacterial cell and which mediates binding to a mammalian cell, for example, Protein A from Staphylococcus aureus is known to bind to

immunoglobulins.

In another embodiment, the mammalian host cell is genetically

engineered to express a receptor which specifically binds to a ligand. Thus, one can

design mammalian host cell-carrier virus systems that promote highly specific

binding of the carrier virus to the mammalian host cell. For example, one may

engineer a mammalian host cell line to express a growth factor receptor, such as the

EPO receptor, and design the carrier vector to comprise a ligand nucleic acid

comprising the EPO gene. One of skill in the art, in light of the instant specification, would be able to identify a large number of mammalian host cell- carrier virus interactive receptor-ligand systems.

In one embodiment the ligand DNA is the VSV-G gene This gene may be placed under the control of the baculovirus polyhedrin (pPH) early

promoter The VSV-G protein, when expressed, modifies the mature carrier virus

such that it may bind to mammalian host cells and thereby infect them [Barsoum,

supra] In another embodiment of the present invention, the ligand DNA is the

BSV env gene, which functions in the context of the invention in a similar manner.

In another preferred embodiment, the present invention exploits the

fact that nonmammalian viruses normally do not terminate glycoproteins with sialic

acid Thus, the ligand DNA is a gene which expresses an asialoglycoprotein, which

binds to mammalian lectins (e.g., the hepatic asialoglycoprotein receptor), which

would then facilitate entry into the mammalian cell

Replication and Encapsidation Nucleic Acids

The replication and encapsidation functions are required for

replication, excision and encapsidation of the recombinant viral genome into an

infectious recombinant virion or virus. Each type of recombinant virus will require

a different type of replication and encapsidation function. For instance, if the

recombinant virus is a retrovirus, then the replication and encapsidation functions

include the retroviral gag, pol and env genes (and in the case of lentiviruses will also include regulatory or accessory genes such as HIV tat, rev, nef, vpu or vpr), while if the recombinant virus is an AAV, then the replication and encapsidation functions include the rep and cap genes from an AAV. As discussed above, either the carrier vector or the mammalian host cell may comprise nucleic acids encoding those replication and encapsidation

functions required for a particular recombinant virus. Mammalian host cells such as

A64 cell line described in U.S. Pat. No. 5,658,785 and the B50 cell line described in

PCT US98/19463) express AAV rep and cap genes for replication and packaging

of recombinant AAV. Similarly, mammalian host cells expressing adenoviral genes

required for replication and packaging of recombinant adenovirus are known [see,

e.g., U.S. Pat. No. 5,851,806 and Amaltifano et al., Proc. Natl. Acad. Sci. USA

93 :3352-6 (1996)] or may be constructed, and a number of mammalian host cells expressing retroviral genes required for replication and packaging of recombinant

retroviruses have been constructed [see, e.g., Cone et al., Proc. Natl. Acad. Sci.

USA 81 :6349-6353 (1984); Miller et al., Mol. Cell. Biol. 6:2895-2902 (1986); Miller et al, Mol. Cell. Biol. 5:431-437 (1985); and Sorge et al., Mol. Cell. Biol.

4: 1730-1737 (1984)]. Cell lines comprising genes required for packaging of

herpesviruses (see, e.g., U.S. Pat. No. 5,851,826) are also known.

If a cell line comprises all the necessary replication and encapsidation

functions to replicate, excise and package a particular recombinant viral genome,

then the carrier vector need not comprise any replication and/or encapsidation

nucleic acid sequences. The cell line may comprise the necessary replication and

encapsidation functions either by being transiently or stably transduced with the

nucleic acid encoding the appropriate proteins. In a preferred embodiment, the cell

line stably comprises the replication and encapsidation functions. Furthermore, the

cell line may express the replication and encapsidation functions constitutively or inducibly Constitutive or inducible expression may be controlled by using any of

the expression regulatory sequences known in the art or as discussed above under

"Expression Regulatory Sequences." In a preferred embodiment, the expression of

the replication and encapsidation functions is inducible. In a more preferred

embodiment, the replication and encapsidation functions are stably transfected or

infected and are inducibly expressed In an even more preferred embodiment, the

expression of the replication and encapsidation functions is regulated by their native

promoters

A mammalian cell line used in the instant invention may comprise none of the functions required for replication or encapsidation, or may comprise

only a part of the functions required for replication or encapsidation If a

mammalian cell line comprises none of the functions required for replication or

encapsidation, these functions must be introduced into the cell by a vector for production of the recombinant virus. In a preferred embodiment, one or more

carrier viruses of the instant invention are used to transduce the mammalian cell line

with the nucleic acids encoding the replication and encapsidation functions. In a

more preferred embodiment, a single carrier virus comprising the replication and

encapsidation functions are used to transduce the mammalian cell line In an even

encapsidation functions, the embedded recombinant viral genome, and any other

nucleic acid sequences required for recombinant virus production are used to transduce the mammalian cell line.

If the mammalian cell line comprises some of the replication or encapsidation functions, these functions must be introduced into the cell by a vector

for production of the recombinant virus. In a preferred embodiment, one or more

carrier viruses are used to transduce the mammalian cell line with the nucleic acids

encoding the missing replication and encapsidation functions. In a more preferred

embodiment, a single carrier virus comprising the missing replication and

encapsidation functions are used to transduce the mammalian cell line. In an even more preferred embodiment, a single carrier virus comprising the missing replication

and encapsidation functions, the embedded recombinant viral genome, and any

other nucleic acid sequences required for recombinant virus production are used to

transduce the mammalian cell line.

The replication and encapsidation functions required for a

recombinant virus differ depending upon the type of recombinant virus. In general, the required replication and encapsidation functions are known in the art for the

various recombinant viruses. In preferred embodiment of recombinant vectors,

recombinant AAV requires rep and cap for replication and encapsidation,

recombinant retroviruses require gag,pol and env (and tat, rev and nef Tor

lentiviruses), recombinant adenoviruses require all of part of the functions encoded

by El, E2, E4, L1-L5, pIX and IVa2 genes, alone or in combination, and

recombinant herpesviruses require a large number of genes, which may be provided

by a helper herpesvirus or by a carrier vector comprising the required herpesvirus

genes. Together the host mammalian cell and the carrier virus must contribute the necessary replication and encapsidation functions for the particular recombinant virus in order to obtain infectious recombinant virus from the mammalian host cells. In one embodiment, the replication and encapsidation functions are encoded by nucleic acids encoding the naturally-occurring proteins having the

replication and encapsidation functions In another embodiment, the replication and

encapsidation functions are encoded by nucleic acids encoding fragments or mutems

of the naturally-occurring proteins but which retain their respective replication and

encapsidation functions In another embodiment of the invention, other

recombinant viruses may be produced using nucleic acids encoding the appropriate

replication and encapsidation functions for the particular recombinant virus desired

Other types of recombinant viruses and the replication and encapsidation functions they require are known in the art

In a preferred embodiment, when production of a recombinant AAV

is desired, the rep and cap sequences are regulated by a native AAV p5 promoter

In another preferred embodiment, when production of a recombinant adenovirus is

desired, the nucleic acid sequences encoding the replication and encapsidation

functions for adenovirus are regulated by their native adenovirus promoters Native promoters may also be used for regulating the expression of replication and

encapsidation functions of other recombinant viruses, including, without limitation,

herpesvirus and HBV

In a more preferred embodiment, the replication and encapsidation

functions are encoded by nucleic acid sequences inserted in the carrier vector The advantage of having these sequences on the carrier vector is that no cell line has to

be constructed before infection by the carrier virus It is often difficult to create and

maintain cell lines expressing replication and encapsidation functions because many of the proteins that provide these functions are toxic to mammalian cells. Thus,

another advantage of inserting the replication and encapsidation sequences on the

carrier vector is that the replication and encapsidation functions are only expressed

in the mammalian cells when the cells are infected with the carrier virus when the

production of a recombinant virus is desired. In a more preferred embodiment, the

carrier virus has an embedded recombinant viral genome comprising a transgene

and the ITRs from AAV and further has rep and cap gene sequences for replication

and encapsidation of the embedded recombinant AAV genome. In an even more

preferred embodiment, the expression of the rep and cap genes is regulated by their

native promoters or rep/cap is separated from the promoter to decrease or eliminate

homologous or non-homologous recombination to form wt AAV. Similarly, in a

preferred embodiment of carrier viruses that produce recombinant retrovirus,

adenovirus, herpesvirus and HBV, the carrier viruses contain nucleic acid sequences that encode replication and encapsidation functions. In a more preferred

embodiment, the nucleic acid sequences encoding the replication and encapsidation

functions are regulated by their native promoters.

Helper Functions

A number of viruses are unable to replicate, excise and package on their own, and require helper functions to do so. Helper functions may also be

required for the production of recombinant viruses which have had a large amount

of their genome deleted for insertion of the transgene. The nature of the helper function may differ depending upon the type of recombinant virus and/or the amount of genome that has been deleted. Helper functions include viral proteins,

non-viral proteins, as well as physical and/or chemical agents. One may identify which helper functions are required from what is known in the art. For instance, it

is known that AAV requires helper functions from adenovirus or herpesvirus or

from different chemical or physical agents. Alternatively, one of skill in the art may

determine what helper functions are required by producing recombinant viruses

using the composition and methods disclosed in the instant specification

To identify which helper functions are required for high levels of recombinant virus production, one may infect mammalian host cells with the carrier

virus in the absence of helper functions and measure the titer of infectious

recombinant virus One may then transduce the mammalian host cells with various

nucleic acids encoding potential helper functions. Such helper functions may be any nucleic acid that is known or thought to encode a helper function. In a preferred

embodiment, the helper function is one or more viral proteins. In a more preferred

embodiment, the helper virus proteins are insufficient to produce a mature helper

virus After transducing the mammalian host cell with the nucleic acid encoding the

potential helper function, one may then measure the titer of the recombinant virus.

If the carrier virus comprises a recombinant AAV genome, helper

functions are required for production of infectious recombinant AAV In a

preferred embodiment, the helper functions are nucleic acids derived from a virus

In a more preferred embodiment, the helper functions are derived from adenovirus,

herpes simplex virus (HSV) HSV-1, HSV-2, cytomegalovirus (CMV) or pseudorabies virus (PRV). In an even more preferred embodiment, the helper functions are at least El a, Elb and E2a from adenovirus, and may also include E4ORF6 and VAI In another preferred embodiment, the nucleic acid encodes the

helper functions from the helicase-primase complex of HSV (UL5, UL8 and UL52)

and the major single-stranded DNA binding protein of HSV (UL29) The helper

functions may also include all 7 HSV DNA replication genes (UL5, 8, 52, 29, 30, 9

and 42) Alternatively, helper functions for recombinant AAV may be provided by chemical or physical agents, including ultraviolet light, cycloheximide, hydroxyurea

and various carcinogens.

The required helper functions for production of a recombinant virus

may be delivered to the mammalian host cell by any method known in art The

helper functions may be delivered by transfection with a vector, such as a plasmid, by infection with a viral vector comprising the helper functions, or by any other

method known in the art, including those discussed above (e.g., biolistic injection of

DNA, use of DNA conjugates, etc.). The transfection or infection may be stable or

transient Alternatively, the mammalian cell line may stably express (either on an

extrachromosomal episome or through integration in the cell's genome) the helper functions In addition, some of the helper functions may be expressed by the

mammalian cell line while other helper functions are introduced by a vector. For

example, 293 cells (ATCC CRL-1573) constitutively produce adenoviral El a and

Elb proteins. Thus, for production of recombinant AAV, the helper functions required for the production of infectious recombinant AAV, such as E2A, E4ORF6 and VAI, are introduced into the host cell by transfection or infection of a vector.

In a preferred embodiment, the helper functions are transduced into the mammalian cells by a carrier virus. In a more preferred embodiment, some or all of the helper functions are transduced into the mammalian cell by a carrier virus

comprising the embedded recombinant viral genome. In an even more preferred

embodiment, all of the helper functions are transduced into the mammalian cell by a carrier virus comprising the embedded recombinant viral genome, any required

replication and encapsidation functions, and, optionally, a ligand DNA. In the most

preferred embodiment, the carrier vector has a baculovirus backbone. An internal

ribosome entry site (IRES) sequence may be placed between E2A and E4orf6 if

only a single promoter is to be used for these two proteins. Alternatively, each

helper function gene may be supplied with its own promoter. These genes may be

under the regulatory control of a variety of promoters, constitutive or inducible,

such as the CMV immediate-early promoter/enhancer or the MMTV LTR,

respectively. Whether the helper functions are provided on the carrier vector itself

or are provided by the host cells, the promoters regulating those genes may be constitutive or inducible.

The expression of the helper functions may be regulated by any of

the expression regulatory sequences known in the art or as described above,

including cis or trans regulation. The expression regulatory sequences may provide

for constitutive expression, inducible expression, tissue-, cell type- or differentiation

state-specific expression, or expression from the helper function protein's native

promoter. In a preferred embodiment, the native promoter of the helper function

protein is used. In another preferred embodiment, an inducible promoter of a helper

function protein is used. In another preferred embodiment, a constitutive promoter of a helper function protein is used. In a further preferred embodiment, the

constitutive promoter is the CMV promoter. In another preferred embodiment, one

or more constitutive promoters are used for certain helper function proteins, and one or more native promoters are used for other helper function proteins.

In one embodiment, each protein or polypeptide required for helper

function is encoded by a nucleic acid whose expression is regulated by its own

promoter and polyadenylation signal, as well as optional sequences such as

enhancers. In another embodiment, a nucleic acid is transcribed to a single

transcript that encodes more than one protein or polypeptide required for helper

function. In this case, an IRES may be placed between the coding sequences of

each of the individual proteins or polypeptide to permit subsequent translation of

the polycistronic mRNA. If only a single polycistronic transcript is produced, only a single promoter, optional enhancer, and polyadenylation signal are required for

regulation of the transcription of the nucleic acid encoding the helper function. One

may also encode the helper function by using both monocistronic mRNAs that

encode single proteins and polycistronic mRNAs encoding multiple proteins.

In a preferred embodiment of the instant invention, the carrier vector

comprises a embedded recombinant AAV genome and helper functions. In a

further preferred embodiment, the helper functions comprise adenovirus El a, Elb

and E2a, and more preferably include E4ORF6 and VAI. In an even more preferred

embodiment, the helper functions are encoded by a single polycistronic transcript, and the promoter for the helper functions is a constitutive promoter, preferably the CMV promoter. Other recombinant viruses would require different helper functions

or none at all, but in all cases those helper functions may be provided on the carrier

vector that carries the embedded recombinant viral genome, on a separate carrier

virus, on a different type of vector capable of transducing a mammalian host cell, or

is endogenously expressed in the mammalian host cell itself.

Mammalian Host Cells

Any type of mammalian host cell which can be adapted to cell

culture may be used to produce the recombinant viral genome. In general, a

mammalian host cell used in this invention is one that may be infected by a

nonmammalian carrier virus. The mammalian host cell may be one that may be

infected by a nonmammalian carrier virus that does not express a ligand encoded by a ligand nucleic acid, may be one that may be infected by a nonmammalian carrier

virus that expresses a ligand encoded by a ligand nucleic acid, or may be a cell that

is infected by a carrier vector that either expresses or does not express a ligand

nucleic acid. Alternatively, the mammalian host cell may be one that is not usually

infected by a carrier virus, but which can be transduced with a cellular receptor such

that it may bind to a nonmammalian host cell. For instance, a mammalian host cell

may be transduced with a growth factor receptor such that it can be infected by a

carrier virus that expresses the particular growth factor as its ligand.

In addition to the ability to be infected by the carrier virus, another preferred characteristic of the mammalian host cell is that it is able to uncoat the

nonmammalian carrier virus. A third preferred characteristic of the mammalian host cell is its ability to replicate the recombinant virus at high levels. In a preferred

embodiment, the mammalian host cell is one that takes up the nonmammalian

carrier virus at high levels, uncoats the carrier virus efficiently, and replicates the

recombinant virus at high levels.

Appropriate mammalian host cells include, without limitation, CHO,

BHK, MDCK and various murine cells, e.g., 10T1/2 and WEHI cells, African green

monkey cells such as COS 1, COS 7, BSC 1, BSC 40, and BMT 10, and human

cells such as VERO, WI38, MRC5, A549, and HT1080 cells. In a preferred

embodiment, appropriate mammalian cell include 293 cells (human embryonic

kidney cells which express adenoviral Ela and Elb proteins), B-50 cells (HeLa cells

which express AAV rep and cap, see PCT US98/19463), 3T3 cells (mouse

embryonic fibroblast cell line), NIH3T3 cells (subline of 3T3 cells), HepG2 cells

(human liver carcinoma cell line), Saos-2 cells (human osteogenic sarcoma cell line),

HuH7 cells or HeLa cells (human carcinoma cell line).

In addition to the mammalian host cells listed above, other mammalian host cells may be used. One may determine whether a cell line would

be suited for use as a mammalian host cell by infecting the cell line with a carrier

virus containing all the required components to produce a recombinant virus,

culturing the cells under conditions in which recombinant virus is produced, and then measuring the titer of infectious recombinant virus that is produced. One may

then compare the titer of infectious virus produced in the potential host cell with the

titers produced by other host cells to determine whether the cell line is good for recombinant virus production. Although the receptor(s) for nonmammalian carrier virus such as

baculovirus on both insect and mammalian cell is/are unknown, it is thought that the

baculovirus may bind to the cell, at least in part, via heparan sulfate expressed on

the cell surface. Without wishing to be bound by any theory, cells which express

high levels of heparan sulfate on their cell surface may be more easily infected by

carrier viruses, especially baculovirus, than cells which express low levels of

heparan sulfate on their cell surface. Thus, one method of identifying whether a

particular cell line is a potential mammalian host cell is to measure the level of

heparan sulfate on the cell surface.

Method of Making and Producing Carrier Viruses

The present invention includes methods of constructing the novel

carrier vectors described above and producing large quantities of the carrier vector.

This method comprises the steps of:

1. Modifying a nonmammalian virus backbone DNA, or a

replication-proficient portion thereof, by inserting one or more nucleic acid inserts

comprising 1 ) a recombinant viral genome comprising a transgene operably linked

to expression regulatory sequences and flanked by flanking elements; 2) nucleic acid

sequences encoding helper functions operably linked to expression regulatory

sequences; 3) nucleic acid sequences encoding replication and/or encapsidation

functions for the recombinant virus; 4) a ligand DNA operably linked to expression

regulatory sequences that are active in nonmammalian cells; and 5) regulatory

control sequences that regulate sequences in the nonmammalian virus backbone, a odified nonmammalian virus backbone or a replication-proficient portion of the

backbone or modified backbone;

2 transducing the resulting carrier vector into nonmammalian host

cells, 3 growing the nonmammalian host cells under conditions in which

carrier virus is produced; and

4 collecting the carrier virus from the nonmammalian host cells

In a preferred embodiment, the carrier vector will be modified such

that it comprises the recombinant viral genome. In a more preferred embodiment,

the carrier vector will be modified such that it comprises the recombinant viral

genome and either or both of the nucleic acid inserts encoding the replication and/or

encapsidation functions and the helper functions required for production of a

recombinant virus In an even more preferred embodiment, the carrier vector will

be modified such that it comprises the recombinant viral genome, all of the nucleic

acid inserts encoding the replication and/or encapsidation functions and the helper

functions required for production of a recombinant virus, and the nucleic acid insert

encoding the ligand

The nonmammalian host cell may be any host cell known in the art

or described in Table 1 of U.S. Pat. No. 5,731,182. The nonmammalian virus

backbone DNA may be derived from any virus that infects nonmammalian species,

including those known in the art or described in Table 1 of U.S. Pat. No. 5,731,182

In a preferred embodiment, the nonmammalian backbone of the carrier vector is

derived from a baculovirus and the nonmammalian host cells are insect cells. In a more preferred embodiment, the carrier virus produced by the baculoviral carrier

virus in the insect cells is produced at a high titer Preferably, when baculovirus is used, the titers of the carrier baculovirus produced in any embodiment are greater

than 10⁸ pfu/ml in insect cells or IO⁹ pfu/ml, more preferably, the titers are greater

than 10¹⁰ pfu/ml or 10¹¹ pfu/ml, and even more preferably, the titers are greater than

10'² pfu/ml The instant invention also encompasses lysates and supernatants of

nonmammalian host cells comprising baculoviral carrier viruses having similar titers

The nonmammalian host cells comprising the carrier vector may be

grown by any method known in the art or as described herein Methods for

producing large amounts of nonmammalian viruses are well known in the art and are described in U S Pat No 5,871,986 The nonmammalian earner virus may be

purified from the supernatant produced by the nonmammalian host cells or from

lysed cells by any method known in the art or as described herein Methods for

collecting and purifying nonmammahan viruses are well known in the art and are

described in U S Pat No 5,871,986 A method of collecting and purifying the

nonmammalian viruses is described in Example 6

The carrier virus produced when the carrier vector is encapsidated

has the normal wild-type capsid optionally modified by addition of the ligand In

general, the expression of the ligand nucleic acid is regulated by expression

regulatory sequences which promote transcription and translation in the

nonmammahan host cells Such expression regulatory sequences may include a nonmammalian promoter active in the nonmammahan host cells of interest, and may

optionally include enhancer sequences, polyadenylation signals, or any other expression regulatory sequences known in the art or described above In a

preferred embodiment, the other nucleic acid inserts in the nonmammahan backbone

may not be expressed or may be expressed at lower levels because their promoters

are inactive or less active in nonmammahan cells Because potentially toxic viral components, such as helper functions or rephcation encapsidation functions, are

either not expressed or expressed at lower levels, a high titer of carrier virus may be

produced in nonmammahan cells

Methods of Producing Recombinant Virus from the Carrier Vector

Another aspect of the instant invention is a method of producing

recombinant virus by using a carrier virus, produced by the method described

above, to infect mammalian cells and subsequently collecting and purifying the

recombinant virus from the mammalian cells The method comprises the steps of

1 Infecting mammalian host cells with a carrier virus, wherein he carrier virus optionally expresses a ligand on the surface of the carrier virus,

2 growing the infected mammalian host cells under conditions in

which the embedded recombinant viral genome is replicated, excised and

encapsidated, and

3 collecting the recombinant virus from the mammalian host cells

The mammalian host cells may be any mammalian host cell known in the art, described in the specification above under "Mammalian Host Cells," or

identified by the method descnbed under "Mammalian Host Cells" as an appropriate

host cell The mammalian host cell, prior to infection, may be one that expresses one or more of the following: 1) replication and/or encapsidation functions (e.g., B-

50 cells or one of the retroviral cell lines described previously); 2) some or all necessary helper functions (e.g., 293 cells); and/or 3) an embedded recombinant

viral genome stably integrated in the mammalian host cell genome. Alternatively,

the mammalian host cell comprises none of these other elements before infection by

the carrier virus.

The mammalian host cells may be infected and grown by any method

known in the art or as described herein. Methods for infecting mammalian host

cells with nonmammalian viruses are described herein and in Barsoum et al., supra.

Once the mammalian host cell has been infected, the expression regulatory

sequences that are operably linked to any required replication and/or encapsidation

functions and helper functions are activated. Expression of the replication and/or encapsidation functions and helper functions, along with the mammalian host cell's

native transcriptional and translational components, permits replication, excision

and encapsidation of the embedded recombinant viral genome, thereby causing the

manufacture of the recombinant virus.

In general, the nonmammalian carrier virus is capable of infecting a mammalian cell, but the carrier virus will not replicate in the mammalian cell

because the components required for replication of the nonmammalian carrier virus

are not present in the mammalian cell. If the carrier virus comprises a ligand nucleic

acid, the expression regulatory sequences controlling ligand expression generally will not function in mammalian cells, such that ligand expression does not occur in

the mammalian host cell. However, if replication of the carrier virus or if expression of the ligand is desired in the mammalian host cell, then additional expression regulatory sequences may be operably linked to the sequences required for replication, excision and/or packaging of the nonmammalian carrier virus and/or

expression of the ligand.

The recombinant virus may be purified from the supernatant

produced by the mammalian host cells or from lysed cells by any method known in

the art or as described herein. Methods for collecting and purifying various types of

recombinant viruses from mammalian host cells are well known in the art and are

described in PCT US97/15716. A method of collecting and purifying the

recombinant viruses is also described in Example 6.

As discussed above, in a preferred embodiment, one or more carrier

viruses comprises all those nucleic acid inserts required for production of recombinant virus in a particular mammalian host cell. Thus, if the host cell

comprises replication and encapsidation functions, then the carrier viruses comprise

the embedded recombinant viral genome and any necessary helper functions.

Similarly, if the host cell comprises the embedded recombinant viral genome, then one or more carrier viruses will comprise the required replication and encapsidation

functions and any necessary helper functions, while if the host cell comprises the

necessary helper functions, then one or more carrier viruses will comprise the

required replication and encapsidation functions and the embedded recombinant viral genome.

In a preferred embodiment, a single carrier virus comprises all of the nucleic acid inserts required for production of a recombinant virus in a particular mammalian host cell. For example, if a recombinant AAV is to be produced in B-

50 cells, the carrier virus will comprise the embedded recombinant viral genome and

those helper functions required for AAV production. Similarly, if a recombinant

AAV is to be produced in a mammalian host cell that does not express any of the

required functions for AAV production, the carrier virus will comprise the

embedded recombinant viral genome, the replication and encapsidation functions

and the helper functions required for AAV production.

The method of producing recombinant virus described is useful

because it produces an essentially homogeneous recombinant virus that is free from helper virus and wild-type virus without purification. The recombinant virus is free

from helper virus because there are insufficient helper virus genes to produce a

mature helper virus. The recombinant virus is free of wild-type virus because

homologous recombination is avoided by a variety of techniques. For instance,

wild-type AAV produced through homologous recombination may be avoided using

several strategies. The rep/cap sequences and the embedded recombinant viral

genome may be positioned at separate loci on the carrier vector, minimizing the

likelihood of a recombination event. The rep/cap sequences and the embedded

recombinant viral genome also may be designed so that they have no regions of

homology. Additionally, because AAV is intolerant of packaging greater than 5.0

kb, one may incorporate a "stuffer" nucleic acid sequence to be inserted between a required sequence, such as rep or cap and its promoter. Thus, even if

recombination took place, the resulting AAV genome would be too large to

package and no wtAAV would be produced. In order to maintain the integrity of translation of rep, the stuffer sequence may be constructed using splice donor and

acceptor sites, such that the resulting mRNA and ultimately the rep protein

produced would be unaffected. Similar methods may be employed for other types

of recombinant viruses to avoid recombination and production of wild-type virus. The method is also easily scaled to industrial production because it

may require only a single infection of mammalian host cells by a carrier virus that

can be produced in large amounts at high titers. In a preferred embodiment, the

recombinant virus produced by the instantly described method is produced at a high

titer. For recombinant AAV, the titer is preferably greater than IO⁴ particles per producing cell, more preferably, greater than 10⁵ to IO⁶ particles per producing cell,

and even more preferably, greater than IO⁷ particles per producing cell. For

recombinant adenovirus, the titer is preferably greater than IO⁴ particles per producing cell, more preferably, greater than 10⁵ particles per producing cell, and

even more preferably, greater than IO⁶ particles per producing cell. For recombinant herpesvirus, the titer preferably is greater than 10¹⁰ pfu per ml, more

preferably, greater than 10¹¹ pfu per ml and even more preferably, greater than IO¹³

pfu per ml. For retroviruses, the titer preferably is greater than IO⁶ to IO⁷ colony

forming units (cfu) per ml, more preferably, 10⁸ cfu per ml, and even more

preferably, 10⁹ cfu per ml. The instant invention also encompasses lysates and

supernatants of mammalian host cells comprising recombinant viruses. These

lysates and supernatants differ from those produced by prior art methods because

they do not contain wild-type virus or helper virus.

In a preferred embodiment, the method is used to manufacture recombinant AAV at high titers and in the absence of helper virus or wild-type

AAV The desired transgene, with appropriate expression regulatory sequences

operably linked thereto, is placed between the AAV ITRs, by means known in the

art In order to maintain the length of the insert at a length compatible with

eventual packaging, spacer DNA may optionally be inserted therein This

recombinant viral genome is then embedded in a baculovirus, in a non-essential

locus by means known in the art The required helper functions, replication and

encapsidation functions, and/or embedded recombinant viral genome may be placed

in the polyhedrin gene site, the plO gene site, or one could be placed at the

polyhedrin gene site and the other may be placed at the plO gene site (see Figure 1)

The baculovirus backbone also may be modified to comprise a ligand nucleic acid,

such as the VSV-G gene The baculovirus may also be modified to comprise rep and cap sequences and helper functions from adenovirus, comprising Ela, Elb,

E2a, E4ORF6 and VAI, or HSV genes UL5, UL8, UL52 and UL29 The carrier

vector is transduced into insect cells, such as Sf9 cells, the cells are grown under

conditions in which baculovirus is produced, and the baculovirus is collected and

purified The baculovirus is then used to infect mammalian cells, the mammahan

cells are grown under conditions in which the recombinant virus is replicated,

excised and encapsidated, and the recombinant AAV is collected and, optionally,

purified

In another preferred embodiment, the method is used to manufacture recombinant "gutless" adenovirus deleted of all adenoviral genes at high titers and

in the absence of helper virus or wild-type adenovirus Previously, one would make a "gutted" adenovirus plasmid from the adenovirus genome in which all of the

adenovirus genes were removed except for the ITRs and the cis-acting packaging

signal Foreign DNA containing the transgene of interest, transcriptional regulatory

sequences, and, optionally, stuffer DNA would be added to obtain an insert of

approximately 36 kb The plasmid is designed such that a DNA cassette contains

the packaging signal upstream of the transgene and stuffer DNA, and the Ad ITRs

flank such DNA cassette. The plasmid was transfected into cells, such as 293 cells

A helper adenovirus lacking the adenoviral El and E3 genes, as well as sequences

within the adenoviral packaging signal was used to infect the 293 cells transfected

with the gutted Ad plasmid to provide replication and encapsidation functions in

trans Using this method, low levels of homologous recombination would rescue

the deletion in the helper Ad's packaging signal, thus both helper and "gutless"

adenovirus would be produced. CsCl gradients would have to be performed to

separate the helper adenovirus from the recombinant "gutless" adenovirus vector. In addition, other disadvantages included high levels of contaminating helper virus

and low yields of the gutless Ad vector.

Using the method of the instant invention, homologous

recombination resulting in generation of contaminating helper Ad can be avoided

Rather than using helper adenovirus, one may construct a carrier vector comprising

the adenoviral functions necessary for replication and packaging of the gutted Ad

genome. In one embodiment, the carrier vector contains the complete genome of

adenovirus without the ITR's, El, the packaging signal, and, optionally, without

E3 Then, one may infect mammalian cells with the carrier virus and transfect the cells with the plasmid described above containing the transgene, ITRs and packaging signal In another embodiment, one may construct two separate carrier

vectors, one comprising helper adenoviral functions described above and the other comprising the gutted Ad construct containing the Ad ITR's, packaging signal and

the transgene cassette Alternatively, one may construct a single carrier vector comprising both the helper adenoviral functions and the transgene cassette

comprising the ITRs, packaging signal and transgene/stuffer DNA The adenoviral

functions and transgene cassette may be placed in the polyhedrin gene locus, the

p 10 gene locus, or one could be placed at the polyhedrin gene locus and the other may be placed at the pi 0 gene locus (see Figure 1).

In another preferred embodiment, the method is used to manufacture

recombinant herpesvirus amplicon vectors As discussed above, herpesvirus

amplicons require the "α" sequence for packaging, and the HSV origin of

replication Either the ori_s or ori_L origin of replication may be used, but the ori_s

origin is preferred One may construct a carrier vector comprising a herpesvirus

amplicon In one embodiment, the cassette would contain, in the 5' to 3' direction,

the "α" sequence, followed by the transgene of interest, followed by the HSV origin

of replication, followed by an optional spacer, and followed by another "a"

sequence This may be inserted into either the polyhedrin or the plO gene loci in

baculovirus, for instance. The carrier virus that is subsequently produced may be

used to infect mammalian cells that have been coinfected with helper herpesvirus.

Alternatively, the helper herpesvirus functions may be placed on the same or a

separate carrier vector and used to infect the mammalian cells. Recombinant herpesvirus amplicon vectors may then be isolated and purified from the mammalian

cells

Recombinant Virus Compositions

Another embodiment of the present invention is the recombinant

virus produced by the methods of the invention Unlike other preparations of

recombinant virus, the preparations produced by the methods of this invention yield

high titers of essentially homogeneous recombinant virus which is helper-free and

wild-type virus free The recombinant virus may be formulated as a

pharmacological composition for use for any form of transient and stable gene

transfer in vivo and in vitro The recombinant virus may be used for in vivo and ex

vivo gene therapy, genetic immunization, in vitro protein production and diagnostic

assays

For gene therapy, the recombinant virus may be introduced into cells

ex vivo or in vivo Where the virus is introduced into a cell ex vivo, the

recombinant virus may be used to infect a cell in vitro, and then the cell may

subsequently be introduced into a mammal (e g., into the portal vein or into the

spleen), if desired Alternatively, the recombinant virus may be administered to a

mammal directly, e g , intravenously or intraperitoneally. A slow-release device,

such as an implantable pump, may be used to facilitate delivery of the virus to a cell

Where the virus is administered to a mammal, the specific cells to be infected may

be targeted by controlling the method of delivery For example, intravascular

administration of the recombinant virus to the portal vein or to the hepatic artery may be used to facilitate targeting the recombinant virus to a liver cell.

The recombinant virus produced by the above-described method

may be administered to a patient, preferably suspended in a biologically compatible

solution or pharmaceutically acceptable delivery vehicle. A suitable vehicle includes

sterile saline. Other aqueous and non-aqueous sterile suspensions known to be pharmaceutically acceptable carrier and well known to those of skill in the art may

be employed for this purpose.

The recombinant virus is administered in sufficient amounts to infect

the desired cells and provide sufficient levels of transduction and expression of the

selected transgene (or viral gene products in the case of a vaccine) to provide a

corrective effect without undue adverse or with medically acceptable physiological

effects, which can be determined by those skilled in the medical arts. Conventional

and pharmaceutically acceptable routes of administration include direct

administration to the target organ, tissue or site; intranasal; intravenous;

intramuscular; subcutaneous; intradermal; oral and other parenteral routes of

administration. Routes of administration may be combined, if desired.

Dosages of the recombinant virus will depend primarily on factors

such as the type of recombinant virus (i.e., whether the virus is AAV, adenovirus,

retrovirus, etc.), the condition being treated and the selected gene. The dosage may

also vary depending upon the age, weight and health of the patient. For example,

an effective human dosage of a recombinant adenovirus is generally in the range of from about 0.5 ml to 50 ml of saline solution containing adenovirus at

concentrations of 1 x 10⁷ or 1 x 10⁸ or 1 x IO⁹ or 1 x 10¹⁰ or 1 x IO¹¹ or 1 x IO¹² or 1 x I O¹³ or 1 x 10^!4 or 1 x IO¹⁵ particles per dose administered. The dosage will be

adjusted to balance the corrective benefits against any adverse side effects. The

levels of expression of the selected gene may be monitored to determine the type

and frequency of dosage administration.

The following examples of the present inventions are illustrative

only, and are not intended to limit the scope of the invention.

EXAMPLE 1 Cell Line Maintenance and Virus Propagation

The human embryonic kidney cell line 293 (ATCC CRL 1573) was

maintained in Dulbecco's Modification of Eagle's Medium (DMEM; GIBCO BRL)

supplemented with 10% FBS (Hyclone) and 50 μg of penicillin, 50 μg of

streptomycin, and 10 μg of neomycin/ml (GIBCO BRL). Insect cell line IPLB-Sf21

(CLONTECH Laboratories, Inc.) was maintained in SF900-II medium (GIBCO

BRL) supplemented with 10% FBS and 50 μg of penicillin, 50 μg of streptomycin,

and 10 μg of neomycin/ml. Human adenovirus type 5 (ATCC VR-5) was

propagated on 293 cells and purified through CsCl gradient centrifugation (Jones

and Shenk, 1978).

EXAMPLE 2 Recombinant Plasmid Construction

Standard DNA recombinant techniques were employed to create

recombinant plasmids (Sambrook et al, 1989). The Rep and Cap sequence of pAV2 (ATCC 37216) between the Drain site upstream of the p5 promoter and the Ncol

site downstream of the polyadenylation signal was removed The Rep and Cap

sequence was replaced through multiple cloning steps with a cassette containing

GFP under the control of elongation factor 1 alpha (EFlα) promoter to create

pAV2cisEFGFP (Fig 2) The entire cassette containing both AAV ITRs and the

GFP gene was then cloned into the Spel and Bglll sites of BV-CZPG (baculovirus

shuttle plasmid with VSV-G gene under control of polyhedrin promoter, kindly

provided by Dr Jim Barsoum of Biogen, Ine ) through multiple cloning steps to

obtain pBV-cisEFGFP (Fig 3)

Adenovirus helper genes E2A, E4ORF6, and VAI were subcloned

from Ad5 DNA Briefly, E4ORF6 was first inserted into the Smal and Xbal sites of

pIRESlneo (CLONTECH Laboratories, Ine ) to obtain pIRESORFό Next, a

Sau3AI-BsrGI fragment containing E2A coding sequences was inserted into the BamHI/BstXI sites of the plasmid pIRESORF6 through multiple cloning steps to

obtain the plasmid pE2 A ORF6 In this construct, E2A and E4ORF6 genes are

separated by an encephalomyocarditis virus (ECMV)-derived IRES, and both genes

are under the transcriptional control of a single human cytomegalovirus (CMV)

promoter upstream of the E2A gene Next, a NcoI-BamHJ fragment of Ad5 DNA

containing the VAI gene was inserted into the Xhol site of pE2AiORF6 through

blunt-end cloning to obtain pE2AiORF6-VAI The entire cassette containing

CMV-E2AORF6-VAI was cloned into the Hpal and Spel sites of the baculovirus shuttle plasmid BV-CZPG to obtain pBV-EiOV (Fig. 2).

AAV-2 rep and cap genes located between a Dra III site, which is upstream of the AAV-2 p5 promoter and a Bsal site, which is downstream of the

polyadenylation signal (Fig 2), were cloned into the Spel and Pad sites of pBV-

EiOV through multiple cloning steps to obtain pBV-EiOV-RC (Fig 3) Ad5 El

and cisEFGFP were cloned into pBV-EiOV through multiple steps to obtain the

pBV-EiOV-cisEFGFP-El plasmid (Fig 3) Plasmid pAc-cisEFGFP was

constructed by inserting a cassette containing the GFP gene flanked by AAV-2

ITRs into pAcUWl (Pharmingen) through several cloning steps The Xbal-Sspl

fragment of EBVOπ from pEBVHisA (Invitrogen) was inserted into pBV-

cisEFGFP and pBV-EiOV-RC to create pBV-cisEFGFP-EBVOn (Fig 3) and

pBV-EiOV-RC-EBVOri (Fig 3) AAV-2 rep and cap genes were cloned into

pAdΔF6 (plasmid carrying Ad helper genes E2A, the entire E4, and VAI, kindly

provided by Dr Guangping Gao of the University of Pennsylvania) to obtain

pAdΔF6-RC (Fig 3)

Reference to a construct preceded by a "p" refers to a plasmid, while

reference to a construct without a "p" preceding it refers to a virus For example,

pBV-EiOV-RC refers to a plasmid, while BV-EiOV-RC refers to a modified

baculovirus

EXAMPLE 3 Transfection of 293 Cells and Selection for 293-CG3 Stable Cell Line

293 cells were grown to -70% confluency in 6-cm dia tissue culture

dishes and co-transfected overnight with 1 μg pIRESlneo and 10 μg

pAV2cιsEFGFP by the calcium phosphate transfection method (Sambrook et al , 1989) Cells were fed with fresh medium containing 10% FBS and cultured for 24 hours Following trypsinization, cells were seeded at a 1 20 dilution in fresh

medium containing 10% FBS After incubation for another 24 hours, fresh medium

containing 1,250 μg/ml of G418 (GIBCO BRL) was added to the cell monolayer to

select for G418-resιstant cells The medium containing G418 was replaced every 3-

4 days until most of the original G418-resιstant cell colonies had formed A total of

fifty colonies were picked, six of which demonstrated constitutive GFP expression

These six clones were expanded in the presence of G418 and tested for their ability

to rescue functional rAAV by transfection with plasmid pBV-EiOV-RC Normally, when a clone was established, it was maintained in G418-contamιng medium for 3

to 5 passages to ensure that all nonresistant cells had been killed Then, the cells

were maintained in G418-free medium One cell clone, 293-CG3, showed high

efficiency of rAAV rescue and was expanded and used for further experiments

EXAMPLE 4 Functional Test of 293-CG3 for rAAV Production

Several plasmids were used to test the efficiency of 293-CG3 cells

for rAAV production The cells were first seeded on 6-well plates at a density of 1

X 10⁶ cells/well at 2 to 4 hours before transfection The cells in each well received

5 μg of plasmid DNA in a final volume of 167 μl of CaPO₄ (Sambrook et al , 1989)

After incubation for 16 hours, cells were fed with fresh medium Three days later,

cells were harvested and rAAV titers (transducing units) were determined The

results are presented in Table 1 as an average of values determined from two separate experiments. They indicate that the 293-CG3 cell line is very efficient for rAAV production, producing approximately 30 to 170 transducing units of rAAV

per cell depending on the configuration of helper plasmid used.

Table 1.

EXAMPLE 5 Generation of Recombinant Baculoviruses

To create VSV-G pseudotyped recombinant baculoviruses, the

BacPAK baculovirus expression system (CLONTECH Laboratories, Inc.) was

used. Plasmid DNA, one of pBV-EiOV-RC, pBV-cisEFGFP, or pBV-EiOV-

cisEFGFP-El, was cotransfected with Bsu36I-digested BacPAKό DNA into Sf21

cells according to the manufacturer's protocol. The medium was harvested 3 days

after transfection and recombinant baculoviruses were screened on 96-well plates by

limited dilution assay. Briefly, the medium harvested from transfection was diluted

to I O^"2, IO^"3, IO^"4, and 10^"5 each in 10 ml of insect medium containing Sf21 cells at 2

X 10⁵ cells/ml. The mixture was then plated on 96-well plates at 100 μl/well.

After infection for 5-7 days, cells were examined for signs of viral

infection (cell fusion mediated by VSV-G expression; see Eidelman et al., 1984).

The weels that showed viral infection in the lowest dilution were marked and the

virus harvested (Chen et al., 1994). The cells were lysed and used for DNA hybridization to verify the presence of recombinant DNA Positive clones were

amplified into 10 ml, and 1 ml of each clone was used to transduce 293 cells grown in 6-well plates The 293 cells were transfected with a plasmid carrying the

elements not provided by the recombinant baculovirus for rAAV rescue After

transduction for 3 days, cells were lysed and the lysates were used to transduce 84-

31 cells (E1/E4 double complementing cell lines derived from 293 cells, see Fischer

et al , J Virol , 70 8934-8943, 1996) The expression of a marker gene indicated

the rescuing of rAAV The cloned that could best support rAAV rescue was

screened for 3 to 4 more rounds in order to obtain pure recombinant baculovirus

and tested for their support of rAAV rescue Functional clones were further

screened on 96-well plates for 3 to 4 rounds to obtain pure recombinant

baculoviruses

To create non-VSV-G pseudotyped recombinant baculoviruses, a Baculovirus Expression Vector System (Pharmingen) was used Plasmid DNA was

co-transfected with baculoviral DNA into Sf21 cells according to manufacturer's

protocol Recombinant baculovirus was screened on 96-well plates the same as

described for the VSV-G pseudotyped baculoviruses above except that X-gal staining was used to distinguish recombinant baculovirus from wild type

baculovirus EXAMPLE 6 Production of rAAV by Using the Methods of this Invention

Method to Transduce Cells

For transduction, recombinant baculoviruses were first pelleted by

centrifugation at 4"C at 20,000 rpm for 30 minutes. The pellets were then

resuspended in serum-free DMEM. The medium was removed from the cell

monolayer and baculovirus was added to the cells. After incubating for 8-16 hours,

cells were fed with fresh medium containing 10% FBS. Cells were harvested 72

hours after transduction. Baculovirus-transduced cells were harvested and lysed in

DOC lysis buffer (50 mM Tris-HCl, pH 7.4, 1 mM MgCl₂, 0.5% sodium

deoxycholate) by sonication on ice water (three sonication pulses for 1 minute

each). Cell debris was removed by centrifugation at 13,000 rpm for 5 minutes at

4°C and the supernatant was collected. The supernatant was used for rAAV

titration as described in Example 7.

Transduction of 293 cells by Baculoviruses BV-EiOV-RC and BV-cisEFGFP

BV-EiOV-RC provides Ad helper genes E2A, E4ORF6, and VAI as well as AAV rep and cap genes. BV-cisEFGFP provides the AAV vector sequence

with both AAV ITRs flanking the marker gene GFP. 293 cells express Ela and

Elb. Thus, transduction of 293 cells with both BV-EiOV-RC and BV-cisEFGFP

provides to the cells the embedded AAV viral genome comprising the GFP transgene operably linked to the EFlα promoter and flanked by the AAV ITRs; a

VSV-G ligand; helper functions comprising Ela, Elb, E2a, E4ORF6, and VAI; and the replication and encapsidation functions, rep and cap. These functions allow the

cells to produce recombinant AAV.

Transduction of 29 -CG 3 Cells by Baculovirus BV-EiOV-RC

Because the AAV vector was stably integrated in the 293-CG3 cells,

only BV-EiOV-RC was needed to provide a ligand nucleic acid, helper functions

and replication and encapsidation functions to produce recombinant AAV

Transduction of Rep-Cap Expressing Cells by Baculovirus BV-EiOV-cisEFGFP-El

The baculovirus BV-EiOV-cisEFGFP-El provides the Ad helper

genes El, E2A, E4ORF6, and VAI, as well as the AAV vector with both AAV-

ITRS flanking the marker gene GFP. The AAV rep-cap genes are provided by

stable rep-cap cell lines such as B50 (Gao et al. 1998).

EXAMPLE 7 Titration of rAAV Produced by Baculovirus Transduction

An rAAV lysate from baculovirus-transduced cells prepared as

described in Example 6, was diluted at IO^"2, IO^"3 and IO^"4 with DMEM containing

10% FBS and used for the titration assay. 24-well plates were first coated with

0 1% gelatin for 30 minutes and then plated with 2 X 10⁵ cells/well of 293 -based

84-31 cells (Fischer, et al., 1996). After 3 to 4 hours of incubation, the cells were

infected with adenovirus at 100 particles/cell for 30 minutes (adenovirus helps the

conversion of single stranded AAV into double stranded AAV and is widely used for AAV titration), and then the diluted rAAV lysate was added After transduction

by the rAAV for 24 hours, the cells were fixed with 4% paraformaldehyde in PBS

for 30 minutes The paraformaldehyde was replaced with PBS, and GFP-

expressing cells were counted under by fluorescent microscopy

EXAMPLE 8

Production of rAAV Using VSV-G Pseudotyped Baculovirus

Recombinant baculovirus BV-EiOV-RC was used to transduce 293-

CG3 cells for rAAV production The cells were first plated on 6-well plates at a

density of 1 X IO⁶ cells/well at 2 to 4 hours prior to transduction Baculovirus BV-

EiOV-RC was concentrated by centrifugation at 20,000 rpm at 4°C for 30 minutes,

resuspended in serum-containing DMEM, and then added to the cells at the

indicated amounts as shown in Table 2 After incubation for 16 hours, cells were

fed with fresh medium Following transduction for a total of 3 days, cells were

harvested and rAAV titers (transducing units) determined The results are

presented in Table 2 as an average of values determined from two separate

experiments They results indicate that recombinant baculovirus carrying Ad helper

and AAV rep-cap genes can successfully transduce 293-CG3 cells and produce rAAV By increasing the multiplicity of infection (moi) of input baculovirus, higher titers of rAAV were produced Table 2

EXAMPLE 9

Transduction Efficiency of Different Mammalian Cell Lines by VSV-G Pseudotyped and Non-Pseudotvped Baculoviruses

In order to identify a suitable cell line that is efficiently transduced by

baculovirus, a number of cell lines were tested. Cells were seeded on 6-well plates

and grown to -80% confluency. Baculoviruses were added to the cells at the

indicated moi's in serum-free DMEM, incubated with the cells overnight, and

replaced with fresh medium 12-15 hours later. GFP-expressing cells were scored as

a percentage of all cells in the monolayer at 48 hours post-transduction by the

recombinant baculovirus.

The results presented in Table 3 indicate that, in general, VSV-G pseudotyped baculovirus (BV-cisEFGFP) transduce mammalian cells much more

efficiently than the non-pseudotyped baculovirus (Ac-cisEFGFP). However, HepG2

and Saos-2 cell lines were found to be more transducible than HeLa and 293 cell

lines by baculovirus. Insertion of Ad El genes into the chromosome of these cell,

similar to the scenario in 293 cells, should further facilitate production of rAAV

from these cells using the recombinant baculoviruses cited in previous examples. It

is noteworthy that Saos-2 cells are highly permissive for infection by baculovirus irrespective of the presence or absence of the VSV-G glycoprotein on the baculoviral coat. The use of this cell line could provide an advantage for rAAV

production using non-pseudotyped baculovirus

All documents cited above are incorporated by reference herein.

Numerous modifications and variations of the present invention are included in

the above-identified specification and are expected to be obvious to one of skill

in the art. Such modifications and alterations to the processes of the present

invention are believed to be encompassed in the scope of the claims appended

hereto.

Table 3

References

1 Jones N, Shenk T. Isolation of deletion and substitution mutants of

adenovirus type 5 Cell 1978 Jan;13(l): 181-8

2 Sambrook, J , Fritsch, E.F., and Maniatis, T "Molecular Cloning — A

Laboratory Manual" Cold Spring Harbor Laboratory Press. 1989

3 Gao GP, Qu G, Faust LZ, Engdahl RK, Xiao W, Hughes JV, Zoltick PW,

Wilson JM High-titer adeno-associated viral vectors from a Rep/Cap cell line and hybrid shuttle virus Hum Gene Ther 1998 Nov l;9(16).2353-62

4 Fisher KJ, Gao GP, Weitzman MD, DeMatteo R, Burda JF, Wilson JM

Transduction with recombinant adeno-associated virus for gene therapy is limited

by leading-strand synthesis. J Virol 1996 Jan;70(l):520-32.

5 Eidelman, O , Schlegel, R., Tralka, T.S., and Blumenthal, R. J Biol Chem 1996, 259 4622-4628.

6 Chen, H. and Padmanabhan, R. Biotechniques 1994, 17.40-42

Claims

1 A carrier vector for the manufacture of a recombinant virus,

wherein the carrier vector comprises a nonmammalian virus backbone, or a portion

or a modification thereof which is capable of replication in a nonmammalian cell

2 The carrier vector of claim 1 further comprising one or more of

the following elements' 1) an embedded recombinant viral genome, 2) nucleic acid

sequences which encode proteins required for replication and encapsidation of the

recombinant viral genome, 3) nucleic acid sequences encoding helper functions, 4)

nucleic acid sequences that encode a ligand that can interact with a mammalian cell,

and 5) regulatory control sequences that regulate sequences in the nonmammalian

virus backbone or in a replication-proficient portion or modification thereof

3 The carrier vector according to claim 2 which comprises nucleic

acid sequences that encode a ligand that can bind to a mammalian cell receptor

4 The carrier vector according to either of claims 1, 2 or 3 which

further comprises an embedded recombinant viral genome

5. The carrier vector according to either of claims 1, 2 or 3 which

further comprises nucleic acid sequences which encode proteins required for

replication and encapsidation of the recombinant viral genome.

6. The carrier vector according to either of claims 1, 2 or 3 which

further comprises nucleic acid sequences encoding helper functions.

7. The carrier vector according to either of claims 1, 2 or 3 which

further comprises regulatory control sequences that regulate expression of nucleic acid sequences in the nonmammalian virus backbone or in a replication-proficient

portion or modification thereof.

8. The carrier vector according to either of claims 1, 2 or 3 which

further comprises nucleic acid sequences which encode proteins required for

replication and encapsidation of the recombinant viral genome and nucleic acid

sequences encoding helper functions.

9. The carrier vector according to either of claims 1, 2 or 3 which

further comprises an embedded recombinant viral genome and nucleic acid sequences which encode proteins required for replication and encapsidation of the

recombinant viral genome and/or nucleic acid sequences encoding helper functions.

10. The carrier vector according to either of claims 1, 2 or 3 which

comprises all those elements which are required by a mammalian host cell to

produce an infectious recombinant virus.

11. The carrier vector according to claim 2 or 3, wherein the nucleic acid sequences that encode a ligand that can interact with a mammalian cell are

under the regulatory control of a non-mammalian promoter.

12 The carrier vector according to claim 11, wherein the ligand can

bind to a mammalian cell receptor.

13 The carrier vector according to claim 2 or 3, wherein the

embedded recombinant viral genome comprises flanking sequences derived from an

adeno-associated virus (AAV), an adenovirus, a retrovirus or a herpesvirus.

14. The carrier vector according to claim 13, wherein the embedded

recombinant viral genome comprises flanking sequences derived from AAV and the carrier vector further comprises helper sequences encoding a protein providing a

helper function required for replication of AAV.

15. The carrier vector according to claim 14, wherein said helper

sequences are derived from adenovirus (Ad) DNN herpes simplex virus (HSV)

type I or type II DNA, pseudorabies virus (PRV), cytomegalovirus (CMV) or vaccinia virus.

16. The carrier vector according to claim 15, wherein said helper

sequences encode at least one gene product selected from the group consisting of

adenoviral genes El A, E1B, E2A, E4orf6 and VAI, or at least one gene product selected from the group consisting of HSV type 1 genes UL5, UL8, UL52, and

UL29

17 The carrier vector according to claim 14, further comprising a

nucleic acid sequence encoding the AAV rep and cap proteins

18 The carrier vector according to claim 13, wherein the embedded

recombinant viral genome comprises flanking sequences and packaging signals

derived from adenovirus.

19 The carrier vector according to claim 13, wherein the embedded

recombinant viral genome comprises a herpesvirus "a" packaging sequence and a

herpesvirus origin of replication.

20 The carrier vector according to claim 2 or 3, wherein the

embedded recombinant viral genome comprises a transgene whose expression is regulated by expression regulatory sequences operably linked to said transgene.

21 A method for producing a carrier virus, comprising the steps of:

a) modifying a nonmammalian virus backbone DNA, or a

replication-proficient portion or modification thereof, by inserting one or more

nucleic acid inserts comprising

i) a recombinant viral genome comprising a transgene operably linked to expression regulatory sequences and flanked by flanking

elements,

ii) nucleic acid sequences encoding helper functions operably

linked to expression regulatory sequences, iii) nucleic acid sequences encoding replication and/or

encapsidation functions for the recombinant virus, iv) a ligand DNA operably linked to expression regulatory

sequences that are active in nonmammalian cells, and

v) regulatory control sequences that regulate sequences in

the nonmammalian virus backbone, a modified nonmammalian virus backbone or a

replication-proficient portion of the backbone or modified backbone;

b) transducing the resulting carrier vector into nonmammalian host

cells, c) growing the nonmammalian host cells under conditions in which

carrier virus is produced; and d) collecting the carrier virus from the nonmammalian host cells.

22 The method according to claim 21, wherein the nonmammalian

virus backbone is derived from baculovirus and the nonmammalian host cells are

insect cells.

23. A lysate or supernatant comprising the carrier virus produced by

the method according to either of claims 21 or 22. 24 The method according to either of claims 21 or 22, further

comprising the step of purifying the carrier virus

25 A purified preparation of carrier virus produced by the method according to any one of claims 21, 22 or 24

26 A method for producing a recombinant virus, comprising the

steps of

a) infecting mammalian host cells with a carrier virus, wherein the

carrier virus optionally expresses a ligand on its surface;

b) growing the infected mammalian host cells under conditions in

which the embedded recombinant viral genome is replicated, excised and

encapsidated, and

c) collecting the recombinant virus from the mammalian host cells

27 The method according to claim 26, wherein the mammalian host

cells are selected from CHO, BHK, MDCK, 10T1/2, WEHI cells, COS, BSC 1, BSC 40, BMT 10, VERO, WI38, MRC5, A549, HT1080, 293, B-50, 3T3,

NIH3T3, HepG2, Saos-2, Huh7 or HeLa cells.

28 A lysate or supernatant comprising the recombinant virus produced by the method according to either of claims 26 or 27. 29 The method according to either of claims 26 or 27 further comprising the step of purifying the recombinant virus from the mammalian host

cells

30 A purified recombinant virus produced by the method according

to any one of claims 26, 27 or 29.

31 A pharmaceutical composition comprising the carrier virus

according to claim 25 or the recombinant virus according to claim 30 and further

comprising a pharmaceutically acceptable carrier.

32 A method for transient or stable gene transfer of a desired

transgene to a mammalian cell, comprising the step of infecting the mammalian cell

with the recombinant virus according to claim 30.

33 The method according to claim 32, wherein said transient or stable gene transfer is for genetic immunization, correction of genetic defects or

production of proteins in vitro, in vivo, or ex vivo.

34 A method of using a recombinant virus comprising a point

mutation or deletion as a vaccine, comprising the steps of producing an attenuated

replication-proficient recombinant virus or a replication-deficient recombinant virus

by the method of claim 26 and administering the recombinant virus to a patient in a dose effective to induce an immunogenic response.

35 The pharmaceutical composition according to claim 31, wherin

the carrier virus further comprises adenoviral sequences required for replication and

encapsidation of the recombinant adenovirus.