US20020194630A1

US20020194630A1 - Use of recombinant gene delivery vectors for treating or preventing diseases of the eye

Info

Publication number: US20020194630A1
Application number: US10/090,983
Authority: US
Inventors: William Manning; Varavani Dwarki; Katherine Rendahl; Shangzhen Zhou; Laura McGee; Dana Lau; John Flannery; Sheldon Miller; Fei Wang; Adriana Di Polo
Original assignee: Individual
Current assignee: Individual
Priority date: 1999-03-15
Filing date: 2002-03-04
Publication date: 2002-12-19
Also published as: US6943153B1

Abstract

Gene delivery vectors, such as, for example, recombinant adeno-associated viral vectors, and methods of using such vectors are provided for use in treating or preventing diseases of the eye.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of U.S. patent application Ser. No. 09/525,956, filed Mar. 15, 2000, which application claims priority to U.S. Provisional Application No. 60/124,460, filed Mar. 15, 1999, and U.S. Provisional Application No. 60/174,984, filed Jan. 6, 2000, all of which applications are incorporated by reference in their entirety.[0001]

TECHNICAL FIELD

The present invention relates generally to compositions and methods for treating diseases of the eye, and more specifically, to the use of various gene delivery vectors which direct the expression of selected gene products suitable for treating or preventing diseases of the eye.

BACKGROUND OF THE INVENTION

Eye diseases represent a significant health problem in the United States and world-wide. Presently, over 80 million Americans are affected with potentially blinding eye disease, with 1.1 million being legally blind. Twelve million individuals suffer from some degree of visual impairment that cannot be corrected. The total economic impact of eye disease is also very significant. In 1981, the estimated economic impact of visual impairment on the U.S. economy was 14 billion per year. By 1995, this impact had grown to an estimated 38.4 billion (National Eye Institute NIH).

A wide variety of eye diseases can cause visual impairment, including for example, macular degeneration, diabetic retinopathies, inherited retinal degeneration such as retinitis pigmentosa, glaucoma, retinal detachment or injury and retinopathies (whether inherited, induced by surgery, trauma, a toxic compound or agent, or, photically).

One structure in the eye that can be particularly affected by disease is the retina. Briefly, the retina, which is found at the back of the eye, is a specialized light-sensitive tissue that contains photoreceptor cells (rods and cones) and neurons connected to a neural network for the processing of visual information (see FIG. 10). This information is sent to the brain for decoding into a visual image.

The retina depends on cells of the adjacent retinal pigment epithelium (RPE) for support of its metabolic functions. Photoreceptors in the retina, perhaps because of their huge energy requirements and highly differentiated state, are sensitive to a variety of genetic and environmental insults. The retina is thus susceptible to an array of diseases that result in visual loss or complete blindness.

Retinitis pigmentosa (RP), which results in the destruction of photoreceptor cells, the RPE, and choroid typify inherited retinal degenerations. This group of debilitating conditions affects approximately 100,000 people in the United States.

A great deal of the progress made in addressing this important clinical problem has depended on advances in research on photoreceptor cell biology, molecular biology, molecular genetics, and biochemistry over the past two decades. Animal models of hereditary retinal disease have been vital in helping unravel the specific genetic and biochemical defects that underlie abnormalities in human retinal diseases. It now seems clear that both genetic and clinical heterogeneity underlie many hereditary retinal diseases.

The leading cause of visual loss in the elderly is Age-related Macular Degeneration (AMD). The social and economic impact of this disease in the United States is increasing. The macula is a structure near the center of the retina that contains the fovea. This specialized portion of the retina is responsible for the high-resolution vision that permits activities such as reading. The loss of central vision in AMD is devastating. Degenerative changes to the macula (maculopathy) can occur at almost any time in life but are much more prevalent with advancing age. With growth in the aged population, AMD will become a more prevalent cause of blindness than both diabetic retinopathy and glaucoma combined. Laser treatment has been shown to reduce the risk of extensive macular scarring from the “wet” or neovascular form of the disease. The effects of this treatment are short-lived, however, due to recurrent choroidal neovascularization. Thus, there are presently no effective treatments in clinical use for the vast majority of AMD patients.

Other diseases of the eye, such as glaucoma, are also major public health problems in the United States. In particular, blindness from glaucoma is believed to impose significant costs annually on the U.S. Government in Social Security benefits, lost tax revenues, and healthcare expenditures.

Briefly, glaucoma is not a uniform disease but rather a heterogeneous group of disorders that share a distinct type of optic nerve damage that leads to loss of visual function. The disease is manifest as a progressive optic neuropathy that, if left untreated, leads to blindness. It is estimated that as many as 3 million Americans have glaucoma and, of these, as many as 120,000 are blind as a result. Furthermore, it is the number one cause of blindness in African-Americans. Its most prevalent form, primary open-angle glaucoma, can be insidious. This form usually begins in midlife and progresses slowly but relentlessly. If detected early, disease progression can frequently be arrested or slowed with medical and surgical treatment.

Glaucoma can involve several tissues in the front and back of the eye. Commonly, but not always, glaucoma begins with a defect in the front of the eye. Fluid in the anterior portion of the eye, the aqueous humor, forms a circulatory system that brings nutrients and supplies to various tissues. Aqueous humor enters the anterior chamber via the ciliary body epithelium (inflow), flows through the anterior segment bathing the lens, iris, and cornea, and then leaves the eye via specialized tissues known as the trabecular meshwork and Schlemm's canal to flow into the venous system. Intraocular pressure is maintained vis-à-vis a balance between fluid secretion and fluid outflow. Almost all glaucomas are associated with defects that interfere with aqueous humor outflow and, hence, lead to a rise in intraocular pressure. The consequence of this impairment in outflow and elevation in intraocular pressure is that optic nerve function is compromised. The result is a distinctive optic nerve atrophy, which clinically is characterized by excavation and cupping of the optic nerve, indicative of loss of optic nerve axons.

Primary open-angle glaucoma is, by convention, characterized by relatively high intraocular pressures believed to arise from a blockage of the outflow drainage channel or trabecular meshwork in the front of the eye. However, another form of primary open-angle glaucoma, normal-tension glaucoma, is characterized by a severe optic neuropathy in the absence of abnormally high intraocular pressure. Patients with normal-tension glaucoma have pressures within the normal range, albeit often in the high normal range. Both these forms of primary open-angle glaucoma are considered to be late-onset diseases in that, clinically, the disease first presents itself around midlife or later. However, among African-Americans, the disease may begin earlier than middle age. In contrast, juvenile open-angle glaucoma is a primary glaucoma that affects children and young adults. Clinically, this rare form of glaucoma is distinguished from primary open-angle glaucoma not only by its earlier onset but also by the very high intraocular pressure associated with this disease. Angle-closure glaucoma is a mechanical form of the disease caused by contact of the iris with the trabecular meshwork, resulting in blockage of the drainage channels that allow fluid to escape from the eye. This form of glaucoma can be treated effectively in the very early stages with laser surgery. Congenital and other developmental glaucomas in children tend to be severe and can be very challenging to treat successfully. Secondary glaucomas result from other ocular diseases that impair the outflow of aqueous humor from the eye and include pigmentary glaucoma, pseudoexfoliative glaucoma, and glaucomas resulting from trauma and inflammatory diseases. Blockage of the outflow channels by new blood vessels (neovascular glaucoma) can occur in people with retinal vascular disease, particularly diabetic retinopathy.

Primary open-angle glaucoma can be insidious. It usually begins in midlife and progresses slowly but relentlessly. If detected, disease progression can frequently be arrested or slowed with medical and surgical treatment. However, without treatment, the disease can result in absolute irreversible blindness. In many cases, even when patients have received adequate treatment (e.g., drugs to lower intraocular pressure), optic nerve degeneration and loss of vision continues relentlessly.

The present invention provides compositions and methods for treating and preventing a number of diseases of the eye, including for example, retinal diseases and degenerations such as RP and AMD, as well as other diseases such as neovascular disease. The present invention also provides other, related advantages.

SUMMARY OF THE INVENTION

Briefly stated, the present invention provides compositions and methods for treating, preventing, or, inhibiting diseases of the eye. Within one aspect of the present invention, methods are provided for treating or preventing diseases of the eye comprising the step of intraocularly administering a gene delivery vector which directs the expression of one or more neurotrophic factors, or, anti-angiogenic factors, such that the disease of the eye is treated or prevented. Within related aspects of the present invention, gene delivery vectors are provided which direct the expression of one or more neurotrophic factors such as FGF, as well as gene therapy vectors which direct the expression of one or more anti-angiogenic factors. Within certain embodiments of the invention, a viral promoter (e.g., CMV) or an inducible promoter (e.g., tet) is utilized to drive the expression of the neurotrophic factor.

Representative examples of gene delivery vectors suitable for use within the present invention may be generated from viruses such as retroviruses (e.g., FIV or HIV), herpesviruses, adenoviruses, adeno-associated viruses, and alphaviruses, or from non-viral vectors.

Utilizing the methods and gene delivery vectors provided herein a wide variety of diseases of the eye may be readily treated or prevented, including for example, glaucoma, macular degeneration, diabetic retinopathies, inherited retinal degeneration such as retinitis pigmentosa, retinal detachment or injury and retinopathies (whether inherited, induced by surgery, trauma, a toxic compound or agent, or, photically). Similarly, a wide variety of neurotrophic factors may be utilized (either alone or in combination) within the context of the present invention, including for example, NGF, BDNF, CNTF, NT-3, NT-4, FGF-2, FGF-5, FGF-18, FGF-20 and FGF-21.

Within certain embodiments of the invention, it is preferred that the gene delivery vector be utilized to deliver and express an anti-angiogenic factor for the treatment, prevention, or, inhibition of diabetic retinopathy, wet AMD, and other neovascular diseases of the eye (e.g., ROP). Within other embodiments it is desirable that the gene delivery vector be utilized to deliver and express a neurotrophic growth factor to treat, prevent, or, inhibit diseases of the eye, such as, for example, glaucoma, retinitis pigmentosa, and dry AMD. Within yet other embodiments, it may be desirable to utilize either a gene delivery vector which expresses both an anti-angiogenic molecule and a neurotrophic growth factor, or two separate vectors which independently express such factors, in the treatment, prevention, or inhibition of an eye disease (e.g., for diabetic retinopathy).

Within further embodiments of the invention, the above-mentioned methods utilizing gene delivery vectors may be administered along with other methods or therapeutic regimens, including for example, photodynamic therapy (e.g., for wet AMD), laser photocoagulation (e.g., for diabetic retinopathy and wet AMD), and intraocular pressure reducing drugs (e.g., for glaucoma).

Also provided by the present invention are isolated nucleic acid molecules comprising the sequence of FIG. 2, vectors which contain, and/or express this sequence, and host cells which contain such vectors.

Within further aspects of the present invention gene delivery vectors are provided which direct the expression of a neurotrophic factor, or, an anti-angiogenic factor. As noted above, representative examples of neurotrophic factors include NGF, BDNF, CNTF, NT-3, NT-4, FGF-2, FGF-5, FGF-18, FGF-20 and FGF-21. Representative examples of anti-angiogenic factors include soluble Flt-1, soluble Tie-2 receptor, and PEDF. Representative examples of suitable gene delivery vectors include adenovirus, retroviruses (e.g., HIV or FIV-based vectors), alphaviruses, AAV vectors, and naked DNA vectors.

Within yet other aspects of the invention non-human animal models of neovascular diseases of the eye are provided, comprising an animal having an angiogenic (i.e., pro-angiogenic) transgene in the eye. Within various embodiments, the neovascularization may be retinal or choroidal neovascularization. Within other embodiments, the animal may be a mouse or rat. As noted herein, a wide variety of angiogenic transgenes may be utilized to generate the non-human animal model, including for example, angiogenic transgenes that encode VEGF and/or an angiopoietin such as angiopoietin-1.

Also provided are methods of making such non-human animal models comprising the general steps of administering to a non-human animal a gene delivery vector which directs the expression of an angiogenic transgene. As noted above, a wide variety of gene delivery vectors (e.g., rAV and rAAV) can be utilized, as well as nucleic acid molecules which encode the angiogenic transgene (e.g., nucleic acid molecules encoding VEGF or angiopoietin). Within certain embodiments, the gene delivery vector can be administered subretinally or intravitreally. Within further embodiments the animal model can be utilized as a model for Age-related Macular Degeneration (AMD), diabetic retinopathy, or, retinopathy of prematurity (ROP).

Also provided are methods for determining the ability of an anti-angiogenic factor to inhibit neovascularization of the eye, comprising the general steps of (a) administering to an animal model as described herein an anti-angiogenic factor, and (b) determining the ability of the anti-angiogenic factor to inhibit neovascularization of the eye. As noted herein, the anti-angiogenic factor may be administered by a variety of routes, including for example, topically, subretinally, or, intravitreally. Further, the animal model may be utilized to test the efficacy of drugs, compounds, or other factors or agents for a wide variety of eye-related neovascular diseases (including AMD and ROP).

These and other aspects of the present invention will become evident upon reference to the following detailed description and attached drawings. In addition, various references are set forth herein which describe in more detail certain procedures or compositions (e.g., plasmids, etc.), and are therefore incorporated by reference in their entirety.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic illustration of pKm201bFGF-2. [0027]
FIGS. 2A and 2B are the nucleic acid sequence of pKm201bFGF-2 (SEQ I.D. No. ______). [0028]
FIG. 3 is a schematic illustration of pD10-CMV-FGF-5. [0029]
FIG. 4 is a western analysis of FGF-5 rAAV infected 293 cells. [0030]
FIG. 5 is a schematic illustration of pD10-CMV-FGF-5 (sig−). [0031]
FIG. 6 is a western analysis of pD10-CMV-FGF-5 (sig−) transfected 293 cells. [0032]
FIG. 7 is a schematic illustration of pD10-CMV-FGF-18. [0033]
FIG. 8 western analysis of 293 cells transfected pD10-CMV-FGF-18. [0034]
FIGS. 9A and 9B are photographs which show that bluo-gal staining is visible across 40% of a retina transfected with AAV-CMV-lacZ. All photoreceptors appear to express lacZ at the injection site, except at the edge where individual cells are visible. [0035]
FIG. 10 is a schematic illustration which shows the retina within the eye, and the organization of cells within the retina. [0036]
FIGS. 11A and 11B are photographs of wild-type and degenerated S334ter rat retinas. S33 4ter is a rat model for retinitis pigmentosa. [0037]
FIGS. 12A, 12B and [0038] 12C are photographs of degenerated S334ter, FGF-2 20 injected S334ter and PBS injected S334ter rat retinas. As can be seen in these figures, FGF-2 injected into the S334ter rat retina substantially slows the progression of disease.
FIG. 13 is a graph which plots Outer Nuclear Layer (ONL) thickness for FGF-2 subretinally injected, PBS subretinally injected, and an uninjected control. [0039]
FIG. 14 is a bar graph which plots ONL thickness at p60. [0040]
FIGS. 15A, 15B and [0041] 15C are photographs of FGF-2 expressing cells stained with an anti-FGF-2 antibody.
FIGS. 16A and 16B are photographs which show gene delivery to cells in the ganglion cell layer following intraocular injection of recombinant rAAV-CMV-lacZ. a) superior quadrant of a retinal flat-mount processed for Bluo-Gal staining to visualize AAV-infected infected neurons. Notice the large number of axons converging at the optic nerve head (asterisk). b) Retinal radial section showing the AAV-mediated LacZ gene product in cells of the ganglion cell layer. A large number of these cells can be identified as RGCs because of the intense LacZ staining in axons projecting to the optic nerve head (asterisk). RPE: retinal pigment epithelium, PS: photoreceptor segments, ONL: outer nuclear layer, OPL: outer plexiform layer, INL: inner nuclear layer, IPL: inner plexiform layer, GCL: ganglion cell layer. Scale bars: a) 0.5 mm, b) 50 μm. [0042]
FIG. 17 is a graph which shows the time-course of AAV-mediated transgene expression in the ganglion cell layer of the adult rat retina. A recombinant AAV vector (rAAV-CMV-lacZ) was injected into the vitreous chamber of adult rats and 2, 4 and 8 weeks later, Lac-Z positive neurons in the ganglion cell layer (GCL) were counted in retinal flat-mounts. The values are the mean of 3-4 retinas per time point +standard deviation (p<0.001). [0043]
FIGS. 18A and 18B are photographs which show the localization of the AAV-mediated LacZ gene product in retrogradely labeled RGCs. a) Retinal radial section showing LacZ immunopositive RGCs transduced with AAV (excitation 520-560, barrier 580, emission 580); b) Same section examined under a different fluorescent filter (excitation 355-425, barrier 460, emission 470) to visualize RGCs backlabeled with Fluorogold from the superior colliculus. Notice that the vast majority of LacZ immunopositive neurons are also labeled with Fluorogold. An exception, a LacZ positive cell that is not Fluorogold labeled, is shown (arrow), and could represent a displaced amacrine cell or RGC that did not incorporate the retrograde tracer. INL: inner nuclear layer, IPL: inner plexiform layer; GCL: ganglion cell layer. Scale bar: 10 μm. [0044]
FIG. 19 is a graph which quantifies Fluorogold- and LacZ-positive cells in the ganglion cell layer following intravitreal injection of rAAV-CMV-lacZ. The number of Fluorogold-positive cells (FG+) was compared to the number of cells that expressed both the Fluorogold and LacZ markers (FG+, LacZ+) and the number of cells expressing only the reporter gene (LacZ+). Values represent the mean of 4-5 retinal radial sections per animal (n=4)±standard deviation (S.D.) (p<0.001). [0045]
FIG. 20 is a photograph which shows the localization of the heparan sulfate (HS) proteoglycan receptor, the cellular receptor for AAV, in the intact adult rat retina. Retinal cryosection immunostained with a polyclonal antibody against the heparan sulfate (HepSS-1; diluted 1:200) followed by biotinylated anti-rabbit Fab fragment, avidin-biotin-peroxidase reagent (ABC Elite Vector Labs, Burlingame, Calif.). The section was reacted in a solution containing 0.05% diaminobenzidine tetrahydrochloride (DAB) and 0.06% hydrogen peroxide in PB (pH 7.4) for 5 min. Notice the strong labeling in RGCs in the ganglion cell layer (GCL). RPE: retinal pigment epithelium, PS: photoreceptor segments, ONL: outer nuclear layer, OPL: outer plexiform layer, INL: inner nuclear layer, IPL: inner plexiform layer. Scale bar: 50 μm. [0046]
FIG. 21 is a schematic illustration of pD10-VEGFuc. [0047]
FIGS. 22A and 22B are the nucleotide sequence of pD10-VEGFUC. [0048]
FIG. 23 is a bar graph which shows pD10-VEGFUC rAAV virus infection of 293 cells. [0049]
FIG. 24 is a three dimensional bar-graph which shows VEGF secretion by hfRPE after infection with VEGF AAV. [0050]
FIG. 25 is a three dimensional bar-graph which shows VEGF secretion by hfRPE after infection with VEGF AV [0051]
FIG. 26 is a three dimensional bar-graph which shows resistance of hfRPE after infection with VEGF AV. [0052]
FIG. 27 is a schematic illustration of pD10-sFlt-1. [0053]
FIGS. 28A and 28B provide the nucleotide sequence of pD10-sFlt-1. [0054]
FIG. 29 is the nucleotide sequence of FGF-20. [0055]
FIG. 30 is the nucleotide sequence of FGF-21. [0056]
FIG. 31 is a schematic illustration of pD10K-FGF-2Sc. [0057]
FIGS. 32A and 32B are the nucleotide sequence of pD10K-FGF-2Sc. [0058]
FIG. 33 is a graph that compares ONL thickness (um) after injection of various vectors into the eye. [0059]
FIG. 34 is a bar graph that shows inhibition of HMVEC proliferation by sFlt-1 rAAV. [0060]
FIGS. 35A and 35B are photographic images showing retinal blood vessels from a live animal, before sacrifice. [0061]
FIGS. 36A, 36B, [0062] 36C, and 36D are a series of images showing epoxy sections of an eye at various distances from an AAV-VEGF injection site.
FIGS. 37A, 37B, [0063] 37C, and 37D are photographs which show lectin/BrdU double-staining of the rat retina.
FIGS. 38A and 38B are bar graphs which show sFlt-1 and PEDF rescue of ERGs. [0064]
FIG. 39 is a graph which shows the ERG of a test and control eye of sFlt-1 treated rats.[0065]

DETAILED DESCRIPTION OF THE INVENTION

Definitions

Prior to setting forth the invention, it may be helpful to an understanding thereof to first set forth definitions of certain terms that will be used hereinafter. [0066]
“Gene delivery vector” refers to a construct which is capable of delivering, and, within preferred embodiments expressing, one or more gene(s) or sequencers) of interest in a host cell. Representative examples of such vectors include viral vectors, nucleic acid expression vectors, naked DNA, and certain eukaryotic cells (e.g., producer cells). [0067]
“Recombinant adeno-associated virus vector” or “rAAV vector” refers to a gene delivery vector based upon an adeno-associated virus. The rAAV vectors, should contain 5′ and 3′ adeno-associated virus inverted terminal repeats (ITRs), and a transgene or gene of interest operatively linked to sequences which regulate its expression in a target cell. Within certain embodiments, the transgene may be operably linked to a heterologous promoter (such as CMV), or, an inducible promoter such as (tet). In addition, the rAAV vector may have a polyadenylation sequence. [0068]
“Neurotrophic Factor” or “NT” refers to proteins which are responsible for the development and maintenance of the nervous system. Representative examples of neurotrophic factors include NGF, BDNF, CNTF, NT-3, NT-4, and Fibroblast Growth Factors. [0069]
“Fibroblast Growth Factor” or “FGF” refers to a family of related proteins, the first of which was isolated from the pituitary gland (see Gospodarowicz, D., Nature, 249:123-127, 1974). From this original FGF (designated basic FGF) a family of related proteins, protein muteins, and protein analogs have been identified (see, e.g., U.S. Pat. Nos. 4,444,760, 5,155,214, 5,371,206, 5,464,774, 5,464,943, 5,604,293, 5,731,170, 5,750,365, 5,851,990, 5,852,177, 5,859,208, and 5,872,226), all of which are generally referred to as Fibroblast Growth Factors within the context of the present invention. [0070]
“Anti-anziogenic Factor” refers to a factor or molecule which is able to inhibit the proliferation of vascular growth. A variety of assays may be utilized to assess the anti-angiogenic activity of a given molecule, including for example, the assay provided in Example 15, which measures HMVEC (human dermal microvascular endothelial cell) proliferation. Representative examples of anti-angiogenic factors include for example, Angiostatin, 1,25-Di-hydroxy-vitamn D[0071] ₃, Endostatin, IGF-1 receptor antagonists, Interferons alpha, beta and gamma, Interferon gamma-inducible protein IP-10, Interleukin 1 alpha and beta, Interleukin 12, 2-Methoxyestradiol, PEDF, Platelet factor 4, Prolactin (16kd fragment), Protamin, Retinoic acid, Thrombospondin-1 and 2, Tissue inhibitor of metalloproteinase-1 and -2, Transforming growth factor beta, anti-VEGF antibodies (which should be understood to include fragments of antibodies such as a single chain antibodies, Fab fragements, or, CDR regions), soluble Tie-2 receptor, soluble Tie-2 receptor, soluble Flt-1 and Tumor necrosis factor-alpha.
“Diseases of the Eve” refers to a broad class of diseases wherein the functioning of the eye is affected due to damage or degeneration of the photoreceptors; ganglia or optic nerve; or neovascularization. Representative examples of such diseases include macular degeneration, diabetic retinopathies, inherited retinal degeneration such as retinitis pigmentosa, glaucoma, retinal detachment or injury and retinopathies (whether inherited, induced by surgery, trauma, a toxic compound or agent, or, photically). [0072]
As noted above, the present invention provides compositions and methods for treating, preventing, or, inhibiting diseases of the eye, comprising the general step of administering intraocularly a recombinant adeno-associated viral vector which directs the expression of one or more neurotrophic factors, such that the disease of the eye is treated or prevented. In order to further an understanding of the invention, a more detailed discussion is provided below regarding (A) gene delivery vectors; (B) Neurotrophic Factors; (C) Anti-angiogenic factors; and (D) methods of administering the rAAVs in the treatment or prevention of diseases of the eye. [0073]
A. Gene Delivery Vectors [0074]
1. Construction of Retroviral Gene Delivery Vectors [0075]
Within one aspect of the present invention, retroviral gene delivery vectors are provided which are constructed to carry or express a selected gene(s) or sequence(s) of interest. Briefly, retroviral gene delivery vectors of the present invention may be readily constructed from a wide variety of retroviruses, including for example, B, C, and D type retroviruses as well as spumaviruses and lentiviruses (see RNA Tumor Viruses, Second Edition, Cold Spring Harbor Laboratory, 1985). Such retroviruses may be readily obtained from depositories or collections such as the American Type Culture Collection (“ATCC”; Rockville, Md.), or isolated from known sources using commonly available techniques. [0076]
Any of the above retroviruses may be readily utilized in order to assemble or construct retroviral gene delivery vectors given the disclosure provided herein, and standard recombinant techniques (e.g., Sambrook et al., [0077] Molecular Cloning: A Laboratory Manual, 2d ed., Cold Spring Harbor Laboratory Press, 1989; Kunkel, PNAS 82:488, 1985). In addition, within certain embodiments of the invention, portions of the retroviral gene delivery vectors may be derived from different retroviruses. For example, within one embodiment of the invention, retrovirus LTRs may be derived from a Murine Sarcoma Virus, a tRNA binding site from a Rous Sarcoma Virus, a packaging signal from a Murine Leukemia Virus, and an origin of second strand synthesis from an Avian Leukosis Virus.
Within one aspect of the present invention, retrovector constructs are provided comprising a 5′ LTR, a tRNA binding site, a packaging signal, one or more heterologous sequences, an origin of second strand DNA synthesis and a 3′ LTR, wherein the vector construct lacks gaglpol or env coding sequences. [0078]
Other retroviral gene delivery vectors may likewise be utilized within the context of the present invention, including for example EP 0,415,731; WO 90/07936; WO 91/0285, WO 9403622; WO 9325698; WO 9325234; U.S. Pat. No. 5,219,740; WO 9311230; WO 9310218; Vile and Hart, [0079] Cancer Res. 53:3860-3864, 1993; Vile and Hart, Cancer Res. 53:962-967, 1993; Ram et al., Cancer Res. 53:83-88, 1993; Takamiya et al., J. Neurosci. Res. 33:493-503, 1992; Baba et al., J. Neurosurg. 79:729-735, 1993 (U.S. Pat. No. 4,777,127, GB 2,200,651, EP 0,345,242 and WO91/02805).
Packaging cell lines suitable for use with the above described retrovector constructs may be readily prepared (see U.S. Ser. No. 08/240,030, filed May 9, 1994; see also U.S. Ser. No. 07/800,921, filed Nov. 27, 1991), and utilized to create producer cell lines (also termed vector cell lines or “VCLs”) for the production of recombinant vector particles. [0080]
2. Recombinant Adeno-Associated Virus Vectors [0081]
As noted above, a variety of rAAV vectors may be utilized to direct the expression of one or more desired neurotrophic factors. Briefly, the rAAV should be comprised of, in order, a 5′ adeno-associated virus inverted terminal repeat, a transgene or gene of interest operatively linked to a sequence which regulates its expression in a target cell, and a 3′ adeno-associated virus inverted terminal repeat. In addition, the rAAV vector may preferably have a polyadenylation sequence. [0082]
Generally, rAAV vectors should have one copy of the AAV ITR at each end of the transgene or gene of interest, in order to allow replication, packaging, and efficient integration into cell chromosomes. The ITR consists of [0083] nucleotides 1 to 145 at the 5′ end of the AAV DNA genome, and nucleotides 4681 to 4536 (i.e., the same sequence) at the 3′ end of the AAV DNA genome. Preferably, the rAAV vector may also include at least 10 nucleotides following the end of the ITR (i.e., a portion of the “D region”).
Within preferred embodiments of the invention, the transgene sequence will be of about 2 to 5 kb in length (or alternatively, the transgene may additionally contain a “stuffer” or “filler” sequence to bring the total size of the nucleic acid sequence between the two ITRs to between 2 and 5 kb). Alternatively, the transgene may be composed of same heterologous sequence several times (e.g., two nucleic acid molecules which encode FGF-2 separated by a ribosome readthrough, or alternatively, by an Internal Ribosome Entry Site or “IRES”), or several different heterologous sequences (e.g., FGF-2 and FGF-5, separated by a ribosome readthrough or an IRES). [0084]
Recombinant AVV vectors of the present invention may be generated from a variety of adeno-associated viruses, including for example, serotypes 1 through 6. For example, ITRs from any AAV serotype are expected to have similar structures and functions with regard to replication, integration, excision and transcriptional mechanisms. [0085]
Within certain embodiments of the invention, expression of the transgene may be accomplished by a separate promoter (e.g., a viral promoter). Representative examples of suitable promoters in this regard include a CMV promoter, RSV promoter, SV40 promoter, or MoMLV promoter. Other promoters that may similarly be utilized within the context of the present invention include cell or tissue specific promoters (e.g., a rod, cone, or ganglia derived promoter), or inducible promoters. Representative examples of suitable inducible promoters include tetracycline-response promoters (“Tet”, see, e.g., Gossen and Bujard, [0086] Proc. Natl. Acad. Sci. USA. 89:5547-5551, 1992; Gossen et al., Science 268, 1766-1769, 1995; Baron et al., Nucl. Acids Res. 25:2723-2729, 1997; Blau and Rossi, Proc. Natl. Acad Sci USA. 96:797-799, 1999; Bohl et al., Blood 92:1512-1517, 1998; and Haberman et al., Gene Therapy 5:1604-1611, 1998), the ecdysone system (see e.g., No et al., Proc. Natl. Acad. Sci. USA. 93:3346-3351, 1996), and other regulated promoters or promoter systems (see, e.g., Rivera et al., Nat. Med. 2:1028-1032, 1996;).
The rAAV vector may also contain additional sequences, for example from an adenovirus, which assist in effecting a desired function for the vector. Such sequences include, for example, those which assist in packaging the rAAV vector in adenovirus-associated virus particles. [0087]
Packaging cell lines suitable for producing adeno-associated viral vectors may be readily accomplished given readily available techniques (see e.g., U.S. Pat. No. 5,872,005). [0088]
Particularly preferred methods for constructing and packaging rAAV vectors are described in more detail below in Examples 1, 2, 3, and 4. [0089]
3. Alphavirus Delivery Vectors [0090]
The present invention also provides a variety of Alphavirus vectors which may function as gene delivery vectors. For example, the Sindbis virus is the prototype member of the alphavirus genus of the togavirus family. The unsegmented genomic RNA (49S RNA) of Sindbis virus is approximately 11,703 nucleotides in length, contains a 5′ cap and a 3′ poly-adenylated tail, and displays positive polarity. Infectious enveloped Sindbis-virus is produced by assembly of the viral nucleocapsid proteins onto the viral genomic RNA in the cytoplasm and budding through the cell membrane embedded with viral encoded glycoproteins. Entry of virus into cells is by endocytosis through clatharin coated pits, fusion of the viral membrane with the endosome, release of the nucleocapsid, and uncoating of the viral genome. During viral replication the genomic 49S RNA serves as template for synthesis of the complementary negative strand. This negative strand in turn serves as template for genomic RNA and an internally initiated 26S subgenomic RNA. The Sindbis viral nonstructural proteins are translated from the genomic RNA while structural proteins are translated from the subgenomic 26S RNA. All viral genes are expressed as a polyprotein and processed into individual proteins by post translational proteolytic cleavage. The packaging sequence resides within the nonstructural coding region, therefore only the genomic 49S RNA is packaged into virions. [0091]
Several different Sindbis vector systems may be constructed and utilized within the present invention. Representative examples of such systems include those described within U.S. Pat. Nos. 5,091,309 and 5,217,879, and PCT Publication No. WO 95/07994. [0092]
4. Other Viral Gene Delivery Vectors [0093]
In addition to retroviral vectors and alphavirus vectors, numerous other viral vectors systems may also be utilized as a gene delivery vector. Representative examples of such gene delivery vectors include viruses such as pox viruses, such as canary pox virus or vaccinia virus (Fisher-Hoch et al., [0094] PNAS 86:317-321, 1989; Flexner et al., Ann. N.Y Acad. Sci. 569:86-103, 1989; Flexner et al., Vaccine 8:17-21, 1990; U.S. Pat. Nos. 4,603,112, 4,769,330 and 5,017,487; WO 89/01973); SV40 (Mulligan et al., Nature 277:108-114, 1979); influenza virus (Luytjes et al., Cell 59:1107-1113, 1989; McMicheal et al., N. Eng. J. Med. 309:13-17, 1983; and Yap et al., Nature 273:238-239, 1978); herpes (Kit, Adv. Exp. Med. Biol. 215:219-236, 1989; U.S. Pat. No. 5,288,641); HIV (Poznansky, J. Virol. 65:532-536, 1991); measles (EP 0 440,219); Semliki Forest Virus, and coronavirus, as well as other viral systems (e.g., EP 0,440,219; WO 92/06693; U.S. Pat. No. 5,166,057). In addition, viral carriers may be homologous, non-pathogenic(defective), replication competent virus (e.g., Overbaugh et al., Science 239:906-910,1988), and nevertheless induce cellular immune responses, including CTL.
5. Non-viral gene delivery vectors [0095]
In addition to the above viral-based vectors, numerous non-viral gene t delivery vectors may likewise be utilized within the context of the present invention. Representative examples of such gene delivery vectors include direct delivery of nucleic acid expression vectors, naked DNA alone (WO 90/11092), polycation condensed DNA linked or unlinked to killed adenovirus (Curiel et al., [0096] Hum. Gene Ther. 3:147-154, 1992), DNA ligand linked to a ligand with or without one of the high affinity pairs described above (Wu et al., J. of Biol. Chem 264:16985-16987, 1989), nucleic acid containing liposomes (e.g., WO 95/24929 and WO 95/12387) and certain eukaryotic cells (e.g., producer cells—see U.S. Ser. No. 08/240,030, filed May 9, 1994, and U.S. Ser. No. 07/800,921).
B. Neurotrophic Factors [0097]
As noted above, the term neurotrophic factor refers to proteins which are responsible for the development and maintenance of the nervous system. Representative examples of neurotrophic factors include NGF, BDNF, CNTF, NT-3, NT-4, and Fibroblast Growth Factors. [0098]
Fibroblast Growth Factor refers to a family of related proteins, the first of which was isolated from the pituitary gland (see Gospodarowicz, D., Nature, 249:123-127, 1974). From this original FGF (designated basic FGF) a family of related proteins, protein muteins, and protein analogs have been identified (see, e.g., U.S. Pat. Nos. 4,444,760, 5,155,214, 5,371,206, 5,464,774, 5,464,943, 5,604,293, 5,731,170, 5,750,365, 5,851,990, 5,852,177, 5,859,208, and 5,872,226; see generally Baird and Gospodarowicz, D. [0099] Ann N. Y Acad. Sci. 638:1, 1991. The first two members of the family to be identified were acidic fibroblast growth factor (aFGF/FGF-1) and basic fibroblast growth factor (bFGF/FGF-2). Additional members of the FGF family include: i-nt-2/FGF-3, (Smith et al., EMBO J. 7: 1013, 1988); FGF-4 (Delli-Bovi et al., Cell 50: 729, 1987); FGF-6 (Marics et al., Oncogene 4: 335 (1989); keratinocyte growth factor/FGF-7, (Finch et al., Science 245: 752, 1989); FGF-8 (Tanaka et al., Proc. Natl. Acad Sci. USA 89: 8928, 1992); and FGF-9 (Miyamoto et al., Mol. Cell Biol. 13: 4251, 1993).
FGF-5 was originally isolated as an oncogene. See Goldfarb et al. U.S. Pat. Nos. 5,155,217 and 5,238,916, Zhan et al. “Human Oncogene Detected by a Defined Medium Culture Assay” ([0100] Oncogene 1:369-376, 1987), Zhan et al. “The Human FGF-5 Oncogene Encodes a Novel Protein Related to Fibroblastic Growth Factors” (Molecular and Cellular Biology 8:3487-3495, 1988), and Bates et al. “Biosynthesis of Human Fibroblast Growth Factor 5”: (Molecular and Cellular Biology 11:1840-1845, 1991).
Other FGFs include those disclosed in U.S. Pat. Nos. 4,444,760, 5,155,214, 5,371,206, 5,464,774, 5,464,943, 5,604,293, 5,731,170, 5,750,365, 5,851,990, 5,852,177, 5,859,208, and 5,872,226. 5,852,177, and 5,872,226, as well as FGF-20 (U.S. Provisional Application No. 60/161,162) and FGF-21 (U.S. Provisional Application No. 60/166,540). [0101]
C. Anti-Angiogenic Factors [0102]
A wide variety of anti-angiogenic factors may also be expressed from the gene delivery vectors of the present invention, including for example, Angiostatin (O'Reilly et al., [0103] Cell 79:315-328, 1994; O'Reilly et al., Nat. Med. 2:689-92, 1996; Sim et al., Cancer Res. 57:1329-34, 1997), 1,25-Di-hydroxy-vitamn D₃(Shibuya et al., Oncogene 5:519-24, 1990; Oikawa et al., Eur. J Pharmacol. 178:247-50, 1990; and 182:616, 1990), Endostatin (O'Reilly et al., Cell 88:277-85, 1997), Interferons alpha and beta (Sidky et al., Cancer Res. 47:5155-61, 1987; Singh et al., Proc. Natl. Acad. Sci. USA 92:4562-6, 1995), Interferon gamma (Friesel et al., J. Cell. Biol. 104:689-96, 1987), IGF-1 receptor antagonists, Interferon gamma-inducible protein IP-10 (Arenberg et al., J. Exp. Med. 1996;184:981-92; Strieter et al., J. Leukoc. Biol. 1995;57:752-62; Angiolillo et al., J. Exp. Med. 182:155-62, 1995), Interleukin 1alpha and beta (Cozzolino et al., Proc. Natl. Acad. Sci. USA 87:6487-91, 1990), Interleukin 12 (Kerbel and Hawley, J. Natl Cancer Inst. 87:557-9, 1995; Majewski et al., J. Invest. Dermatol 106:1114-8, 1996; Voest et al., J. Natl Cancer Inst. 87:581-6, 1995), 2-Methoxyestradiol (Fotsis et al., Nature 368:237-9, 1994), Platelet factor 4 (Taylor and Folkman, Nature 297:307-12, 1982; Gengrinovitch et al., J. Biol. Chem 270:15059-65, 1995), Prolactin (16kd fragment) (Clapp et al., Endocrinology 133:1292-9, 1993; Ferrara, Endocrinology 129:896-900, 1991), Protamin, Retinoic acid (Lingen et al., Lab. Invest 74:476-83, 1996), Thrombospondin-1 and 2 (Lawler, Blood, 67:1197-209, 1986; Raugi and Lovett, Am. J. Pathol 129:364-72, 1987; Volpert et al., Biochem. Biophys. Res. Commun 217:326-32, 1995), Tissue inhibitor of metalloproteinase-1 and -2 (Moses and Langer, J. Cell Biochem 47:230-5, 1991; Ray and Stetler-Stevenson, Eur. Respir. J. 7:2062-72, 1994), Transforming growth factor beta (RayChaudhury, J. Cell. Biochem 47:224-9, 1991; Roberts et al., Proc. Natl Acad. Sci USA 83:4167-71, 1986), and Tumor necrosis factor—alpha (Frater-Schroeder et al., Proc. Natl. Acad. Sci. USSA 84:5277-81, 1987; Leibovich et al., Nature 329:630-2, 1987).
Other anti-angiogenic factors that can be utilized within the context of the present invention include VEGF antagonists such as soluble Flt-1 (Kendall and Thomas, [0104] PNAS 90: 10705, 1993), pigment epithelium-derived factor or “PEDF” (Dawson et al., Science 285:245, 1999), and Ang-1 antagonists such as soluble Tie-2 receptor (Thurston et al., Science 286:2511, 1999; see also, generally Aiello et al., PNAS 92:10457, 1995; Robinson et al., PNAS 93:4851, 1996; Seo et al., Am. J. Pathol. 154:1743, 1999).
The ability of a given molecule to be “anti-angiogenic” can be readily assessed utilizing a variety of assays, including for example, the HMVEC assay provided in Example 15. [0105]
D. Method for Treating and/or Preventing Diseases of the Eye, and Pharmaceutical Compositions [0106]
As noted above, the present invention provides methods which generally comprise the step of intraocularly administering a gene delivery vector which directs the expression of one or more neurotrophic factor to the eye, or an anti-angiogenic factor to the eye in order to treat, prevent, or inhibit the progression of an eye disease. As utilized herein, it should be understood that the terms “treated, prevented, or, inhibited” refers to the alteration of a disease course or progress in a statistically significant manner. Determination of whether a disease course has been altered may be readily assessed in a variety of model systems, discussed in more detail below, which analyze the ability of a gene delivery vector to delay, prevent or rescue photoreceptors, as well as other retinal cells, from cell death. [0107]
1. Diseases of the Eye [0108]
A wide variety of diseases of the eye may be treated given the teachings provided herein. For example, within one embodiment of the invention gene delivery vectors are administered to a patient intraocularly in order to treat or prevent macular degeneration. Briefly, the leading cause of visual loss in the elderly is macular degeneration (MD), which has an increasingly important social and economic impact in the United States. As the size of the elderly population increases in this country, age related macular degeneration (AMD) will become a more prevalent cause of blindness than both diabetic retinopathy and glaucoma combined. Although laser treatment has been shown to reduce the risk of extensive macular scarring from the “wet” or neovascular form of the disease, there are currently no effective treatments for the vast majority of patients with MD. [0109]
Within another embodiment, gene delivery vectors can be administered to a patient intraocularly in order to treat or prevent an inherited retinal degeneration. One of the most common inherited retinal degenerations is retinitis pigmentosa (RP), which results in the destruction of photoreceptor cells, and the RPE. Other inherited conditions include Bardet-Biedl syndrome (autosomal recessive); Congenital amaurosis (autosomal recessive); Cone or cone-rod dystrophy (autosomal dominant and X-linked forms); Congenital stationary night blindness (autosomal dominant, autosomal recessive and X-linked forms); Macular degeneration (autosomal dominant and autosomal recessive forms); Optic atrophy, autosomal dominant and X-linked forms); Retinitis pigmentosa (autosomal dominant, autosomal recessive and X-linked forms); Syndromic or systemic retinopathy (autosomal dominant, autosomal recessive and X-linked forms); and Usher syndrome (autosomal recessive). This group of debilitating conditions affects approximately 100,000 people in the United States alone. [0110]
As noted above, within other aspects of the invention, gene delivery vectors which direct the expression of a neurotrophic growth factor can be administered to a patient intraocularly in order to treat or prevent glaucoma. Briefly, glaucoma is not a uniform disease but rather a heterogeneous group of disorders that share a distinct type of optic nerve damage that leads to loss of visual function. The disease is manifest as a progressive optic neuropathy that, if left untreated leads to blindness. It is estimated that as many as 3 million Americans have glaucoma and, of these, as many as 120,000 are blind as a result. Furthermore, it is the number one cause of blindness in African-Americans. Its most prevalent form, primary open-angle glaucoma, can be insidious. This form usually begins in midlife and progresses slowly but relentlessly. If detected early, disease progression can frequently be arrested or slowed with medical and surgical treatment. Representative factors that may be expressed from the vectors of the present invention to treat glaucoma include neurotrophic growth factors such as FGF-2, 5, 18, 20, and, 21. [0111]
Within yet other embodiments gene delivery vectors can be administered to a patient intraocularly in order to treat or prevent injuries to the retina, including retinal detachment, photic retinopathies, surgery-induced retinopathies, toxic retinopathies, retinopathies due to trauma or penetrating lesions of the eye. [0112]
As noted above, the present invention also provides methods of treating, preventing, or, inhibiting neovascular disease of the eye, comprising the step of administering to a patient a gene delivery vector which directs the expression of an anti-angiogenic factor. Representative examples of neovascular diseases include diabetic retinopathy, AMD (wet form), and retinopathy of prematurity. Briefly, choroidal neovascularization is a hallmark of exudative or wet Age-related Macular Degeneration (AMD), the leading cause of blindness in the elderly population. Retinal neovascularization occurs in diseases such as diabetic retinapathy and retinopathy of prematurity (ROP), the most common cause of blindness in the young. [0113]
Particularly preferred vectors for the treatment, prevention, or, inhibition of neovascular diseases of the eye direct the expression of an anti-angiogenic factor such as, for example, soluble tie-2 receptor or soluble Flt-1. [0114]
2. Animal Models [0115]
In order to assess the ability of a selected gene therapy vector to be effective for treating diseases of the eye which involve neovascularization, a novel model for neovascularization (either choroidal or subretinal) can be generated by subretinal injection of a recombinant virus (e.g., rAV or rAAV) containing an angiogenic transgene such as VEGF and/or angiopoietin. Within certain embodiments, an angiogenic transgene such as angiopoietin-1 can be used in combination with another factor such as VEGF, in order to generate neovascularization. The extent and duration of neovascularization induced by the gene delivery vectors containing an angiogenic transgene such as VEGF can be determined using fundus photography, fluorescein angiography and histochemistry. [0116]
To assess the ability of anti-angiogenic molecules to prevent neovascularization in the model described above, a D10-sFlt-1 rAAV (or other gene delivery vector which directs the expression of an anti-angiogenic factor) is intraocularly injected, either by subretinal or intravitreal routes of injection. Generally, subretinal injection of the gene delivery vector may be utilized to achieve delivery to both the choroidal and inner retinal vasculature. Intravitreal injection can be utilized to infect Muller cells and retinal ganglion cells (RGCs), which deliver anti-angiogenic protein to the retinal vasculature. Muller cells span the retina and would secrete the therapeutic protein into the subretinal space. [0117]
Such injections may be accomplished either prior to, simultaneous with, or subsequent to administration of an angiogenic factor or gene delivery vector which expresses an angiogenic factor. After an appropriate time interval, inhibition of neovascularization can be determined using fundus photography, fluorescein angiography and/or histochemistry. [0118]
While there are many animal models of retinal neovascularization such as oxygen-induced ischemic retinopathy (Aiello et al., [0119] PNAS 93: 4881, 1996.) and the VEGF transgenic mouse (Okamoto et al., Am. J. Pathol. 151: 281, 1997), there are fewer models of choroidal neovascularization (e.g., laser photocoagulation as described by Murata et al., IOVS 39: 2474, 1998). Subretinal neovascularization from the retinal rather than choroidal blood supply is also observed in VEGF transgenic animals (Okamoto et al., Am. J. Pathol. 151: 281, 1997). Hypoxic stimulation of VEGF expression is known to correlate with neovascularization in human ocular disease.
The pathologic hallmark of glaucomatous optic neuropathy is the selective death of retinal ganglion cells (RGCs) (Nickells, R. W., J. Glaucoma 5:345-356. 1996; Levin, L. A. and Louhab, A., Arch. Ophthalmol. 114:488-491, 1996.; Kerrigan, L. A., Zack, D. J., Quigley, H. A., Smith, S. D. and Pease, M. E., Arch. Ophthalmol. 115:1031-1035, 1997). Recent studies indicate that RGCs die with characteristics of apoptosis after injury to the axons of adult RGCs such as axotomy of the optic nerve (ON), and in glaucoma and anterior ischemic optic neuropathy in humans (Nickells, 1996). Thus, damage to the optic nerve by axotomy is used by many researchers as a model for selective apoptotic cell death of adult RGCs. [0120]
The loss of RGCs caused by ON transection in adult mammals varies from 50% to more than 90% depending on the techniques used to identify RGCs, the proximity of the lesion to the eye, and the age and species of the animal. For example, in a study in adult rats, in which retrogradely transported tracers were used to distinguish RGCs from displaced amacrine cells (Villegas-Perez, M. P., Vidal-Sanz, M., Bray, G. M. and Aguayo, A. J., [0121] J. Neurosci. 8:265-280, 1988). ON transection near the eye (0.5-1 mm) leads to the loss of more than 90% of the RGCs by 2 weeks. In contrast, in adult animals in which the ON was cut nearly 10 mm from the eye, 54% of RGCs survived by 3 months (Richardson, P. M., Issa, V. M. K. and Shemie, S., J. Neurocytol. 11:949-966, 1982.).
Briefly, the posterior pole of the left eye and the origin of the optic nerve (ON) are exposed through a superior temporal intraorbital approach. A longitudinal excision of the ON dural sheath is performed. The ON is then gently separated from the dorsal aspect of this sheath and completely transected within the orbit, within 1 mm of the optic disc. Care is taken to avoid damage to the ophthalmic artery, which is located on the inferomedial dural sheath of the ON. [0122]
RGC survival and death following gene delivery can also be examined using two alternative models of ON injury: 1) ON crush; and (2) increased intraocular pressure. In the first model the ON is exposed, and then clamped at a distance of about one millimeter from the posterior pole using a pair of calibrated forceps as previously described (Li et al., [0123] Invest. Ophthalmol. Vis. Sci. 40:1004, 1999). In the second model, chronic moderately elevated intraocular pressure can be produced unilaterally by cauterization of three episcleral vessels as described by Neufeld et al. in PNAS 17:9944, 1999).
A variety of animal models can be utilized for photoreceptor degeneration, including the RCS rat model, P23H transgenic rat model, the rd mouse, and the S334ter transgenic rat model. [0124]
Briefly, in the S334ter transgenic rat model, a mutation occurs resulting in the truncation of the C-[0125] terminal 15 amino acid residues of rhodopsin (a seven-transmembrane protein found in photoreceptor outer segments, which acts as a photopigment). The S334ter mutation is similar to rhodopsin mutations found in a subset of patients with retinitis pigmentosa (RP). RP is a heterogeneous group of inherited retinal disorders in which individuals experience varying rates of vision loss due to photoreceptor degeneration. IN many RP patients, photoreceptor cell death progresses to blindness. Transgenic S334ter rats are born with normal number of photoreceptors. The mutant rhodopsin gene begins expression at postnatal day 5 in the rat, and photoreceptor cell death begins at postnatal day 10-15. In transgenic line S334ter-3, approximately 70% of the outer nuclear layer has degenerated by day 60 in the absence of any therapeutic intervention. The retinal degeneration in this model is consistent from animal to animal and follows a predictable and reproducible rate. This provides an assay for therapeutic effect by morphological examination of the thickness of the photoreceptor nuclear layer and comparison of the treated eye to the untreated (contralateral) eye in the same individual animal.
S334ter rats are utilized as a model for RP as follows. Briefly, S334ter transgenic rats are euthanized by overdose of carbon dioxide inhalation and immediately perfused intracardially with a mixture of mixed aldehydes (2% formaldehyde and 2.5% glutaraldehyde). Eyes are removed and embedded in epoxy resin, and 1 μm thick histological sections are made along the vertical meridian. Tissue sections are aligned so that the ROS and Müller cell processes crossing the inner plexiform layer are continuous throughout the plane of section to assure that the sections are not oblique, and the thickness of the ONL and lengths of RIS and ROS are measured. These retinal thickness measurements are plotted and establish the baseline retinal degeneration rates for the animal model. The assessment of retinal thickness is as follows: briefly, 54 measurements of each layer or structure were made at set points around the entire retinal section. These data were either averaged to provide a single value for the retina, or plotted as a distribution of thickness or length across the retina. The greatest 3 contiguous values for ONL thickness in each retina is also compared in order to determine if any region of retina (e.g., nearest the injection site) showed proportionally greater rescue; although most of these values were slightly greater than the overall mean of all 54 values, they were no different from control values than the overall mean. Thus, the overall mean was used in the data cited, since it was based on a much larger number of measurements. [0126]
One particularly preferred line of transgenic rats, TgN(s3 34ter) line 4 (abbreviated s334ter 4) can be utilized for in vivo experiments. Briefly, in this rat model expression of the mutated opsin transgene begins at postnatal day P5 in these rats, leading to a gradual death of photoreceptor cells. These rats develop an anatomically normal retina up to P15, with the exception of a slightly increased number of pyknotic photoreceptor nuclei in the outer nuclear layer (ONL) than in non-transgenic control rats. In this animal model , the rate of photoreceptor cell death is approximately linear until P60, resulting in loss of 40-60% of the photoreceptors. After P60, the rate of cell loss decreases, until by one year the retinas have less than a single row of photoreceptor nuclei remaining. [0127]
3. Methods of Administration [0128]
Gene delivery vectors of the present invention may be administered intraocularly to a variety of locations depending on the type of disease to be treated, prevented, or, inhibited, and the extent of disease. Examples of suitable locations include the retina (e.g., for retinal diseases), the vitreous, or other locations in or adjacent to the eye. [0129]
Briefly, the human retina is organized in a fairly exact mosaic. In the fovea, the mosaic is a hexagonal packing of cones. Outside the fovea, the rods break up the close hexagonal packing of the cones but still allow an organized architecture with cones rather evenly spaced surrounded by rings of rods. Thus in terms of densities of the different photoreceptor populations in the human retina, it is clear that the cone density is highest in the foveal pit and falls rapidly outside the fovea to a fairly even density into the peripheral retina (see Osterberg, G. (1935) Topography of the layer of rods and cones in the human retina. [0130] Acta Ophthal. (suppl.) 6, 1-103; see also Curcio, C. A., Sloan, K. R., Packer, O., Hendrickson, A. E. and Kalina, R. E. (1987) Distribution of cones in human and monkey retina: individual variability and radial asymmetry. Science 236, 579-582).
Access to desired portions of the retina, or to other parts of the eye may be readily accomplished by one of skill in the art (see, generally Medical and Surgical Retina: Advances, Controversies, and Management, Hilel Lewis, Stephen J. Ryan, Eds., medical illustrator, Timothy C. Hengst. St. Louis: Mosby, c1994. xix, 534; see also [0131] Retina, Stephen J. Ryan, editor in chief,. 2nd ed., St. Louis, Mo.: Mosby, c1994. 3 v. (xxix, 2559 p.)
The amount of the specific viral vector applied to the retina is uniformly quite small as the eye is a relatively contained structure and the agent is injected directly into it. The amount of vector that needs to be injected is determined by the intraocular location of the chosen cells targeted for treatment. The cell type to be transduced will be determined by the particular disease entity that is to be treated. [0132]
For example, a single 20-microliter volume (of 10[0133] ¹³physical particle titer/ml rAAV) may be used in a subretinal injection to treat the macula and fovea. A larger injection of 50 to 100 microliters may be used to deliver the rAAV to a substantial fraction of the retinal area, perhaps to the entire retina depending upon the extent of lateral spread of the particles.
A 100-ul injection will provide several million active rAAV particles into the subretinal space. This calculation is based upon a titer of 10[0134] ¹³physical particles per milliliter. Of this titer, it is estimated that {fraction (1/1000)} to {fraction (1/10,000)} of the AAV particles are infectious. The retinal anatomy constrains the injection volume possible in the subretinal space (SRS). Assuming an injection maximum of 100 microliters, this would provide an infectious titer of 10⁸to 10⁹rAAV in the SRS. This would have the potential of infecting all of the 150×10 6 photoreceptors in the entire human retina with a single injection.
Smaller injection volumes focally applied to the fovea or macula may adequately transfect the entire region affected by the disease in the case of macular degeneration or other regional retinopathies. [0135]
Gene delivery vectors can alternately be delivered to the eye by intraocular injection into the vitreous. In this application, the primary target cells to be transduced are the retinal ganglion cells, which are the retinal cells primarily affected in glaucoma. In this application, the injection volume of the gene delivery vector could be substantially larger, as the volume is not constrained by the anatomy of the subretinal space. Acceptable dosages in this instance can range from 25 ul to 1000 ul. [0136]
4. Assays [0137]
A wide variety of assays may be utilized in order to determine appropriate dosages for administration, or to assess the ability of a gene delivery vector to treat or prevent a particular disease. Certain of these assays are discussed in more detail below. [0138]
a. Electroretinographic Analysis [0139]
Electroretinographic analysis can be utilized to assess the effect of gene delivery administration into the retina. Briefly, rats are dark adapted overnight and then in dim red light, then anesthetized with intramuscular injections of xylazine (13 mg/kg) and ketamine (87 mg/kg). Full-field scotopic ERGs are elicited with 10-μsec flashes of white light and responses were recorded using a UTAS-[0140] E 2000 Visual Electrodiagnostic System (LKC Technologies, Inc., Gaithersburg, Md.). The corneas of the rats are the anesthetized with a drop of 0.5% proparacaine hydrochloride, and the pupils dilated with 1% atropine and 2.5% phenylephrine hydrochloride. Small contact lenses with gold wire loops are placed on both corneas with a drop of 2.5% methylcellulose to maintain corneal hydration. A silver wire reference electrode is placed subcutaneously between the eyes and a ground electrode is placed subcutaneously in the hind leg. Stimuli are presented at intensities of −1.1, 0.9 and 1.9 log cd m⁻²at 10-second, 30-second and 1-minute intervals, respectively. Responses are amplified at a gain of 4,000, filtered between 0.3 to 500 Hz and digitized at a rate of 2,000 Hz on 2 channels. Three responses are averaged at each intensity. The a-waves are measured from the baseline to the peak in the cornea-negative direction, and b-waves are measured from the cornea-negative peak to the major cornea-positive peak. For quantitative comparison of differences between the two eyes of rats, the values from all the stimulus intensities are averaged for a given animal.
b. Retinal Tissue Analysis [0141]
As described in more detail above and below, retinal tissue analysis can also be utilized to assess the effect of gene delivery administration into the retina. [0142]
5. Pharmaceutical Compositions [0143]
Gene delivery vectors may be prepared as a pharmaceutical product suitable for direct administration. Within preferred embodiments, the vector should be admixed with a pharmaceutically acceptable carrier for intraocular administration. Examples of suitable carriers are saline or phosphate buffered saline. [0144]

Deposit Information

The following material was deposited with the American Type Culture Collection: [0145]

Name Deposit Date Accession No.

PKm201bFGF-2 3/11/99 #207160

PD10-Kan-FGF-2-Sc
The above material was deposited by Chiron Corporation with the American Type Culture Collection (ATCC), 10801 University Blvd., Manassas, Va. 20110-2209, telephone 703-365-2700. This deposit will be maintained under the terms of the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for purposes of Patent Procedure. The deposit will be maintained for a period of 30 years following issuance of this patent, or for the enforceable life of the patent, whichever is greater. Upon issuance of the patent, the deposits will be available to the public from the ATCC without restriction. [0146]
This deposit is provided merely as a convenience to those of skill in the art, and is not an admission that a deposit is required under 35 U.S.C. §112. The nucleic acid sequence of this deposit, as well as the amino acid sequence of the polypeptide encoded thereby, are incorporated herein by reference and should be referred to in the event of an error in the sequence described herein. A license may be required to make, use, or sell the deposited materials, and no such license is granted hereby. [0147]
The following examples are offered by way of illustration, and not by way of limitation. [0148]

EXAMPLES

Example 1

Construction of a rAAV Vector Expressing FGF-2

pKm201CMV is an AAV cloning vector in which an expression cassette, consisting of a CMV immediate early promoter/enhancer and a bovine growth hormone (BGH) polyadenylation site, is flanked by inverted terminal repeat (ITR) sequences from AAV-2. Briefly, pKm201CMV was derived from pKm201, a modified AAV vector plasmid in which the ampicillin resistance gene of pEMBL-AAV-ITR (see Srivastava, (1989) [0149] Proc. Natl. Acad. Sci. USA 86:8078-8082) had been replaced with the gene for kanamycin resistance. The expression cassette from pCMVlink, a derivative of pCMV6c (see Chapman, Nucleic Acids Res. 19:193-198 (1991)) in which the BGH poly A site has been substituted for the SV40 terminator, was inserted between the ITRs of pKm201 to generate pKm201 CMV.
pKm201 bFGF-2 was constructed by cloning the following, in order, into the multiple cloning site of pKm201 CMV: the encephalomyocarditis virus (EMCV) internal ribosome entry site (IRES), the bovine FGF-2 cDNA, and the human growth hormone polyadenylation sequence. The cDNA for FGF-2 has two mutations that change amino acid 121 from serine to threonine and amino acid 137 from proline to serine. The DNA sequence of pKm201bFGF-2 is shown in FIG. 2 and the plasmid has been deposited with the American Type Culture Collection (ATCC). [0150]
rAAV vector particles were produced by a triple transfection protocol ([0151] Nucleic Acids Res. 24:596-601, 1996; J. Exp. Med. 179:1867-1875, 1994). Briefly, human embryonic kidney 293 cells, grown to 50% confluence in a 10 layer Nunclon cell factory (Nalge Nunc, Int., Naperville, Ill.), were co-transfected with 400 μg of helper plasmid pKSrep/cap (Hum. Gene Ther. 9:477-485, 1998) 400 μg of vector plasmid, and 800 μg of adenovirus plasmid pBHG10 (Microbix Biosystems, Inc., Toronto, Ontario) using the calcium phosphate co-precipitation method. Forty-eight hours after co-transfection, media was replaced with IMDM+10% FB S containing adenovirus type 5 dl312 at a multiplicity of infection (MOI) of 2. Seventy-two hours after infection cells were harvested and resuspended in HEPES buffer (200 ml total) and lysed by three cycles of freezing and thawing. Cell debris was removed by centrifugation at 12,000× g for 20 min. Packaged rAAV was purified from adenovirus by two rounds of cesium chloride equilibrium density gradient centrifugation. Residual adenovirus contamination was inactivated by heating at 56° C. for 45 min. Though three plasmids were used in the production of rAAV vector in this example, it is possible to combine the rAAV vector construct and the AAV helper gene construct on one plasmid. This would allow rAAV to be produced by transfecting 293 cells with two plasmids. Alternatively, one could add the adenovirus helper genes to this plasmid to make a single plasmid containing all that is required to make rAAV particles.
To estimate total number of rAAV particles, the virus stock was treated with DNAse I, and encapsidated DNA was extracted with phenol-chloroform, and precipitated with ethanol. DNA dot blot analysis against a known standard was used to determine titer ([0152] Blood 76:1997-2000, 1990).
To assay for adenovirus contamination, 293 cells were infected with 10 μl of purified rAAV stock and followed for any signs of cytopathic effect. All stocks were negative for adenovirus contamination (level of detection greater than or equal to 100 PFU/ml). [0153]
To assay for wild type AAV, 293 cells were co-infected with serial dilutions of rAAV stocks and adenovirus dl312 at a MOI of 2. Three days later the cells were harvested, lysed by three cycles of freezing/thawing, and centrifuged to remove cell debris. The supernatant was heat inactivated (56° C. for 10 min) and fresh plates of 293 cells (6×10[0154] ⁶) were infected in the presence of adenovirus dl312 at a MOI of 2. Forty-eight hours after infection, low molecular-weight DNA was isolated (J Mol. Biol. 26:365-369, 1967) subjected to agarose gel electrophoresis, and transferred to a nylon membrane. The membrane was hybridized with a biotinylated oligonucleotide probe specific for the AAV capsid region. The wild type AAV titer was defined as the highest dilution of rAAV vector stock demonstrating a positive hybridization signal. The rAAV preparations contained less than 1 wild type AAV genome per 109 rAAV genomes.

Example 2

Infection of Cells with RAAV-CMV-FGF-2 Results in the Expression of FGF-2

293 cells were plated the day before infection at 5×10 ⁵cells/well in 6-well plates and were infected with rAAV-CMV-bFGF-2 virus, prepared as described above in Example 1, at different multiplicities of infection (MOI) with and without etoposide (3μM). Etoposide is a topoisomerase inhibitor which has been shown to increase transduction efficiency of rAAV vectors (Proc. Natl. Acad. Sci. USA, 92:5719-5723, 1995). Forty-eight hours after infection, culture supernatant was collected and cells were lysed in 0.5 mL 1× lysis buffer (100 mM NaCl, 20 mM Tris pH 7.5, 1 mM EDTA, 0.5% NP40, and 0.5% deoxycholate). FGF-2 in the supernatants and lysates was assayed by ELISA (cat. #DFB00, R & D Systems, Minneapolis, Minn.) following manufacturer's instructions. The results are shown below in Table 1.

TABLE 1


FGF-2 PRODUCTiON IN 293 CELLS FOLLOWING INFECTION
WITH RAAV-FGF-2

sample	infection MOI	Etoposide	FGF2 protein

Culture Medium Supernatant (1.5 ml)

1	0	−	<5	pg/ml
2	2 × 10⁵	−	<5	pg/ml
3	2 × 10⁴	−	<5	pg/ml
4	2 × 10³	−	<5	pg/ml
1	0	+	<5	pg/ml
2	2 × 10⁵	+	106	pg/ml ≈ 300 pg/24 h/
				10⁶ cells
3	2 × 10⁴	+	<5	pg/ml
4	2 × 10³	+	<5	pg/ml

Cell Lysate (0.5 ml)

1	0	−	8.95	ng/ml
2	2 × 10⁵	−	114.	ng/ml
3	2 × 10⁴	−	18.8	ng/ml
4	2 × 10³	−	11.3	ng/ml
1	0	+	5.05	ng/ml
2	2 × 10⁵	+	296.	ng/ml ≈ 300 ng/24 h/
				10⁶ cells
3	2 × 10⁴	+	48.0	ng/ml
4	2 × 10³	+	13.2	ng/ml

Example 3

Construction of rAAV Vectors

A. Construction of pD10-bFGF-2 [0156]
The pD10 AAV vector is constructed by replacing the AAV gene encoding sequences of pD-10 (see Wang, X. et al. [0157] J. Virol. 71:3077 (1997), with the CMV promoter, multiple cloning site, and BGH polyadenylation sequences from pKm201CMV. Briefly, tides 5′-ggtatttaaa acttgcggcc gcggaatttc gactctaggc c-3′ (SEQ I.D. No. ______) and 5′-gctgcccggg acttgctagc tggatgatcc tccagcgcgg ggatctcatg-3′(SEQ I.D. No. ______) are used to amplify the CMV expression cassette from pKm201 CMV. The product of this PCR amplification is digested with SmaI and DraI and cloned into pD-10 digested with is new vector is named pD10-CMV.
To construct pD10-bFGF-2, the synthetic gene for bovine FGF-2 (see U.S. Pat. No. 5,464,774 for sequence) is digested with EcoRI and SalI, treated with T4 polymerase to blunt the ends, and then cloned into the StuI site of pD10-CMV. The synthetic gene described above encodes the mature, processed form of bovine FGF-2. [0158]
B. Construction of a rAAV Vector Expressing FGF-2-Sc. [0159]
pD10-K-FGF -2-Sc (see FIG. 31) was constructed by cloning the FGF-2 humanized bovine cDNA obtained from Scios, into the pD10 vector backbone containing the kanamycin (Kan) resistance gene. This cDNA contains the mutations at amino acid positions 121 and 137 described in example 1. Briefly, the FGF-2-Sc cDNA was digested from the parent plasmid with the enzyme NdeI, the ends blunted with T4 DNA polymerase, cut with the restriction enzyme HindIII, and cloned into the pD10-CMV vector which had been digested with the enzymes StuI and HindIII. The nucleotide sequence of [0160] pD 1 0-K-FGF-2-Sc is illustrated in FIG. 32.
C. Infection of Cells with rAAV-FGF-2-Sc Results in the Expression of FGF-2 293 cells were infected as in example 2, with the following modifications: 4×10e5 cells/well were plated in a 12 well dish, and all wells contained 3 uM etoposide. Three different particle numbers of FGF-2 virus, and a negative control CMV-lacZ virus were used to infect the cells. 48 hours after infection, tissue culture media was collected and cells lysed in 100 ul lysis buffer containing Triton-[0161] X 100 and Complete™ protein inhibitor cocktail (Boehringer Mannheim, Germany). FGF-2 protein in the media and lysates was assayed by ELISA. The results are shown below in Table 2 below. TABLE 2.

TABLE 2

FGF-2 PRODUCTION IN 293 CELLS FOLLOWING INFECTION

WITH RAAV D10-K-FGF-2-Sc

Viral Culture media

Vector Particles Lysates (pg/mL) (pg/mL)

D10-K-FGF-2-Sc 1 × 10e10 324492.919 438.621

D10-K-FGF-2-Sc 1 × 10e9 32876.106 46.984

D10-K-FGF-2-Sc 1 × 10e8 6950.039 14.649

CMV-lacz 1 × 10e10 2327.527 17.096

Example 4

Construction of rAAV Vectors Which Express FGF5 and FGF18

A. Cloning FGF-5 into the PD10-CMV rAAV Vector. [0162]
The FGF-5 coding region (see U.S. Serial No. 08,602,147) was cloned into the rAAV pD10-CMV vector by digestion with the enzymes SacII and Xmnl, resulting in an 814 bp fragment. This removed an ORF (ORF-1) upstream of and overlapping with the FGF-5 coding region. The ends of the FGF-5 fragment were then blunted with T4 DNA polymerase, and it was cloned into the rAAV pD10-CMV vector linearized with StuI. This vector contains a 1353 bp insertion of a bacteriophage Phi X174 HaeIII fragment. [0163]
The pD10-CMV-FGF-5 vector is illustrated schematically in FIG. 3. In summary, this plasmid contains the CMV immediate/early enhancer+promoter, the CMV intron A, an FGF-5 coding region, the bovine growth hormone polyA site, and AAV ITR sequences. There is a 1353 bp insertion of PhiX 174 bacteriophage DNA cloned into the NotI site between one ITR and the CMV immediate early enhancer +promoter region. [0164]
B. Packaging and Functional Analysis of FGF-5 rAAV. [0165]
rAAV virus was packaged using a triple transfection method as described in Example 1. However, rather than cesium chloride equilibrium density gradient centrifugation, heparin sulfate column chromatography is utilized. More specifically, a cell pellet is resuspended in TNM buffer: 20 mM Tris pH 8.0, 150 mM NaCl, 2 mM MgCl[0166] ₂. Deoxycholic Acid is added to 0.5% to lyse the cells. 50 U/ml Benzonase is added and the lysed cells are incubated at 37 degrees to digest any nucleic acids. The cell debris is pelleted and the supernatant is filtered through a 0.45 um filter and then a 0.22 um filter. The virus is then loaded onto a 1.5 ml Heparin sulfate column using the Biocad HPLC. The column is then washed with 20 mM Tris pH 8.0, 100 mM NaCl. The rAAV particles are eluted with a gradient formed with increasing concentrations of NaCl. The fractions under the peak are pooled and filtered through a 0.22 um filter before overnight precipitation with 8% PEG 8000. CaCl₂is added to 25 mM and the purified particles are pelleted and then resuspended in HBS#2: 150 mM NaCl, 50 mM Hepes pH 7.4.
Briefly, 8×10[0167] ⁸or 8×10⁹particles of the resulting FGF-5 virus were used to infect 293 cells, which were simultaneously treated with 3 uM etoposide to enhance viral expression levels. At 24 hours post-infection, tissue culture media and cell lysates were harvested and analysed by Western blotting. Briefly, protein samples were run on a 4-20% tris-glycine gradient gel, and transferred to nitrocellulose by standard procedures. After blocking with 5% milk in PBS, the membrane was incubated with an anti-human FGF-5 antibody (R and D systems, made in goat) at a dilution of 1:1,000 for one hour at room temperature. After the membrane was washed 3 times in PBS+0.05% Tween-20, it was incubated with an anti-goat secondary antibody conjugated to peroxidase (1:5,000 dilution). The membrane was then washed and the FGF-5 protein detected by chemiluminescence.
Results of the Western blot are shown in FIG. 4. Briefly, [0168] lane 1 represents 50 ng of the 29.5 Kd recombinant FGF-5 protein (R and D systems). Lane 2, media from cells infected with 8×10⁹viral particles and treated with etoposide, shows no FGF-5 expression. Lane 3 is an uninfected cell lysate control. Lane 4 and 5 are lysates from cells infected with 8×108 or 8×10⁹viral particles, respectively, and Lanes 6 and 7 are lysates from cells infected with 8×10⁸or 8×10⁹viral particles and treated with 3 uM etoposide. Lanes 4-7 all show positive FGF-5 expression. Lane 8 is a negative control of lysate from uninfected cells.
In summary, although the FGF-5 signal sequence was intact, FGF-5 protein was detected in the cell lysate only. [0169]
C. Cloning FGF-5 Lacking a Signal Sequence into rAAV pD10-CMV. [0170]
Oncogenic activity is associated with the wild-type FGF-5 molecule (Zhan et al., 1988; Bates et al., 1991). To improve its safety, the codons for the first 21 amino acids of FGF-5's signal sequence were removed by PCR amplification of the above pD10-CMV-FGF-5 plasmid with the following primers: AGA/TAT/AAG/CTT/AC C/ATG/GGT/GAA/AAG/CG T/CTC/GCC/CCC/AAA (5′, 5FGFMUTB; SEQ I.D. No.______) and CGC/GCG/CTC/GAG/AC C/ATG/AGG/AAT/ATT/ATC/CAA/AGC/GAA/ACT (3′, 3FGF5WT; SEQ I.D. No. ______). The 5′ primer contains point mutations which destabilize G/C rich hairpin structures of the FGF-5 mRNA, and should increase levels of gene expression. The PCR product was digested with HindIII and XhoI (restriction sites introduced by the primers), and cloned by standard methods, into the [0171] pD 10 vector digested with the same enzymes. The pD10-CMV-FGF-5 (sig−) vector is illustrated schematically in FIG. 5.
In summary, the pD10-CMV-FGF-5 (sig−) plasmid contains the CMV immediate/early enhancer+promoter, the CMV intron A, the FGF-5 coding region with the modifications described in Example C above, the bovine growth hormone polyA site, and the AAV ITR sequences. There is a 1353 bp insertion of PhiX 174 bacteriophage DNA clones into the NotI site between one ITR and the CMV immediate early enhancer +promoter region. [0172]
D. Western Analysis of 293 Cells Transfected with pD10-CMV-FGF-5 (sig−). [0173]
Expression of FGF-5 protein was demonstrated by transient transfection of 293 cells with the plasmid pD10-CMV-FGF-5 (sig−), by standard methods. After 48 hours, tissue culture media and cell lysates were harvested. Western analysis was performed with an anti-human FGF-5 antibody (R and D systems) as described above. [0174]
Results of the Western analysis are provided below in FIG. 6. Briefly, [0175] lane 1 represents 50 ng of the 29.5 Kd recombinant FGF-5 protein (R and D systems). Lanes 2 and 3, showing FGF-5 expression, are cell lysates from 293 cells transfected with two different clones of the pD10-CMV-FGF-5 sig− plasmid. Lane 4 is lysate from cells transfected with a negative control plasmid CMV-Epo. Lanes 5, 6 and 7 represent media from cells transfected with different clones of the pD10-CMV-FGF-5 sig− plasmid, respectively, and the CMV-Epo plasmid. As is evident from this figure, FGF-5 protein was detected in the cell lysate only.
E. Generation of FGF-5 (signal −) rAAV. [0176]
FGF-5 (sig−) rAAV virus is packaged using the triple transfection method described in more detail above. [0177]
F. Cloning FGF-18 into the pD10-CMV rAAV Vector. [0178]
The FGF-18 coding region (see U.S. Provisional Application Serial No. 60/083,553) was cloned into the pD10-CMV vector as a PstI to EcoRV fragment, using restriction sites found in both the FGF-18 and the multiple cloning site of the pD 10-CMV vector. The vector contains a 1353 bp insertion of PhiX174 bacteriophage DNA (see Example A). [0179]
A schematic illustration of pD10-CMV-FGF-18 is provided in FIG. 7. Briefly, this plasmid contains the CMV immediate/early enhancer+promoter, the CMV intron A, the FGF-18 coding region, the bovine growth hormone polyA site, and the AAV ITR sequences. There is a 1353 bp insertion of PhiX 174 bacteriophage DNA cloned into the NotI site between one ITR and the CMV immediate early enhancer+promoter region. [0180]
G. Analysis of 293 Cells Transfected with pD10-CMV-FGF-18 Plasmid. [0181]
Expression of FGF-1 8 protein was assessed by transient transfection of 293 cells followed by Western analysis, using standard methods. Cell lysates and tissue culture media were harvested at 48 hours post transfection. An anti-peptide FGF-18 rabbit polyclonal antibody, generated against a selected polypeptide from recombinant FGF-1 8, was used at a dilution of 1:2,500 for one hour at room temperature. The secondary antibody, an anti-rabbit IgG conjugated to peroxidase, was used at a dilution of 1:25,000. [0182]
Results of the Western analysis are provided in FIG. 8. Briefly, lanes 1-3 represent 1, 2 and 10 ul of tissue culture media from cells transfected with the pD 110-CMV-FGF-18 plasmid. [0183] Lane 4 is blank. Lanes 5, 6 and 7 contain 2, 10 and 20 ul of lysate from the transfected cells. Lanes 8 and 9 are negative controls; 20 ul of tissue culture media and cell lysate, respectively, from uninfected cells. Lane 10 contains a positive control; an FGF-18-maltose binding protein fusion ((MBP); predicted size =80 Kd, larger than the FGF-18 protein).
H. Packaging of the pD10CMV-FGF-18 Plasmid into rAAV Particles [0184]
FGF-1 8 rAAV virus was generated by the triple transfection method. [0185]

Example 5

AAV—LacZ Injected Retina

A. Subretinal Injection of rAAV [0186]
Albino Sprague-Dawley rats were injected at 14-15 days postnatal (P14-P15). Animals were anesthetized by ketamine/xylazine injection, and a local anesthetic (proparacain HCl) was applied topically to the cornea. An aperture was made through the inferior cornea of the eye with a 28 gauge needle. Subretinal injections of 2-3μl of AAV-CMV-Lac-Z were then made by inserting a blunt 32 gauge needle through the opening and delivering the rAAV suspension into the subretinal space in the posterior retina. The contralateral eye was either uninjected, injected subretinally with PBS, or with a control rAAV containing a reporter gene. [0187]
B. Staining Protocol [0188]
Cryosections of the retina were stained with Bluo-gal for b-galactosidase reaction product of lacZ. In all wild type rats tested (3), positive staining was visible in the interior of the whole eyecup upon gross examination (see FIG. 9). 100 μm thick agarose or 20 μm thick cryosections of retinas indicated that most of the b-gal positive staining localized to the photoreceptors. There were a small number of LacZ positive retinal ganglion cells observed. [0189]
C. Anti-b-galactosidase Immunocytochemistry [0190]
Sections from 3 wildtype and 2 transgenic rats were stained with a polyclonal antibody against b-galactosidase. These results were comparable to the bluo-gal results, primarily demonstrating photoreceptor-specific staining. Two out of five rats showed no positive staining. [0191]
D. Results [0192]
Subretinal injection of 2 ul of AAV-CMV-lacZ effectively transduced a large number of photoreceptor and retinal pigment epithelial (rpe) cells following a single intraocular inoculation of AAV-CMV-lacZ into the subretinal space (SRS) of the rat eye. The lateral extent of lacZ reporter gene expression was typically ⅓ to ½ of the retinal expanse following a single AAV-CMV-LacZ injection. This finding was confirmed by bluo-gal staining of the b-galactosidase reaction product of the lacZ gene as well as by immunocytochemistry using an antibody specific for b-galactosidase. The AAV-CMV-lacZ vector was effective at transducing photoreceptor and RPE cells in both the normal (wildtype) and affected, degenerating (transgenic) rat retina. [0193]

Example 6

Retinal Tissue Analysis OF rAAV-FGF-2 infected cells, vs. Controls [0194]
A. Subretinal Injection of rAAV [0195]
[0196] Line 3 albino transgenic rats (P23H-3) on an albino Sprague-Dawley background (produced by Chrysalis DNX Transgenic Sciences, Princeton, N.J.) were injected at the ages of P14 or P15. Animals were anesthetized by ketamine/xylazine injection, and a local anesthetic (proparacain HCl) was applied topically to the cornea. An aperture was made through the inferior cornea of the eye with a 28 gauge needle. The subretinal injections of 2 μl were then made by inserting a blunt 32 gauge needle through the opening and delivering the rAAV suspension into the subretinal space in the posterior retina. The intent was to inject into the subretinal space of the posterior superior hemisphere, but sometimes upon histological examination it was found that the injection site was located just inferior to the optic nerve head. The opposite eye was either uninjected, injected subretinally with PBS, with control rAAV containing no neurotrophin or containing proteins not known to possess neurotrophic properties.
B. Histopathology Protocol/Retinal Tissue Analysis [0197]
The rats were euthanized by overdose of carbon dioxide inhalation and immediately perfused intracardially with a mixture of mixed aldehydes (2% formaldehyde and 2.5% glutaraldehyde). Eyes were removed and embedded in epoxy resin, and 1 μm thick histological sections were made along the vertical meridian. Tissue sections were aligned so that the ROS and Muller cell processes crossing the inner plexiform layer were continuous throughout the plane of section to assure that the sections were not oblique, and the thickness of the ONL and lengths of RIS and ROS were measured as described (see e.g., LaVail, et al. PNAS 1992, 89(23:11249-53 and LaVail et al., Invest. Ophthamlmol. Vis. Sci 1998, 39(3):592-602). Briefly, 54 measurements of each layer or structure were made at set points around the entire retinal section. These data were either averaged to provide a single value for the retina, or plotted as a distribution of thickness or length across the retina. The 3 greatest contiguous values for ONL thickness was also compared in each retina, to determine if any region of retina (e.g., nearest the injection site) showed proportionally greater rescue; although most of these values were slightly greater than the overall mean of all 54 values, they were no different from control values than the overall mean. Thus, the overall mean was used in the data cited, since it was based on a much larger number of measurements. [0198]
C. Results [0199]
Two surgical methods of delivery of rAAV-CMV-FGF2 were completed, intravitreal and subretinal injection. [0200]
1. Intravitreal injection [0201]
RAAV-CMV-FGF-2 was injected into the right eye of nine transgenic S334ter rats after day P15 (the left eye was not injected). S334(4) transgenic animals were used to assess the rescue effect of rAAV-CMV-FGF-2 on degenerating photoreceptor cells when delivered by intravitreal injection. The rats were all sacrificed at age p60 and the embedded in plastic and sectioned to assess morphology and therapeutic effect as assayed by the preservation of thickness of outer nuclear layer. Superior and inferior regions of eyecup are quantitated by measuring the ONL thickness using a BioQuant morphometric measuring system (BioQuant). Injected eyes were evaluated along with uninjected control eyes. [0202]
Control Left superior—16.52+/−2.77 urn [0203]
Injected Right superior-19.71+/−5.27 urn [0204]
Control Left inferior -22.64+/−2.11 um [0205]
Injected Right inferior -26.47+/−3.55 um [0206]
Based upon these results it was evident that there is a rescue effect of AAV -CMV-FGF-2 when delivered intraocularly into the vitreous cavity. [0207]
2. Subretinal Injection of rAAV-CMV-FGF-2 [0208]
Experiment A.—Location of injection—subretinal, 7 rats-both right and left eyes injected, 3 rats-(left eye =uninjected). Number of rats injected—10 rats all wild type p15 on day of injection. One rat was sacrificed every week starting at [0209] week 2. Expression of FGF-2 was assessed, as well as any signs of inflammation or neovascularization.
Experiment B.—Location of injection—subretinal, 5 rats—right eyes injected w/vector left eyes injected with PBS, 4 rats—right eyes injected w/vector (left eye=uninjected). Number of rats injected—11 transgenic S334(4) rats—all were p15 on day of injection. The rats were sacrificed at age p60 and the embedded in plastic and sectioned to assess histopathology and number of surviving photoreceptor cells. . [0210]
Anatomic indication of therapeutic effect (photoreceptor rescue) was assessed histologically. Briefly, eyes injected with rAAV-CMV-FGF2 retained significantly more photoreceptors at P60, P75 and P90 than uninjected contralateral control eyes of the same animal. Retinas receiving a subretinal injection of AAV-CMV-FGF2 at P14-15 retained 71% of the normal ONL thickness, compared to about 47% in the uninjected controls (see FIGS. 11, 12, [0211] 13 and 14).
There was little or no rescue in PBS-injected control eyes (p>0.169 in all cases). This is consistent with previous reports that needle injury to the retina in young rats (P14-P15) does not rescue photoreceptors or up-regulate bFGF mRNA expression. [0212]
3. Subretinal injection of rAAV-CMV-FGF-2 [0213]
Two to three microliters of rAAV-CMV-FGF-2 vector was injected into the subretinal space between the photoreceptors and the adjacent retinal pigment epithelium at P14 or P15. Rats were sacrificed and eyes examined at time points between P60-P90. At these ages in uninjected control eyes of S334ter rats, the ONL thickness, which is an index of photoreceptor cell number, was reduced to about 60% of normal. [0214]
Evidence of anatomic rescue was found to be significant to the p=.005 confidence level in retinas transfected by rAAV-CMV-FGF-2 when compared to the control AAV vectors or sham injection of PBS by ANOVA (analysis of Variance statistical measures). JMP statistical analysis software (Copyright (c) 1999 SAS Institute Inc. Cary, N.C., USA). [0215]

Example 7

Antibody Staining OF RAAV-FGF-2 Infected Cells

A. Injection Protocol [0216]
Albino Sprague-Dawley rats were injected with rAAV-CMV-FGF-2 at the ages of P14 or P15 essentially as follows. Briefly, wild-type animals were anesthetized by ketamine/xylazine injection, and a local anesthetic (proparacain HCl) was applied topically to the cornea. An aperture was made through the inferior cornea of the eye with a 28 gauge needle. The subretinal injections of 2-3 ul of rAAV-CMV-FGF-2 were then made by inserting a blunt 32 gauge needle through the opening and delivering the rAAV suspension into the subretinal space in the posterior retina. The contralateral eye was either uninjected, injected subretinally with PBS, wild-type rAAV, or with rAAV-CMV-lacZ. [0217]
B. Staining Protocol [0218]
Fixed eyecups were embedded in OCT and cryosectioned in 20um thick sections. Sections from 10 wt rats were stained with antibody to FGF-2. (primary-anti-FGF-2 1:500 (commercial antibody purchased from R&D systems) (secondary-anti-goat Cy3 conjugate (Sigma, St. Louis. Mo.) [0219]
C. Results [0220]
Immunohistochemistry was used to look for expression of FGF-2 in the eye. Two rats were examined every week starting at 3 weeks post-injection. Retinas were examined for expression of FGF-2 and also examined histopathologically for signs of inflammation or neovascularization. [0221]
Results are shown in FIG. 15. Briefly, expression of FGF-2 was found in retinal photoreceptor cells as well as RPE cells at 35 days following inoculation with 2-3 ul of rAAV-CMV-FGF-2. Less significant expression was noted in retinal bipolar interneurons and retinal ganglion cells (RGCs) following injection into the subretinal space (SRS). No significant staining above background was observed in sections injected with PBS or rAAV-CMV-lacZ vectors. [0222]

Example 8

Retinal Tissue Analysis OF rAAV-FGF-5 (SIG−) AND −18 Infected Cells, vs. Controls

A. Subretinal Injection of rAAV [0223]
[0224] Line 4 albino transgenic rats (S334ter-4) on an albino Sprague-Dawley background (produced by Chrysalis DNX Transgenic Sciences, Princeton, N.J.) were injected at age P15. Animals were anesthetized by ketamine/xylazine injection, and a local anesthetic (proparacain HCl) was applied topically to the cornea. An aperture was made through the inferior cornea of the eye with a 28 gauge needle. The subretinal injections of 2.5 μl were then made by inserting a blunt 32 gauge needle through the opening and delivering the rAAV suspension into the subretinal space in the posterior retina. The opposite eye was either uninjected, injected subretinally with PBS, with control rAAV containing no neurotrophin or containing proteins not known to possess neurotrophic properties.
B. Histopathology Protocol/Retinal Tissue Analysis [0225]
The rats were euthanized by overdose of carbon dioxide inhalation and immediately perfused intracardially with a mixture of mixed aldehydes (2% formaldehyde and 2.5% glutaraldehyde). Eyes were removed and embedded in epoxy resin, and 1 μm thick histological sections were made along the vertical meridian. Tissue sections were aligned so that the ROS and Müller cell processes crossing the inner plexiform layer were continuous throughout the plane of section to assure that the sections were not oblique, and the thickness of the ONL was measured as described (LaVail, et al). Briefly, 54 measurements of each layer or structure were made at set points around the entire retinal section. The 27 measurements from the inferior region and the superior region of the retina were averaged separately to give two values for each eye. This separation was made because the retina degenerates at different rates in these two regions of the S334ter-4 animal model. [0226]
C. Results [0227]
Sub-retinal injections of both rAAV-CMV-FGF-5 (sig−) and rAAV-CMV-FGF-18 were performed. [0228]
1. Sub-Retinal Injection of rAAV-CMV-FGF-5 (sig−) [0229]
Experiment.—Location of injection—subretinal, 3 rats—right eyes injected w/vector left eyes injected with PBS, 8 rats—right eyes injected w/vector left eyes injected with rAAV-CMV-LacZ, 4 rats—right eyes injected w/vector (left eye=uninjected). Number of rats injected—15 transgenic S334ter-4 rats—all were p15 on day of injection. The rats were sacrificed at age p60. The retinas were embedded in plastic and sectioned to assess histopathology and number of surviving photoreceptor cells. [0230]
Anatomic indication of therapeutic effect (photoreceptor rescue) was assessed histologically. The injection of rAAV-CMV-FGF-5 (sig−) resulted in significant rescue of photoreceptors, compared to PBS injected, rAAV-CMV-LacZ injected, and uninjected eyes (see FIG. 33). The rescue was significant to the p=0.05 confidence level for all three comparisons, by ANOVA (analysis of Variance statistical measures). JMP statistical analysis software (Copyright (c) 1999 SAS Institute Inc. Cary, N.C., USA). [0231]
2. Sub-Retinal Injection of rAAV-CMV-FGF-18 [0232]
Experiment.—Location of injection—subretinal, 3 rats—right eyes injected w/vector left eyes injected with PBS, 3 rats—right eyes injected w/vector left eyes injected with rAAV-CMV-LacZ, 4 rats—right eyes injected w/vector (left eye=uninjected). Number of rats injected—10 transgenic S334ter-4 rats —all were p15 on day of injection. The rats were sacrificed at p60, and the retinas embedded in plastic and sectioned. [0233]
Eyes injected with rAAV-CMV-FGF-18 retained significantly more photoreceptors at P60 than PBS injected, rAAV-CM-LacZ injected, or uninjected control eyes. Each comparison, by ANOVA, was statistically significant to the p=0.05 confidence level. [0234]

Example 9

In Vivo Delivery to Retinal Ganglion Cells (RGCS)

A. Intra-Vitreal Injection of AAV Vectors [0235]
All surgical procedures were performed in female adult Sprague-Dawley rats (180-200 g; Charles River Breeders) under general anesthesia (7% chloral hydrate; 0.42 mg per g of body weight, i.p.) in accordance with the Use of Animals in Neuroscience Research and McGill University Animal Care Committee guidelines for the use of experimental animals. [0236]
Briefly, rAAV-CMV-lacZ (5 μl; see above) was injected into the vitreous chamber in the superior (dorsal) hemisphere of the retina using a posterior approach as described (Di Polo, PNAS, 1998). Control eyes were injected with equal volumes of Hepes-buffered saline (HBS, virus vector). [0237]
B. Identification of RPCs [0238]
For visualization of RGCs, neurons were retrogradely labeled with the fluorescent tracer Fluorogold (Fluorochrome, Englewood, Colo.) at 2% in 0.9% NaCl containing 10% dimethyl sulfoxide by application of the tracer to both [0239] superior colliculi 7 days prior to analyses as described (Vidal-Sanz et al., 1988). Anesthetized rats were then perfused intracardially with 4% paraformaldehyde in 0.1 M phosphate buffer (PB, pH 7.4) and the eyes were immediately enucleated. The anterior part of the eye and the lens were removed and the remaining eye cup was immersed in the same fixative for 2 hr at 4° C. Eye cups were cryoprotected in graded sucrose solutions (10-30% in PB) for several hours at 4° C., embedded in O.C.T. compound (Tissue-Tek, Miles Laboratories, Elkhart, IN) and frozen in a 2-methylbutane/liquid nitrogen bath. Retinal radial cryosections (12-15 em), obtained along the vertical meridian of the eye, were collected onto gelatin-coated slides and processed for immunocytochemistry. Alternatively, entire eyes were rinsed three times (15 min each) in PBS at room temperature with gentle shaking, to whole-mount histochemical staining as described below.
C. Histochemical Analysis [0240]
Expression of the bacterial LacZ gene in whole retinas was detected by standard histochemical staining reactions using halogenated indoyl-β-D-galactoside (Bluogal; GIBCO BRL). Following removal of the anterior eye structures and lens, eye cups were incubated overnight in a staining solution containing 5 mM K-ferricyanide, 5 mM K-ferrocyanide, 2 mM MgCl[0241] ₂, and 0.5 mg/ml Bluo-gal at 37° C. Retinas were then dissected, fixed for an additional 30 min and flat-mounted vitreal side up on glass slides.
For visualization of the AAV-mediated lacZ gene product in retinal radial sections, cryosections were incubated in 10% normal goat serum (NGS) in 0.2% Triton X-100 (Sigma, St. Louis, Mo.) in phosphate buffer saline (PBS) for 30 min at room temperature to block non-specific binding. Two primary antibodies raised against the lacZ gene product were used with similar results. A polyclonal anti-betagal antibody (diluted 1:1000; 5 prime→3 prime, Inc., Boulder, Colo.) and a monoclonal anti-LacZ antibody (diluted 1:500; Promega, Madison, Wis.). Primary antibodies were added in 2% NGS in 0.2% Triton X-100 and incubated overnight at 4° C. Sections were subsequently processed with anti-rabbit Cy3-conjugated IgG (diluted 1:500, Jackson Immunoresearch, West Grove, Pa.) or anti-mouse Cy3-conjugated IgG (diluted 1:500, Jackson Immunoresearch) and mounted. Control sections were treated in the same way but with omission of the primary antibody. Sections were visualized by fluorescent microscopy (Polyvar, Reichert-Jung). [0242]
Expression of the heparan sulfate proteoglycan receptor in the retina was examined using a monoclonal anti-heparan sulfate antibody (HepSS-1, diluted 1:1,000, Seikagaku Corporation, Tokyo, Japan). Following overnight incubation at 4° C., sections were processed with biotinylated anti-mouse Fab fragment (Jackson Immunoresearch), avidin-biotin-peroxidase reagent (ABC Elite Vector Labs, Burlingame, Calif.), followed by reaction in a solution containing 0.05% diaminobenzidine tetrahydrochloride (DAB) and 0.06% hydrogen peroxide in PB (pH 7.4) for 5 min. For analysis of co-localization of heparan sulfate in Fluorogold-labeled neurons, sections were processed with Cy3-coupled anti-mouse IgG (Jackson Immunoresearch) after incubation in primary antibody. In all cases, the primary antibody was omitted in control sections. Sections were mounted and visualized by light or fluorescent microscopy. [0243]
Quantification of AAV-transduced cells in the ganglion cell layer of retinal flat-mounts was performed in two ways: i) by counting the entire number of Bluo-gal positive cells in each of the retinal quadrants (superior, inferior, temporal and nasal); and ii) by counting the number of cells in three standard areas (at 1, 2 and 3 mm from the optic disc) of each quadrant as previously described (Villegas-Perez et al., 1993). [0244]
For quantification of Fluorogold, Bluo-gal or HepSS-1 positive cells in retinal radial sections, the entire number of labeled cells per section was counted under fluorescent microscopy. Four to five serial sections per eye were routinely counted and a mean value per animal was obtained, followed by the calculation of a mean value for the entire experimental group which consisted of 4-5 rats. Results were analyzed using the Sigmastat program (Jandel, San Rafael Madera, Calif.) by a student's t test (paired groups). [0245]
D. Results [0246]
Analysis of retinas from eyes that received a single intravitreal injection of rAAV-CMV-lacZ demonstrated a large number of LacZ-positive cells throughout the entire GCL as assessed by histochemical LacZ staining of both flat-mounts (FIG. 16A) and radial sections (FIG. 16B). In many cases, RGCs transduced by AAV could be unequivocally identified because the LacZ reaction product filled their axons that converged at the level of the optic nerve head. In addition, LacZ-positive photoreceptor nuclei were observed but were always restricted to the vicinity of the injection site (not shown). No staining was observed in control eyes injected with virus vector. No signs of cytotoxic damage or cellular immune reaction to the viral vector were observed in any of the retinas examined. [0247]
Quantification of LacZ-positive cells in the GCL of retinal flat-mounts demonstrated a 2.8-fold increase between 2 and 4 weeks after intravitreal injection of the rAAV-CMV-lacZ vector (FIG. 17). For example, it was found that 27,569±7,646 cells/retina (mean±S.D.;n=3) and 79,043±10,321 cells/retina (n=4) expressed the LacZ gene product at 2 and 4 weeks after intraocular administration of the vector, respectively. A comparable number of cells expressing the AAV-mediated transgene at 4 weeks was observed at 8 weeks (70,221±12,500; n=3) following rAAV-CMV-lacZ injection. Although the majority of LacZ-positive cells were observed in the superior hemisphere at 2 weeks after virus administration, there was robust transgene expression throughout the entire retina by 4 and 8 weeks as assessed by quantification of Lac-Z positive cell densities in all retinal quadrants at these time points (FIG. 17). [0248]
To identify the cellular localization of the AAV-mediated LacZ gene product, immunocytochemical staining of LacZ was combined with retrograde tracing of RGC bodies using Fluorogold backlabeling from the superior colliculi. Double-labeling experiments indicated that the majority of cells in the GCL expressing the LacZ gene product were also Fluorogold-positive (FIG. 18). Analysis of the number of Fluorogold-labeled cells in the GCL expressing the LacZ gene product indicated that 300±29 (mean ±S.D.; n=4) expressed both markers out of 330±32 Fluorogold-labeled cells (the average RGC population per retinal radial section). This indicates that ˜92% of RGCs, identified by the Fluorogold label, also expressed the AAV-mediated LacZ gene product (FIG. 19). In all retinas examined, it was routinely observed that a number of Lac-Z positive cells that were not labeled with Fluorogold (FIGS. 18 and 19). Thus, it is possible that these cells are displaced amacrine cells or RGCs that failed to incorporate the retrograde tracer. Together, these results indicate that RGCs are preferentially transduced by recombinant AAV following intravitreal injection of this viral vector. [0249]
To investigate the molecular mechanisms underlying preferential transduction of RGCs by AAV, expression of the heparan sulfate proteoglycan (which mediates both AAV attachment and infection of target cells (Summerford et al., 1998)) in the adult retina was observed. Immunostaining of retinal radial sections with a specific antibody against heparan sulfate (HepSS-1) demonstrated robust staining in the GCL (FIG. 20). Positive immunolabeling was clearly visualized in both neuronal somata and axonal bundles in the fiber layer. More diffuse and sparse staining was observed in some photoreceptor nuclei and cells in the inner nuclear layer. No staining was observed in control retinal sections in which the primary antibody was omitted (not shown). [0250]
To determine the cell type within the GCL that express the heparan sulfate proteoglycan receptor, a double-labeling study was performed in which RGCs were first retrogradely labeled from the superior colliculi followed by immunostaining of retinal sections with HepSS-1. Our analysis showed that 299+23 (mean ±S.D.; n—4) cells in the GCL expressed both Fluorogold and HepSS-1 markers out of 315+34 Fluorogold-labeled cells which represent the average RGC population visualized per retinal radial section. The large population of RGCs (˜95%) expressing heparan sulfate proteoglycan receptor correlated well with the number of RGCs expressing the AAV-mediated transgene product (˜92%). Together, these data suggest that preferential transduction of adult RGCs by recombinant AAV is mediated by the heparan sulfate proteoglycan receptor expressed by these neurons. [0251]

Example 10

Construction of a rAAV Vector Expressing Vascular Endothelial Growth Factor (VEGF) 165

The human VEGF-165 cDNA was cloned from the PCR-Blunt II Topo Vector (Invitrogen) into the pD10-CMV rAAV vector as an EcoRI fragment (pD10 -VEGFuc). The pD10-VEGFuc vector is illustrated schematically in FIG. 21, and its nucleotide sequence is shown in FIG. 22. The VEGFuc rAAV virus was packaged using the triple transfection method and purified by column chromatography. [0252]
Briefly, a cell pellet is resuspended in TNM buffer: 20 mM Tris pH 8.0, 150 mM NaCl, 2 mM MgCl[0253] ₂. Deoxycholic Acid is added to 0.5% to lyse the cells. 50u/ml Benzonase is added and the lysed cells are incubated at 37 degrees to digest any nucleic acids. The cell debris is pelleted and the supernatant is filtered through a 0.45 um filter and then a 0.22 um filter. The virus is then loaded onto a 1.5 ml Heparin sulfate column using the Biocad. The column is then washed with 20 mM Tris pH 8.0, 100 mM NaCl. The rAAV particles are eluted with a gradient formed with increasing concentrations of NaCl. The fractions under the peak are pooled and filtered through a 0.22 um filter before overnight precipitation with 8% PEG 8000. CaCl₂is added to 25 mM and the purified particles are pelleted and then resuspended in HBS#2: 150 mM NaCl, 50 mM Hepes pH 7.4.

Example 11

Infection of 293 Cells with D10-VEGF rAAV Results in VEGF Protein Expression

The functionality of the viral particles was assessed by infection of 293 cells with 3 different viral multiplicities of infection (MOIs); 1×10e7, 1×10e8 and 1×10e9 viral particles per 4×10e5 293 cells, in the presence of 1.5 uM etoposide. At 48 hours post infection, tissue culture media (sups) and cell lysates were harvested. VEGF protein levels were determined using a Quantikine human VEGF sandwich ELI SA kit (R and D Systems, see FIG. 23). VEGF protein concentrations are given in pg/ml. The two highest MOIs gave values significantly above that of the cells infected with a negative control virus. The levels of secreted VEGF were approximately 4-7 fold higher than those of the lysates. [0254]

Example 12

Infection of Retinal Pigment Epithelial (RPE) Cells with D 10-VEGF rAAV Results in VEGF Protein Secretion

VEGF expression levels in a monolayer of cultured primary (or very early passage) human fetal RPE cells infected with D10-VEGF 165 rAAV were clearly elevated relative to endogenous levels. Cells were infected with a range of rAAV particles from 0 to 1×10e5 per cell. VEGF expression was dose dependent, increased over time, and secretion appeared to be somewhat higher from the apical surface. In a representative experiment, RPE cells infected with 1×10e5 viral particles secreted >100 ng/1×10e6 cells from the apical surface and 50 ng/1×10e6 cells from the basal surface at 8 days post infection. The polarity of VEGF secretion from human fetal RPE cells infected with 3 different MOIs is shown in FIG. 24. [0255]

Example 13

Infection of Retinal Pigment Epithelial (RPE) Cells with VEGF rAV Results In VEGF Protein Secretion and Decreased Membrane Conductance

Infection of cultured human fetal RPE cells with recombinant VEGF adenovirus (AV) results in secretion of very high levels of VEGF from both the apical and basal surfaces of the RPE. MOI's of 0 to 1,000 or 0 to 10,000 particles per cell were used in two separate experiments. In both cases, expression levels increased over time, peaking at approximately 100-200 ug/1×10e6 cells at the highest MOI's (see FIG. 25). In addition, the total transepithelial membrane resistance of the RPE monolayer decreased significantly at all MOIs, and by approximately 4-5 fold at the highest MOIs (see FIG. 26). [0256]

Example 14

Construction of a rAAV Vector Expressing Soluble FLT-1 (SFLT-1) Receptor

The sFlt-1 cDNA was cloned from the Blunt II Topo Vector (Invitrogen) into the pD10-CMV rAAV vector as an EcoRI fragment (pD10-sFlt-1). The pD10-sFlt-1 vector is illustrated schematically in FIG. 27, and its nucleotide sequence is shown in FIG. 28. The human sFlt-1 rAAV virus was packaged using the triple transfection technique and purified by column chromatography. [0257]

Example 15

In Vitro Assay for Anti-Angiogenic Activity

This example describes the HMVEC (human dermal microvascular endothelial cell) proliferation assay, which can be utilized to determine the anti-angiogenic activity of a molecule by inhibition of VEGF stimulated proliferation (see Kupprion et al., 1998. JBC 273:29635-29640). [0258]
Briefly, HMVEC cells obtained from Clonetics (catalog #2543), are seeded in a 96 well culture dish at a density of 2,000 cells per well in 100 ul assay media and incubated at 37° C. for 3-5 hours. The assay media is EBM media, or endothelial basal media (Clonetics, catalog #CC-3121) containing 5% FBS and 1% pen/strep. Dilutions of anti-angiogenic samples are added in triplicate (50 ul each, for final well volume of 200 ul), immediately followed by 50 [0259] ul 20 ng/ml recombinant VEGF (R and D Systems, final concentration 5 ng/ml, or 0.1 nM). The samples are conditioned media from 293 cells transiently transfected with a pD 10 rAAV plasmid, by standard methods, or from 293 cells infected with an rAAV virus. Culture media is collected from 24-48 hours post-transfection or post-infection. After the addition of sample and recombinant VEGF, the cells are incubated for 48 hours at 37° C., when they are pulsed with 1 uCi/well H-thymidine (Amersham, catalog #TRK300). The stock of 1 mCi/ml ³H-thymidine is diluted 1:10 in assay media, and 10 ul added per well. The cells are incubated for an additional 18 hours, at which point 100 ul media is removed and the cells are lysed by the addition of 40 ul of 1M NaOH per well. Finally, the cells are harvested with a Tomtec Harvestor, transferred to Filtermat paper (Wallac), 10 ml of scintillation fluid added and the incorporation of ³H-thymidine determined by scintillation counting.
Inhibition of HMVEC proliferation by conditioned media from sFlt-1 rAAV infected 293 cells is shown in FIG. 34. Complete inhibition of proliferation (induced by 0.1 nM VEGF) was observed at approximately at 1 nM sFlt-1, and partial inhibition at approximately 0.3 nM and 0.1 nM sFlt-1 protein. This inhibition was not seen with HMVEC cells treated with conditioned media from lacZ rAAV infected cells, or cells treated with recombinant VEGF alone. To generate conditioned media, 4×10e5 293 cells were infected with 1×10e11total particles sFlt-1 rAAV or a CMV-lacZ control rAAV. If one assumes an infectious particle ratio of 1:1,000 to 1:10,000, this is an MOI of less than or equal to 2.5×10e2 per cell. All samples were run in triplicate, and means and standard deviations are shown. Background incorporation of [0260] ³H-thymidine in cells not stimulated with exogenous VEGF was subtracted from all samples, leading to a negative value in one case. The total amount of sFlt-1 protein in the conditioned media was determined by a sandwich Elisa (antibodies purchased from R and D Systems).

Example 16

Animal Model for Neovascularization by Subretinal Injection of VEGF rAAV

This example describes an animal model that, after subretinal injection of a recombinant virus (rAAV) containing an angiogenic transgene (VEGF), generates subretinal neovascularization and choroidal neovascularization. As noted above, choroidal neovascularization is a hallmark of exudative or wet Age-related Macular Degeneration (AMD), the leading cause of blindness in the elderly population. Retinal neovascularization occurs in diseases such as diabetic retinopathy and retinopathy of prematurity (ROP), the most common cause of blindness in the young. [0261]
Briefly, subretinal injections of 2 μl AAV-VEGF (titer: 5.8×0.1013 particles/ml) were made in a bleb under the retina just outside the apical membrane of the RPE. These injections were made 3-3.5 months before the animals were sacrificed. After sacrifice animals were examined for the extent and duration of neovascularization induced by rAAV vectors using fundus photography, fluorescein angiography (FIG. 35), histology (FIG. 36), and immunochemistry (FIG. 37). As described in more detail below, these figures demonstrate in three different ways that AAV mediated overexpression of VEGF in the RPE can generate choroidal neovascularization. [0262]
More specifically, FIG. 35A is an image of the fundus showing retinal blood vessels from a live animal before it was sacrificed for the serial sectioning shown in FIG. 36. Note that the blood vessels are larger in diameter in the AAV-VEGF injected area (black arrow). FIG. 35B, is a fluorescein angiogram from the same animal taken shortly after the fundus image in 35A. Two minutes after fluorescein injection (intramuscular) significant leakage of fluorescein was observed at the AAV-VEGF injection site (black arrows). [0263]
FIG. 36 (panels A-D) are a series of epoxy sections taken after sacrifice of the animal. FIG. 36A is a section taken from half of the eye furthest from AAV-VEGF injection site, showing normal photoreceptors and blood vessels (the arrow points to photoreceptors with normal morphology). Moving from this section toward the AAV-VEGF injection site, monotonically increasing photoreceptor disorganization and new blood vessel formation was observed (data not shown). [0264]
FIGS. 36B and C are epoxy sections from the AAV-VEGF injection site. The short arrows show new blood vessel growth and the long arrows show a pathologically disorganized photoreceptor layer. FIG. 36D is also an epoxy section from the AAV-VEGF injection site. The arrow points to a blood vessel breaking through Bruch's Membrane, probably from the choroid. [0265]
FIGS. [0266] 37(A-D) show lectin/BrdU double-staining of rat retina (A-B) and choroid (C-D). Green staining is the lectin staining of endothelial cells, and red staining is BrdU staining of dividing cells. Green cells with red dots are dividing endothelial cells, which are part of the newly formed blood vessels.
More specifically, FIG. 37A is an image of the at the AAV-VEGF injection site showing extensive BrdU staining. Note that there are many more blood vessels compared to that seen at points distant from the AAV-VEGF injection site in panel B. The lectin staining is fuzzy because the blood vessels are bloated with dividing endothelial cells. FIG. 37B is an image of the retina furthest from the AAV-VEGF injection site. This image shows minimal BrdU staining. In contrast, lectin staining is clear and sharply defined. FIG. 37C is an image of the choroids at the AAV-VEGF injection site, which also shows extensive BrdU staining. The lectin image is not shown since it binds indiscriminately throughout choroid and sclera. FIG. 37D is an image of the choroids furthest from the AAV-VEGF injection site, and shows minimal BrdU staining. [0267]

Example 17

Injection of Therapeutic Anti-Angiogenic rAAV into an Animal Model for Ocular Neovascularization

This example demonstrates the ability of anti-angiogenic molecules to prevent neovascularization in the rat model described above. Briefly, in four animals rAAV-sFlt-1 or rAAV-PEDF were injected together with rAAV-VEGF into the subretinal space of one eye; the contralateral eye received an injection of rAAV-VEGF and rAAV-GFP. Six weeks after injection, electroretinographic analysis (ERGs) were obtained from both eyes of each animals simultaneously. The a- or b-wave amplitude from the test eye (AAV-VEGF+AAV-sFlt) is designated as A[0268] _tor B_t. The a- or b-wave amplitude from the control eye (AAV-VEGF+AAV-GFP) is designated as A_cor B_c, respectively. In each eye ERG a- and b-waves were measured and for each animal the amplitude ratio was calculated as percent change in the test eye relative to the control eye:
ERG Amplitude Ratio=(A _t −A _c)/A _cor (B _t −B _c)/B _c
The amplitude ratio for a- and b-waves are plotted in FIG. 38. Briefly, significant functional rescue was obtained in three/four animals using sFlt-1 and two/four animals using PEDF. FIG. 39 shows comparison ERGs of test and control eye of sFlt-l treated rats. The dark-solid line shows that the eye rescued with sFlt-1 has a- and b-wave amplitudes approximately twice as large as the control eye (light-dashed line). This data indicates that sFlt-1 or PEDF can be used to rescue retinal function that is lost during neovascularization. [0269]
From the foregoing, it will be appreciated that, although specific embodiments of the invention have been described herein for purposes of illustration, various modifications may be made without deviating from the spirit and scope of the invention. Accordingly, the invention is not limited except as by the appended claims. [0270]
1 12 1 6514 DNA Homo sapien 1 accatgtagc ggccctgcgc gctcgctcgc tcactgaggc cgcccgggca aagcccgggc 60 gtcgggcgac ctttggtcgc ccggcctcag tgagcgagcg agcgcgcaga gagggagtgg 120 ccaactccat cactaggggt tccttgtagt taatgattaa cccgccatgc tacttatcta 180 cgtagccatg ctctagggaa ttggccgcgg aatttcgact ctaggccatt gcatacgttg 240 tatctatatc ataatatgta catttatatt ggctcatgtc caatatgacc gccatgttga 300 cattgattat tgactagtta ttaatagtaa tcaattacgg ggtcattagt tcatagccca 360 tatatggagt tccgcgttac ataacttacg gtaaatggcc cgcctggctg accgcccaac 420 gacccccgcc cattgacgtc aataatgacg tatgttccca tagtaacgcc aatagggact 480 ttccattgac gtcaatgggt ggagtattta cggtaaactg cccacttggc agtacatcaa 540 gtgtatcata tgccaagtcc gccccctatt gacgtcaatg acggtaaatg gcccgcctgg 600 cattatgccc agtacatgac cttacgggac tttcctactt ggcagtacat ctacgtatta 660 gtcatcgcta ttaccatggt gatgcggttt tggcagtaca ccaatgggcg tggatagcgg 720 tttgactcac ggggatttcc aagtctccac cccattgacg tcaatgggag tttgttttgg 780 caccaaaatc aacgggactt tccaaaatgt cgtaataacc ccgccccgtt gacgcaaatg 840 ggcggtaggc gtgtacggtg ggaggtctat ataagcagag ctcgtttagt gaaccgtcag 900 atcgcctgga gacgccatcc acgctgtttt gacctccata gaagacaccg ggaccgatcc 960 agcctccgcg gccgggaacg gtgcattgga acgcggattc cccgtgccaa gagtgacgta 1020 agtaccgcct atagactcta taggcacacc cctttggctc ttatgcatgc tatactgttt 1080 ttggcttggg gcctatacac ccccgctcct tatgctatag gtgatggtat agcttagcct 1140 ataggtgtgg gttattgacc attattgacc actcccctat tggtgacgat actttccatt 1200 actaatccat aacatggctc tttgccacaa ctatctctat tggctatatg ccaatactct 1260 gtccttcaga gactgacacg gactctgtat ttttacagga tggggtccat ttattattta 1320 caaattcaca tatacaacaa cgccgtcccc cgtgcccgca gtttttatta aacatagcgt 1380 gggatctccg acatctcggg tacgtgttcc ggacatgggc tcttctccgg tagcggcgga 1440 gcttccacat ccgagccctg gtcccatccg tccagcggct catggtcgct cggcagctcc 1500 ttgctcctaa cagtggaggc cagacttagg cacagcacaa tgcccaccac caccagtgtg 1560 ccgcacaagg ccgtggcggt agggtatgtg tctgaaaatg agctcggaga ttgggctcgc 1620 acctggacgc agatggaaga cttaaggcag cggcagaaga agatgcaggc agctgagttg 1680 ttgtattctg ataagagtca gaggtaactc ccgttgcggt gctgttaacg gtggagggca 1740 gtgtagtctg agcagtactc gttgctgccg cgcgcgccac cagacataat agctgacaga 1800 ctaacagact gttcctttcc atgggtcttt tctgcagtca ccgtcgtcga cctaagaatt 1860 caggcctaag cttcctaggt atcgatctcg agcaagtcta gagggagacc acaacggttt 1920 ccctctagcg ggatcaattc cgcccccccc cctaacgtta ctggccgaag ccgcttggaa 1980 taaggccggt gtgcgtttgt ctatatgtta ttttccacca tattgccgtc ttttggcaat 2040 gtgagggccc ggaaacctgg ccctgtcttc ttgacgagca ttcctagggg tctttcccct 2100 ctcgccaaag gaatgcaagg tctgttgaat gtcgtgaagg aagcagttcc tctggaagct 2160 tcttgaagac aaacaacgtc tgtagcgacc ctttgcaggc agcggaaccc cccacctggc 2220 gacaggtgcc tctgcggcca aaagccacgt gtataagata cacctgcaaa ggcggcacaa 2280 ccccagtgcc acgttgtgag ttggatagtt gtggaaagag tcaaatggct ctcctcaagc 2340 gtattcaaca aggggctgaa ggatgcccag aaggtacccc attgtatggg atctgatctg 2400 gggcctcggt gcacatgctt tacatgtgtt tagtcgaggt taaaaaaacg tctaggcccc 2460 ccgaaccacg gggacgtggt tttcctttga aaaacacgat aataccatgg ccgccgggag 2520 catcaccacg ctgccagccc tgccggagga cggcggcagc ggcgctttcc cgccgggcca 2580 cttcaaggac cccaagcggc tgtactgcaa gaacgggggc ttcttcctgc gcatccaccc 2640 cgacggccga gtggacgggg tccgcgagaa gagcgaccca cacatcaaac tacaacttca 2700 agcagaagag agaggggttg tgtctatcaa aggagtgtgt gcaaaccgtt accttgctat 2760 gaaagaagat ggaagattac tagcttctaa atgtgttaca gacgagtgtt tcttttttga 2820 acgattggag tctaataact acaatactta ccggtcaagg aaatacacca gttggtatgt 2880 ggcactgaaa cgaactgggc agtataaact tggatccaaa acaggacctg ggcagaaagc 2940 tatacttttt cttccaatgt ctgctaagag ctgatcttaa tggcagcatc tgatctcatt 3000 ttacatgaag ctggtggcat ccctgtgacc cctccccagt gcctctcctg gccctggaag 3060 ttgccactcc agtgcccacc agccttgtcc taataaaatt aagttgcatc attttgtctg 3120 actaggtgtc cttctataat attatggggt ggaggggggt ggtatggagc aaggggcaag 3180 ttgggaagac aacctgtagg gcctgcgggg tctattggga accaagctgg agtgcagtgg 3240 cacaatcttg gctcactgca atctccgcct cctgggttca agcgattctc ctgcctcagc 3300 ctcccgagtt gttgggattc caggcatgca tgaccaggct cagctaattt ttgttttttt 3360 ggtagagacg gggtttcacc atattggcca ggctggtctc caactcctaa tctcaggtga 3420 tctacccacc ttggcctccc aaattgctgg gattacaggc gtgaaccact gctcccttcc 3480 ctgtccttct gattttaaaa taactatacc agcaggagga cgtccagaca cagcataggc 3540 tacctggcca tgcccaaccg gtgggacatt tgagttgctt gcttggcact gtcctctcat 3600 gcgttgggtc cactcagtag atgcctgttg aattatcgga tccactacgc gttagagctc 3660 gctgatcagc ctcgactgtg ccttctagtt gccagccatc tgttgtttgc ccctcccccg 3720 tgccttcctt gaccctggaa ggtgccactc ccactgtcct ttcctaataa aatgaggaaa 3780 ttgcatcgca ttgtctgagt aggtgtcatt ctattctggg gggtggggtg gggcaggaca 3840 gcaaggggga ggattgggaa gacaatagca ggggggtggg cgaagaactc cagcatgaga 3900 tccccgcgct ggaggatcat ccagccaatt ccctagagca tggctacgta gataagtagc 3960 atggcgggtt aatcattaac tacaaggaac ccctagtgat ggagttggcc actccctctc 4020 tgcgcgctcg ctcgctcact gaggccgggc gaccaaaggt cgcccgacgc ccgggctttg 4080 cccgggcggc ctcagtgagc gagcgagcgc gcagggggtg ggcgaagaac tccagcatga 4140 gatccccgcg ctggaggatc atccagccgg cgtcccggaa aacgattccg aagcccaacc 4200 tttcatagaa ggcggcggtg gaatcgaaat ctcgtgatgg caggttgggc gtcgcttggt 4260 cggtcatttc gaaccccaga gtcccgctca gaagaactcg tcaagaaggc gatagaaggc 4320 gatgcgctgc gaatcgggag cggcgatacc gtaaagcacg aggaagcggt cagcccattc 4380 gccgccaagc tcttcagcaa tatcacgggt agccaacgct atgtcctgat agcggtccgc 4440 cacacccagc cggccacagt cgatgaatcc agaaaagcgg ccattttcca ccatgatatt 4500 cggcaagcag gcatcgccat gggtcacgac gagatcctcg ccgtcgggca tgcgcgcctt 4560 gagcctggcg aacagttcgg ctggcgcgag cccctgatgc tcttcgtcca gatcatcctg 4620 atcgacaaga ccggcttcca tccgagtacg tgctcgctcg atgcgatgtt tcgcttggtg 4680 gtcgaatggg caggtagccg gatcaagcgt atgcagccgc cgcattgcat cagccatgat 4740 ggatactttc tcggcaggag caaggtgaga tgacaggaga tcctgccccg gcacttcgcc 4800 caatagcagc cagtcccttc ccgcttcagt gacaacgtcg agcacagctg cgcaaggaac 4860 gcccgtcgtg gccagccacg atagccgcgc tgcctcgtcc tgcagttcat tcagggcacc 4920 ggacaggtcg gtcttgacaa aaagaaccgg gcgcccctgc gctgacagcc ggaacacggc 4980 ggcatcagag cagccgattg tctgttgtgc ccagtcatag ccgaatagcc tctccaccca 5040 agcggccgga gaacctgcgt gcaatccatc ttgttcaatc atgcgaaacg atcctcatcc 5100 tgtctcttga tcagatcttg atcccctgcg ccatcagatc cttggcggca agaaagccat 5160 ccagtttact ttgcagggct tcccaacctt accagagggc gccccagctg gcaattccgg 5220 ttcgcttgct gtccataaaa ccgcccagtc tagctatcgc catgtaagcc cactgcaagc 5280 tacctgcttt ctctttgcgc ttgcgttttc ccttgtccag atagcccagt agctgacatt 5340 catccggggt cagcaccgtt tctgcggact ggctttctac gtgttccgct tcctttagca 5400 gcccttgcgc cctgagtgct tgcggcagcg tgaagctgtc aattccgcgt taaatttttg 5460 ttaaatcagc tcatttttta accaataggc cgaaatcggc aaaatccctt ataaatcaaa 5520 agaatagccc gagatagggt tgagtgttgt tccagtttgg aacaagagtc cactattaaa 5580 gaacgtggac tccaacgtca aagggcgaaa aaccgtctat cagggcgatg gcggatcagc 5640 ttatgcggtg tgaaataccg cacagatgcg taaggagaaa ataccgcatc aggcgctctt 5700 ccgcttcctc gctcactgac tcgctgcgct cggtcgttcg gctgcggcga gcggtatcag 5760 ctcactcaaa ggcggtaata cggttatcca cagaatcagg ggataacgca ggaaagaaca 5820 tgtgagcaaa aggccagcaa aaggccagga accgtaaaaa ggccgcgttg ctggcgtttt 5880 tccataggct ccgcccccct gacgagcatc acaaaaatcg acgctcaagt cagaggtggc 5940 gaaacccgac aggactataa agataccagg cgtttccccc tggaagctcc ctcgtgcgct 6000 ctcctgttcc gaccctgccg cttaccggat acctgtccgc ctttctccct tcgggaagcg 6060 tggcgctttc tcatagctca cgctgtaggt atctcagttc ggtgtaggtc gttcgctcca 6120 agctgggctg tgtgcacgaa ccccccgttc agcccgaccg ctgcgcctta tccggtaact 6180 atcgtcttga gtccaacccg gtaagacacg acttatcgcc actggcagca gccactggta 6240 acaggattag cagagcgagg tatgtaggcg gtgctacaga gttcttgaag tggtggccta 6300 actacggcta cactagaagg acagtatttg gtatctgcgc tctgctgaag ccagttacct 6360 tcggaaaaag agttggtagc tcttgatccg gcaaacaaac caccgctggt agcggcggtt 6420 ttttgtttgc aagcagcaga ttacgcgcag aaaaaaagga tctcaagaag atcctttgat 6480 cttttcttac tgaacggtga tccccaccgg aatt 6514 2 5610 DNA Homo sapien 2 aaaacttgcg gccgcggaat ttcgactcta ggccattgca tacgttgtat ctatatcata 60 atatgtacat ttatattggc tcatgtccaa tatgaccgcc atgttgacat tgattattga 120 ctagttatta atagtaatca attacggggt cattagttca tagcccatat atggagttcc 180 gcgttacata acttacggta aatggcccgc ctggctgacc gcccaacgac ccccgcccat 240 tgacgtcaat aatgacgtat gttcccatag taacgccaat agggactttc cattgacgtc 300 aatgggtgga gtatttacgg taaactgccc acttggcagt acatcaagtg tatcatatgc 360 caagtccgcc ccctattgac gtcaatgacg gtaaatggcc cgcctggcat tatgcccagt 420 acatgacctt acgggacttt cctacttggc agtacatcta cgtattagtc atcgctatta 480 ccatggtgat gcggttttgg cagtacacca atgggcgtgg atagcggttt gactcacggg 540 gatttccaag tctccacccc attgacgtca atgggagttt gttttggcac caaaatcaac 600 gggactttcc aaaatgtcgt aataaccccg ccccgttgac gcaaatgggc ggtaggcgtg 660 tacggtggga ggtctatata agcagagctc gtttagtgaa ccgtcagatc gcctggagac 720 gccatccacg ctgttttgac ctccatagaa gacaccggga ccgatccagc ctccgcggcc 780 gggaacggtg cattggaacg cggattcccc gtgccaagag tgacgtaagt accgcctata 840 gactctatag gcacacccct ttggctctta tgcatgctat actgtttttg gcttggggcc 900 tatacacccc cgctccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 960 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1020 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1080 tgacacggac tctgtatttt tacaggatgg ggtccattta ttatttacaa attcacatat 1140 acaacaacgc cgtcccccgt gcccgcagtt tttattaaac atagcgtggg atctccgaca 1200 tctcgggtac gtgttccgga catgggctct tctccggtag cggcggagct tccacatccg 1260 agccctggtc ccatccgtcc agcggctcat ggtcgctcgg cagctccttg ctcctaacag 1320 tggaggccag acttaggcac agcacaatgc ccaccaccac cagtgtgccg cacaaggccg 1380 tggcggtagg gtatgtgtct gaaaatgagc tcggagattg ggctcgcacc tggacgcaga 1440 tggaagactt aaggcagcgg cagaagaaga tgcaggcagc tgagttgttg tattctgata 1500 agagtcagag gtaactcccg ttgcggtgct gttaacggtg gagggcagtg tagtctgagc 1560 agtactcgtt gctgccgcgc gcgccaccag acataatagc tgacagacta acagactgtt 1620 cctttccatg ggtcttttct gcagtcaccg tcgtcgacct aagaattcgc ccttcgaaac 1680 catgaacttt ctgctgtctt gggtgcattg gagccttgcc ttgctgctct acctccacca 1740 tgccaagtgg tcccaggctg cacccatggc agaaggagga gggcagaatc atcacgaagt 1800 ggtgaagttc atggatgtct atcagcgcag ctactgccat ccaatcgaga ccctggtgga 1860 catcttccag gagtaccctg atgagatcga gtacatcttc aagccatcct gtgtgcccct 1920 gatgcgatgc gggggctgct gcaatgacga gggcctggag tgtgtgccca ctgaggagtc 1980 caacatcacc atgcagatta tgcggatcaa acctcaccaa ggccagcaca taggagagat 2040 gagcttccta cagcacaaca aatgtgaatg cagaccaaag aaagatagag caagacaaga 2100 aaatccctgt gggccttgct cagagcggag aaagcatttg tttgtacaag atccgcagac 2160 gtgtaaatgt tcctgcaaaa acacagactc gcgttgcaag gcgaggcagc ttgagttaaa 2220 cgaacgtact tgcagatgtg acaagccgag gcggtgagcc gggcaggagg aaggagcctc 2280 cctcagggtt tcgggaacca gatctctcac caggaaagac tgatacagaa agggcgaatt 2340 caggcctaag cttcctaggt atcgatctcg agcaagtcta gaaagccatg gatatcggat 2400 ccactacgcg ttagagctcg ctgatcagcc tcgactgtgc cttctagttg ccagccatct 2460 gttgtttgcc cctcccccgt gccttccttg accctggaag gtgccactcc cactgtcctt 2520 tcctaataaa atgaggaaat tgcatcgcat tgtctgagta ggtgtcattc tattctgggg 2580 ggtggggtgg ggcaggacag caagggggag gattgggaag acaatagcag gggggtgggc 2640 gaagaactcc agcatgagat ccccgcgctg gaggatcatc cagctagcaa gtcccatcag 2700 tgatggagtt ggccactccc tctctgcgcg ctcgctcgct cactgaggcc gggcgaccaa 2760 aggtcgcccg acgcccgggc tttgcccggg cggcctcagt gagcgagcga gcgcgccagc 2820 gattctcttg tttgctccag actctcaggc aatgacctga tagcctttgt agagacctct 2880 caaaaatagc taccctctcc ggcatgaatt tatcagctag aacggttgaa tatcatattg 2940 atggtgattt gactgtctcc ggcctttctc acccgtttga atctttacct acacattact 3000 caggcattgc atttaaaata tatgagggtt ctaaaaattt ttatccttgc gttgaaataa 3060 aggcttctcc cgcaaaagta ttacagggtc ataatgtttt tggtacaacc gatttagctt 3120 tatgctctga ggctttattg cttaattttg ctaattcttt gccttgcctg tatgatttat 3180 tggatgttgg aattcctgat gcggtatttt ctccttacgc atctgtgcgg tatttcacac 3240 cgcatatggt gcactctcag tacaatctgc tctgatgccg catagttaag ccagccccga 3300 cacccgccaa cacccgctga cgcgccctga cgggcttgtc tgctcccggc atccgcttac 3360 agacaagctg tgaccgtctc cgggagctgc atgtgtcaga ggttttcacc gtcatcaccg 3420 aaacgcgcga gacgaaaggg cctcgtgata cgcctatttt tataggttaa tgtcatgata 3480 ataatggttt cttagacgtc aggtggcact tttcggggaa atgtgcgcgg aacccctatt 3540 tgtttatttt tctaaataca ttcaaatatg tatccgctca tgagacaata accctgataa 3600 atgcttcaat aatattgaaa aaggaagagt atgagtattc aacatttccg tgtcgccctt 3660 attccctttt ttgcggcatt ttgccttcct gtttttgctc acccagaaac gctggtgaaa 3720 gtaaaagatg ctgaagatca gttgggtgca cgagtgggtt acatcgaact ggatctcaac 3780 agcggtaaga tccttgagag ttttcgcccc gaagaacgtt ttccaatgat gagcactttt 3840 aaagttctgc tatgtggcgc ggtattatcc cgtattgacg ccgggcaaga gcaactcggt 3900 cgccgcatac actattctca gaatgacttg gttgagtact caccagtcac agaaaagcat 3960 cttacggatg gcatgacagt aagagaatta tgcagtgctg ccataaccat gagtgataac 4020 actgcggcca acttacttct gacaacgatc ggaggaccga aggagctaac cgcttttttg 4080 cacaacatgg gggatcatgt aactcgcctt gatcgttggg aaccggagct gaatgaagcc 4140 ataccaaacg acgagcgtga caccacgatg cctgtagcaa tggcaacaac gttgcgcaaa 4200 ctattaactg gcgaactact tactctagct tcccggcaac aattaataga ctggatggag 4260 gcggataaag ttgcaggacc acttctgcgc tcggcccttc cggctggctg gtttattgct 4320 gataaatctg gagccggtga gcgtgggtct cgcggtatca ttgcagcact ggggccagat 4380 ggtaagccct cccgtatcgt agttatctac acgacgggga gtcaggcaac tatggatgaa 4440 cgaaatagac agatcgctga gataggtgcc tcactgatta agcattggta actgtcagac 4500 caagtttact catatatact ttagattgat ttaaaacttc atttttaatt taaaaggatc 4560 taggtgaaga tcctttttga taatctcatg accaaaatcc cttaacgtga gttttcgttc 4620 cactgagcgt cagaccccgt agaaaagatc aaaggatctt cttgagatcc tttttttctg 4680 cgcgtaatct gctgcttgca aacaaaaaaa ccaccgctac cagcggtggt ttgtttgccg 4740 gatcaagagc taccaactct ttttccgaag gtaactggct tcagcagagc gcagatacca 4800 aatactgtcc ttctagtgta gccgtagtta ggccaccact tcaagaactc tgtagcaccg 4860 cctacatacc tcgctctgct aatcctgtta ccagtggctg ctgccagtgg cgataagtcg 4920 tgtcttaccg ggttggactc aagacgatag ttaccggata aggcgcagcg gtcgggctga 4980 acggggggtt cgtgcacaca gcccagcttg gagcgaacga cctacaccga actgagatac 5040 ctacagcgtg agctatgaga aagcgccacg cttcccgaag ggagaaaggc ggacaggtat 5100 ccggtaagcg gcagggtcgg aacaggagag cgcacgaggg agcttccagg gggaaacgcc 5160 tggtatcttt atagtcctgt cgggtttcgc cacctctgac ttgagcgtcg atttttgtga 5220 tgctcgtcag gggggcggag cctatggaaa aacgccagca acgcggcctt tttacggttc 5280 ctggcctttt gctggccttt tgctcacatg ttctttcctg cgttatcccc tgattctgtg 5340 gataaccgta ttaccgcctt tgagtgagct gataccgctc gccgcagccg aacgaccgag 5400 cgcagcgagt cagtgagcga ggaagcggaa gagcgcccaa tacgcaaacc gcctctcccc 5460 gcgcgttggc cgattcatta atgcagctgg cgcgctcgct cgctcactga ggccgcccgg 5520 gcaaagcccg ggcgtcgggc gacctttggt cgcccggcct cagtgagcga gcgagcgcgc 5580 agagagggag tggccaactc catcactgat 5610 3 7096 DNA Homo sapien 3 aaaacttgcg gccgcggaat ttcgactcta ggccattgca tacgttgtat ctatatcata 60 atatgtacat ttatattggc tcatgtccaa tatgaccgcc atgttgacat tgattattga 120 ctagttatta atagtaatca attacggggt cattagttca tagcccatat atggagttcc 180 gcgttacata acttacggta aatggcccgc ctggctgacc gcccaacgac ccccgcccat 240 tgacgtcaat aatgacgtat gttcccatag taacgccaat agggactttc cattgacgtc 300 aatgggtgga gtatttacgg taaactgccc acttggcagt acatcaagtg tatcatatgc 360 caagtccgcc ccctattgac gtcaatgacg gtaaatggcc cgcctggcat tatgcccagt 420 acatgacctt acgggacttt cctacttggc agtacatcta cgtattagtc atcgctatta 480 ccatggtgat gcggttttgg cagtacacca atgggcgtgg atagcggttt gactcacggg 540 gatttccaag tctccacccc attgacgtca atgggagttt gttttggcac caaaatcaac 600 gggactttcc aaaatgtcgt aataaccccg ccccgttgac gcaaatgggc ggtaggcgtg 660 tacggtggga ggtctatata agcagagctc gtttagtgaa ccgtcagatc gcctggagac 720 gccatccacg ctgttttgac ctccatagaa gacaccggga ccgatccagc ctccgcggcc 780 gggaacggtg cattggaacg cggattcccc gtgccaagag tgacgtaagt accgcctata 840 gactctatag gcacacccct ttggctctta tgcatgctat actgtttttg gcttggggcc 900 tatacacccc cgctccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 960 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1020 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1080 tgacacggac tctgtatttt tacaggatgg ggtccattta ttatttacaa attcacatat 1140 acaacaacgc cgtcccccgt gcccgcagtt tttattaaac atagcgtggg atctccgaca 1200 tctcgggtac gtgttccgga catgggctct tctccggtag cggcggagct tccacatccg 1260 agccctggtc ccatccgtcc agcggctcat ggtcgctcgg cagctccttg ctcctaacag 1320 tggaggccag acttaggcac agcacaatgc ccaccaccac cagtgtgccg cacaaggccg 1380 tggcggtagg gtatgtgtct gaaaatgagc tcggagattg ggctcgcacc tggacgcaga 1440 tggaagactt aaggcagcgg cagaagaaga tgcaggcagc tgagttgttg tattctgata 1500 agagtcagag gtaactcccg ttgcggtgct gttaacggtg gagggcagtg tagtctgagc 1560 agtactcgtt gctgccgcgc gcgccaccag acataatagc tgacagacta acagactgtt 1620 cctttccatg ggtcttttct gcagtcaccg tcgtcgacct aagaattcgc cctttcacca 1680 tggtcagcta ctgggacacc ggggtcctgc tgtgcgcgct gctcagctgt ctgcttctca 1740 caggatctag ttcaggttca aaattaaaag atcctgaact gagtttaaaa ggcacccagc 1800 acatcatgca agcaggccag acactgcatc tccaatgcag gggggaagca gcccataaat 1860 ggtctttgcc tgaaatggtg agtaaggaaa gcgaaaggct gagcataact aaatctgcct 1920 gtggaagaaa tggcaaacaa ttctgcagta ctttaacctt gaacacagct caagcaaacc 1980 acactggctt ctacagctgc aaatatctag ctgtacctac ttcaaagaag aaggaaacag 2040 aatctgcaat ctatatattt attagtgata caggtagacc tttcgtagag atgtacagtg 2100 aaatccccga aattatacac atgactgaag gaagggagct cgtcattccc tgccgggtta 2160 cgtcacctaa catcactgtt actttaaaaa agtttccact tgacactttg atccctgatg 2220 gaaaacgcat aatctgggac agtagaaagg gcttcatcat atcaaatgca acgtacaaag 2280 aaatagggct tctgacctgt gaagcaacag tcaatgggca tttgtataag acaaactatc 2340 tcacacatcg acaaaccaat acaatcatag atgtccaaat aagcacacca cgcccagtca 2400 aattacttag aggccatact cttgtcctca attgtactgc taccactccc ttgaacacga 2460 gagttcaaat gacctggagt taccctgatg aaaaaaataa gagagcttcc gtaaggcgac 2520 gaattgacca aagcaattcc catgccaaca tattctacag tgttcttact attgacaaaa 2580 tgcagaacaa agacaaagga ctttatactt gtcgtgtaag gagtggacca tcattcaaat 2640 ctgttaacac ctcagtgcat atatatgata aagcattcat cactgtgaaa catcgaaaac 2700 agcaggtgct tgaaaccgta gctggcaagc ggtcttaccg gctctctatg aaagtgaagg 2760 catttccctc gccggaagtt gtatggttaa aagatgggtt acctgcgact gagaaatctg 2820 ctcgctattt gactcgtggc tactcgttaa ttatcaagga cgtaactgaa gaggatgcag 2880 ggaattatac aatcttgctg agcataaaac agtcaaatgt gtttaaaaac ctcactgcca 2940 ctctaattgt caatgtgaaa ccccagattt acgaaaaggc cgtgtcatcg tttccagacc 3000 cggctctcta cccactgggc agcagacaaa tcctgacttg taccgcatat ggtatccctc 3060 aacctacaat caagtggttc tggcacccct gtaaccataa tcattccgaa gcaaggtgtg 3120 acttttgttc caataatgaa gagtccttta tcctggatgc tgacagcaac atgggaaaca 3180 gaattgagag catcactcag cgcatggcaa taatagaagg aaagaataag atggctagca 3240 ccttggttgt ggctgactct agaatttctg gaatctacat ttgcatagct tccaataaag 3300 ttgggactgt gggaagaaac ataagctttt atatcacaga tgtgccaaat gggtttcatg 3360 ttaacttgga aaaaatgccg acggaaggag aggacctgaa actgtcttgc acagttaaca 3420 agttcttata cagagacgtt acttggattt tactgcggac agttaataac agaacaatgc 3480 actacagtat tagcaagcaa aaaatggcca tcactaagga gcactccatc actcttaatc 3540 ttaccatcat gaatgtttcc ctgcaagatt caggcaccta tgcctgcaga gccaggaatg 3600 tatacacagg ggaagaaatc ctccagaaga aagaaattac aatcagaggt gagcactgca 3660 acaaaaaggc tgttttctct cggatctcca aatttaaaag cacaaggaat gattgtacca 3720 cacaaagtaa tgtaaaacat taaaggactc attaaaaagt aacagttgtc tcatatcatc 3780 ttgatttatt gtcactgttg ctaactttca ggctcaaggg cgaattcagg cctaagcttc 3840 ctaggtatcg atctcgagca agtctagaaa gccatggata tcggatccac tacgcgttag 3900 agctcgctga tcagcctcga ctgtgccttc tagttgccag ccatctgttg tttgcccctc 3960 ccccgtgcct tccttgaccc tggaaggtgc cactcccact gtcctttcct aataaaatga 4020 ggaaattgca tcgcattgtc tgagtaggtg tcattctatt ctggggggtg gggtggggca 4080 ggacagcaag ggggaggatt gggaagacaa tagcaggggg gtgggcgaag aactccagca 4140 tgagatcccc gcgctggagg atcatccagc tagcaagtcc catcagtgat ggagttggcc 4200 actccctctc tgcgcgctcg ctcgctcact gaggccgggc gaccaaaggt cgcccgacgc 4260 ccgggctttg cccgggcggc ctcagtgagc gagcgagcgc gccagcgatt ctcttgtttg 4320 ctccagactc tcaggcaatg acctgatagc ctttgtagag acctctcaaa aatagctacc 4380 ctctccggca tgaatttatc agctagaacg gttgaatatc atattgatgg tgatttgact 4440 gtctccggcc tttctcaccc gtttgaatct ttacctacac attactcagg cattgcattt 4500 aaaatatatg agggttctaa aaatttttat ccttgcgttg aaataaaggc ttctcccgca 4560 aaagtattac agggtcataa tgtttttggt acaaccgatt tagctttatg ctctgaggct 4620 ttattgctta attttgctaa ttctttgcct tgcctgtatg atttattgga tgttggaatt 4680 cctgatgcgg tattttctcc ttacgcatct gtgcggtatt tcacaccgca tatggtgcac 4740 tctcagtaca atctgctctg atgccgcata gttaagccag ccccgacacc cgccaacacc 4800 cgctgacgcg ccctgacggg cttgtctgct cccggcatcc gcttacagac aagctgtgac 4860 cgtctccggg agctgcatgt gtcagaggtt ttcaccgtca tcaccgaaac gcgcgagacg 4920 aaagggcctc gtgatacgcc tatttttata ggttaatgtc atgataataa tggtttctta 4980 gacgtcaggt ggcacttttc ggggaaatgt gcgcggaacc cctatttgtt tatttttcta 5040 aatacattca aatatgtatc cgctcatgag acaataaccc tgataaatgc ttcaataata 5100 ttgaaaaagg aagagtatga gtattcaaca tttccgtgtc gcccttattc ccttttttgc 5160 ggcattttgc cttcctgttt ttgctcaccc agaaacgctg gtgaaagtaa aagatgctga 5220 agatcagttg ggtgcacgag tgggttacat cgaactggat ctcaacagcg gtaagatcct 5280 tgagagtttt cgccccgaag aacgttttcc aatgatgagc acttttaaag ttctgctatg 5340 tggcgcggta ttatcccgta ttgacgccgg gcaagagcaa ctcggtcgcc gcatacacta 5400 ttctcagaat gacttggttg agtactcacc agtcacagaa aagcatctta cggatggcat 5460 gacagtaaga gaattatgca gtgctgccat aaccatgagt gataacactg cggccaactt 5520 acttctgaca acgatcggag gaccgaagga gctaaccgct tttttgcaca acatggggga 5580 tcatgtaact cgccttgatc gttgggaacc ggagctgaat gaagccatac caaacgacga 5640 gcgtgacacc acgatgcctg tagcaatggc aacaacgttg cgcaaactat taactggcga 5700 actacttact ctagcttccc ggcaacaatt aatagactgg atggaggcgg ataaagttgc 5760 aggaccactt ctgcgctcgg cccttccggc tggctggttt attgctgata aatctggagc 5820 cggtgagcgt gggtctcgcg gtatcattgc agcactgggg ccagatggta agccctcccg 5880 tatcgtagtt atctacacga cggggagtca ggcaactatg gatgaacgaa atagacagat 5940 cgctgagata ggtgcctcac tgattaagca ttggtaactg tcagaccaag tttactcata 6000 tatactttag attgatttaa aacttcattt ttaatttaaa aggatctagg tgaagatcct 6060 ttttgataat ctcatgacca aaatccctta acgtgagttt tcgttccact gagcgtcaga 6120 ccccgtagaa aagatcaaag gatcttcttg agatcctttt tttctgcgcg taatctgctg 6180 cttgcaaaca aaaaaaccac cgctaccagc ggtggtttgt ttgccggatc aagagctacc 6240 aactcttttt ccgaaggtaa ctggcttcag cagagcgcag ataccaaata ctgtccttct 6300 agtgtagccg tagttaggcc accacttcaa gaactctgta gcaccgccta catacctcgc 6360 tctgctaatc ctgttaccag tggctgctgc cagtggcgat aagtcgtgtc ttaccgggtt 6420 ggactcaaga cgatagttac cggataaggc gcagcggtcg ggctgaacgg ggggttcgtg 6480 cacacagccc agcttggagc gaacgaccta caccgaactg agatacctac agcgtgagct 6540 atgagaaagc gccacgcttc ccgaagggag aaaggcggac aggtatccgg taagcggcag 6600 ggtcggaaca ggagagcgca cgagggagct tccaggggga aacgcctggt atctttatag 6660 tcctgtcggg tttcgccacc tctgacttga gcgtcgattt ttgtgatgct cgtcaggggg 6720 gcggagccta tggaaaaacg ccagcaacgc ggccttttta cggttcctgg ccttttgctg 6780 gccttttgct cacatgttct ttcctgcgtt atcccctgat tctgtggata accgtattac 6840 cgcctttgag tgagctgata ccgctcgccg cagccgaacg accgagcgca gcgagtcagt 6900 gagcgaggaa gcggaagagc gcccaatacg caaaccgcct ctccccgcgc gttggccgat 6960 tcattaatgc agctggcgcg ctcgctcgct cactgaggcc gcccgggcaa agcccgggcg 7020 tcgggcgacc tttggtcgcc cggcctcagt gagcgagcga gcgcgcagag agggagtggc 7080 caactccatc actgat 7096 4 636 DNA Homo sapien 4 atggctccct tagccgaagt cgggggcttt ctgggcggcc tggagggctt gggccagcag 60 gtgggttcgc atttcctgtt gcctcctgcc ggggagcggc cgccgctgct gggcgagcgc 120 aggagcgcgg cggagcggag cgcgcgcggc gggccggggg ctgcgcagct ggcgcacctg 180 cacggcatcc tgcgccgccg gcagctctat tgccgcaccg gcttccacct gcagatcctg 240 cccgacggca gcgtgcaggg cacccggcag gaccacagcc tcttcggtat cttggaattc 300 atcagtgtgg cagtgggact ggtcagtatt agaggtgtgg acagtggtct ctatcttgga 360 atgaatgaca aaggagaact ctatggatca gagaaactta cttccgaatg catctttagg 420 gagcagtttg aagagaactg gtataacacc tattcatcta acatatataa acatggagac 480 actggccgca ggtattttgt ggcacttaac aaagacggaa ctccaagaga tggcgccagg 540 tccaagaggc atcagaaatt tacacatttc ttacctagac cagtggatcc agaaagagtt 600 ccagaattgt acaaggacct actgatgtac acttga 636 5 211 PRT Homo sapien 5 Met Ala Pro Leu Ala Glu Val Gly Gly Phe Leu Gly Gly Leu Glu Gly 1 5 10 15 Leu Gly Gln Gln Val Gly Ser His Phe Leu Leu Pro Pro Ala Gly Glu 20 25 30 Arg Pro Pro Leu Leu Gly Glu Arg Arg Ser Ala Ala Glu Arg Ser Ala 35 40 45 Arg Gly Gly Pro Gly Ala Ala Gln Leu Ala His Leu His Gly Ile Leu 50 55 60 Arg Arg Arg Gln Leu Tyr Cys Arg Thr Gly Phe His Leu Gln Ile Leu 65 70 75 80 Pro Asp Gly Ser Val Gln Gly Thr Arg Gln Asp His Ser Leu Phe Gly 85 90 95 Ile Leu Glu Phe Ile Ser Val Ala Val Gly Leu Val Ser Ile Arg Gly 100 105 110 Val Asp Ser Gly Leu Tyr Leu Gly Met Asn Asp Lys Gly Glu Leu Tyr 115 120 125 Gly Ser Glu Lys Leu Thr Ser Glu Cys Ile Phe Arg Glu Gln Phe Glu 130 135 140 Glu Asn Trp Tyr Asn Thr Tyr Ser Ser Asn Ile Tyr Lys His Gly Asp 145 150 155 160 Thr Gly Arg Arg Tyr Phe Val Ala Leu Asn Lys Asp Gly Thr Pro Arg 165 170 175 Asp Gly Ala Arg Ser Lys Arg His Gln Lys Phe Thr His Phe Leu Pro 180 185 190 Arg Pro Val Asp Pro Glu Arg Val Pro Glu Leu Tyr Lys Asp Leu Leu 195 200 205 Met Tyr Thr 210 6 659 DNA Homo sapien 6 gagcgcagcc ctgatggaat ggatgagatc tagagttggg accctgggac tgtgggtccg 60 actgctgctg gctgtcttcc tgctgggggt ctaccaagca taccccatcc ctgactccag 120 ccccctcctc cagtttgggg gtcaagtccg gcagaggtac ctctacacag atgacgacca 180 agacactgaa gcccacctgg agatcaggga ggatggaaca gtggtaggcg cagcacaccg 240 cagtccagaa agtctcctgg agctcaaagc cttgaagcca ggggtcattc aaatcctggg 300 tgtcaaagcc tctaggtttc tttgccaaca gccagatgga gctctctatg gatcgcctca 360 ctttgatcct gaggcctgca gcttcagaga actgctgctg gaggacggtt acaatgtgta 420 ccagtctgaa gcccatggcc tgcccctgcg tctgcctcag aaggactccc caaaccagga 480 tgcaacatcc tggggacctg tgcgcttcct gcccatgcca ggcctgctcc acgagcccca 540 agaccaagca ggattcctgc ccccagagcc cccagatgtg ggctcctctg accccctgag 600 catggtagag cctttacagg gccgaagccc cagctatgcg tcctgactct tcctgaatc 659 7 210 PRT Homo sapien 7 Met Glu Trp Met Arg Ser Arg Val Gly Thr Leu Gly Leu Trp Val Arg 1 5 10 15 Leu Leu Leu Ala Val Phe Leu Leu Gly Val Tyr Gln Ala Tyr Pro Ile 20 25 30 Pro Asp Ser Ser Pro Leu Leu Gln Phe Gly Gly Gln Val Arg Gln Arg 35 40 45 Tyr Leu Tyr Thr Asp Asp Asp Gln Asp Thr Glu Ala His Leu Glu Ile 50 55 60 Arg Glu Asp Gly Thr Val Val Gly Ala Ala His Arg Ser Pro Glu Ser 65 70 75 80 Leu Leu Glu Leu Lys Ala Leu Lys Pro Gly Val Ile Gln Ile Leu Gly 85 90 95 Val Lys Ala Ser Arg Phe Leu Cys Gln Gln Pro Asp Gly Ala Leu Tyr 100 105 110 Gly Ser Pro His Phe Asp Pro Glu Ala Cys Ser Phe Arg Glu Leu Leu 115 120 125 Leu Glu Asp Gly Tyr Asn Val Tyr Gln Ser Glu Ala His Gly Leu Pro 130 135 140 Leu Arg Leu Pro Gln Lys Asp Ser Pro Asn Gln Asp Ala Thr Ser Trp 145 150 155 160 Gly Pro Val Arg Phe Leu Pro Met Pro Gly Leu Leu His Glu Pro Gln 165 170 175 Asp Gln Ala Gly Phe Leu Pro Pro Glu Pro Pro Asp Val Gly Ser Ser 180 185 190 Asp Pro Leu Ser Met Val Glu Pro Leu Gln Gly Arg Ser Pro Ser Tyr 195 200 205 Ala Ser 210 8 5974 DNA Homo sapien 8 aaaacttgcg gccgcggaat ttcgactcta ggccattgca tacgttgtat ctatatcata 60 atatgtacat ttatattggc tcatgtccaa tatgaccgcc atgttgacat tgattattga 120 ctagttatta atagtaatca attacggggt cattagttca tagcccatat atggagttcc 180 gcgttacata acttacggta aatggcccgc ctggctgacc gcccaacgac ccccgcccat 240 tgacgtcaat aatgacgtat gttcccatag taacgccaat agggactttc cattgacgtc 300 aatgggtgga gtatttacgg taaactgccc acttggcagt acatcaagtg tatcatatgc 360 caagtccgcc ccctattgac gtcaatgacg gtaaatggcc cgcctggcat tatgcccagt 420 acatgacctt acgggacttt cctacttggc agtacatcta cgtattagtc atcgctatta 480 ccatggtgat gcggttttgg cagtacacca atgggcgtgg atagcggttt gactcacggg 540 gatttccaag tctccacccc attgacgtca atgggagttt gttttggcac caaaatcaac 600 gggactttcc aaaatgtcgt aataaccccg ccccgttgac gcaaatgggc ggtaggcgtg 660 tacggtggga ggtctatata agcagagctc gtttagtgaa ccgtcagatc gcctggagac 720 gccatccacg ctgttttgac ctccatagaa gacaccggga ccgatccagc ctccgcggcc 780 gggaacggtg cattggaacg cggattcccc gtgccaagag tgacgtaagt accgcctata 840 gactctatag gcacacccct ttggctctta tgcatgctat actgtttttg gcttggggcc 900 tatacacccc cgctccttat gctataggtg atggtatagc ttagcctata ggtgtgggtt 960 attgaccatt attgaccact cccctattgg tgacgatact ttccattact aatccataac 1020 atggctcttt gccacaacta tctctattgg ctatatgcca atactctgtc cttcagagac 1080 tgacacggac tctgtatttt tacaggatgg ggtccattta ttatttacaa attcacatat 1140 acaacaacgc cgtcccccgt gcccgcagtt tttattaaac atagcgtggg atctccgaca 1200 tctcgggtac gtgttccgga catgggctct tctccggtag cggcggagct tccacatccg 1260 agccctggtc ccatccgtcc agcggctcat ggtcgctcgg cagctccttg ctcctaacag 1320 tggaggccag acttaggcac agcacaatgc ccaccaccac cagtgtgccg cacaaggccg 1380 tggcggtagg gtatgtgtct gaaaatgagc tcggagattg ggctcgcacc tggacgcaga 1440 tggaagactt aaggcagcgg cagaagaaga tgcaggcagc tgagttgttg tattctgata 1500 agagtcagag gtaactcccg ttgcggtgct gttaacggtg gagggcagtg tagtctgagc 1560 agtactcgtt gctgccgcgc gcgccaccag acataatagc tgacagacta acagactgtt 1620 cctttccatg ggtcttttct gcagtcaccg tcgtcgacct aagaattcag gtatggctgc 1680 tggttctatc actaccctgc cagctctgcc agaagacggt ggttctggtg ccttcccacc 1740 aggtcacttc aaagacccaa aacgtctgta ctgcaaaaac ggtggtttct tcctgcgcat 1800 ccaccccgac ggccgagtgg acggggtccg cgagaagagc gacccacaca tcaaactaca 1860 acttcaagca gaagagagag gggttgtgtc tatcaaagga gtgtgtgcaa accgttacct 1920 tgctatgaaa gaagatggaa gattactagc ttctaaatgt gttacagacg agtgtttctt 1980 ttttgaacga ttggagtcta ataactacaa tacttaccgg tcaaggaaat acaccagttg 2040 gtatgtggca ctgaaacgaa ctgggcagta taaacttgga tccaaaacag gacctgggca 2100 gaaagctata ctttttcttc caatgtctgc taagagctga tcttaatggc agcatctgat 2160 ctcattttac atgaagcttc ctaggtatcg atctcgagca agtctagaaa gccatggata 2220 tcggatccac tacgcgttag agctcgctga tcagcctcga ctgtgccttc tagttgccag 2280 ccatctgttg tttgcccctc ccccgtgcct tccttgaccc tggaaggtgc cactcccact 2340 gtcctttcct aataaaatga ggaaattgca tcgcattgtc tgagtaggtg tcattctatt 2400 ctggggggtg gggtggggca ggacagcaag ggggaggatt gggaagacaa tagcaggggg 2460 gtgggcgaag aactccagca tgagatcccc gcgctggagg atcatccagc tagcaagtcc 2520 catcagtgat ggagttggcc actccctctc tgcgcgctcg ctcgctcact gaggccgggc 2580 gaccaaaggt cgcccgacgc ccgggctttg cccgggcggc ctcagtgagc gagcgagcgc 2640 gccagcgatt ctcttgtttg ctccagactc tcaggcaatg acctgatagc ctttgtagag 2700 acctctcaaa aatagctacc ctctccggca tgaatttatc agctagaacg gttgaatatc 2760 atattgatgg tgatttgact gtctccggcc tttctcaccc gtttgaatct ttacctacac 2820 attactcagg cattgcattt aaaatatatg agggttctaa aaatttttat ccttgcgttg 2880 aaataaaggc ttctcccgca aaagtattac agggtcataa tgtttttggt acaaccgatt 2940 tagctttatg ctctgaggct ttattgctta attttgctaa ttctttgcct tgcctgtatg 3000 atttattgga tgttggaatt cctgatgcgg tattttctcc ttacgcatct gtgcggtatt 3060 tcacaccgca tatggtgcac tctcagtaca atctgctctg atgccgcata gttaagccag 3120 ccccgacacc cgccaacacc cgctgacgcg ccctgacggg cttgtctgct cccggcatcc 3180 gcttacagac aagctgtgac cgtctccggg agctgcatgt gtcagaggtt ttcaccgtca 3240 tcaccgaaac gcgcgagacg aaagggcctc gtgatacgcc tatttttata ggttaatgtc 3300 atgataataa tggtttctta gacgtcaggt ggcacttttc ggggaaatgt gcgcggaacc 3360 cctatttgtt tatttttcta aatacattca aatatgtatc cgctcatgag acaataaccc 3420 tgataaatgc ttcaataatg tacccgtcaa gaaggcgata gaaggcgatg cgctgcgaat 3480 cgggagcggc gataccgtaa agcacgagga agcggtcagc ccattcgctt cagcaatatc 3540 acgggtagcc aacgctatgt cctgatagcg gtccgccaca cccagccggc cacagtcgat 3600 gaatccagaa aagcggccat tttccaccat gatattcggc aagcaggcat cgccatgggt 3660 cacgacgaga tcctcgccgt cgggcatgcg cgccttgagc ctggcgaaca gttcggctgg 3720 cgcgagcccc tgatgctctt cgtccagatc atcctgatcg acaagaccgg cttccatccg 3780 agtacgtgct cgctcgatgc gatgtttcgc ttggtggtcg aatgggcagg tagccggatc 3840 aagcgtatgc agccgccgca ttgcatcagc catgatggat actttctcgg caggagcaag 3900 gtgagatgac aggagatcct gccccggcac ttcgcccaat agcagccagt cccttcccgc 3960 ttcagtgaca acgtcgagca cagctgcgca aggaacgccc gtcgtggcca gccacgatag 4020 ccgcgctgcc tcgtcctgca gttcattcag ggcaccggac aggtcggtct tgacaaaaag 4080 aaccgggcgc ccctgcgctg acagccggaa cacggcggca tcagagcagc cgattgtctg 4140 ttgtgcccag tcatagccga atagcctctc cacccaagcg gccggagaac ctgcgtgcaa 4200 tccatcttgt tcaatcatgc gaaacgatcc tcatcctgtc tcttgatcag atcttgatcc 4260 cctgcgccat cagatccttg gcggcaagaa agccatccag tttactttgc agggcttccc 4320 aaccttacca gagggcgccc cagctggcaa ttccggttcg cttgctgtcc ataaaaccgc 4380 ccagtctagc tatcgccatg taagcccact gcaagctacc tgctttctct ttgcgcttgc 4440 gttttccctt gtccagatag cccagtagct gacattcatc cggggtcagc accgtttctg 4500 cggactggct ttctacgtgt tccgcttcct ttagcagccc ttgcgccctg agtgcttgcg 4560 gcagcgtgaa gctgtcaatt ccgcgttaaa tttttgttaa atcagctcat tttttaacca 4620 ataggccgaa atcggcaaaa tcccttataa atcaaaagaa tagcccgaga tagggttgag 4680 tgttgttcca gtttggaaca agagtccact attaaagaac gtggactcca acgtcaaagg 4740 gcgaaaaacc gtctatcagg gcgatggcgg atcagcttat gcggtgtgaa ataccgcaca 4800 gatgcgtaag gagaaaatac cgcatcaggc gctcttccgc ttcctcgctc actgactcgc 4860 tgcgctcggt cgttcggctg cggcgagcgg tatcagctca ctcaaaggcg gtaatacggt 4920 tatccacaga atcaggggat aacgcaggaa agaacatgcg gcgcgccaca tgtgagcaaa 4980 aggccagcaa aaggccagga accgtaaaaa ggccgcgttg ctggcgtttt tccataggct 5040 ccgcccccct gacgagcatc acaaaaatcg acgctcaagt cagaggtggc gaaacccgac 5100 aggactataa agataccagg cgtttccccc tggaagctcc ctcgtgcgct ctcctgttcc 5160 gaccctgccg cttaccggat acctgtccgc ctttctccct tcgggaagcg tggcgctttc 5220 tcatagctca cgctgtaggt atctcagttc ggtgtaggtc gttcgctcca agctgggctg 5280 tgtgcacgaa ccccccgttc agcccgaccg ctgcgcctta tccggtaact atcgtcttga 5340 gtccaacccg gtaagacacg acttatcgcc actggcagca gccactggta acaggattag 5400 cagagcgagg tatgtaggcg gtgctacaga gttcttgaag tggtggccta actacggcta 5460 cactagaagg acagtatttg gtatctgcgc tctgctgaag ccagttacct tcggaaaaag 5520 agttggtagc tcttgatccg gcaaacaaac caccgctggt agcggcggtt ttttgtttgc 5580 aagcagcaga ttacgcgcag aaaaaaagga tctcaagaag atcctttgat cttttcttac 5640 tgaacggtga tccccaccgg aattgcggcc catgttcttt cctgcgttat cccctgattc 5700 tgtggataac cgtattaccg cctttgagtg agctgatacc gctcgccgca gccgaacgac 5760 cgagcgcagc gagtcagtga gcgaggaagc ggaagagcgc ccaatacgca aaccgcctct 5820 ccccgcgcgt tggccgattc attaatgcag ctggcgcgct cgctcgctca ctgaggccgc 5880 ccgggcaaag cccgggcgtc gggcgacctt tggtcgcccg gcctcagtga gcgagcgagc 5940 gcgcagagag ggagtggcca actccatcac tgat 5974 9 41 DNA Artificial Sequence Oligonucleotide used for PCR amplification 9 ggtatttaaa acttgcggcc gcggaatttc gactctaggc c 41 10 50 DNA Artificial Sequence Oligonucleotide used for PCR amplification 10 gctgcccggg acttgctagc tggatgatcc tccagcgcgg ggatctcatg 50 11 42 DNA Artificial Sequence PCR primer 11 agatataagc ttaccatggg tgaaaagcgt ctcgccccca aa 42 12 42 DNA Artificial Sequence PCR primer 12 cgcgcgctcg agaccatgag gaatattatc caaagcgaaa ct 42

Claims

We claim:

1. A method of treating or preventing diseases of the eye, comprising, administering intraocularly a gene delivery vector which directs the expression of a neurotrophic factor, such that said disease of the eye is treated or prevented.

2. The method according to claim 1 wherein said neurotrophic factor is NGF, BDNF, CNTF, NT-3, or, NT-4.

3. The method according to claim 1 wherein said neurotrophic factor is a FGF.

4. The method according to claim 3 wherein said FGF is FGF-2, FGF-5, FGF-18, FGF-20, or, FGF-21.

5. The method according to claim 1 wherein said disease of the eye is macular degeneration.

6. The method according to claim 1 wherein said disease of the eye is diabetic retinopathy.

7. The method according to claim 1 wherein said disease of the eye is an inherited retinal degeneration.

8. The method according to claim 7 wherein said inherited retinal degeneration is retinitis pigmentosa.

9. The method according to claim 1 wherein said disease of the eye is glaucoma.

10. The method according to claim 1 wherein said disease of the eye is a surgery-induced retinopathy.

11. The method according to claim 1 wherein said disease of the eye is retinal detachment.

12. The method according to claim 1 wherein said disease of the eye is a photic retinopathy.

13. The method according to claim 1 wherein said disease of the eye is a toxic retinopathy.

14. The method according to claim 1 wherein said disease of the eye is a trauma-induced retinopathy.

15. The method according to claim 1 wherein said gene delivery vector is a retrovirus selected from the group consisting of HIV and FIV.

16. The method according to claim 1 wherein said gene delivery vector is a recombinant adeno-associated viral vector.

17. A method of inhibiting neovascular disease of the eye, comprising, administering intraocularly a gene delivery vector which directs the expression of an anti-angiogenic factor, such that said neovascular disease of the eye is inhibited.

18. The method according to claim 17 wherein said anti-angiogenic factor is soluble Flt-1, PEDF, soluble Tie-2 receptor, or, a single chain anti-VEGF antibody.

19. The method according to claim 17 wherein said neovascular disease of the eye is diabetic retinopathy, wet AMD, and retinopathy of prematurity.

20. The method according to claim 17 wherein said gene delivery vector is a retrovirus selected from the group consisting of HIV and FIV.

21. The method according to claim 17 wherein said gene delivery vector is a recombinant adeno-associated viral vector.

22. A gene delivery vector which directs the expression of a neurotrophic factor, or an anti-angiogenic factor.

23. The gene delivery vector according to claim 22 wherein said neurotrophic factor is NGF, BDNF, CNTF, NT-3, or, NT-4.

24. The gene delivery vector according to claim 22 wherein said neurotrophic factor is a FGF.

25. The gene delivery vector according to claim 22 wherein said FGF is FGF-2, FGF-5, FGF-18, FGF-20, or, FGF-21.

26. The gene delivery vector according to claim 22 wherein said anti-angiogenic factor is soluble Flt-1, PEDF, soluble Tie-2 receptor, or, a single chain anti-VEGF antibody.

27. The gene delivery vector according to claim 22 wherein said vector is generated from a retrovirus.

28. The gene delivery vector according to claim 27 wherein said retrovirus is HIV or FIV.

29. The gene delivery vector according to claim 22 wherein said vector is generated from a recombinant adeno-associated virus.

30. A non-human animal model of neovascularization of the eye, comprising an animal having an angiogenic transgene in the eye.

31. The non-human animal model according to claim 30 wherein said neovascularization is retinal neovascularization.

32. The non-human animal model according to claim 30 wherein said neovascularization is choroidal neovascularization.

33. The non-human animal model according to claim 30 wherein said animal is a mouse or rat.

34. The non-human animal model according to claim 30 wherein said angiogenic transgene encodes VEGF.

35. The non-human animal model according to claim 30 wherein said angiogenic transgene encodes an angiopoietin.

36. A method for making a non-human animal model of neovascularization of the eye, comprising administering to a non-human animal a gene delivery vector which directs the expression of an angiogenic transgene.

37. The method according to claim 36 wherein said gene delivery vector is administered subretinally.

38. The method according to claim 36 wherein said gene delivery vector is administered intravitreally.

39. The method according to claim 36 wherein said gene delivery vector is rAV or rAAV.

40. The method according to claim 36 wherein said angiogenic transgene is a nucleic acid molecule which encodes VEGF.

41. The method according to claim 36 wherein said angiogenic transgene is a nucleic acid molecule which encodes an angiopoietin.

42. A method for determining the ability of an anti-angiogenic factor to inhibit neovascularization of the eye, comprising: (a) administering to an animal model according to any one of claims 30 to 35 an anti-angiogenic factor, and (b) determining the ability of said anti-angiogenic factor to inhibit neovascularization of the eye.

43. The method according to claim 42 wherein said anti-angiogenic factor is administered subretinally.

44. The method according to claim 42 wherein said anti-angiogenic factor is administered intravitreally.