Codon-optimized recombinant plasmid, method of stimulating peripheral nerve regeneration, and method of treating nerve damage in humans

Abstract

Provided is a method for treating a peripheral nervous system damage or injury, or for regenerating peripheral nervous system tissue that involves administering to a subject in need thereof a vector that comprises polynucleotide sequences that encode a modified vascular endothelia growth factor (VEGF) and a fibroblast growth factor (FGF2) and further a polynucleotide that encodes resistance to kanamycin. A gene-therapeutic structure encoding modified vascular endothelial growth factors (VEGF) and (FGF-2) is also provided. The gene-therapeutic structure can be administered directly to a damaged nerve and paraneural tissues both in intraoperative and post-operative period to stimulate peripheral nerve regeneration. The structure and method significantly advance existing methods for reconstructive treatment for damaged peripheral nerves.

Claims

1. A method for treating peripheral nervous system damage or injury, or for regenerating peripheral nervous system tissue, the method comprising: administering to a subject in need thereof an effective amount of a vector that comprises polynucleotide sequences that encode a vascular endothelia growth factor (VEGF) and a fibroblast growth factor 2 (FGF2), wherein the administration is performed by injecting the vector (i) directly at a damage or injury site, (ii) at a site proximal to the injury or damage site, (iii) at a site distal to the injury or damage site, or a combination of (i)-(iii), of the median nerve in the middle third of the forearm of the subject, wherein the peripheral nervous system damage or injury is neurotmesis, wherein the vector comprises FGF2 encoding nucleotides at positions 699-1166 and VEGF165 encoding nucleotides at positions 3723-4298 of SEQ ID NO: 4, and wherein the vector expresses the VEGF and FGF2, thereby treating peripheral nervous system damage or injury, or regenerating peripheral nervous system tissue.

2. The method of claim 1, wherein the vector is administered (i) directly at a damage or injury site.

3. The method of claim 1, wherein the vector is administered (ii) at a site proximal to the injury or damage site, (iii) at a site distal to the injury or damage site, or a combination of (ii)-(iii).

4. The method of claim 1, comprising administering the vector intra-, peri- and/or paraneurally.

5. The method of claim 1, comprising contacting the vector with a neuron, a Schwann cell, astrocyte, or microglia.

6. The method of claim 1, wherein the subject is human.

7. The method of claim 1, wherein the vector further comprises a polynucleotide sequence that encodes resistance to kanamycin.

8. The method of claim 1, wherein the vector comprises resistance to kanamycin nucleotides at positions 1469-2511 of SEQ ID NO: 4.

9. The method of claim 1, wherein the vector is pBud(Kan)-coVEGF165-coFGF2 having the nucleotide sequence of SEQ ID NO: 4.

Description

BRIEF DESCRIPTION OF THE FIGURES

(1) The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the office upon request and payment of the necessary fee.

(2) A more complete appreciation of the invention and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings, wherein:

(3) FIG. 1 provides the repeated approach. The entire sciatic nerve with an autologous graft is visualized. Results after injection of plasmid pBud(Kan)-VEGF-FGF2.

(4) FIG. 2 shows a view of the upper extremity prior to surgery. Post-traumatic and post-operative indented irregular scars are seen on the anterior and posterolateral surfaces of the lower, middle, and upper third of the right upper arm.

(5) FIG. 3 shows lack of active movements in the middle phalanges of fingers 2-5.

(6) FIG. 4 shows the impaired prehension function by all fingers.

(7) FIG. 5 shows high-grade atrophy of the hand muscle within a zone innervated by the median and ulnar nerves and the ability to oppose finger 1 to finger 2 only.

(8) FIG. 6 shows injection of the recombinant plasmid pBud (Kan)-VEGF-FGF2 into the repaired nerve into the suture zone and also proximally and distally over the length of 10 cm.

(9) FIG. 7 shows application of fibrin glue to prevent leakage of the recombinant plasmid.

(10) FIG. 8 shows atrophy of hand and forearm muscles. Nail changes: hypoplastic. Secretory function (sweating): decreased. Figure demonstrates post-surgical improvement in patient's condition.

(11) FIG. 9 shows a hook grasp (a purse handle). Figure demonstrates post-surgical improvement in patient's condition.

(12) FIG. 10 shows a fist grasp. Figure demonstrates post-surgical improvement in patient's condition.

(13) FIG. 11 shows tip prehension (finger Figure demonstrates post-surgical improvement in patient's condition.

(14) FIG. 12 shows tip prehension (finger Figure demonstrates post-surgical improvement in patient's condition.

(15) FIG. 13 shows tip prehension (finger I-IV). Figure demonstrates post-surgical improvement in patient's condition.

(16) FIG. 14 shows a diagram of electromyography results for the thenar muscle group. Based on the electromyography results the thenar muscle response amplitude had increased over the year from 0 mV to 5 mV and almost achieved the value of the contralateral extremity.

(17) FIG. 15 shows electromyography findings for the hypothenar muscle group.

(18) FIG. 16 A, B, Cshow the mmunofluorescence analysis of VEGF and FGF2 expression in genetically modified HEK293T cells 48 hours after transfection by fluorescence microscopy. A) Staining with primary antibodies to FGF2 and secondary antibodies conjugated to the fluorescent label Alexa-488. B) Staining with primary antibodies to VEGF and secondary antibodies conjugated to the fluorescent label Alexa-555. C) Staining with a fluorescent dye DAPI and matching the fluorescence of FGF2 and VEGF. Scale: 50 m.

(19) FIG. 17 shows a 7 cm defect of a median nerve replaced by a sural nerve.

(20) FIGS. 18 and 19 show injection of the recombinant plasmid pBud (Kan)-coVEGF-coFGF2 into the grafted nerve into the suture zone and also proximally and distally over the length of 10 cm.

(21) FIG. 20 shows application of fibrin glue to prevent leakage of the recombinant plasmid.

(22) FIG. 21 shows a cylindrical grip. Figure demonstrates post-surgical improvement in patient's condition.

(23) FIG. 22 shows a hook grasp (a purse handle). Figure demonstrates post-surgical improvement in patient's condition.

(24) FIG. 23 shows a fist grasp. Figure demonstrates post-surgical improvement in patient's condition.

DETAILED DESCRIPTION OF THE INVENTION

(25) The present invention is used in medicine, preferably in neurosurgery, traumatology and maxillofacial surgery, and in treatment of peripheral nerve injuries.

(26) As used herein the words a, an and the like generally carry a meaning of one or more, unless stated otherwise.

(27) A goal of the inventors' research has been to create, based on their experience in the development of gene therapeutic agents, an effective product for treating patients with peripheral nerve injuries. For this purpose, the inventors have developed various gene therapeutic constructions that differ from each other by the number of encoded transgenes and the transgenes, as well as by the nucleotide sequences of the same transgenes.

(28) In one embodiment, an object of the present invention is to provide an improved or enhanced method for reconstructive treatment involving delivery of a therapeutic polynucleotide construct into or in the vicinity of a damaged peripheral nervous system tissue. An example of this embodiment is the delivery of genetic sequences encoding VEGF and FGF-2 into such tissue using the recombinant plasmid pBud(Kan)-VEGF-FGF2. In another embodiment, genetic sequences encoding modified VEGF and FGF-2 are delivered into such tissue using the recombinant plasmid pBud(Kan)-coVEGF165-coFGF2.

(29) An object of the present invention is to provide a method for treating a peripheral nervous system damage or injury, or for regenerating peripheral nervous system tissue, comprising administering to a subject in need thereof a vector that comprises polynucleotide sequences that encode vascular endothelia growth factor (VEGF) and fibroblast growth factor (FGF2).

(30) A range of the injected plasmid could be from 200 to 500 g per nerve in 2.5 ml of a physiologic saline solution. The ranges include all values and subranges therebetween, including 250, 300, 350, 400, and 450 g per nerve in 2.5 ml of a physiologic saline solution and any amount in between.

(31) The vector could be administered in vivo. In another embodiment, the vector is administered to a site of the peripheral nervous system damage or injury or to a tissue to be regenerated. In a different embodiment, the vector is administered to a site of the peripheral nervous system damage or injury at a site proximal or distal to the peripheral nervous system damage, or at sites proximal and distal to said damage. The vector could be administered intra-, peri- and/or paraneurally.

(32) In yet another embodiment, the vector is contacted with a neuron or a Schwann cell, astrocyte, microglia and/or neuron.

(33) In one embodiment, the subject has neurotmesis. In another embodiment, the subject has a diastatic peripheral nerve damage. In a different embodiment, the subject has peripheral nerve damage other than neurotmesis or diastatic peripheral nerve damage. The subject could be human or animal.

(34) In one embodiment, the vector comprises a polynucleotide sequence that encodes resistance to kanamycin.

(35) In another embodiment, the vector comprises FGF2 encoding nucleotides at positions 699-1166 and VEGF165 encoding nucleotides at positions 3723-4298 of SEQ ID NO: 1. The vector further could comprise resistance to kanamycin nucleotides at positions 1469-2511 of SEQ ID NO: 1. In yet another embodiment, the vector is pBud(Kan)-VEGF-FGF2 that has SEQ ID NO: 1.

(36) In another embodiment, a vector comprises codon optimized polynucleotide sequences that encode vascular endothelia growth factor (coVEGF) and codon optimized fibroblast growth factor (coFGF2), and resistance to kanamycin. In one embodiment, the vector is pBud(Kan)-coVEGF165-coFGF2 that has SEQ ID NO: 4. In one embodiment, the vector comprises coFGF2 encoding nucleotides at positions 699-1166 and coVEGF165 encoding nucleotides at positions 3723-4298 of SEQ ID NO: 4. The vector further could comprise resistance to kanamycin nucleotides at positions 1469-2511 of SEQ ID NO: 4.

(37) A different object of the present invention is to provide a cell that has been transformed with the vectors.

(38) Having generally described this invention, a further understanding can be obtained by reference to certain specific examples which are provided herein for purposes of illustration only and are not intended to be limiting unless otherwise specified.

EXAMPLES

Comparative Example 1. Treatment of Diastatic Peripheral Nerve Injury with VEGF/FGF2 Gene Therapy

(39) An animal model of a diastatic peripheral nerve injury was used to evaluate effects of gene therapy with the plasmid vector encoding both VEGF and FGF2 described by Masgutov [26].

(40) Test animals (rats), were divided into three groups: (i) intact group, (ii) a test group where a gene therapeutic construction was administered, and (iii) a control group where a phosphate-buffered saline (PBS) solution was injected instead of the gene therapeutic construction.

(41) In test group (ii) a total dose of 45 g of a gene therapeutic construction was directly injected equally into distal and proximal ends of an autologous nerve graft. In control group (iii) a phosphate-buffered saline (PBS) solution was injected into these locations instead of the gene therapeutic construction.

(42) The evaluation criteria of the regeneration dynamics of the peripheral nerve included neurophysiological parameters such as the nerve conduction velocity and the muscle response amplitude as well as the histological examination findings such as the number of myelinated fibers and the capillary network density.

(43) On day 56 following the injection of the plasmid construction, the neurophysiological parameters in the test group (ii) were superior to those in the control group (iii); however, they were significantly inferior to those in the intact animals of group (i).

(44) A histological examination revealed that myelinated fiber numbers per unit of the cross-section area of the graft were significantly higher in the experimental group (ii) compared to the control group (iii). However, no effective recovery of the extremity function was observed. These experiment results show that the use of plasmid-based constructions containing genetic sequences of growth factors provides a stimulating effect on the regeneration of peripheral nerves.

Example 1. Construction and Evaluation of Vector Encoding VEGF and FGF2 in Animal Model

(45) The inventors have sought to determine whether the effect observed in Comparative Example 1 was attributable to the construction of the used plasmid. The inventors have engineered a new plasmid encoding VEGF and FGF2 which replaced the tag sequences in the prior vector with a gene encoding kanamycin resistance. Among other constructs, plasmid pBud(Kan)-VEGF-FGF2 (SEQ ID NO: 1) was constructed. This plasmid has been engineered to include a sequence encoding resistance to kanamycin at nucleotides 1469-2511 of SEQ ID NO: 1; cDNA of a gene encoding FGF2 at nucleotides 699-1166 in SEQ ID NO: 1; cDNA of the gene encoding VEGF165 at nucleotides 3723-4298 in SEQ ID NO: 1; and the Kozak sequence at nucleotides 695-698 and 3719-3722.

(46) The rat animal model of a peripheral nerve injury substantially as described in Comparative Example 1 was used to evaluate the effect of administering the new plasmid constructs, including plasmid pBud(Kan)-VEGF-FGF2 (SEQ ID NO: 1). Gene therapeutic constructions were administrated intraneurally immediately after the peripheral nerve suturing. The results were evaluated after 60 days following the surgical intervention and therapeutic constructs administration. Of all the plasmid DNAs that were used, the best results were obtained for the plasmid pBud(Kan)-VEGF-FGF2 (SEQ ID NO: 1) containing genetic sequences of FGF2 and VEGF. The results for the plasmid pBud(Kan)-VEGF-FGF2 are depicted by FIG. 1. Based on these favorable non-clinical results, the inventors evaluated whether peripheral nerve regeneration could be attained in the clinical setting using the gene therapeutic construction pBud(Kan)-VEGF-FGF2 (SEQ ID NO: 1), as described below.

Example 2. Clinical Evaluation of Regenerative Effects of pBud(Kan)-VEGF-FGF2 (SEQ ID NO: 1)

(47) Patient B., born in 1985, was admitted to the trauma center of the Republic Clinical Hospital of MoH of the Republic of Tatarstan on Apr. 4, 2011, with the diagnosis of sequelae of the median and ulnar nerve injury in the middle third of the right upper arm as shown by FIG. 2. From the patient's history, it was known that in 2009 the patient had a glass cut of the middle third of the upper arm, with the median and ulnar nerves damaged.

(48) The median and ulnar nerves were sutured end-to-end immediately after the injury. However, both motor and sensitivity functions were completed absent in the immediate post-operation period. A course of rehabilitation therapy had produced no visible results.

(49) After 7 months, in 2010, neurolysis of the median and ulnar nerves was performed due to the lack of positive changes in the motor and sensitivity functional recovery. Slight changes in nerve regeneration were observed in the post-operative follow-up, namely, complete lack of sensitivity, at the same time, the motor function appeared which was characterized by the mild bending of the injured hand and fingers. It was decided to perform a surgical treatment.

(50) Prior to surgery, on Apr. 21, 2011, the patient had an examination with the following results:

(51) Trophic Disturbances a) skin status: normal color, decreased fingers' temperature, increased feeling of chillness; b) atrophy of the hand and forearm muscles, as compared to the normal arm: more than 2 cm as shown by FIGS. 2 and 3. c) nail changes: hypoplastic; and d) secretory function (sweating): decreased.

(52) Sensitivity Testing in the Patient in the Autonomous Zone of Innervation by the Nerve:

(53) TABLE-US-00001 No. Kinds of Sensitivity Brief Description 1. Pain Absent 2. Temperature Absent 3. Tactile Absent 4. Discriminative Absent 5. Sense of two-dimension space Absent 6. Stereognosis Absent 7. Sense of pressure Absent 8. Sense of weight Absent

(54) TABLE-US-00002 Degree Motor function recovery M2 Distinct contractions without movements in joints

(55) Motor Function Testing

(56) TABLE-US-00003 Degree Sensitivity recovery S0 Lack of sensitivity within the nerve autonomous zone

(57) Hand prehension patterns: the hand is unable to perform any type of prehension (FIG. 3-4).

(58) Diagnosis: the injury of the median and ulnar nerves in the middle third of the forearm sustained 2 years ago. The status post suturing and neurolysis of the median and ulnar nerves are shown in FIG. 5.

(59) A surgery was performed on Apr. 26, 2011, including neurolysis of the median and ulnar nerves with the intraneural administration of plasmid pBud(Kan)-VEGF-FGF2 (SEQ ID NO: 1) containing the vegf and fgf-2 genes.

(60) The surgery was conducted under the nerve block anaesthesia. Following triple treatment of the surgical field, an arcuate incision was made on the inner surface of the right upper arm. The median and ulnar nerves were isolated with technical difficulties. The suture lines had been found. There were no neuroma signs observed; however, the nerves were involved in a scar-forming process and adhered to the surrounding tissue.

(61) The plasmid pBud(Kan)-VEGF-FGF2 was injected with an insulin needle, 250 g per nerve in 2.5 ml of a physiologic saline solution. The injection was administered into the suture zone and also proximally and distally over the length of 10 cm (FIG. 6). After that 2 ml of the two-component fibrin glue TISSUCOL was applied to the isolated nerves (FIG. 7).

(62) The post-surgical case included hemostasis, wound suturing, placement of a rubber tube drainage, and application of an antiseptic dressing and a plaster cast. A re-examination was performed one month after the surgery.

(63) The results of the physical examination dated on May 25, 2011, are presented below:

(64) Trophic Disturbances

(65) a) skin status: normal color;

(66) b) atrophy of the injured hand and forearm muscles, compared to the normal arm: more than 2 cm (FIG. 8);

(67) c) nail changes: hypoplastic; and

(68) d) secretory function (sweating): decreased.

(69) Sensitivity Testing in the Patient in the Autonomous Zone of Innervation by the Nerve:

(70) TABLE-US-00004 No. Kinds of Sensitivity Brief Description 1. Pain Absent 2. Temperature Hot - absent Cold - distal phalanges of fingers 1, 2 3. Tactile Fingers 1, 2 - distal phalange 4. Discriminative Absent 5. Sense of two-dimension space Absent (Moberg pickup test) 6. Sense of pressure Present 7. Sense of weight present

(71) TABLE-US-00005 Degree Sensitivity recovery S1 Recovery of deep pain sensitivity within the nerve autonomous zone

(72) Motor Function Testing

(73) TABLE-US-00006 Degree Motor function recovery M2 Distinct contractions without movements in joints

(74) Hand prehension patterns: the hand is unable to perform any type of prehension.

(75) A regular examination was performed in 6 months after the surgery. The results of the physical examination dated on Nov. 15, 2012, are presented below:

(76) Trophic Disturbances a) skin status: of normal color; b) atrophy of the hand and forearm muscles, compared to the normal arm: moderate (1-2 cm) and severe (more than 2 cm); c) nail changes: within normal limits; and d) secretory function (sweating): normal.

(77) Sensitivity Testing in the Patient in the Autonomous Zone of Innervation by the Nerve:

(78) TABLE-US-00007 No. Kinds of Sensitivity Brief Description 1. Pain Present, including distal phalanges of all fingers 2. Temperature Hot - distal phalanges of finger 1, middle phalanges of fingers 3, 4 Cold - distal phalanges of fingers 1, 3; distal phalanges of fingers 2, 4, 5 3. Tactile Fingers 1, 3 - distal phalange, middle phalange 2, 4, 5 4. Discriminative finger 1 - 10 mm finger 2 - 30 mm finger 3 - 20 mm finger 4 - 30 mm finger 5 - 30 mm 5. Sense of two-dimension space Identifies large objects (a box of (Moberg pickup test) cigarettes, glue, tube for blood collection), a pencil, glue tube 6. Sense of pressure Present 7. Sense of weight present

(79) TABLE-US-00008 Degree Sensitivity recovery S3 Recovery of surface pain and tactile sensitivity within the entire autonomous zone with complete hyperpathia disappearance

(80) Motor Function Testing

(81) TABLE-US-00009 Degree Motor function recovery M3 Mild movements in joints (useful recovery)

(82) Hand Prehension Patterns: 1) cylindrical graspYES; 2) spherical graspYES; 3) hook grasp (a bag handle)YES; 4) first graspYES; 5) tip prehension a) terminal oppositionYES; b) subterminal oppositionNO; 6) lateral prehension a) pinch gripNO; b) scissor gripcigaretteNO.

(83) A year after the surgery, the patient had a regular examination. The results of the physical examination dated on Apr. 20, 2012, are presented below:

(84) Trophic Disturbances a) skin status: of normal color; b) atrophy of the injured hand and forearm muscles, compared to the normal arm: moderate (1-2 cm); c) nail changes: within normal limits; and d) secretory function: within normal limits.

(85) Sensitivity Testing in the Patient in the Autonomous Zone of Innervation by the Nerve:

(86) TABLE-US-00010 No. Kinds of Sensitivity Brief Description 1. Pain Present, including distal phalanges of all fingers 2. Temperature Hot - distal phalanges of fingers 1 and 3, middle phalanges of fingers 4, 5 Cold - distal phalanges of fingers 1, 3; distal phalanges of fingers 1, 2, 3, 4, 5 3. Tactile Fingers 1, 2, 3, 4, 5 - distal phalange 4. Discriminative finger 1 - 5 mm finger 2 - 5 mm finger 3 - 10 mm finger 4 - 5 mm finger 5 - 10 mm 5. Sense of two-dimension space Identifies large objects (a box of (Moberg pickup test) cigarettes, glue, tube for blood collection), as well as small objects (rubber, button, coin, clip) 6. Sense of pressure Present 7. Sense of weight present

(87) TABLE-US-00011 Degree Sensitivity recovery S3+ Recovery of surface pain and tactile sensitivity within the entire autonomous zone with complete hyperpathia disappearance, but with some recovery of two-point discrimination within the autonomous zone (from 12 to 15 mm)

(88) Motor Function Testing

(89) TABLE-US-00012 Degree Motor function recovery M4 Movements with overcoming some resistance

(90) Hand Prehension Patterns: 1) spherical graspYES; 2) spherical graspYES; 3) hook graspYES (FIG. 9); 4) first graspYES (FIG. 10); 5) tip prehension: (FIG. 11-13) a) terminal oppositionYES; b) subterminal oppositionYES; 6) lateral prehension a) pinch gripYES; 6) scissor gripYES.

(91) These clinical results show that the extremity function was significantly improved one year after the intraneural administration of the gene-therapeutic construction containing a plasmid expressing VEFG and FGF2. The improved functional state of the extremity was manifested as the decreased severity of the trophic disturbances, as the development of various sensitivities within the area of innervation of the median and ulnar nerves, and as a significant improvement of the motor function. Based on the electromyography results the thenar muscle response amplitude had increased over the year from 0 mV to 5 mV and almost achieved the value of the contralateral extremity (FIGS. 14 and 15).

(92) An animal model and clinical results show that a plasmid that expresses two growth factors, VEGF and FGF2, provides a more effective induction of the peripheral nerve regeneration that prior plasmid constructs.

(93) The efficacy of using a gene therapeutic construction to improve results of surgical treatment of peripheral nerve injuries has been determined and demonstrated by the present inventors in the above described experiments and clinical observations. While not being bound to any particular mechanism, the inventors believe that the achieved clinical effects when using the plasmid pBud(Kan)-VEGF-FGF2 (SEQ ID NO: 1) were likely obtained due to the combination of these two growth factors. However, a full understanding of the influence of genetic constructs requires further studies.

Example 3. Codon Optimization

(94) (A) Codon optimization is based on the degeneracy of genetic code when the most commonly used synonymous codons of degenerate genetic code are used as optimal codons. The higher the frequency of occurrence of a codon used to encode an amino acid in the body the more rapidly it could be translated by ribosomes due to the high intracellular concentration of tRNA recognizing such codon. To optimize the codon composition of VEGF165 and FGF2 genes, the OptimumGene algorithm was used, which takes into account various factors affecting gene expression levels such as codon shift, GC composition, CpG dinucleotide content, secondary mRNA structure, tandem repeats, restriction sites that can interfere with the cloning, premature polyadenylation sites, additional minor ribosome binding sites, etc. All these optimizations can result in increased target transgene transcription, mRNA stability and translation.

(95) The nucleotide sequences of mRNA of VEGF165 gene (GeneBank #AF486837.1, 576 bp) and FGF2 gene (GeneBank #DD406196.1, 468 bp) were used as a template for the codon optimization. The codon usage bias in VEGF165 and FGF2 genes was changes by upgrading the codon adaptation index (CAI) from 0.81 to 0.87 and from 0.77 to 0.87, respectively. The GC content and unfavorable peaks have been optimized to prolong the half-life of mRNA. Stem-Loop structures that impact ribosomal binding and stability of mRNA were disturbed. In addition, the applied optimization process has screened and successfully modified the negative cis-acting sites as listed in the introduction. As a result of the codon optimization, the amino acid sequences of FGF2 and VEGF165 genes have not changed and were 155 and 191 amino acid residues, respectively.

(96) De novo synthesis of codon-optimized VEGF165 and FGF2 cDNAs and subsequent subcloning into plasmid pBud (Kan)-coVEGF165-coFGF2 was performed by GenScript (USA).

(97) (B) A functional activity of the obtained genetic construct was confirmed by the analysis of transgenes expression in vitro.

(98) A genetic modification (transfection) of HEK293T cells with plasmid pBud(Kan)-coVEGF165-coFGF2 was performed using TurboFect transfection reagent (Thermo Fisher Scientific Inc., USA) according to the procedure recommended by the manufacturer. To evaluate efficiency of transfection plasmid vector pEGFPN2 (BD Biosciences Clontech, Germany) expressing the green fluorescent protein GFP was used as a positive control.

(99) To evaluate expression of VEGF165 and FGF2 in the transfected HEK293T cells immunofluorescence and xMap Luminex (multiplex) assays were performed.

(100) Immunofluorescence analysis of the expression of VEGF165 and FGF2 in the genetically modified HEK293T cells was performed 48 hours after transfection using a standard protocol using specific antibodies to VEGF (VEGF Antibody (A-20), #sc-152, Santa Cruz Biotechnology, Inc.) and FGF2 (FGF-2 Antibody (N-19), #sc-1390, Santa Cruz Biotechnology, Inc.). Results were analyzed by fluorescence microscopy on an inverted AxioOberver.Z1 fluorescence microscope (Carl Zeiss, Germany) using AxyoVision Rel software. 4.8. Immunofluorescence analysis of the HEK293T cells transfected with plasmid pBud (Kan)-coVEGF165-coFGF2 has revealed a positive reaction with specific antibodies to the vascular endothelial growth factor and the fibroblast growth factor (FIG. 16).

(101) A level of secretion of VEGF and FGF2 by the genetically modified HEK293T cells was determined using Bio-Plex Pro Human Cytokine 27-plex Assay (BioRad) xMap Luminex multiplex assay kit on the Luminex200 multiplex analyzer. The concentrations of FGF2 and VEGF in a conditioned medium of HEK293T cells transfected with plasmid pBud(Kan)-coVEGF165-coFGF2 were 825.21 pg/ml and 2145.8 pg/ml, respectively.

(102) TABLE-US-00013 Concentration of Concentration of Sample FGF2, pg/ml VEGF, pg/ml pBud(Kan)-coVEGF165- 825.21 2145.8 coFGF2 pEGFP-N2 3.01 37.74 Without plasmid 3.05 24.75

Example 4. Clinical Evaluation of Regenerative Effects of pBud(Kan)-coVEGF165-coFGF2 (SEQ ID NO: 4)

(103) Patient M., born in 1979, was admitted to the trauma center of the Republic Clinical Hospital of MoH of the Republic of Tatarstan in October 2014, with the diagnosis of sequelae of the median nerve injury in the middle third of the right upper arm.

(104) From the patient's history, it was known that in December 2013, the patient had a knife cut of the middle third of the upper arm, with the median nerve damaged. Primary surgical treatment of the wound without suture of the median nerve was performed in the ambulance hospital in the patient's place of residence. In 10 months, the patient came to the clinic.

(105) At the time of admission, there was a complete loss of function of the median nervelack of flexion of 1 and 2 fingers, lack of sensitivity. With palpation, there was a sharp soreness in the field of a trauma with characteristic shooting pain. Prior to surgery, on Oct. 20, 2014, the patient had an examination with the following results:

(106) Trophic Disturbances: a) skin status: normal color, decreased fingers' temperature, increased feeling of chillness; b) atrophy of the hand and forearm muscles, as compared to the normal arm: more than 2 cm. c) nail changes: hypoplastic; and d) secretory function (sweating): decreased.

(107) Sensitivity Testing in the Patient in the Autonomous Zone of Innervation by the Nerve:

(108) TABLE-US-00014 No. Kinds of Sensitivity Brief Description 1. Pain Absent 2. Temperature Absent 3. Tactile Absent 4. Discriminative Absent 5. Sense of two-dimension space Absent 6. Stereognosis Absent 7. Sense of pressure Absent 8. Sense of weight Absent

(109) TABLE-US-00015 Degree Sensitivity recovery SO Lack of sensitivity within the nerve autonomous zone

(110) Motor Function Testing

(111) TABLE-US-00016 Degree Motor function recovery M2 Distinct contractions without movements in joints

(112) Hand prehension patterns: the hand is unable to perform any type of prehension.

(113) Diagnosis: the injury of the median nerve in the middle third of the forearm sustained 10 months ago.

(114) A surgery was performed on Oct. 21, 2014, including a 7 cm defect autonerve grafting by sural nerve (FIG. 17) of the median nerve with the intraneural administration of plasmid pBud(Kan)-coVEGF165-coFGF2 (SEQ ID NO: 4) containing the VEGF165 and FGF2 genes.

(115) The surgery was conducted under the nerve block anaesthesia. Following triple treatment of the surgical field, an arcuate incision was made on the inner surface of the right upper arm. The median nerve was isolated with technical difficulties. There were neuroma signs observed and the nerve was involved in a scar-forming process and adhered to the surrounding tissue.

(116) The plasmid pBud(Kan)-coVEGF165-coFGF2 was injected with an insulin needle, 250 pg in 2.5 ml of a physiologic saline solution. The injection was administered into the graft zones and also proximally and distally over the length of 10 cm (FIG. 18, 19). After that 2 ml of the two-component fibrin glue TISSUCOL was applied to the isolated nerves (FIG. 20).

(117) The post-surgical case included hemostasis, wound suturing, placement of a rubber tube drainage, and application of an antiseptic dressing and a plaster cast. A re-examination was performed one month after the surgery.

(118) The results of the physical examination dated Nov. 21, 2014, are presented below:

(119) Trophic Disturbances: a) skin status: normal color; b) atrophy of the injured hand and forearm muscles, compared to the normal arm: more than 2 cm; c) nail changes: hypoplastic; and d) secretory function (sweating): decreased.

(120) Sensitivity Testing in the Patient in the Autonomous Zone of Innervation by the Nerve:

(121) TABLE-US-00017 No. Kinds of Sensitivity Brief Description 1. Pain Absent 2. Temperature Hot - absent Cold - distal phalanges of fingers 1, 2 3. Tactile Fingers 1, 2 - distal phalange 4. Discriminative Absent 5. Sense of two-dimension space Absent (Moberg pickup test) 6. Sense of pressure Present 7. Sense of weight Present

(122) TABLE-US-00018 Degree Sensitivity recovery SI Recovery of deep pain sensitivity within the nerve autonomous zone

(123) Motor Function Testing:

(124) TABLE-US-00019 Degree Motor function recovery M2 Distinct contractions without movements in joints

(125) Hand prehension patterns: the hand is unable to perform any type of prehension.

(126) A regular examination was performed in 6 months after the surgery. The results of the physical examination dated Apr. 20, 2015, are presented below:

(127) Trophic Disturbances: a) skin status: of normal color; b) atrophy of the hand and forearm muscles, compared to the normal aim: moderate (1-2 cm) and severe (more than 2 cm); c) nail changes: within normal limits; and d) secretory function (sweating): normal.

(128) Sensitivity Testing in the Patient in the Autonomous Zone of Innervation by the Nerve:

(129) TABLE-US-00020 No. Kinds of Sensitivity Brief Description 1. Pain Present, including distal phalanges of all fingers 2. Temperature Hot - distal phalanges of finger 1, middle phalanges of fingers 3, 4 Cold - distal phalanges of fingers 1, 3; distal phalanges of fingers 2, 4, 5 3. Tactile Fingers 1, 3 - distal phalange, middle phalange 2, 4, 5 4. Discriminative Finger 1 - 10 mm Finger 2 - 30 mm Finger 3 - 20 mm Finger 4 - 30 mm Finger 5 - 30 mm 5. Sense of two-dimension Identifies large objects (a box of space (Moberg pickup test) cigarettes, glue, tube for blood collection), a pencil, glue tube 6. Sense of pressure Present 7. Sense of weight Present

(130) TABLE-US-00021 Degree Sensitivity recovery S3 Recovery of surface pain and tactile sensitivity within the entire autonomous zone with complete hyperpathia disappearance

(131) Motor Function Testing

(132) TABLE-US-00022 Degree Motor function recovery M3 Mild movements in joints (useful recovery)
Hand Prehension Patterns: 1) cylindrical graspYES; 2) spherical graspYES; 3) hook grasp (a bag handle)YES; 4) first graspYES; 5) tip prehension a) terminal oppositionYES; b) subterminal oppositionNO; 6) lateral prehension a) pinch gripNO; b) scissor gripcigaretteNO.

(133) A 1 year after the surgery, the patient had a regular examination. The results of the physical examination dated Oct. 26, 2015, are presented below:

(134) Trophic Disturbances: a) skin status: of normal color; b) atrophy of the injured hand and forearm muscles, compared to the normal arm: moderate (1-2 cm) and severe (more than 2 cm);; c) nail changes: within normal limits; and d) secretory function: within normal limits.

(135) Sensitivity Testing in the Patient in the Autonomous Zone of Innervation by the Nerve:

(136) TABLE-US-00023 No. Kinds of Sensitivity Brief Description 1. Pain Present, including distal phalanges of all fingers 2. Temperature Hot-distal phalanges of fingers 1 and 3, middle phalanges of fingers 4, 5 Cold-distal phalanges of fingers 1, 3; distal phalanges of fingers 1, 2, 3, 4, 5 3. Tactile Fingers 1, 2, 3, 4, 5-distal phalange 4. Discriminative Finger 1-5 mm Finger 2-5 mm Finger 3-10 mm Finger 4-5 mm Finger 5-10 mm 5. Sense of two- Identifies large objects (a box of cigarettes, dimension space glue, tube for blood collection), as well as (Moberg pickup test) small objects (rubber, button, coin, dip) 6. Sense of pressure Present 7. Sense of weight present

(137) TABLE-US-00024 Degree Sensitivity recovery S3+ Recovery of surface pain and tactile sensitivity within the entire autonomous zone with complete hyperpathia disappearance, but with some recovery of two-point discrimination within the autonomous zone (from 12 to 15 mm)

(138) Motor Function Testing

(139) TABLE-US-00025 Degree Motor function recovery M4 Movements with overcoming some resistance

(140) Hand Prehension Patterns: 1) spherical graspYES (FIG. 21); 2) hook graspYES (FIG. 22); 3) first graspYES (FIG. 23); 4) tip prehension: a) terminal oppositionYES; b) subterminal oppositionYES; 5) lateral prehension a) pinch gripYES; 6) scissor gripYES.

(141) These clinical results show that the extremity function was significantly improved one year after the intraneural administration of the gene-therapeutic construction containing a plasmid expressing VEFG165 and FGF2. The improved functional state of the extremity was manifested as the decreased severity of the trophic disturbances, as the development of various sensitivities within the area of innervation of the median nerve, and as a significant improvement of the motor function.

(142) The in vitro experiments and clinical results show that a plasmid that expresses two growth factors, VEGF165 and FGF2, provides a more effective induction of the peripheral nerve regeneration that prior plasmid constructs.

(143) The efficacy of using a gene therapeutic construction to improve results of surgical treatment of peripheral nerve injuries has been determined and demonstrated by the present inventors in the above described experiments and clinical observations. While not being bound to any particular mechanism, the inventors believe that the achieved clinical effects when using the plasmid pBud(Kan)-coVEGF165-coFGF2 (SEQ ID NO: 4) were likely obtained due to the combination of these two growth factors. However, a full understanding of the influence of genetic constructs requires further studies.

(144) All publications, patent applications, patents, and other references mentioned herein are incorporated by reference herein in their entirety. Further, the materials, methods, and examples are illustrative only and are not intended to be limiting, unless otherwise specified.

(145) Numerous modification and variations on the present invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein.

REFERENCES

(146) 1. Hudso, A. R. Timing of peripheral nerve repair: important local and neuropathological factors/A. R. Hudson/Clinical Neurosurgery.-1977.-Vol. 24.-C. 391-405. 2. Deitch, E. A. Experience with 112 shotgun wounds of the extremities/E. A. Deitch, W. R. Grimes/J Trauma.-1984.-Vol. 24.-P. 600-603. 3. Analysis of upper and lower extremity peripheral nerve injuries in a population of patients with multiple injuries/C. A. Munro/J. Trauma.-1998.-Vol. 45.-P. 116-122. 4. Terenghi, G. Peripheral nerve regeneration and neurotrophic factors/G. Terenghi/J. Anat. 1999.-Vol. 194.-P. 5. Vascular endothelial growth factor has neurotrophic activity and stimulates axonal outgrowth, enhancing cell survival and Schwann cell proliferation in the peripheral nervous system/M. Sondell, M. Kanje. G. Lundborg/J Neurosci.-1999.-Vol. 19, No 14-P. 5731-40. 6. VEGF-A165b is an endogenous neuroprotective splice isoform of vascular endothelial growth factor A in vivo and in vitro/N. Beazley-Long [et al.]/J Pathol.-2013.-Vol. 183, No 3-P. 918-29. 7. Sondell, M. Vascular endothelial growth factor stimulates Schwann cell invasion and neovascularisation of acelular nerve grafts/M. Sondell, G. Lundborg, M. Kanje/Brain Res.-1999.-Vol. 846-P. 219-228. 8. Vascular, glial and neuronal effects of vascular endothelial growth factor in mesencephalic expiants cultures/W. F. Silverman [et al.]/Neuroscience.-1999.Vol. 90-P. 1529-1541. 9. Forstreuter, F. Vascular endothelial growth factor induces chemotaxis and proliferation of microglial cells/F. Forstreuter, R. Lucius, R. Mentlein/J. Neuroimmunol.-2002.-Vol. 132-P. 93-98. 10. Zhu, Y. Vascular endothelial growth factor promotes proliferation of cortical neuron precursors by regulating E2F expression/Y. Zhu [et al.]/J FASEB.-2003. Vol. 17-P. 186-193. 11. Induction of VEGF and its Flt-1 receptor after sciatic nerve crush injury/R. R. Islamov [et al.]/Neuroreport.-2004. Vol. 15, No 13-P. 2117-21. 12. Effects of vascular endothelial growth factor on nerve regeneration in acellular nerve grafts/J. M. Rovak [et al.]/J Reconstr Microsurg.-2004. Vol. 20, No 1-P. 53-58. 13. Vascular endothelial growth factor-loaded poly (lactic-co-glycolic acid) microspheres-induced lateral axonal sprouting into the vein graft bridging two healthy nerves: nerve graft prfabrication using controlled release system/H. Karagoz [et al.]/J Microsurgery.-2012. Vol. 32, No 8-P. 635-41. 14. Sondell, M. Vascular endothelial growth factor stimulates Schwann cell invasion and neovascularization of acellular nerve grafts/M. Sondell, G. Lundborg, M. Kanje/Brain Res.-1999. Vol. 846, No 2-P. 219-28. 15. The effect of vascular endothelial growth factor and brain-derived neurotrophic factor on cavernosal nerve regeneration in a nerve-crush rat model/P S. Hsieh [et al.]/BJU Int.-2003. Vol. 92, No 4-P. 470-5. 16. Grothe, C. Physiological function and putative therapeutic impact of the FGF-2 system in peripheral nerve regeneration-lessons from in vivo studies in mice and rats/K. Haastert, J. Jungnickel, C. Grothe/Brain Res Rev.-2006. Vol. 51-P. 293-299. 17. Furushol, M. Disruption of Fibroblast growth factor receptor signaling in non-myelinating Schwann cells causes sensory axonal neuropathy and impairment of thermal pain sensitivity/M. Furushol [et al.]/J Neurosci.-2009. Vol. 29, No 6-P. 1608-1614. 18. Tulio, V. R. Bone marrow-derived fibroblast growth factor-2 induces glial cell proliferation in the regenerating peripheral nervous system/V. R. Tulio [et al.]/Molecular Neurodegeneration.-2012. Vol. 7, No 34-P. 1-17. 19. Sciatic nerve grafting and inoculation of FGF-2 promotes improvement of motor behavior and fiber regrowth in rats with spinal cord transaction/F. P. Guzen, [et al.]/Restorative Neurology and Neuroscience.-2012. Vol. 30-P. 265-275. 20. Zeng, W. Ionically cross-linked chitosan microspheres for controlled release of bioactive nerve growth factor/W. Zeng [et al.]/Int J Pharm.-2011. Vol. 421-P. 283-290. 21. Enhancement of musculocutaneous nerve reinnervation after vascular endothelial growthfactor (VEGF) gene therapy/P. Haninec [et al.]/BMC Neuroscience.-2012. Vol. 13, No 57-P. 22. Effect of VEGF gene therapy and hyaluronic acid film sheath on peripheral nerve regeneration/F. Zor [et al.]/-2014. Vol. 34, No 3-P. 209-16. 23. Favorable effect of local VEGF gene injection on axonal regeneration in the rat sciatic nerve/C. Fu [et al.]/J Huazhong University Scince Technology.-2007. Vol. 2-P. 186-9. 24. Double gene therapy with granulocyte colony-stimulating factor and vascular endothelial growth factor acts synergistically to improve nerve regeneration and functional outcome after sciatic nerve injury in mice/F. Pereira Lopes [et al.]/Neuroscience.2013. Vol. 230-P. 184-97. 25. Pat. 2459630 RF, IPC A61K 48/00, A61P 25/28, C12N 15/79, C1. Stimulation Technique for Neuroregeneration with Genetic Constructions/Yu. A. Chelyshev; Federal State Educational Institution Kazan Federal University.-No 2011116853/10; 27 Apr. 2011; published 27 Oct. 2009, Bull. No 30.-11 p. [in Russian] 26. Stimulation of post-traumatic regeneration of a rat sciatic nerve with a plasmid expressing the vascular endothelial growth factor and the basic fibroblast growth factor./R. F. Masgutov [et al]/Cell Technologies and Tissue Engineering.-2011.-6(3): 67-70. [in Russian].