Patent Application
20180296729
This document relates to decellularized nerve allografts. For example, this document provides methods and materials for using decellularized nerve allografts to repair nerve injuries or bridge a severed nerve, thereby restoring motor function of the nerve.
Traumatic injuries to peripheral nerves can cause considerable disability and economic burden (Jaquet et al., J. Trauma, 51(4):687-92 (2001)). Although highly prevalent in military conflicts, peacetime injuries commonly result from trauma secondary to motor vehicle accidents, penetrating trauma, industrial injuries, and falls. It is estimated that 5% of the patients admitted to Level I trauma centers have a peripheral nerve injury (Noble et al., J. Trauma, 45(1):116-22 (1998); Taylor et al., Am. J. Phys. Med. Rehab., 87(5):381-5 (2008); and Campbell et al., Connecticut Med., 73(7):389-94 (2009)). The treatment of peripheral nerve injuries is dependent on mechanism of injury, time between injury and treatment, and concomitant injuries. The majority of peripheral nerve injuries require surgical reconstruction to restore sensation and function (Kovachevich et al., J. Hand Surg., 35(12):1995-2000 (2010)). For nerve injuries that cannot be directly repaired, a bridging nerve graft is necessary.
The gold standard for nerve reconstruction is the autograft (Millesi, Clin. Plast. Surg., 11(1):105-13 (1984)). Typically, the sural nerve is harvested and sectioned into cables to fit the diameter and length of the defect (Berger and Millesi, Clin. Orthop. Relat. Res., 133:49-55 (1978)). However, the use of the autograft is limited by supply, diameter, and length, and is accompanied by associated donor site morbidity (IJmpa et al., Annals Plast. Surg., 57(4):391-5 (2006)). This has constrained the ability to optimally reconstruct nerves of patients with multiple segmental defects where length of nerve graft needed far exceeds the availability and results in the need to prioritize the nerves to be reconstruct.
This document relates to decellularized nerve allografts. For example, this document provides decellularized nerve allografts and methods and materials for using decellularized nerve allografts to repair nerve injuries or bridge a severed nerve. As described herein, decellularized nerve allografts that are prepared using elastase and stored under cold conditions (e.g., about 2 to 6° C.) without being frozen can be used to repair nerve injuries or bridge a severed nerve in a manner that restores motor function of the nerve. This restored motor function can be evident at 12 weeks, 16 weeks, 20 weeks, or longer following nerve reconstruction. Having the ability to repair injured or severed nerves in a manner that restores motor function using the methods and materials provided herein can allow surgeons and patients to minimize the disabilities and economic burden associated with nerve injuries.
In general, one aspect of this document features a method for reconstructing an injured or severed nerve in a mammal. The method comprises, or consists essentially of, (a) providing a decellularized nerve graft of the same species as the mammal, wherein the decellularized nerve graft was prepared by contacting nerve tissue with from about 0.01 units/mL to about 1 unit/mL (e.g., about 0.05 units/mL) of elastase for at least about four hours (e.g., about 16 hours) to prepare the decellularized nerve graft, and wherein the decellularized nerve graft was not frozen and was stored under cold conditions of from about 1.5° C. to about 6.5° C., and (b) implanting the decellularized nerve graft into the mammal to repair the injured or severed nerve, wherein motor function of the nerve is observed after the implanting step. The mammal can be a human. The function of the nerve can be observed six months after the implanting step. The decellularized nerve graft can be prepared by contacting nerve tissue with from about 0.03 units/mL to about 0.07 units/mL of elastase. The decellularized nerve graft can be prepared by contacting nerve tissue with from about 0.03 units/mL to about 0.07 units/mL of elastase for from about 10 hours to about 20 hours. The decellularized nerve graft can be one that was stored under cold conditions of from about 3° C. to about 5° C.
In another aspect, this document features a method for making a decellularized nerve graft. The method comprises, or consists essentially of, (a) providing a nerve tissue from a mammal, and (b) contacting the nerve tissue with from about 0.01 units/mL to about 1 unit/mL (e.g., about 0.05 units/mL) of elastase and from about 0.5 units/mL to about 5 units/mL (e.g., about 2 units/mL) of a chondroitin-sulfate-ABC endolyase to form the decellularized nerve graft, wherein, when the decellularized nerve graft is implanted into a member of the same species as the mammal to repair an injured or severed nerve of the member, motor function of the injured or severed nerve is observed after being implanted. The mammal can be a human. The motor function of the injured or severed nerve can be observed six months after being implanted. The nerve tissue can be contacted with the elastase for from about 10 hours to about 20 hours (e.g., about 16 hours). The nerve tissue can be contacted with from about 0.03 units/mL to about 0.07 units/mL of elastase. The decellularized nerve graft can be one that was not frozen. The decellularized nerve graft can be one that was stored under cold conditions of from about 1.5° C. to about 6.5° C.
In another aspect, this document features a decellularized nerve graft produced by contacting nerve tissue obtained from a mammal with from about 0.01 units/mL to about 1 unit/mL (e.g., about 0.05 units/mL) of elastase and from about 0.5 units/mL to about 5 units/mL (e.g., about 2 units/mL) of a chondroitin-sulfate-ABC endolyase to form the decellularized nerve graft, wherein, when the decellularized nerve graft is implanted into a member of the same species as the mammal to repair an injured or severed nerve of the member, motor function of the injured or severed nerve is observed after being implanted. The mammal can be a human. The motor function of the injured or severed nerve can be observed six months after being implanted. The nerve tissue can be nerve tissue that was contacted with the elastase for from about 10 hours to about 20 hours (e.g., about 16 hours). The nerve tissue can be nerve tissue that was contacted with from about 0.03 units/mL to about 0.07 units/mL of elastase. The decellularized nerve graft can be one that was not frozen. The decellularized nerve graft can be one that was stored under cold conditions of from about 1.5° C. to about 6.5° C.
Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, suitable methods and materials are described below. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.
Other features and advantages of the invention will be apparent from the following detailed description, and from the claims.
This document provides decellularized nerve allografts. For example, this document provides decellularized nerve allografts prepared using elastase as well as methods and materials for using decellularized nerve allografts to repair nerve injuries or bridge a severed nerve.
As described herein, using elastase to prepare a decellularized nerve allograft and storing the decellularized nerve allograft under cold conditions (e.g., about 2 to 6° C.) without freezing can result in a decellularized nerve allograft that, when implanted into a recipient to repair nerve injuries or bridge a severed nerve, restores motor function of the nerve. In some cases, a decellularized nerve allograft produced using elastase can exhibit reduce immunogenicity (e.g., reduced immunogenicity (MHC-I), a reduced number of Schwann cells (e.g., S100-positive Schwann cells), and/or positive structural properties (e.g., basal lamina and overall structural properties).
Any appropriate mammal having an injured or severed nerve can be treated using a decellularized nerve allograft provided herein. For example, humans, monkeys, horses, pigs, dogs, cats, rabbits, mice, and rats having an injured or severed nerve can be treated using a decellularized nerve allograft provided herein.
Any appropriate nerve tissue can be obtained from a donor. Examples of nerve tissue that can be obtained from one member of a species (e.g., a human) to create a decellularized nerve allograft for implantation into another member of that same species include, without limitation, peripheral nerve tissues. In some cases, the length of nerve tissue obtained from a donor is selected based on the length of the nerve injury being treated. For example, when a 15 mm section of damaged or severed nerve is to be repaired, then a section at least about 20 mm can be obtained from a donor.
Once obtained, the fresh nerve tissue can be processed to create a decellularized nerve allograft. Briefly, nerve segments can be immediately after harvest placed in RPMI 1640 solution at 4° C. overnight. The next day, the nerve tissues can be placed in deionized distilled water. After about 8 hours, the water can be replaced by a solution containing about 125 mM sulfobetaine-10 (SB-10), about 10 mM phosphate, and about 50 mM sodium. The nerves can be agitated for about 15 hours and rinsed for about 15 minutes in a washing solution of about 10 mM phosphate and about 50 mM sodium. Next, the washing solution can be replaced by a solution containing about 0.14% Triton X-200, about 0.6 mM sulfobetaine-16 (SB-16), about 10 mM phosphate, and about 50 mM sodium and agitated for about 24 hours. Next, the tissues can be rinsed with a washing solution containing about 50 mM phosphate and about 100 mM sodium. The washing solution can be replaced by an SB-10 solution, and the nerves can be agitated for about 8 hours. Next, the nerves can be washed with a washing solution once and put into a solution of SB-16/Triton X-200. The nerves can be agitated for about 15 hours and then washed in a solution containing about 10 mM phosphate and about 50 mM sodium. At this point, the nerves can be incubated in a solution containing about 2 U/mL chondroitinase ABC for about 16 hours at room temperature and then washed in a solution containing about 10 mM phosphate and about 50 mM sodium. In some cases, 1-3 U/mL of chondroitinase ABC can be used. Then, nerve segments can be incubated in a solution containing about 0.05 U/mL elastase at about 37° C. for about 16 hours. After that, the nerves can be sterilized with gamma radiation of about 2.5 kGray.
Once prepared, the decellularized nerve allograft can be stored under cold conditions (e.g., about 2 to 6° C., about 3 to 5° C., or about 4° C.) without freezing until the time of implantation. In some cases, a decellularized nerve allograft can be stored under cold conditions (e.g., about 2 to 6° C., about 3 to 5° C., or about 4° C.) without freezing for about 8 hours to about one month prior to being implanted into a recipient. Any appropriate surgical technique can be used to prepare the recipient's existing injured or severed nerve for repair with a decellularized nerve allograft provided herein. In general, an injured or severed nerve is repaired by removing scarred injured nerve ends to fresh nerve, placing a decellularized nerve allograft between the freshened nerve ends, and sewing them in place with microsutures or by using fibrin glue or by another coaptation method. Once implanted, the decellularized nerve allograft can restore motor function to the nerve being repaired. This restored motor function can be evident by 6 months or longer, depending on the distance of the nerve injury from the end organ.
The invention will be further described in the following examples, which do not limit the scope of the invention described in the claims.
66 Lewis rats (weighing 250-300 grams) were used, and 22 Sprague Dawley rats served as full major histocompatibility complex mismatch nerve donors. Lewis rats were used as they are known for their reduced tendency for autotomy (Carr et al., Annals Plast. Surg., 28(6):538-44 (1992)). Animals were randomly divided into three groups each treated for a 10 mm sciatic nerve gap. Group I (n=22) had a unilateral nerve gap reconstructed with a processed nerve allograft that was cold stored (‘Allograft Cold’). Group II (n=22) had a similar procedure except the processed allograft was freeze-stored (‘Allograft Frozen’). Group III (n=22) served as a control using a nerve autograft. The rats were given food and water ad libitum and were individually housed with a 12 hour light-dark cycle.
Twenty-two Sprague-Dawley rats, weighing 300-350 grams, were sacrificed with an intraperitoneal injection of pentobarbital after which 15 mm nerve segments were harvested aseptically. Nerve allografts were prepared as follows. Briefly, nerve segments were placed in RPMI medium (Roswell Park Memorial Institute), followed by subsequent steps with different detergents, two enzymatic steps, and gamma irradiation. In particular, nerves segments were immediately after harvest placed in RPMI 1640 solution at 4° C. overnight. The next day, the nerve tissues were placed in deionized distilled water. After 8 hours, the water was replaced by a solution containing 125 mM sulfobetaine-10 (SB-10), 10 mM phosphate, and 50 mM sodium. The nerves were agitated for 15 hours and rinsed for 15 minutes in a washing solution of 10 mM phosphate and 50 mM sodium. Next, the washing solution was replaced by a solution containing 0.14% Triton X-200, 0.6 mM sulfobetaine-16 (SB-16), 10 mM phosphate, and 50 mM sodium, and the nerves agitated for 24 hours. Next, the tissues were rinsed with the washing solution containing 50 mM phosphate and 100 mM sodium. The washing solution was replaced by SB-10 solution, and the nerves were agitated for 8 hours. Next, they were washed with the washing solution once and put into a solution of SB-16/Triton X-200. The nerves were agitated for 15 hours and then washed in a solution containing 10 mM phosphate and 50 mM sodium. Subsequently, nerves were incubated in a solution containing 2 U/mL chondroitinase ABC for 16 hours at room temperature and then washed in a solution containing 10 mM phosphate and 50 mM sodium. Subsequently, nerve segments were incubated in a solution containing 0.05 U/mL elastase at 37° C. for 16 hours. After that, the nerves were sterilized with gamma radiation of 2.5 kGray.
At the end, the processed allografts were either stored in phosphate buffered saline (PBS) at 4° C. (‘allograft cold’) or stored in Ringers Lactate at −80° C. (‘allograft frozen’) for 14 days.
Rats were anesthetized with an intraperitoneal cocktail of ketamine (Ketaset®, 100 mg/mL; Fort Dodge Animal Health, Fort Dodge, Iowa) and xylazine (Vettek™, 100 mg/mL, Bluesprings, Mo.) 10:1 mixture, respectively at a dose of 1 mL/kg body weight after initial induction with Isoflurane. Anesthesia was maintained with additional doses of ketamine only. Ringer's lactate solution was administrated subcutaneously to prevent dehydration, and body temperature was maintained with a heating pad. The left sciatic nerve was exposed with a mid-gluteal incision. A 10 mm sciatic nerve segment was excised under an operating microscope (Zeiss OpMi6, Carl Zeiss Surgical GmbH, Oberkochen, Germany). In group I and II, a 10 mm nerve allograft cold or frozen, respectively, was used to bridge the 10 mm nerve gap using 10-0 nylon epineural sutures. In the control group (group III), the nerve segment was reversed and put back. The muscle was approximated with 5-0 Vicryl rapid sutures, and the skin was closed with the same sutures. Postoperatively, trimethoprim/sulfadiazine 30 mg/kg (Tribrissen, Five Star Compounding Pharmacy, Clive, Iowa) was administered to prevent infection, and buprenorphine (Buprinex®, 0.1 mL/kg, Reckitt Benckiser Pharmaceuticals Inc., Richmond, Va.) served as an analgesic.
The motor functional outcome and histomorphometry of the nerve was tested at 12 and 16 weeks. During both time points, eleven animals per group were tested. The passive ankle angle, compound muscle action potential (CMAP), isometric tetanic force, and wet muscle weight were tested bilaterally. Distal nerve segments were analyzed for histomorphometry.
For the sacrificial procedure, at 12 and 16 weeks, the animals were anesthetized.
The maximum passive plantar flexion angle of the ankle was measured bilaterally in all animals to determine the ankle contracture angle as described elsewhere (Lee et al., Plast. Reconstr. Surg., 132(5):1173-80 (2013)).
The sciatic nerve was exposed. A miniature bipolar electrode (Harvard Apparatus, Holliston, Mass.) was attached proximal to the nerve graft. Recording electrodes were placed subcutaneous to the tibialis anterior muscle, and a ground electrode was placed in the surrounding tissue. Compound muscle action potential (CMAP) was measured using an EMG (VikingQuest, Nicolet Biomedical, Madison, Wis.). The maximal amplitude was recorded. In a similar fashion, the contralateral side was measured. The skin was re-approximated upon further testing.
For obtaining the maximum isometric tetanic force, the peroneal nerve, distal of the nerve graft, was exposed. The force measurements were executed as described elsewhere (Shin et al., Microsurgery, 28(6):452-7 (2008)). Briefly, the tibial muscle was carefully freed from its insertion while preserving the neurovascular pedicle. The hindlimb was stabilized with two Kirschner wires (DePuy Orthopedics) in the distal femur and ankle joint. The distal tendon of the tibial muscle was attached to a force transducer (MDB-0.5, Transducer Techniques, Temecula, Calif.) using a custom clamp with the tendon aligned in the anatomical position. The force transducer signal was processed and analyzed with a computer using LabView software (National Instruments). A miniature bipolar electrode (Harvard Apparatus) was attached to the peroneal nerve. The nerve was stimulated with a stimulator (Grass SD9, Grass Instrument Co., Quincy, Mass.). After establishing the optimal preload or muscle resting length, the stimulus intensity was increased until maximum tetanic muscle force was reached.
After bilateral force testing, animals were sacrificed with an overdose of pentobarbital intraperitoneally. The tibial muscles of both hindlimbs were carefully dissected and weighed immediately to obtain muscle mass ratio.
Nerve segments of the peroneal nerve were excised and stored in Trumps solution (37% formaldehyde and 25% glutaraldehyde) and subsequently embedded in spur resin. 1 μm sections were cut and stained with 1% Toluidine Blue. Images were acquired with a camera (Eclipse 50i; Nikon instruments, Melville, N.Y.) and analyzed using Image ProPlus Software (Media Cybernetics Inc, Bethesda, Md.), where nerve area, total myelin area, number of axons, and total axon area were obtained in semi-automatic fashion.
The sample size of the groups was based on the results of muscle force test obtained from previous studies showing the highest standard deviation being approximately 10%. Assuming that same variability will occur (two tailed distribution, α=0.05), the number of animals to provide an 80% power to detect 10% difference between the groups was estimated to be 19. To guard against potential attrition and to overpower the study, the sample size was increased to 22 per group. The three groups were compared with respect to ankle contracture, electrophysiology, maximum isometric tetanic force, wet muscle weight, and nerve histomorphometry. Data were expressed as a percentage of the contralateral (healthy) side to diminish intra-animal differences. One-way analysis of variance (ANOVA) followed by a Bonferroni correction for multiple testing was used for statistical analysis. All results are presented as mean±Standard Deviation (SD). A p-value of 0.05 was considered significant.
All animals survived the surgical procedure, and no complications were observed. All animals were used for final analysis. A summary of all results is presented in Table 1.
The percentage of recovery of the ankle angle contracture of the experimental side compared to the contralateral side was 80.2±3.1% in group I, 73.7±3.9% in group II, and 73.1±4.2% in group III at 12 weeks. At 16 weeks, the recovery was 88.0±3.1% in group I, 77.4±3.6% in group II, and 74.1±3.1% in group III. Significant difference was observed between group I and III (p<0.001) at both 12 and 16 weeks postoperatively (
Recovery of the compound muscle action potentials (CMAP) at 12 weeks was 41.9±14.4% in group I, 44.5±15.1% in group II, and 40.8±5.3% in group III. At 16 weeks, the recovery increased to 44.0±21.9% in group I, 56.2±14.0% in group II, and 53.5±12.7% in group III. Group comparison showed no statistically significant difference between all groups at both time points (
In group I, the percentage of muscle force recovery was found to be 42.3±5.8%. Group II exhibited the highest recovery with 48.7±7.6%. In group III, it was 43.2±10.1%. In the late follow-up time, at 16 weeks, the muscle force was recovered to 53.9±12.0% in group I, 55.4±12.7% in group II, and 50.0±11.4% in group III. No statistical significant difference was found when the groups were compared at the early and late follow up times (
The muscle mass ratio of the tibial muscle at 12 weeks was 63.7±4.9%, 60.2±4.7%, and 58.3±4.1% for groups I, II, and III, respectively. At 16 weeks, the muscle weight revealed a recovery up to 71.1±4.8% in group I, 67.0±6.6% in group II, and 64.7±3.7% in group III. At both time points, a statistically significant difference was observed between groups I and III (p<0.05 at both weeks). The autograft performed better than the frozen allograft. No difference was found when comparing the autograft to the cold allograft (
Twenty-five Sprague-Dawley rats, weighing 250-350 grams (Harlan, Indianapolis, Ind.), were used. After initial Isoflurane induction, all animals were sacrificed with an overdose of pentobarbital. Bilateral, 15 mm nerve segments of the sciatic nerve were aseptically harvested. A total of 50 nerve segments were collected.
A total of 5 groups were compared in this study. All groups consisted of 10 nerves. The first group was processed following a standard protocol based on previous studies (Hudson et al., Tissue Engineering, 10(9-10):1346-58 (2004); Neubauer et al., Exp. Neurol., 207(1):163-70 (2007); and Giusti et al., J. Bone Joint Surg. Am., 7; 94(5):410-7 (2012)). The second and third group underwent the same processing only with the addition of the enzyme elastase in two different time periods (i.e., 8 and 16 hours; Group II and III, respectively). The effect of freeze storage (−80° C.) was also studied in Group IV. A native unprocessed nerve (Group V) was analyzed as a negative control.
An overview of the studied groups is depicted in Table 2.
Briefly, nerves segments were immediately after harvest placed in RPMI 1640 solution at 4° C. overnight. The next day, the nerve tissues were placed in deionized distilled water. After 8 hours, the water was replaced by a solution containing 125 mM sulfobetaine-10 (SB-10), 10 mM phosphate, and 50 mM sodium. The nerves were agitated for 15 hours and rinsed for 15 minutes in a washing solution of 10 mM phosphate and 50 mM sodium. Next, the washing solution was replaced by a solution containing 0.14% Triton X-200, 0.6 mM sulfobetaine-16 (SB-16), 10 mM phosphate, and 50 mM sodium and agitated for 24 hours. Next, the tissues were rinsed with the washing solution of 50 mM phosphate and 100 mM sodium. The washing solution was replaced by SB-10 solution, and the nerves were agitated for 8 hours. Next, they were washed once using the washing solution and put into a solution of SB-16/Triton X-200. The nerves were agitated for 15 hours and then washed in a solution containing 10 mM phosphate and 50 mM sodium. Subsequently, nerves were incubated in a solution containing 2 U/mL Chondroitinase ABC for 16 hours at room temperature and then washed in a solution containing 10 mM phosphate and 50 mM sodium. In the Groups 2-4, nerves, which underwent elastase treatment, were incubated in a solution containing 0.05 U/mL elastase at 37° C. for 8 hours (Group II) or 16 hours (Groups III and IV). After that, the nerves were sterilized with gamma radiation of 2.5 kGray.
Nerve segments were stored in Ringers solution at −80° C. for the freeze storage (Group IV) for a duration of two weeks before final analysis. The other storage method was cold storage (4° C.), where nerves were placed in PBS solution.
A 5 mm section of each nerve segment was fixed in 2% Trump's solution (37% formaldehyde and 25% glutaraldehyde). 1 μm thin sections were transversally cut and stained with 1% toluidine blue. Another 5 mm section of each nerve segment was suspended in OCT and fast frozen, and 5 μm transverse sections were cut. Nerve sections were stained with hematoxylin and eosin (H&E). Digital images of each sample were taken using a microscope digital camera (Nikon microscopy digital color camera 4.0 mega pixels, Melville, N.Y.).
The organization of the basal lamina was visualized with a laminin staining as described herein. For electron microscopy, ultra-thin section were cut (500 A), placed on copper grids (200 mesh, EMS, Philadelphia, Pa.) and stained with uranyl acetate (EMS) and lead citrate (EMS). Sections were examined under a JEOL 1400 transmission electron microscope (JEOL Ltd, Peabody, Mass., USA). All sections were scored for their structural properties on a 1-5 scale with 1 being worst and 5 being optimal. Three independent and blinded investigators performed the analysis. Validity and reliability of the objective analysis was determined with an intra-class correlation of 0.83 (95% CI; 0.71-0.90).
Intraluminal remnants were examined with immunohistochemical (IHC) stainings on different components of the nerve allograft. Nerve segments were pre-fixed with 4% cold paraformaldehyde and fast frozen. Transverse frozen sections (5 μm thickness) were cut. To identify the remnant axons left in the graft, a S100 staining was performed. To study the immunogenicity of the graft after processing, MHC-I was stained. Additionally, laminin was stained to identify the basal laminae. The IHC staining procedure was performed using the Leica Bond III Stainer (Leica, Buffalo, Ill.). The sections were post fixed in 4% paraformaldehyde and retrieved on-line using Epitope Retrieval 1 (Leica, Buffalo, Ill.) for 5 minutes. The following primary antibodies were used: polyclonal 5100 anti-rabbit (Dako) was used at 1:5000, polyclonal laminin y1 anti-rabbit (Sigma) was used at 1:200, and mouse anti-MHCI (Clone OX18, Novus Biological) was used at 1:100. All antibodies were incubated for 60 minutes. The detection system used was Research detection (Leica DS9455). This system includes the Protein Block (Dako X0909) and secondary antibody AlexFluor488. All sections were nuclear stained with Hoechst33342 (Invitrogen H1399).
Once completed, slides were removed from stainer and rinsed for 5 minutes in distilled water. Slides were coverslipped using ProLong Gold antifade media (Invitrogen). Nerve slides were examined under a fluorescence laser confocal microscope (LSM 780, Zeiss, Germany), and pictures were captured with a camera. The intensity of stainings in the cross section of the nerve was measured with Image J software (NIH, Bethesda, USA).
Data were expressed as mean±SEM. For structural analysis, the results of the three different observers and the three different stainings were averaged to score the structural properties. Statistical analysis of the differences between the groups was performed with one-way analysis of variance (ANOVA) followed by Bonferroni post hoc test with GraphPad Prism 5 software (GraphPad Software, CA, USA). P-values<0.05 were considered to be significant.
An overview of the different stainings is depicted in
The structure of the nerve graft was not significantly influenced by the addition of elastase to the decellularization protocol. Group I, the standard protocol, exhibited a score of 3.9±0.2, and Group II, with the addition of elastase, exhibited a score of 3.5±0.1. There was no significant difference between the groups. A longer exposure of the enzyme, Group III, did not influence the structure of the nerve graft (3.2±0.1). There was no statistical difference between the groups (
The same was observed when the intensity of the laminin was determined. The enzyme did not significantly reduce the presence of laminin in the nerve. Group I (standard protocol) had a laminin intensity of 65.7±8.6, Group II (with elastase) had a laminin intensity of 53.22±6.2, and the group with a longer exposure to elastase, Group III, had a score of 51.5±3.3. No significant difference between those three groups was observed (p=0.20).
Axons were significantly reduced by the addition of the extra enzymatic step (Group I; 9.5±1.0, Group II; 5.0±0.5). Prolonged exposure to elastase (Group III) resulted in an even lower score of axons (3.2±0.4). The difference between the groups was statistically significant (p<0.0001) (
Elastase had a similar significant effect of reduction of the remnants when evaluating immunogenicity. The standard protocol without the enzyme (Group I) had an MHCI score of 18.21±1.8, and the addition of elastase reduced the MHCI score to 9.3±1.0. The observed differences were significant, p<0.0001 (
The effect of cold or freeze storage at either 4° C. or −80° C. revealed a tremendous effect on the structure of the graft. When frozen, the total score for the structure significantly decreased from 3.2±0.1 (Group III) to 1.6±0.2 (Group IV) for the rat nerves. The effect of storage was visualized with electron microscopy in
Storage had no significant effect on the laminin intensity staining. The score of Group III (51.49±3.31) was not significantly different compared to that of Group IV (63.67±2.4, p=0.20).
When examining the effect of storage on the intraluminal remnants, the cold storage nerves exhibited a significantly lower amount of axons, stained with S100 compared to the frozen nerves. The effect of storage was statistically significant. Group III was 3.2±0.3, and the freeze storage group (Group IV) was higher at 5.7±0.3 (
The effect of cold or freeze storage at either 4° C. or −80° C. revealed a severe effect on the structure of the graft. The immunogenicity in the rat nerves of the cold storage group (Group III), stained with MHCI, was statistically significant different (9.3±1.0) from the frozen storage (Group IV; 20.8±1.2) (
The results provided herein demonstrate a reduced immunogenicity, diminished cellular debris, and elimination of Schwann cells, while maintaining ultrastructure, when elastase was added to the nerve processing. Storage at −80° C. after the decellularization process heavily damaged the nerve ultrastructure as compared to cold storage.
It is to be understood that while the invention has been described in conjunction with the detailed description thereof, the foregoing description is intended to illustrate and not limit the scope of the invention, which is defined by the scope of the appended claims. Other aspects, advantages, and modifications are within the scope of the following claims.
This application claims priority to U.S. Application Ser. No. 62/166,432, filed on May 26, 2015. The disclosure of the prior application is considered part of the disclosure of this application, and is incorporated in its entirety into this application.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US16/31313 | 5/6/2016 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62166432 | May 2015 | US |
