ORGAN PRESERVATION SOLUTION AND METHODS OF USE THEREOF IN THE INHIBITION OF ISCHEMIA-REPERFUSION INJURY

Abstract

Compositions and methods for preserving organs, maintaining organ viability and inhibiting ischemia-reperfusion injury and the like are disclosed.

Claims

1. An organ perfusion solution for maintaining donor organ viability and inhibiting ischemia-reperfusion injury comprised of: a) 0.0001-0.002 mg/mL Heparin sodium salt b) 0.015-0.3 mg/mL N-acetyl-L-cysteine c) 7-140 mg/mL Trehalose d) 0.1-1% Sodium chloride.

2. The solution of claim 1, wherein the concentration of heparin sodium salt is 0.001 mg/mL.

3. The solution of claim 1, wherein the concentration of N-acetyl-cysteine is 0.15 mg/mL.

4. The solution of claim 1, wherein the concentration of Trehalose is 70 mg/mL.

5. The solution of claim 1, wherein the concentration of sodium chloride is 0.9%.

6. The solution of claim 1, wherein the concentration of heparin sodium salt is 0.001 mg/mL, N-acetyl-cysteine is 0.15 mg/mL, Trehalose is 70 mg/mL, and sodium chloride is 0.9%.

7. A method for preserving an organ comprising placing the organ in a solution according to claim 1 to maintain viability of the organ and inhibit ischemia-reperfusion injury.

8. The method according to claim 7, wherein the solution has a temperature of between 0° and 10° C.

9. The method according to claim 7, wherein the solution has a temperature of 4° C.

10. The method according to claim 7, further comprising rinsing or flushing the organ with the solution.

11. The method according to claim 7, further comprising placing the organ under continuous or pulsatile perfusion with the solution.

12. The method according to claim 7, wherein the organ is an intestine, a kidney, a liver, a lung, skin, a pancreas, or a heart transplant.

13. The method according to claim 12, wherein the organ is an intestine.

14. The method according to claim 12, wherein the organ is obtained from a heart-beating donor.

15. The method according to claim 12, wherein the organ is obtained from a non-heart-beating donor.

16. The method according to claim 12, wherein the organ is mammalian in origin.

17. The method according to claim 12, wherein the organ is human in origin.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0011] FIG. 1. Quantification of normal intestinal villi following ZL solution, saline and UW solution preservation of mouse intestines (n=1 mice).

[0012] FIG. 2. Quantification of normal intestinal villi following ZL and UW solution preservation of mouse intestines (n=13 mice).

[0013] FIG. 3. Quantification of normal intestinal villi following ZL and UW solution preservation of human intestines (n=5 patients).

DETAILED DESCRIPTION OF THE INVENTION

[0014] Based on previous studies on the mechanism of intestinal ischemia/reperfusion injury, we have developed an intestine preservation solution for the inhibition of ischemia-reperfusion injury. The intestine preservation solution (ZL solution) is comprised of combinations of a complement inhibitor/anti-coagulant, anti-oxidant, and cell membrane stabilizer. Specifically, the preservation solution comprises: heparin, N-acetyl-L-cysteine, trehalose, and sodium chloride. The composition of our solution is distinct from the current standard preservation solution, University of Wisconsin solution (UW solution; U.S. Pat. No. 4,798,824).

[0015] The following ranges of our solution composition have been tested: [0016] 1) Heparin sodium salt: 0.0001-0.002 mg/ml (optimal concentration: 0.001 mg/mL) [0017] 2) N-acetyl-L-cysteine: 0.015-0.3 mg/ml (optimal concentration: 0.15 mg/mL) [0018] 3) Trehalose: 7-140 mg/ml (optimal concentration: 70 mg/mL) [0019] 4) Sodium chloride: 0.1-1% (optimal concentration: 0.9%)

[0020] ZL solution was tested in procured mouse intestine under cold storage preservation conditions. Control groups included intestine preserved with saline or UW solution. Histological analysis quantified the number of normal intestinal villi. The saline preserved intestines lacked normal villi after cold preservation. The UW preserved intestines showed reduced protection compared to the intestines treated with ZL solution which exhibited a statistically significant increase in the number of preserved normal villi.

[0021] Additional studies compared the preservation effect of ZL solution on human intestine. Intestine obtained from patients who had undergone bowel resection surgery was preserved in cold storage with ZL or UW solution. ZL solution preservation resulted in a 3-fold increase in preserved normal intestinal villi compared to intestines stored in the UW solution.

DEFINITIONS

[0022] For purposes of the present invention, “a” or “an” entity refers to one or more of that entity. As such, the terms “a” or “an,” “one or more” and “at least one” can be used interchangeably herein. It is also noted that the terms “comprising,” “including,” and “having” can be used interchangeably. Furthermore, a compound “selected from the group consisting of” refers to one or more of the compounds in the list that follows, including mixtures (i.e. combinations) of two or more of the compounds.

[0023] In this disclosure, “comprises,” “comprising,” “containing” and “having” and the like can have the meaning ascribed to them in U.S. Patent law and can mean “ includes,” “including,” and the like; “consisting essentially of” or “consists essentially” likewise has the meaning ascribed in U.S. Patent law and the term is open-ended, allowing for the presence of more than that which is recited so long as basic or novel characteristics of that which is recited is not changed by the presence of more than that which is recited, but excludes prior art embodiments.

[0024] “Effective amount” is meant the amount of a composition of the invention required to inhibit ischemia-reperfusion injury relative to an untreated organ.

[0025] According to the present invention, an isolated, or biologically pure molecule is a compound that has been removed from its natural milieu. As such, “isolated” and “biologically pure” do not necessarily reflect the extent to which the compound has been purified. An isolated compound of the present invention can be obtained from its natural source, can be produced using laboratory synthetic techniques or can be produced by any such chemical synthetic route.

[0026] Unless specifically stated or obvious from context, as used herein, the term “or” is understood to be inclusive. Unless specifically stated or obvious from context, as used herein, the terms “a”, “an”, and “the” are understood to be singular or plural.

[0027] Unless specifically stated or obvious from context, as used herein, the term “about” is understood as within a range of normal tolerance in the art, for example within 2 standard deviations of the mean. About can be understood as within 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, 0.5%, 0.1%, 0.05%, or 0.01% of the stated value.

[0028] The recitation of a listing of chemical groups in any definition of a variable herein includes definitions of that variable as any single group or combination of listed groups. The recitation of an embodiment for a variable or aspect herein includes that embodiment as any single embodiment or in combination with any other embodiments or portions thereof.

[0029] “Sample” or “patient sample” or “biological sample” generally refers to a sample which may be tested for a particular molecule. Samples may include but are not limited to cells, body fluids, including blood, serum, plasma, bone aspirate, urine, saliva, tears, CSF, pleural fluid, tissue, organs and the like.

[0030] The terms “agent” and “compound” are used interchangeably herein and denote a chemical compound, a mixture of chemical compounds, a biological macromolecule, or an extract made from biological materials such as bacteria, plants, fungi, or animal (particularly mammalian) cells or tissues.

[0031] The term “modulate” as used herein refers to increasing or decreasing. For example, the term modulate refers to the ability of a compound or agent to decrease ischemia-reperfusion injury.

[0032] A “transplant” or “donor organ” can be any organ of the body, such as intestine, a kidney, a liver, a lung, skin, a pancreas, or a heart.

[0033] The term “preserving” denotes placing an organ in a solution, rinsing or flushing an organ with a solution, or placing the organ under continuous or pulsatile perfusion with a solution.

[0034] The following materials and methods are provided to facilitate the practice of the present invention.

EXAMPLE I

Development of a Novel Preservation Solution Against Intestinal Ischemia/Reperfusion Injury

[0035] Intestinal failure is a potentially fatal syndrome associated with a mortality rate as high as 30%. Intestinal transplantation remains the therapy of choice for critically ill patients but early postoperative mortality rates can exceed 30%. One major barrier to intestinal transplantation is the extreme sensitivity of donor intestine to ischemia, resulting in ischemia-reperfusion (IR) injury and poor clinical outcome. We developed a novel preservation solution with an optimal combination of complement inhibitors, anti-oxidants, trehalose, pH and ions that inhibited intestinal I/R injury and preserved intestinal villi. The preservation buffer (ZL solution) consisted of heparin sodium salt (0.001 mg/mL), N-acetyl-L-cysteine (0.15 mg/mL), Trehalose (70 mg/mL), and sodium chloride (0.9%) (normal saline).

[0036] ZL solution was tested in procured mouse intestine stored at 4° C. for 24 hours (n=1). Control groups included intestines stored in saline or UW solution. H & E staining and microscopic analysis was performed to evaluate the number of normal intestinal villi. The numbers of normal villi were quantified microscopically in the preserved tissue slices and normalized with the lengths of tissues analyzed (FIG. 1). The saline preserved group lacked villi following 24 hours cold preservation. While the intestines preserved in UW solution exhibited some protection, the intestines stored in ZL solution showed a 3-fold greater number of normal villi.

[0037] We subsequently performed a larger study. Mouse intestine was procured in ZL or UW solution (n=13 mice) and preserved for 24 hours in cold storage conditions (4° C.). Intestinal histology was evaluated using H & E staining and microscopic analysis. The numbers of normal intestinal villi were counted in the preserved tissue slices and normalized with the lengths of tissues analyzed. The results showed that ZL solution preservation increased the number of normal intestinal villi 5-fold compared to the intestine stored in the UW solution (FIG. 2).

[0038] To evaluate the preservation effect on human intestine, human intestinal tissues were obtained from 5 patients who had undergone bowel resection surgery. Tissue was stored for 24 hours at 4° C. in ZL or UW solution. The intestines preserved in ZL solution showed a 2-fold greater number of normal intestinal villi compared to the intestines stored in UW solution (FIG. 3).

[0039] These results indicate that ZL solution provides superior preservation for procured intestine from mice and humans. An additional advantage of ZL solution over UW solution is the reduced number of chemical components (4 versus 13, respectively), which will translate into lower cost and better applications in clinical situations. The same is true with respect to other organ preservation solutions of the prior art.

REFERENCES

[0040] 1. Cotran, R. S. (1999) in Robbins Pathologic Basis of Disease (Saunders, St. Louis), pp. 7-12. [0041] 2. Lawrence, J. B. (2003) in Current Diagnosis & Treatment in Gastroenterology, ed. Friedman, S. L. (McGraw-Hill, New York), Section 1.9. [0042] 3. Koike, K., Moore, E. E., Moore, F. A., Franciose, R. J., Fontes, B. & Kim, F. J. (1995) J. Trauma 39, 23-27; discussion, 27-28. [0043] 4. Simpson, R., Alon, R., Kobzik, L., Valeri, C. R., Shepro, D. & Hechtman, H. B. (1993) Ann. Surg. 218, 444-453; discussion, 453-454. [0044] 5. Szabo, A., Boros, M., Kaszaki, J. & Nagy, S. (1997) Shock 8, 284-291. [0045] 6. Weisman, H. F., Bartow, T., Leppo, M. K., Marsh, H. C., Jr., Carson, G. R., Concino, M. F. Boyle, M. P., Roux, K. H., Weisfeldt, M. L. & Fearon, D. T. (1990) Science 249, 146-151. [0046] 7. Hill, J., Lindsay, T. F., Ortiz, F., Yeh, C. G., Hechtman, H. B. & Moore, F. D., Jr. (1992) J. Immunol. 149, 1723-1728. [0047] 8. Weiser, M. R., Williams, J. P., Moore, F. D., Kobzik, L., Ma, M., Hechtman, H. B. & Carroll, M. C. (1996) J. Exp. Med. 183, 2343-2348. [0048] 9. Williams, J. P., Pechet, T. T., Weiser, M. R., Reid, R., Kobzik, L., Moore, F. D., Carroll, M. C. & Hechtman, H. B. (1999) J. Appl. Physiol. 86, 938-942. [0049] 10. Fleming, S. D., Shea-Donohue, T., Guthridge, J. M., Kulik, L., Waldschmidt, T. J., Gipson, M. G., Tsokos, G. C. & Holers, V. M. (2002) J. Immunol. 169, 2126-2133. [0050] 11. Reid, R. R., Woodcock, S., Shimabukuro-Vornhagen, A., Austen, W. G., Jr., Kobzik, L., Zhang, M., Hechtman, H. B., Moore, F. D., Jr., & Carroll, M. C. (2002) J. Immunol. 169, 5433-5440. [0051] 12. Ladefoged K, Hessov I, Jarnum S. Scandinavian journal of gastroenterology. Supplement. 1996; 216:122-131 [0052] 13. Howard L, Ament M, Fleming C R, Shike M, Steiger E. Gastroenterology. 1995; 109:355-365 [0053] 14. Roskott A M, Nieuwenhuijs V B, Dijkstra G, Koudstaal L G, Leuvenink H G, Ploeg R J. Transplant international: official journal of the European Society for Organ Transplantation. 2011; 24:107-131

[0054] Furthermore, the transitional terms “comprising”, “consisting essentially of” and “consisting of”, when used in the appended claims, in original and amended form, define the claim scope with respect to what unrecited additional claim elements or steps, if any, are excluded from the scope of the claim(s). The term “comprising” is intended to be inclusive or open-ended and does not exclude any additional, unrecited element, method, step or material. The term “consisting of” excludes any element, step or material other than those specified in the claim and, in the latter instance, impurities ordinary associated with the specified material(s). The term “consisting essentially of” limits the scope of a claim to the specified elements, steps or material(s) and those that do not materially affect the basic and novel characteristic(s) of the claimed invention. Thus, the organ preservation solution of the present invention may suitably comprise, consist essentially of or consist of the above-described heparin sodium salt, N-acetyl-L-cysteine, Trehalose and sodium chloride components.

[0055] While certain of the preferred embodiments of the present invention have been described and specifically exemplified above, it is not intended that the invention be limited to such embodiments. Various modifications may be made thereto without departing from the scope of the present invention, as set forth in the following claims.