IP Library Granted Patent US 8,445,190
Granted Patent B2
US 8,445,190 · App. 13/121,396 · Granted May 21, 2013

Method of inhibiting biomaterial-induced procoagulant activity using complement inhibitors

Inventors: John D. Lambris (Philadelphia, PA); Konstantinos Ritis (Alexandroupolis, GR)
Assignee: The Trustees of the University of Pennsylvania
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Quick Facts
Patent No.
US 8,445,190
App. No.
13/121,396
Granted
May 21, 2013
Kind
B2
Abstract

Methods for reducing or eliminating biomaterial-induced procoagulant activity in blood subjected to extracorporeal treatment that exposes the blood to the biomaterial are disclosed. The methods involve treatment of the blood, or the extracorporeal biomaterial, or both, with a complement inhibitor to inhibit C5a/C5aR-mediated tissue factor formation in the blood.

Claims (18)

1. A method for reducing or eliminating biomaterial-induced procoagulant activity in blood subjected to extracorporeal treatment that exposes the blood to the biomaterial, the method comprising treating the blood, or the biomaterial, or both, with a complement inhibitor in an amount effective to reduce or prevent C5a/C5aR-mediated tissue factor (TF) formation, thereby reducing or eliminating the biomaterial-induced procoagulant activity in the blood.

2. The method of claim 1 , wherein the complement inhibitor comprises one or more of a C5a inhibitor, a C5aR inhibitor, a C3 inhibitor, a factor D inhibitor, a factor B inhibitor, a C4 inhibitor, a C1q inhibitor, or any combination thereof.

3. The method of claim 2 , wherein the complement inhibitor is a C5a inhibitor or a C5aR inhibitor.

4. The method of claim 3 , wherein the C5a inhibitor or C5aR inhibitor is acetyl-Phe-[Orn-Pro-D-cyclohexylalanine-Trp-Arg] (PMX-53), PMX-53 analogs, neutrazumab, TNX-558, eculizumab, pexelizumab or ARC1905, or any combination thereof.

5. The method of claim 2 , wherein the complement inhibitor is a C3 inhibitor.

6. The method of claim 5 , wherein the C3 inhibitor is compstatin, a compstatin analog, a compstatin peptidomimetic, a compstatin derivative, or any combinations thereof.

7. The method of claim 2 , wherein the complement inhibitor is a C4 inhibitor.

8. The method of claim 1 wherein the extracorporeal treatment of blood comprises hemodialysis.

9. The method of claim 8 , wherein the biomaterial comprises hemodialysis filter fibers.

10. The method of claim 8 , wherein the blood is from an individual with renal disease.

11. The method of claim 10 , wherein the renal disease is end stage renal disease (ESDR).

12. The method of claim 1 , wherein the blood is contacted with the complement inhibitor prior to and/or during the extracorporeal treatment.

13. The method of claim 1 , wherein the biomaterial is contacted with the complement inhibitor prior to the extracorporeal treatment.

14. The method of claim 1 , wherein the complement inhibitor treatment is used together or concurrently with, or sequentially before or after, at least one other anti-coagulant or anti-inflammatory treatment of the blood.

15. A kit comprising a complement inhibitor and a biomaterial for use in an extracorporeal treatment device, and, optionally, instructions for using the complement inhibitor in a method such as the one described above.

16. The kit of claim 15 , comprising hemodialysis filtration fibers.

17. An extracorporeal treatment device that includes a complement inhibitor-treated biomaterial, or a biomaterial adapted for or amenable to treatment with a complement inhibitor.

18. The device of claim 17 , which is a hemodialysis unit.

Assignments (1)
CONFIRMATORY LICENSE Recorded Jun 22, 2011
From: UNIVERSITY OF PENNSYLVANIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 026503/0497 →
Continuity (2)
Provisional Application 61101453 · Sep 30, 2008
Related Publication 20110269113A1 · Nov 3, 2011