IP Library Granted Patent US 11,459,545
Granted Patent B2
US 11,459,545 · App. 13/509,409 · Granted Oct 4, 2022

Methods to enhance delivery and engraftment of stem cells including the identification of specific prostaglandin E2 receptors

Inventors: Louis M. Pelus (Indianapolis, IN); Jonathan Hoggatt (Cambridge, MA)
Assignee: INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION
C12N5/0647C12N2501/02
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Quick Facts
Patent No.
US 11,459,545
App. No.
13/509,409
Granted
Oct 4, 2022
Kind
B2
Abstract

The receptor EP 4 is identified as the PGE 2 receptor that is most responsible enhancing the homing and engraftment of hematopoietic stem and progenitor cells. Treatment of graft sources and graft recipients with compounds that preferentially target the EP 4 receptor provide effective methods of increasing engraftment success while minimizing adverse side effects that may be associated with therapies that include the use of less selective molecules such as PGE 2 and dmPGE 2 . One effective molecule used in such therapies is 5-[(1E,3R)-4,4-difluoro-3-hydroxy-4-phenyl-1-buten-1-yl]-1-[6-(2H-tetrazol-5R-yl)hexyl]-2-pyrrolidinone or a pharmaceutically acceptable salt thereof (L-902, 688).

Claims (20)

1. A method of increasing homing of a hematopoietic stem cell or hematopoietic progenitor cell, comprising the steps of:

(a) contacting a hematopoietic stem cell or hematopoietic progenitor cell expressing at least one PGE2 EP4 receptor with at least one compound or a pharmaceutically acceptable salt thereof such that homing potential is increased in the contacted hematopoietic stem cell or hematopoietic progenitor cell,

wherein the at least one compound or the pharmaceutically acceptable salt thereof:

(i) preferentially interacts with the PGE2 EP4 receptor as compared to the PGE2 EP1, EP2, and EP3 receptors, and

(ii) increases the homing of the contacted hematopoietic stem cell or hematopoietic progenitor cell when transplanted into a patient compared to a compound that does not preferentially interact with the PGE2 EP4 receptor, and

(b) washing the contacted hematopoietic stem cell or hematopoietic progenitor cell, and wherein the amount of the compound contacting said hematopoietic stem cell or hematopoietic progenitor cell is about 0.001-10 microMolar.

2. The method according to claim 1 , wherein said hematopoietic stem cell or hematopoietic progenitor cell is isolated from marrow, umbilical cord or peripheral blood.

3. The method according to claim 1 , wherein contacting the compound with said hematopoietic stem cell or hematopoietic progenitor cell increases the homing of said cells.

4. The method according to claim 1 , wherein contacting the compound with said hematopoietic stem cell or hematopoietic progenitor cell increases the engrafting potential of said cells.

5. The method according to claim 1 , wherein the at least one compound is selected from the groups consisting of: 2-[3-[(1R,2S,3R)-3-hydroxy-2-[(E,3S)-3- hydroxy-5-[2-(methoxymethyl)phenyl-]pent-l-enyl]-5-oxocyclopentyl]sulfanylpropylsulfanyl]acetic acid;

methyl 4-[2-[(1R,2R,3R)-3-hydroxy-2-[(E,3S)-3-hydroxy-4-[3-(methoxymethyl)phenyl-]but-1-enyl]-5-oxocyclopentyl]ethylsulfanyl]butanoate; 16-(3-Methoxymethyl)phenyl-w-tetranor-5-thiaPGE; 543-[(2S)-2-{(3R)-3-hydroxy-4-[3-(trifluoromethyl)phenyl]butyl}-5-oxopyrrolidin-1-yl]propyl]thiophene-2-carboxylate; [4′-[3-butyl-5-oxo-1-(2-trifluoromethyl-phenyl)-1,5-dihydro-[1,2,4]triazol-4-ylmethyl]-biphenyl-2-sulfonic acid (3-methyl-thiophene-2-carbonyl)-amide]; and ((Z)-7-{(1R,4S,5R)-5-[(E)-5-(3-chloro-benzo[b]thiophene-2-yl)-3-hydroxy-p-ent-l-enyl]-4-hydroxy-3,3-dimethyl-2-oxo-cyclopentyl}-hept-5-enoic acid) or a pharmaceutically acceptable salt thereof.

6. The methods according to claim 1 , wherein the at least one compound is 5-[(1E,3R)-4,4-difluoro-3-hydroxy -4-phenyl-1-buten-1-yl]-1-[6-(2H-tetrazol-5Ryl) hexyl]-2-pyrrolidinone or a pharmaceutically acceptable salt thereof.

7. The method according to claim 1 , wherein said cell is contacted with said compound or pharmaceutically acceptable salt thereof for 15 minutes to 6 hours.

8. The method according to claim 1 , further comprising administering the washed cell to the patient.

9. A method of increasing homing of a hematopoietic stem cell or hematopoietic progenitor cell, comprising the steps of:

(a) contacting about 1-10 million hematopoietic stem cells or hematopoietic progenitor cells expressing at least one PGE2 EP4 receptor with at least one compound or a pharmaceutically acceptable salt thereof such that homing potential is increased in the contacted hematopoietic stem cell or hematopoietic progenitor cell, wherein the compound or the pharmaceutically acceptable salt thereof:

(i) preferentially interacts with the PGE2 EP4 receptor as compared to PGE2 EP1, EP2, and EP3 receptors, and

(ii) increases the homing potential of the contacted hematopoietic stem cell or hematopoietic progenitor cells compared to a compound that does not preferentially interact with the PGE2 EP4 receptor, and

(b) washing the contacted hematopoietic stem cell or hematopoietic progenitor cell, and wherein the amount of the compound contacting said hematopoietic stem cells or hematopoietic progenitor cells is about 0.001-10 microMolar.

10. The method of claim 1 , wherein the contacted hematopoietic stem cell or hematopoietic progenitor cell has increased engraftment when transplanted into a patient compared to a non-contacted hematopoietic stem cell or hematopoietic progenitor cell.

Assignments (1)
CONFIRMATORY LICENSE Recorded Nov 19, 2012
From: INDIANA UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029321/0772 →
Continuity (3)
Provisional Application 61261349 · Nov 15, 2009
Provisional Application 61261352 · Nov 15, 2009
Related Publication 20120315253A1 · Dec 13, 2012