Increased In Vivo Circulation Time of Platelets After Storage With A Sialidase Inhibitor
The present invention relates to methods, compositions and kits for increasing the in vivo circulation time of isolated platelets by storing the platelets with one or more sialidase inhibitors.
1 ) A method of preparing platelets for storage, wherein isolated platelets are obtained from one or more donors, the method comprises:
contacting the isolated platelets with one or more sialidase inhibitors, and optionally one or more glycan-modifying agents.
2 ) The method of claim 1 , wherein the sialidase inhibitor is selected from the group consisting of: fetuin, 2,3-dehydro-2-deoxy-N-acetylneuraminic acid (DANA) or a pharmaceutically acceptable salt thereof; ethyl (3R,4R,5S)-5-amino-4-acetamido-3-(pentan-3-yloxy)-cyclohex-1-ene-1-carboxylate); (2R,3R,4S)-4-guanidino-3-(prop-1-en-2-ylamino)-2-((1R,2R)-1,2,3-trihydroxypropyl)-3,4-dihydro-2H-pyran-6-carboxylic acid; (4S,5R,6R)-5-acetamido-4-carbamimidamido-6-[(1R,2R)-3-hydroxy-2-methoxypropyl]-5,6-dihydro-4H-pyran-2-carboxylic acid; and (1S,2S,3S,4R)-3-[(1S)-1-acetamido-2-ethyl-butyl]-4-(diaminomethylideneamino)-2-hydroxy-cyclopentane-1-carboxylic acid, or a pharmaceutically acceptable salt thereof.
3 ) The method of claim 2 , wherein the sialidase inhibitor is the sodium salt of 2,3-dehydro-2-deoxy-N-acetylneuraminic acid.
4 ) The method of claim 1 , wherein the glycan-modifying agent is CMP-sialic acid or a CMP-sialic acid precursor.
5 ) The method of claim 4 , further comprising an enzyme that converts the CMP-sialic acid precursor to CMP-sialic acid.
6 ) The method of claim 1 , wherein the glycan-modifying agent is UDP-galactose.
7 ) The method of claim 1 , wherein the glycan-modifying agents are CMP-sialic acid and UDP-galactose.
8 ) A method of preparing platelets for storage, the method comprises:
a) isolating platelets from one or more individuals;
b) contacting the isolated platelets with a sialidase inhibitor in an amount sufficient to reduce hydrolysis of sialic acid residues from platelet surface glycans.
9 ) The method of claim 8 , wherein a reduction in platelet receptors loss occurs.
10 ) The method of claim 9 , wherein the reduction in platelet receptor loss includes a reduction in GPIbα loss, GPV loss or both.
11 ) A method of increasing the in vivo circulation time of isolated platelets comprising:
a) obtaining isolated platelets from one or more individuals;
b) treating the platelets with an amount of one or more sialidase inhibitors, and optionally one or more glycan-modifying agents to thereby obtain treated platelets;
c) transfusing the treated platelets into an individual in need thereof to thereby obtain transfused platelets;
wherein the circulation time of the transfused platelets is longer, as compared to platelets not subjected to step a).
12 ) The method of claim 11 , further comprising storing the platelet composition at room temperature for a period of time.
13 ) The method of claim 11 , further comprising cooling the platelet composition to a temperature below room temperature; storing the platelet composition for a period of time; and then rewarming the platelet composition back to room temperature.
14 ) A platelet preparation comprising a sialidase inhibitor and a population of platelets;
wherein the stable platelet preparation is prepared by the method of:
a) obtaining a population of platelets from a donor; and
b) treating the platelets with an effective amount of a sialidase inhibitor; and
wherein the platelet preparation is suitable for administration to a human after storage without significant loss of hemostatic function or without a significant increase in platelet clearance in the human as compared to untreated platelets.
15 ) A platelet preparation comprising:
i) platelets isolated from a donor; and
ii) an amount of one or more sialidase inhibitors and optionally one or more glycan-modifying agents.
16 ) A kit comprising: a sterile container capable of receiving and containing a population of platelets, the container substantially closed to the environment, and a sterile quantity of a sialidase inhibitor.
17 ) The kit of claim 16 , wherein the container is suitable for the cold storage of platelets.
18 ) The kit of claim 16 , wherein the sialidase inhibitor is selected from the group consisting of: fetuin, 2,3-dehydro-2-deoxy-N-acetylneuraminic acid (DANA) or a pharmaceutically acceptable salt thereof; ethyl (3R,4R,5S)-5-amino-4-acetamido-3-(pentan-3-yloxy)-cyclohex-1-ene-1-carboxylate); (2R,3R,4S)-4-guanidino-3-(prop-1-en-2-ylamino)-2-((1R,2R)-1,2,3-trihydroxypropyl)-3,4-dihydro-2H-pyran-6-carboxylic acid; (4S,5R,6R)-5-acetamido-4-carbamimidamido-6-[(1R,2R)-3-hydroxy-2-methoxypropyl]-5,6-dihydro-4H-pyran-2-carboxylic acid; and (1S,2S,3S,4R)-3-[(1S)-1-acetamido-2-ethyl-butyl]-4-(diaminomethylideneamino)-2-hydroxy-cyclopentane-1-carboxylic acid, or a pharmaceutically acceptable salt thereof.
19 ) The kit of claim 18 , wherein the sialidase inhibitor is the sodium salt of 2,3-dehydro-2-deoxy-N-acetylneuraminic acid.
20 ) The kit of claims 16 , further comprising an effective amount of at least one glycan-modifying agent.
21 ) The kit of claim 20 , wherein the glycan-modifying agent is CMP-sialic acid or a CMP-sialic acid precursor.
22 ) The kit of claim 16 , further comprising an enzyme that converts the CMP-sialic acid precursor to CMP-sialic acid.
23 ) The kit of claim 20 , wherein the glycan-modifying agent is UDP-galactose.
24 ) The kit of claim 20 , wherein the glycan-modifying agents are CMP-sialic acid and UDP-galactose.
25 ) A sterile bag or container that comprises:
a) a sterile bag or container suitable for blood storage; and
b) an amount of one or more sialidase inhibitors and optionally one or more glycan-modifying agents.