Prolonging Survival of Platelets Using CMP-Sialic Acid, UDP-Galactose or Both

a technology of cmpsialic acid and udpgalactose, which is applied in the field of prolonging the survival of platelets using cmpsialic acid, udpgalactose or both, can solve the problems of concomitant loss of hemostatic function, storage lesion defects, etc., and achieve the effect of reducing the incidence of platelet clearan

Inactive Publication Date: 2013-03-07
ROSIELLO KEITH M +5
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent text discusses methods for improving the quality and lifespan of platelets by modifying their surface with glycan modifying agents. These agents can reduce storage lesions, maintain biological function, and decrease clearance when transfused into a mammal. The agents can include UDP-galactose and CMP-sialic acid, and can target a specific molecule on the platelet surface. The modified platelets can then be stored at a low temperature to reduce pathogen growth. Overall, this patent provides technical means for enhancing the quality and lifespan of platelets for use in blood transfusions.

Problems solved by technology

CR3 receptors recognize N-linked sugars with terminal βGlcNAc on the surface of platelets, which have formed GP1bα complexes, and phagocytose the platelets, clearing them from the circulation and resulting in a concomitant loss of hemostatic function.
Room temperature stored-treated platelets also demonstrate ameliorated or substantially reduced storage lesion defects over an extended period of time relative to untreated platelets.

Method used

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  • Prolonging Survival of Platelets Using CMP-Sialic Acid, UDP-Galactose or Both
  • Prolonging Survival of Platelets Using CMP-Sialic Acid, UDP-Galactose or Both
  • Prolonging Survival of Platelets Using CMP-Sialic Acid, UDP-Galactose or Both

Examples

Experimental program
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example 1

Introduction

[0166]Modest cooling primes platelets for activation, but refrigeration causes shape changes and rapid clearance, compromising storage of platelets for therapeutic transfusions. We found that shape change inhibition does not normalize cold-induced clearance. We also found that cooling platelets rearranges the surface configuration of the von Willebrand factor (vWf) receptor complex α subunit (GP1bα) such that it becomes targeted for recognition by complement receptor 3 receptors (CR3) predominantly expressed on liver macrophages, leading to platelet phagocytosis and clearance. GP1bα removal prolongs survival of unchilled platelets. Chilled platelets bind vWf and function normally in vitro and ex vivo after transfusion into CR3-deficient mice. Cooled platelets, however, are not “activated” like platelets exposed to thrombin or ADP, and their vWf-receptor complex reacts normally with activated vWf.

[0167]As the temperature falls below 37° C. platelets become more susceptibl...

example 2

Implication of the αMβ2 (CR3) Lectin Domain in Chilled Platelet Phagocytosis

[0256]αMβ2 (CR3) has a cation-independent sugar-binding lectin site, located “C-T” to its I-domain (Thornton et al, J. Immunol. 156, 1235-1246, 1996), which binds to mannans, glucans and N-Acetyl-D-glucosamine (GlcNAc). Since CD16b / αMβ2 membrane complexes are disrupted by β-glucan, N-Acetyl-D-galactosamine (GalNAc), and methyl-α-mannoside, but not by other sugars, it is believed that this interaction occurs at the lectin site of the αMβ2 integrin (CR3) (Petty et al, J. Leukoc. Biol. 54, 492-494, 1993; Sehgal et al, J. Immunol. 150, 4571-4580, 1993).

[0257]The lectin site of αMβ2 integrin has a broad sugar specificity (Ross, R. Critical Reviews in Immunology 20, 197-222, 2000). Although sugar binding to lectins is usually of low affinity, clustering can cause a more robust interaction by increasing avidity. The clustering of GP1bα following cooling, as shown by electron microscopy, suggests such a mechanism. T...

example 3

Enzymatic Modification of Platelet β-Glycans Inhibit Phagocytosis of Cooled Platelets by Macrophages In Vitro and Accommodate Normal Circulation In Vivo

[0273]Our preliminary experiments have demonstrated the enzymatic covering of GlcNAc residues on GP1bα using galactose-transfer (glycan modification) onto chilled human platelet surfaces greatly reduced their in vitro phagocytosis. One interpretation of these findings is that GP1bα structure is altered on the surface of chilled human and murine platelets. This causes the exposure or clustering of GlcNAc, which is recognized by the lectin binding domain of αMβ2 leading to platelet removal. β-GlcNAc exposure can be measured by WGA binding and possibly by binding of recombinant αMβ2 lectin domain peptides. Resting human platelets bind WGA, which increases greatly after chilling. We propose that galactose transfer (glycan modification) will prevent GP1bα's interaction with αMβ2-lectin but not with vWf. This modification (galactose transf...

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Abstract

The present invention provides modified platelets having a reduced platelet clearance and methods for reducing platelet clearance. Also provided are compositions for the preservation of platelets. The invention also provides methods for making a pharmaceutical composition containing the modified platelets and for administering the pharmaceutical composition to a mammal to mediate hemostasis.

Description

RELATED APPLICATIONS[0001]This application is a continuation of U.S. application Ser. No. 12 / 172,990, filed Jul. 14, 2008, which is a continuation of U.S. application Ser. No. 11 / 577,261, filed Apr. 13, 2007, abandoned, which is the U.S. National stage of International Application No. PCT / US2005 / 037241, filed Oct. 17, 2005, published in English, which claims the benefit of U.S. Provisional Application No. 60 / 619,176, filed Oct. 15, 2004.FIELD OF THE INVENTION[0002]The inventions relate to compositions and methods for reducing the clearance of transfused platelets from circulations in a mammal, and prolonging the biological activity and survival of the transfused platelets.BACKGROUND OF THE INVENTION[0003]Platelets are anucleate bone marrow-derived blood cells that protect injured mammals from blood loss by adhering to sites of vascular injury and by promoting the formation of plasma fibrin clots. Humans depleted of circulating platelets by bone marrow failure suffer from life threat...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C12N5/078A61K35/19
CPCA01N1/00C12N5/0644A61K35/19A61P7/04
Inventor ROSIELLO, KEITH M.CLAUSEN, HENRIKWANDALL, HANSSTOSSEL, THOMAS P.HARTWIG, JOHN H.HOFFMEISTER, KARIN M.
Owner ROSIELLO KEITH M
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