IP Library Granted Patent US 8,137,989
Granted Patent B2
US 8,137,989 · App. 10/672,144 · Granted Mar 20, 2012

Method for delivering a cytokine using a colloidal metal

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Quick Facts
Patent No.
US 8,137,989
App. No.
10/672,144
Granted
Mar 20, 2012
Kind
B2
Abstract

In accordance with the present invention, a composition and method is provided that allows for the administration of a biologically-active factors to a human or animal. The present invention can be used to treat a disease with a biologically-active factor or combination of biologically-active factors, or can be used to safely vaccinate a human or animal against a biologically-active factor. It can also be used as a method for the delivery of biologically-active factors for the treatment of disease. Additionally, the present invention also includes a method of targeted drug delivery for the treatment of disease through the administration of custom complexes containing of one or more biologically active factors bound to a colloidal metal where at least one of the biologically-active factors is capable of binding a high affinity receptor on a cell surface.

Claims (6)

1. A method comprising administering to a human or animal a composition comprising one or more cytokines, a target molecule and a colloidal metal, wherein said one or more cytokines and said target molecule are bound to said colloidal metal.

2. The method of claim 1 , wherein the one or more cytokines are selected from the group consisting of Interleukin-1a (“IL-1a”), Interleukin-1B (“IL-1β”), Interleukin-2 (“IL-2”), Interleukin-3 (“IL-3”), Interleukin-4 (“IL-4”), Interleukin-5 (“IL-5”), Interleukin-6 (“IL-6”), Interleukin-7 (“IL-7”), Interleukin-8 (“IL-8”), Interleukin-9 (“IL-9”), Interleukin-10 (“IL-10”), Interleukin-11 (“IL-11”), Interleukin-12 (“IL-12”), Interleukin-13 (“IL-13”), Type I Interferon, Type II Interferon, Migration Inhibition Factor, Granulocyte-Macrophage Colony-Stimulating Factor (“CSF”), Monocyte-Macrophage CSF, and Granulocyte CSF.

3. The method of claim 1 , wherein the target molecule is selected from the group consisting of Tumor Necrosis Factor (“TNFα”), Transforming Growth Factor-β (“TGFβ), Migration Inhibition Factor, vascular endothelial growth factor (“VEGF”), receptor proteins, glucose, glycogen, phospholipids, monoclonal and/or polycolonal antibodies, cancer cell specific antigen, and transforming growth factor alpha (“TGFα”).

4. The method of claim 3 , wherein the target molecule is a cancer cell specific antigen.

5. The method of claim 4 , wherein the cancer cell specific antigen is MART, MAGE, or BAGE.

6. The method of claim 3 , wherein the target molecule is a polyclonal or monoclonal antibody.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Sep 5, 2014
From: ITANI, HIDETAKA KENTARO
To: CYTIMMUNE SCIENCES, INC.
Reel/Frame 033692/0418 →
SECURITY AGREEMENT Recorded Sep 18, 2009
From: CYTIMMUNE SCIENCES, INC.
To: ITANI, HIDETAKA KENTARO
Reel/Frame 023254/0076 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2009
From: TAMARKIN, LAWRENCE; PACIOTTI, GIULIO F.
To: CYTIMMUNE SCIENCES, INC.
Reel/Frame 023157/0803 →