The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Mar. 10, 2015

Filed:

Dec. 11, 2009
Applicants:

Lori Jeanne West, Edmonton, CA;

Todd Lambert Lowary, Edmonton, CA;

Jillian Mary Buriak, Edmonton, CA;

Brian Daly, Edmonton, IE;

Mylvaganam Jeyakanthan, Alberta, CA;

Peter John Meloncelli, Edmonton, CA;

Vincent Arthur Wright, Edmonton, CA;

Anne Margaret Cooper, Edmonton, CA;

Inventors:

Lori Jeanne West, Edmonton, CA;

Todd Lambert Lowary, Edmonton, CA;

Jillian Mary Buriak, Edmonton, CA;

Brian Daly, Edmonton, IE;

Mylvaganam Jeyakanthan, Alberta, CA;

Peter John Meloncelli, Edmonton, CA;

Vincent Arthur Wright, Edmonton, CA;

Anne Margaret Cooper, Edmonton, CA;

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 39/00 (2006.01); A61L 31/16 (2006.01); A61K 47/48 (2006.01); A61K 49/04 (2006.01); B82Y 5/00 (2011.01);
U.S. Cl.
CPC ...
A61L 31/16 (2013.01); A61K 39/001 (2013.01); A61K 47/48215 (2013.01); A61K 47/48861 (2013.01); A61K 49/0423 (2013.01); B82Y 5/00 (2013.01); A61K 2039/55555 (2013.01); A61K 2039/6093 (2013.01); A61K 2039/627 (2013.01); A61L 2300/438 (2013.01); A61L 2300/80 (2013.01);
Abstract

Described herein are methods and systems that can be used to induce immunologic tolerance to non-self antigens. The methods and systems comprise introducing a tolerogen comprising at least one immunogenic non-self antigen coupled to a carrier, wherein the immunogenic antigen can be a foreign or endogenous antigen or fragments thereof. The non-self antigen can be selected from the group consisting of carbohydrate antigens, full-length antigenic proteins, and fragments and combinations thereof, while the carrier can be selected from nanoparticles and stents. Tolerogen compositions are also provided and can be used to induce immunologic tolerance to non-self antigens. These methods, systems and compositions are particularly advantageous since they can be used to allow for the extension of the window of safety for immunologically-incompatible transplantations to patients who are growing past the age of infancy.


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