IP Library Granted Patent US 10,016,371
Granted Patent B2
US 10,016,371 · App. 13/880,778 · Granted Jul 10, 2018

Antigen-specific, tolerance-inducing microparticles and uses thereof

Inventors: Benjamin George Keselowsky (Gainesville, FL); Jamal Lewis (Tallahassee, FL); Abhinav Acharya (Atlanta, GA); Michael J. Clare-Salzler (Gainesville, FL)
Assignee: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION
A61K9/5031A61K31/59A61K39/0008A61K47/6937A61K2039/55511A61K2039/55522A61K2039/6093A61K2300/00
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Quick Facts
Patent No.
US 10,016,371
App. No.
13/880,778
Granted
Jul 10, 2018
Kind
B2
Abstract

The present invention provides antigen-specific, tolerance-inducing microparticles for the targeted delivery of therapeutic agents to immune cells. In addition, the present invention allows for sustained release of therapeutic agents for a prolonged period of time. Also provided are therapeutic uses of the present invention for the prevention and/or treatment of immune diseases and autoimmune disorders. In a specific embodiment, the present invention provides treatment for type 1 diabetes.

Claims (3)

1. A dual microparticle system for targeting an antigen-presenting immune cell of interest in a subject and for reducing an immune response to an antigen, wherein the microparticle system is a liquid formulation that comprises:

microparticles that are phagocytosable by the antigen-presenting immune cell of interest, and microparticles that are non-phagocytosable by the antigen- presenting immune cell of interest, wherein the phagocytosable microparticles together comprise an antigen and at least one immunomodulatory agent selected from vitamin D3, vitamin D3 analog, glucocorticoid, estrogen, rapamycin, and retinoic acid; wherein the non-phagocytosable microparticles comprise at least one immunosuppressive tolerogenic agent selected from IL-10, TGF-β, and nonsteroidal anti-inflammatory drugs (NSAIDs), and an agent that recruits the antigen-presenting immune cell of interest selected from GM-CSF, G-CFS, and M-CSF; wherein the phagocytosable microparticle and the non-phagocytosable microparticles are made of PLGA.

2. The microparticle system of claim 1 , wherein the phagocytosable microparticle has a diameter of 0.5 μm-5.0 μm and the non-phagocytosable microparticle has a diameter of 15.0 μm-50.0 μm.

Assignments (2)
CONFIRMATORY LICENSE Recorded Sep 7, 2017
From: UNIVERSITY OF FLORIDA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 043775/0179 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 5, 2013
From: KESELOWSKY, BENJAMIN G.; LEWIS, JAMAL; ACHARYA, ABHINAV; CLARE-SALZLER, MICHAEL J.; ATKINSON, MARK A.; WASSERFALL, CLIVE HENRY; XIA, CHANG QING; BRUSKO, TODD M.
To: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC.
Reel/Frame 031721/0860 →
Continuity (2)
Provisional Application 61405999 · Oct 22, 2010
Related Publication 20130287729A1 · Oct 31, 2013