IP Library Granted Patent US 10,987,314
Granted Patent B2
US 10,987,314 · App. 16/024,890 · Granted Apr 27, 2021

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, Inc.
A61K9/5031A61K31/59A61K39/0008A61K47/6937A61K2039/55511A61K2039/55522A61K2039/6093A61K2300/00
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Quick Facts
Patent No.
US 10,987,314
App. No.
16/024,890
Granted
Apr 27, 2021
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 (5)

1. A method for reducing an immune response to an antigen in a subject, wherein the method comprises administering, to a subject in need of such tolerance:

a dual microparticle system for targeting an antigen-presenting immune cell of interest in the 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 together 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 method of claim 1 , wherein the non-phagocytosable microparticles collectively comprise GM-CSF and TGF-β.

3. The method of claim 1 , wherein the subject an autoimmune disease, allergy, chronic inflammation, and/or transplant rejection.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 13, 2019
From: KESELOWSKY, BENJAMIN GEORGE; 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 050036/0941 →
CONFIRMATORY LICENSE Recorded Sep 18, 2018
From: UNIVERSITY OF FLORIDA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 047569/0841 →
Continuity (3)
Continuation 13880778
Provisional Application 61405999 · Oct 22, 2010
Related Publication 20180303760A1 · Oct 25, 2018