IP Library Granted Patent US 10,376,563
Granted Patent B1
US 10,376,563 · App. 15/431,373 · Granted Aug 13, 2019

Methods for systemically delivering polypeptides and microorganisms therefor

Inventors: Jan Peter Van Pijkeren (Madison, WI); Alan Attie (Madison, WI); Mark Keller (McFarland, WI); Jee-Hwan Oh (Madison, WI)
Assignee: WISCONSIN ALUMNI RESEARCH FOUNDATION
A61K38/20A61K9/0053A61K35/747A61K38/02C07K14/54A61K2035/11
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Quick Facts
Patent No.
US 10,376,563
App. No.
15/431,373
Granted
Aug 13, 2019
Kind
B1
Abstract

Methods and microorganisms for systemically introducing a polypeptide in the bloodstream of a subject. The methods of the invention include administering into the gastrointestinal tract of a subject a bacterium configured to express and produce and release the polypeptide. The bacterium is administered in an amount effective to introduce the polypeptide in the bloodstream of the subject, preferably in a detectable amount. The microorganisms of the invention include lactic acid bacteria, such as Lactobacillus reuteri , that comprise a recombinant gene configured to express a polypeptide to be systemically introduced.

Claims (11)

1. A method of systemically introducing a polypeptide into a bloodstream of a subject, the method comprising administering into the gastrointestinal tract of the subject a bacterium that produces and releases the polypeptide, wherein the bacterium comprises a recombinant gene configured to express the polypeptide, wherein the bacterium is administered in an amount effective to introduce the polypeptide in the bloodstream of the subject in a detectable amount without the bacterium being introduced in the bloodstream of the subject in a detectable amount, wherein the bacterium is Lactobacillus reuteri.

2. The method of claim 1 , wherein the bacterium is administered in an amount effective to introduce the polypeptide in the bloodstream in an amount effective to induce at least one direct systemic effect in the subject.

3. The method of claim 1 , wherein the bacterium is administered in an amount effective to introduce the polypeptide in the bloodstream in an amount effective to induce at least one direct effect in a non-gastrointestinal tissue in the subject.

4. The method of claim 1 , wherein the bacterium is administered in an amount effective to introduce the polypeptide in the bloodstream in an amount effective to induce at least one direct effect in a tissue selected from the group consisting of liver, muscles, lungs, kidneys, pancreas, and adipose tissue in the subject.

5. The method of claim 1 , wherein the subject suffers from a condition treatable with systemic introduction of the polypeptide and wherein the polypeptide is introduced in the bloodstream of the subject in an amount effective to treat the condition.

6. The method of claim 1 , wherein the subject suffers from a condition treatable with systemic introduction of the polypeptide but not treatable with local introduction of the polypeptide to the gastrointestinal tract without systemic introduction of the polypeptide, and wherein the polypeptide is introduced in the bloodstream of the subject in an amount effective to treat the condition.

7. The method of claim 1 , wherein the polypeptide is selected from the group consisting of a cytokine, a hormone, an antibody, an antimicrobial peptide, and an antigenic peptide.

8. The method of claim 1 , wherein the polypeptide is selected from the group consisting of interleukin-22 (IL-22), interleukin-35 (IL-35), insulin, leptin, cathelicidin related antimicrobial peptide, a peptide inhibitor of proprotein convertase subtilisin/kexin type 9 (PCSK9), and an endolysin.

9. The method of claim 8 , wherein the subject suffers from at least one condition selected from the group consisting of insulin resistance, hyperglycemia, lipid dysregulation, hyperlipidemia, and obesity, and wherein the polypeptide is introduced in the bloodstream of the subject in an amount effective to treat the at least one condition.

10. The method of claim 1 , wherein the polypeptide is interleukin-22 (IL-22).

11. The method of claim 1 , wherein the polypeptide is a cytokine.

Assignments (2)
CONFIRMATORY LICENSE Recorded May 25, 2018
From: UNIVERSITY OF WISCONSIN-MADISON
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046245/0751 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2017
From: VAN PIJKEREN, JAN PETER; OH, JEE-HWAN; ATTIE, ALAN; KELLER, MARK
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 044162/0975 →
Continuity (1)
Provisional Application 62294578 · Feb 12, 2016
Cited By (2)
US 12,414,971 US 12,473,573