IP Library Granted Patent US 12,318,484
Granted Patent B2
US 12,318,484 · App. 17/560,594 · Granted Jun 3, 2025

Pegylated liposomes and methods of use

Inventors: Christopher B. Fox (Sumner, WA); Susan S. Lin (Kirkland, WA); Darrick Carter (Seattle, WA); Neal Van Hoeven (Seattle, WA); Mayuresh M. Abhyankar (Charlottesville, VA); William A. Petri (Charlottesville, VA)
Assignees: Access to Advanced Health Institute; University of Virginia Patent Foundation
A61K9/1271A61K31/739A61K39/39A61K2039/55555A61K2039/6087
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,318,484
App. No.
17/560,594
Granted
Jun 3, 2025
Kind
B2
Abstract

Provided herein are PEGylated liposomes, and methods of making and using thereof. The PEGylated liposomes comprise at least a cholesterol, a non-PEGylated neutral lipid, and a PEGylated lipid, wherein the average molecular weight of the PEG component in the PEGylated lipid is about 5000 Daltons or less. The PEGylated liposomes are stable and capable of delivery of an agent for the generation of an immune response, for example an agent for vaccine, therapeutic, or diagnostic uses. Compositions and methods related to making the PEGylated liposomes and using the PEGylated liposomes for stimulating an immune response are also provided.

Claims (26)

1. A composition comprising:

an antigen; and

a liposome comprising:

a cholesterol;

a non-PEGylated neutral lipid;

a PEGylated lipid, wherein an average molecular weight of the PEG in the PEGylated lipid is about 2000 Daltons, wherein a lipid molar ratio of the non-PEGylated neutral lipid:cholesterol:PEGylated lipid is about 9.8:5.7:0.8 or about 18:5.5:3; and

agonists comprising GLA and 3M-052, wherein there is at least about twice as much GLA as 3M-052 by weight and wherein the GLA comprises a synthetic GLA of formula:

or a pharmaceutically acceptable salt thereof, wherein R 1 , R 3 , R 5 , and R 6 are C 11 -C 20 alkyl; and R 2 and R 4 are C 12 -C 20 alkyl.

2. The composition of claim 1 , wherein the lipid component of the PEGylated lipid is DSPE, DPPC, DOPC, DLPC, DMPC, DSPC, POPC, DPPE, or DMPE.

3. The composition of claim 1 , wherein the lipid component of the PEGylated lipid comprises a C 14 alkyl chain, a C 16 alkyl chain, or a C 18 alkyl chain.

4. The composition of claim 1 , wherein the non-PEGylated neutral lipid is DPPC, DOPC, DLPC, DMPC, DSPC, POPC, DPPE, or DMPE.

5. The composition of claim 1 , wherein the non-PEGylated neutral lipid comprises a C 14 alkyl chain, a C 16 alkyl chain, or a C 18 alkyl chain.

6. The composition of claim 1 , wherein R 3 , R 5 , and R 6 are C 11 alkyl; and R 2 and R 4 are C 13 alkyl.

7. The composition of claim 1 , wherein the synthetic GLA has the formula:

or a pharmaceutically acceptable salt thereof.

8. The composition of claim 1 , wherein there is at about 2.5 times as much GLA as 3M-052 by weight.

9. The composition of claim 1 , wherein the lipid molar ratio of the non-PEGylated neutral lipid:cholesterol:PEGylated lipid is about 9.8:5.7:0.8.

10. The composition of claim 1 , wherein the lipid molar ratio of the non-PEGylated neutral lipid:cholesterol:PEGylated lipid is about 18:5.5:3.

11. The composition of claim 1 , wherein the cholesterol is present at about 1-50 mol %, the non-PEGylated neutral lipid is present at about 45-98 mol %, and the PEGylated lipid is present at about 1-25 mol %.

12. The composition of claim 11 , wherein the cholesterol is present at about 50 mol %, the non-PEGylated neutral lipid is present at about 45 mol %, and the PEGylated lipid is present at about 5 mol %.

13. The composition of claim 1 , wherein a polydispersity index of the liposome is maintained at about 0.3 or less.

14. The composition of claim 1 , wherein a size of the liposome is less than or about 450 nm.

15. The composition of claim 1 , wherein the antigen comprises H5N1.

16. The composition of claim 1 , wherein the antigen comprises LecA.

17. The composition of claim 1 , further comprising an antioxidant.

18. The composition of claim 17 , wherein the antioxidant comprises ascorbic acid, sodium bisulfite, or α-tocopherol.

Assignments (4)
CHANGE OF NAME Recorded Jun 10, 2022
From: INFECTIOUS DISEASE RESEARCH INSTITUTE
To: ACCESS TO ADVANCED HEALTH INSTITUTE
Reel/Frame 060344/0290 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 23, 2021
From: FOX, CHRISTOPHER B.; LIN, SUSAN S.; CARTER, DARRICK; VAN HOEVEN, NEAL
To: INFECTIOUS DISEASE RESEARCH INSTITUTE
Reel/Frame 058469/0848 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 23, 2021
From: PETRI, WILLIAM A., JR.; ABHYANKAR, MAYURESH M.
To: UNIVERSITY OF VIRGINIA
Reel/Frame 058469/0976 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 23, 2021
From: UNIVERSITY OF VIRGINIA
To: UNIVERSITY OF VIRGINIA PATENT FOUNDATION D/B/A UNIVERSITY OF VIRGINIA LICENSING & VENTURES GROUP
Reel/Frame 058470/0064 →
Continuity (3)
Continuation 16098619
Provisional Application 62337328 · May 16, 2016
Related Publication 20220160632A1 · May 26, 2022
References Cited (44)
US 8609114B2 · Reed et al. · 2013 [cited by applicant]
US 20120014866A1 · Bull et al. · 2012 [cited by applicant]
US 20120148663A1 · Nilssen et al. · 2012 [cited by applicant]
US 20140027182A1 · Wilson · 2014 [cited by applicant]
US 20140030212A1 · Vasconcellos et al. · 2014 [cited by applicant]
US 20140035641A1 · Pasquale et al. · 2014 [cited by applicant]
US 20140271821A1 · McGhee · 2014 [cited by applicant]
US 20140302120A1 · Carson et al. · 2014 [cited by applicant]
US 20140356416A1 · Kesari et al. · 2014 [cited by applicant]
US 20150064265A1 · Fahmy et al. · 2015 [cited by applicant]
JP 2015512950A · 2015 [cited by applicant]
JP 2018559785A · 2019 [cited by applicant]
WO 2012031043A1 · 2012 [cited by applicant]
WO 2015123496A1 · 2015 [cited by applicant]
WO 2015136479A1 · 2015 [cited by applicant]
WO 2017200957A1 · 2017 [cited by applicant]
Office Action from related Canadian Patent Application No. 3,023,672, mailed Mar. 22, 2023, 5 pages. [cited by applicant]
Khantasup, et al., Target Small Interfering RNA-Immunoliposomes as a Promising Therapeutic Agent against Highly Pathogenic Avian Influenza A (H5N1) Virus Infection, Antimicrobial Agents and Chemotherapy, p. 2816-2824, M… [cited by applicant]
Office Action from related Chinese Patent Application No. 2017800302944 mailed Aug. 31, 2023, 16 pages (translation attached). [cited by applicant]
Office Action from related Japanese Patent Application No. 2022-143788, mailed Aug. 31, 2023, 9 pages (translation attached). [cited by applicant]
AU 2017268175—Examination Report, mailed Apr. 1, 2022, 5 pages. [cited by applicant]
KR 10-2018-7034749—Office Action, mailed Jan. 3, 2022, 24 pages. (with English translation). [cited by applicant]
Office action for related patent application in Canada CIPO, application No. 3,023,672, mailed Nov. 27, 2023, 3 pages. [cited by applicant]
Office action for related patent application in Israel PTO, application No. 263030, mailed Oct. 26, 2023, 4 pages. [cited by applicant]
Indian Application No. 202118057586—Exam Report, mailed Apr. 28, 2022, 7 pages. (with English translation). [cited by applicant]
CN 201780030294.4—Second Office Action, mailed Apr. 24, 2022, 13 pages, with English translation. [cited by applicant]
JP 2018-559785—Decision of Refusal, mailed May 9, 2022, 8 pages, with English translation. [cited by applicant]
KR 10-2018-7034749—Notice of Decision for Rejection, mailed Jul. 7, 2022, with English translation. [cited by applicant]
Dmitri Smirnov, et al., “Vaccine Adjuvant Activity of 3M-052: An Imidazoquinoline Designed for Local Activity without Systemic Cytokine Induction”, May 2011, 10 pages. [cited by applicant]
AU 2017268175—Second Examination Report, mailed Aug. 24, 2022, 3 pages. [cited by applicant]
Application No. 10-2018-7034749—Notice of Allowance, mailed Oct. 14, 2022, 4 pages. (with English translation). [cited by applicant]
Application No. MX/a/2018/013640—First Office Action, mailed Oct. 19, 2022, 12 pages. (with English translation). [cited by applicant]
Application No. IL 263030—Second Office Action, mailed Oct. 20, 2022, 9 pages. (with English translation). [cited by applicant]
Application No. JP 2018-559785—Decision to Grant, mailed Nov. 17, 2022, 7 pages. (with English translation). [cited by applicant]
Application No. AU 2017268175—Notice of Acceptance, mailed Feb. 8, 2023, 3 pages. (with English translation). [cited by applicant]
Application No. CN 2017800302944—Third Office Action, mailed Feb. 11, 2023, 17 pages. (with English translation). [cited by applicant]
Application No. MX/a/2018/013640—Second Office Action, mailed Feb. 23, 2023, 8 pages. (with English translation). [cited by applicant]
Notice of Acceptance for Patent Application for related patent Australian Patent Application No. 2023200515 mailed Apr. 9, 2024, 3 pages. [cited by applicant]
Office Action from related patent Japan Patent Application No. 2022-143788 dated Jun. 18, 2024, 9 pages, translation attached. [cited by applicant]
Khantasup, K., et al., “Targeted small interfering RNA-immunoliposomes as a promising therapeutic agent against highly pathogenic Avian Influenza A (H5N1) virus infection.”,Antimicrobial Agents and Chemotherapy, v 58, n… [cited by applicant]
Smirnov, et al., “Vaccine adjuvant activity of 3M-052: An imidazoquinoline designed for local activity without systemic cytokine induction,” Vaccine vol. 29, 2011m pp. 5434 to 5442. [cited by applicant]
Fox, et al., “A nanoliposome delivery system to synergistically trigger TLR4 and TLR7,” Journal of Nanobiologytechnology, 2014, vol. 12:17, pp. 1-9. [cited by applicant]
Goff, et al., “Synthetic Toll-Like Receptor 4 (TLR4) and TLR7 Ligands as Influenza Virus Vaccing Adjuvants Induce Rapid, Sustained, and Broadly Protective Responses,” 15 pages. [cited by applicant]
Related matter Japanese patent application No. 2022-143788, Decision of Refusal mailed Feb. 25, 2025, 8 pages (translation included. [cited by applicant]