IP Library Granted Patent US 12,662,515
Granted Patent B2
US 12,662,515 · App. 18/139,003 · Granted Jun 23, 2026

Fusion protein comprising BP26 and antigenic polypeptide

Inventors: Sangyong Jon (Daejeon, KR); Sukmo Kang (Chungcheongbuk-do, KR); Yujin Kim (Daejeon, KR); Ji-Joon Song (Daejeon, KR)
Assignee: KOREA ADVANCED INSTITUTE OF SCIENCE AND TECHNOLOGY
C07K14/23A61K39/02A61K39/145A61P37/04C07K14/11C12N15/63A61K2039/10
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 12,662,515
App. No.
18/139,003
Granted
Jun 23, 2026
Kind
B2
Abstract

The present disclosure relates to a fusion protein comprising BP26 and an antigenic polypeptide, and to a nanoarchitecture comprising same. A vaccine composition comprising the fusion protein, nanoarchitecture, or combination thereof of the present disclosure can be used to effectively prevent or treat pathogens or cancer, and thus can be used as a multi-purpose vaccine platform.

Claims (14)

1 . A nanoarchitecture comprising a fusion protein comprising BP26 and an antigenic polypeptide,

wherein the antigenic polypeptide is linked to the C-terminus of the BP26, and no antigenic polypeptide is linked to the N-terminus of the BP26; and

wherein the nanoarchitecture comprises 8 or 16 copies of the fusion protein.

2 . A vaccine composition comprising the nanoarchitecture of claim 1 .

3 . The vaccine composition of claim 2 , wherein the vaccine composition is for preventing infection from an infectious pathogen.

4 . The vaccine composition of claim 2 , wherein the vaccine composition is for a cancer vaccine.

5 . The vaccine composition of claim 2 , wherein the vaccine composition further comprises an adjuvant.

6 . The nanoarchitecture of claim 1 , wherein the BP26 comprises the amino acid sequence of SEQ ID NO: 1 or 2.

7 . The nanoarchitecture of claim 1 , wherein the antigen is a pathogen-derived antigen or a tumor-derived antigen.

8 . The nanoarchitecture of claim 7 , wherein the pathogen is selected from the group consisting of a virus, a bacterium, a Rickettsia , a fungus, and a protozoa.

9 . The nanoarchitecture of claim 7 , wherein the pathogen-derived antigenic polypeptide is M2e.

10 . The nanoarchitecture of claim 9 , wherein the M2e comprises the amino acid sequence of SEQ ID NO: 3, 4, 5, or 6.

11 . The nanoarchitecture of claim 1 , wherein the fusion protein comprises at least one copy of the antigenic polypeptide.

12 . The nanoarchitecture of claim 1 , wherein the antigenic polypeptides are continuously or discontinuously linked in the fusion protein.