IP Library › Granted Patent US 12,478,675
Granted Patent B2
US 12,478,675 · App. 18/008,034 · Granted Nov 25, 2025

Pharmaceutical composition for enhancing radiotherapy comprising fusion protein containing IL-2 protein and CD80 protein

Inventors: Myung Ho Jang (Seoul, KR); Su Youn Nam (Seoul, KR); Young Jun Koh (Seoul, KR)
Assignee: GI INNOVATION, INC.
A61K41/0038A61P35/00C07K14/55C07K14/70532A61K38/00C07K2319/00C07K2319/30
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Quick Facts
Patent No.
US 12,478,675
App. No.
18/008,034
Granted
Nov 25, 2025
Kind
B2
Abstract

A pharmaceutical composition for enhancing radiation therapy, containing a fusion protein dimer is disclosed. The fusion protein dimer includes an IL-2 protein and a CD80 protein. A method of radiation therapy for cancer, using the composition is also disclosed. The composition for enhancing radiation therapy may increase the effect of radiation therapy in cancer treatment.

Claims (41)

1 . A pharmaceutical composition for enhancing radiation therapy for cancer, comprising a fusion protein dimer comprising an IL-2 protein and a CD80 protein.

2 . The pharmaceutical composition of claim 1 , wherein the IL-2 protein and the CD80 protein are bound to each other via a linker.

3 . The pharmaceutical composition of claim 1 , wherein the IL-2 protein has the amino acid sequence of SEQ ID NO: 10.

4 . The pharmaceutical composition of claim 1 , wherein the IL-2 protein is an IL-2 variant.

5 . The pharmaceutical composition of claim 4 , wherein the IL-2 variant is obtained by substitution of at least one selected from the group consisting of the 38 th , 42 nd , 45 th , 61 st , and 72 nd amino acid(s) in the amino acid sequence of SEQ ID NO: 10.

6 . The pharmaceutical composition of claim 4 , wherein the IL-2 variant is obtained by at least one substitution selected from the group consisting of R38A, F42A, Y45A, E61R, and L72G in the amino acid sequence of SEQ ID NO: 10.

7 . The pharmaceutical composition of claim 4 , wherein the IL-2 variant is obtained by any one selected from the following substitution combinations (a) to (d) in the amino acid sequence of SEQ ID NO: 10:

(a) R38A/F42A

(b) R38A/F42A/Y45A

(c) R38A/F42A/E61R

(d) R38A/F42A/L72G.

8 . The pharmaceutical composition of claim 4 , wherein the IL-2 variant has the amino acid sequence of SEQ ID NO: 6, 22, 23, or 24.

9 . The pharmaceutical composition of claim 1 , wherein the CD80 has the amino acid sequence of SEQ ID NO: 11.

10 . The pharmaceutical composition of claim 1 , wherein the CD80 protein is a fragment of CD80.

11 . The pharmaceutical composition of claim 10 , wherein the fragment of CD80 consists of the 35 th to 242 nd amino acids in the amino acid sequence of SEQ ID NO: 11.

12 . The pharmaceutical composition of claim 2 , wherein the linker is an albumin or an Fc domain of an immunoglobulin.

13 . The pharmaceutical composition of claim 12 , wherein the Fc domain is a wild type or a variant of an Fc domain.

14 . The pharmaceutical composition of claim 12 , wherein the Fc domain has the amino acid sequence of SEQ ID NO: 4.

15 . The pharmaceutical composition of claim 13 , wherein the variant of the Fc domain has the amino acid sequence of SEQ ID NO: 12.

16 . The pharmaceutical composition of claim 1 , wherein the fusion protein consists of the following structural formula (I) or (II):

N′-X-[linker (1)] n-Fc domain-[linker (2)] m-Y-C′ (I)

N′-Y-[linker (1)] n-Fc domain-[linker (2)] m-X-C′ (II)

in the structural formulas (I) and (II),

N′is the N-terminus of the fusion protein,

C′ is the C-terminus of the fusion protein,

X is the CD80 protein,

Y is the IL-2 protein,

the linkers (1) and (2) are peptide linkers, and

n and m are each independently 0 or 1.

17 . The pharmaceutical composition of claim 16 , wherein the linker (1) is a peptide linker consisting of the amino acid sequence of SEQ ID NO: 3.

18 . The pharmaceutical composition of claim 16 , wherein the linker (2) is a peptide linker consisting of the amino acid sequence of SEQ ID NO: 5.

19 . The pharmaceutical composition of claim 16 , wherein the fusion protein consists of the structural formula (I).

20 . The pharmaceutical composition of claim 1 , wherein the fusion protein has a sequence identity of 85% or higher to the amino acid sequence of SEQ ID NO: 9, 26, 28, or 30.

21 . The pharmaceutical composition of claim 1 , wherein the cancer is any one selected from the group consisting of gastric cancer, liver cancer, lung cancer, colorectal cancer, breast cancer, prostate cancer, ovarian cancer, pancreatic cancer, cervical cancer, thyroid cancer, laryngeal cancer, acute myeloid leukemia, brain tumor, neuroblastoma, retinoblastoma, head and neck cancer, salivary gland cancer, and lymphoma.

22 . A method of radiation therapy for cancer, comprising:

irradiating radiation to a cancer site of a non-human mammal suffering from cancer; and

administering the pharmaceutical composition of claim 1 to the mammal.

23 . The method of claim 22 , wherein the radiation is irradiated in an irradiation amount of 0.1 Gy to 100 Gy.

24 . The method of claim 22 , wherein the pharmaceutical composition is administered before or after radiation irradiation.

25 . The method of claim 24 , wherein the pharmaceutical composition is administered before or after 6 to 48 hours based on the time of radiation irradiation.

26 . The method of claim 22 , wherein the pharmaceutical composition is administered once to 20 times a week.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 2, 2022
From: JANG, MYUNG HO; NAM, SU YOUN; KOH, YOUNG JUN
To: GI INNOVATION, INC.
Reel/Frame 062053/0534 →
Priority Claims (1)
KR 10-2020-0068456 · Jun 5, 2020 · national
Continuity (1)
Related Publication 20230233680A1 · Jul 27, 2023
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