IP Library › Granted Patent US 12,516,290
Granted Patent B2
US 12,516,290 · App. 17/777,746 · Granted Jan 6, 2026

Medium composition for culturing T cells and method for culturing T cells using same

Inventors: Myoung Ho Jang (Seoul, KR); Chun-Pyo Hong (Gyeonggi-do, KR); Young Joo Choi (Gyeonggi-do, KR); June Sub Lee (Gyeonggi-do, KR)
Assignee: GI CELL, INC.
C12N5/0636C12N2501/2302C12N2501/51C12N2506/115
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Quick Facts
Patent No.
US 12,516,290
App. No.
17/777,746
Granted
Jan 6, 2026
Kind
B2
Abstract

The present invention relates to a composition for proliferating a T cells, containing a fusion protein dimer comprising IL-2 protein or a variant thereof and CD80 protein or a fragment thereof, and to a method for culturing T cells using same. The T cells cultured according to the present invention increase the proliferation and activity of T cells even without using CD3/CD28 antibody-bound magnetic beads and proliferate T cells by culturing a patient's own peripheral blood mononuclear cells and are not likely to cause side effects in the human body, and thus will be widely used as a novel T cell therapeutic agent. Furthermore, in the case of CD8+ T cells cultured as described above, the activity thereof increases, and thus, the CD8+ T cells can be used as a more effective therapeutic agent.

Claims (44)

1 . A method for culturing a T cell comprising:

culturing CD8+ T cells in a medium comprising a fusion protein dimer comprising an IL-2 variant and a CD80 protein or a fragment thereof,

wherein the fusion protein comprises the following structural formula (I) or (II):

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

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

wherein

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

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

X is a CD80 protein or a fragment thereof,

Y is the IL-2 variant,

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

n and m are each independently 0 or 1,

wherein the IL-2 variant comprises 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, and

wherein the CD80 protein fragment comprises an extracellular domain of CD80.

2 . The method according to claim 1 , wherein the CD8+ T cell is obtained from peripheral blood mononuclear cells (PBMCs).

3 . The method according to claim 1 , wherein the culturing is performed for 7 to 21 days.

4 . A method for in vitro activation and proliferation of CD8+ T cells comprising:

simultaneously culturing a cell and a cancer antigen in a medium comprising a fusion protein dimer comprising an IL-2 variant and a CD80 protein or a fragment thereof,

wherein the cell is either a peripheral blood mononuclear cell (PBMC) or a T cell,

wherein the fusion protein comprises the following structural formula (I) or (II):

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

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

wherein

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

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

X is a CD80 protein or a fragment thereof,

Y is the IL-2 variant,

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

n and m are each independently 0 or 1,

wherein the IL-2 variant comprises 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,

wherein the CD80 protein fragment comprises an extracellular domain of CD80.

5 . The method according to claim 4 , wherein the T cells are CD8+ T cells.

6 . The method according to claim 1 , wherein the IL-2 variant comprises the amino acid sequence of SEQ ID NO: 6, 22, 23, or 24.

7 . The method according to claim 1 , wherein the CD80 protein has the amino acid sequence of SEQ ID NO: 11.

8 . The method according to claim 1 , wherein the fusion protein comprises the amino acid sequence of SEQ ID NO: 9, 26, 28, or 30.

9 . The method according to claim 1 , wherein the T cells comprise memory T cells.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2022
From: JANG, MYOUNG HO; HONG, CHUN-PYO; CHOI, YOUNG JOO; LEE, JUNE SUB
To: GI CELL, INC.
Reel/Frame 059945/0823 →
Priority Claims (1)
KR 10-2019-0149779 · Nov 20, 2019 · national
Continuity (1)
Related Publication 20230015408A1 · Jan 19, 2023
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