IP Library › Granted Patent US 12,180,258
Granted Patent B2
US 12,180,258 · App. 18/391,486 · Granted Dec 31, 2024

T-cell modulatory multimeric polypeptides and methods of use thereof

Inventors: Ronald D. Seidel, III (Boston, MA); Rodolfo J. Chaparro (Cambridge, MA)
Assignee: Cue Biopharma, Inc.
C07K14/55A61K9/0019A61K35/17C07K14/005C07K14/4748C07K14/70539G01N33/5008A61K38/00A61K2039/505C07K2317/34C07K2319/30
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Quick Facts
Patent No.
US 12,180,258
App. No.
18/391,486
Granted
Dec 31, 2024
Kind
B2
Abstract

The present disclosure provides variant immunomodulatory polypeptides, and fusion polypeptides comprising the variant immunomodulatory peptides. The present disclosure provides T-cell modulatory multimeric polypeptides, and compositions comprising same, where the T-cell modulatory multimeric polypeptides comprise a variant immunomodulatory polypeptide of the present disclosure. The present disclosure provides nucleic acids comprising nucleotide sequences encoding the T-cell modulatory multimeric polypeptides, and host cells comprising the nucleic acids. The present disclosure provides methods of modulating the activity of a T cell; the methods comprise contacting the T cell with a T-cell modulatory multimeric polypeptide of the present disclosure.

Claims (39)

1. A fusion polypeptide comprising:

a) one or more variant IL-2 polypeptides, wherein each of the one or more variant IL-2 polypeptides comprises up to four amino acid substitutions relative to the amino acid sequence set forth in SEQ ID NO:1, wherein amino acid 42 is an amino acid other than a phenylalanine, wherein amino acid 16 is an amino acid other than a histidine, and wherein each of the one or more variant IL2 polypeptides exhibit reduced binding affinity to an IL-2 receptor (IL2R) comprising alpha, beta, and gamma polypeptides having amino acid sequences set forth in SEQ ID NOs: 18-20, compared to the binding affinity of the IL-2 amino acid sequence set forth in SEQ ID NO: 1 for the IL2R; and

b) a heterologous fusion partner comprising an antibody Fc region, wherein the antibody Fc region comprises an amino acid sequence having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:57, wherein the percent sequence identity is determinable by a sequence alignment performed using BLAST,

wherein the fusion polypeptide does not comprise a major histocompatibility complex (MHC) polypeptide.

2. The fusion polypeptide of claim 1 , wherein the antibody Fc region comprises one or more substitutions selected from an L14A substitution, an L15A substitution, an N77A substitution, a P111S substitution based on the amino acid numbering of SEQ ID NO:57.

3. The fusion polypeptide of claim 1 , wherein the fusion polypeptide comprises from 400 to 600 amino acids.

4. The fusion polypeptide of claim 1 , wherein the fusion polypeptide comprises from 500 to 700 amino acids.

5. The fusion polypeptide of claim 1 , wherein the heterologous fusion partner comprises an antibody Fc region and an antigen-binding region of an antibody.

6. The fusion polypeptide of claim 5 , wherein the fusion polypeptide comprises from 400 to 700 amino acids.

7. The fusion polypeptide of claim 5 , wherein the fusion polypeptide comprises from 700 to 900 amino acids.

8. The fusion polypeptide of claim 1 , wherein amino acid 16 of each of the one or more variant IL-2 polypeptides is Ala, Thr, Asp, or Glu; and wherein amino acid 42 of each of the one or more variant IL-2 polypeptides is Ala or Thr.

9. The fusion polypeptide of claim 6 , wherein amino acid 16 of each of the one or more variant IL-2 polypeptides is Ala, Thr, Asp, or Glu; and wherein amino acid 42 of each of the one or more variant IL-2 polypeptides is Ala or Thr.

10. The fusion polypeptide of claim 7 , wherein amino acid 16 of each of the one or more variant IL-2 polypeptides is Ala, Thr, Asp, or Glu; and wherein amino acid 42 of each of the one or more variant IL-2 polypeptides is Ala or Thr.

11. A fusion polypeptide comprising:

a) one or more variant IL-2 polypeptides, wherein each of the one or more variant IL-2 polypeptides comprises up to three amino acid substitutions relative to the amino acid sequence set forth in SEQ ID NO:1, wherein amino acid 42 is an amino acid other than a phenylalanine, wherein amino acid 16 is an amino acid other than a histidine, and wherein each of the one or more variant IL2 polypeptides exhibit reduced binding affinity to an IL-2 receptor (IL2R) comprising alpha, beta, and gamma polypeptides having amino acid sequences set forth in SEQ ID NOs: 18-20, compared to the binding affinity of the IL-2 amino acid sequence set forth in SEQ ID NO: 1 for the IL2R; and

b) a heterologous fusion partner comprising an antibody Fc region, wherein the antibody Fc region comprises an amino acid sequence having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO: 57, wherein the percent sequence identity is determinable by a sequence alignment performed using BLAST,

wherein the fusion polypeptide does not comprise a major histocompatibility complex (MHC) polypeptide.

12. The fusion polypeptide of claim 11 , wherein the antibody Fc region comprises one or more substitutions selected from an L14A substitution, an L15A substitution, an N77A substitution, a P111S substitution based on the amino acid numbering of SEQ ID NO:57.

13. The fusion polypeptide of claim 11 , wherein the fusion polypeptide comprises from 400 to 600 amino acids.

14. The fusion polypeptide of claim 11 , wherein the fusion polypeptide comprises from 500 to 700 amino acids.

15. The fusion polypeptide of claim 11 , wherein the heterologous fusion partner comprises an antibody Fc region and an antigen-binding region of an antibody.

16. The fusion polypeptide of claim 15 , wherein the fusion polypeptide comprises from 400 to 700 amino acids.

17. The fusion polypeptide of claim 15 , wherein the fusion polypeptide comprises from 700 to 900 amino acids.

18. The fusion polypeptide of claim 11 , wherein amino acid 16 of each of the one or more variant IL-2 polypeptides is Ala, Thr, Asp, or Glu; and wherein amino acid 42 of each of the one or more variant IL-2 polypeptides is Ala or Thr.

19. The fusion polypeptide of claim 16 , wherein amino acid 16 of each of the one or more variant IL-2 polypeptides is Ala, Thr, Asp, or Glu; and wherein amino acid 42 of each of the one or more variant IL-2 polypeptides is Ala or Thr.

20. The fusion polypeptide of claim 17 , wherein amino acid 16 of each of the one or more variant IL-2 polypeptides is Ala, Thr, Asp, or Glu; and wherein amino acid 42 of each of the one or more variant IL-2 polypeptides is Ala or Thr.

21. A fusion polypeptide comprising:

a) one or more variant IL-2 polypeptides, wherein each of the one or more variant IL-2 polypeptides comprises two amino acid substitutions relative to the amino acid sequence set forth in SEQ ID NO:1, wherein amino acid 42 is an amino acid other than a phenylalanine, wherein amino acid 16 is an amino acid other than a histidine, and wherein each of the one or more variant IL2 polypeptides exhibit reduced binding affinity to an IL-2 receptor (IL2R) comprising alpha, beta, and gamma polypeptides having amino acid sequences set forth in SEQ ID NOs: 18-20, compared to the binding affinity of the IL-2 amino acid sequence set forth in SEQ ID NO: 1 for the IL2R; and

b) a heterologous fusion partner comprising an antibody Fc region, wherein the antibody Fc region comprises an amino acid sequence having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO: 57, wherein the percent sequence identity is determinable by a sequence alignment performed using BLAST,

wherein the fusion polypeptide does not comprise a major histocompatibility complex (MHC) polypeptide.

22. The fusion polypeptide of claim 21 , wherein the antibody Fc region comprises one or more substitutions selected from an L14A substitution, an L15A substitution, an N77A substitution, a P111S substitution based on the amino acid numbering of SEQ ID NO:57.

23. The fusion polypeptide of claim 21 , wherein the fusion polypeptide comprises from 400 to 600 amino acids.

24. The fusion polypeptide of claim 21 , wherein the fusion polypeptide comprises from 500 to 700 amino acids.

25. The fusion polypeptide of claim 21 , wherein the heterologous fusion partner comprises an antibody Fc region and an antigen-binding region of an antibody.

26. The fusion polypeptide of claim 25 , wherein the fusion polypeptide comprises from 400 to 700 amino acids.

27. The fusion polypeptide of claim 25 , wherein the fusion polypeptide comprises from 700 to 900 amino acids.

28. The fusion polypeptide of claim 21 , wherein amino acid 16 of each of the one or more variant IL-2 polypeptides is Ala, Thr, Asp, or Glu; and wherein amino acid 42 of each of the one or more variant IL-2 polypeptides is Ala or Thr.

29. The fusion polypeptide of claim 26 , wherein amino acid 16 of each of the one or more variant IL-2 polypeptides is Ala, Thr, Asp, or Glu; and wherein amino acid 42 of each of the one or more variant IL-2 polypeptides is Ala or Thr.

30. The fusion polypeptide of claim 27 , wherein amino acid 16 of each of the one or more variant IL-2 polypeptides is Ala, Thr, Asp, or Glu; and wherein amino acid 42 of each of the one or more variant IL-2 polypeptides is Ala or Thr.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 20, 2024
From: SEIDEL, RONALD D., III; CHAPARRO, RODOLFO J.
To: CUE BIOPHARMA, INC.
Reel/Frame 068346/0721 →
Continuity (14)
Continuation 18202596 · May 26, 2023
Continuation 17845583 · Jun 21, 2022
Continuation 17578094 · Jan 18, 2022
Continuation 17507113 · Oct 21, 2021
Continuation 17386109 · Jul 27, 2021
Continuation 17176777 · Feb 16, 2021
Continuation 16812926 · Mar 9, 2020
Continuation 16741202 · Jan 13, 2020
Continuation 16462443
Provisional Application 62582132 · Nov 6, 2017
Provisional Application 62555435 · Sep 7, 2017
Provisional Application 62470774 · Mar 13, 2017
Provisional Application 62438272 · Dec 22, 2016
Related Publication 20240199715A1 · Jun 20, 2024
Cited By (1)
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