IP Library Patent Application 18486563
Patent Application
App. No. 18/486,563

ENGINEERED CHIMERIC FUSION PROTEIN COMPOSITIONS AND METHODS OF USE THEREOF

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Quick Facts
Patent No.
US None
App. No.
18/486,563
Abstract

The present disclosure provides compositions and methods for making and using engineered myeloid cells for immunotherapy in cancer or infection by expressing a chimeric antigen receptor having an enhanced phagocytic activity, wherein the chimeric receptor is encoded by a recombinant nucleic acid.

Claims (50)

1 . A composition comprising a recombinant polynucleic acid, wherein the recombinant polynucleic acid comprises a sequence encoding a cell surface receptor, wherein the cell surface receptor is a chimeric fusion protein (CFP) comprising:

(a) an extracellular domain comprising an antigen binding domain,

(b) a transmembrane domain operatively linked to the extracellular domain, wherein the transmembrane domain is a transmembrane domain from a protein that dimerizes with Fc receptor γ-chain, and wherein the CFP undergoes degradation when expressed in a cell that does not express Fc receptor γ-chain; and

(c) an intracellular domain operatively linked to the transmembrane domain, the intracellular domain comprising:

(i) a therapeutic agent, wherein the therapeutic agent is a transcription factor or transcriptionally functional portion thereof, and

(ii) a protease cleavage site disposed between the transcription factor and the transmembrane domain.

2 . The composition of claim 1 , wherein the recombinant polynucleic acid is expressed in a cell that naturally expresses an Fc receptor γ-chain.

3 . The composition of claim 1 , wherein cleavage of the protease cleavage site by a protease releases the therapeutic agent from the CFP.

4 . (canceled)

5 . The composition of claim 1 , wherein the transcription factor is an inflammatory response transcription factor.

6 . The composition of claim 5 , wherein the transcription factor is IRF3, IRF5 or IRF7.

7 . (canceled)

8 . The composition of claim 1 , wherein the intracellular domain of the CFP lacks a phosphorylated tyrosine residue.

9 . The composition of claim 1 , wherein the intracellular domain of the CFP lacks a phosphotyrosine binding (PTB) domain.

10 . The composition of claim 1 , wherein the protease cleavage site is a viral protease cleavage site.

11 . The composition of claim 10 , wherein the viral protease cleavage site is for a viral protease derived from hepatitis C virus (HCV) nonstructural protein 3 (NS3).

12 . The composition of claim 10 , wherein the viral protease cleavage site is selected from the group consisting of: an NS4A/4B junction cleavage site, an NS3/NS4A junction cleavage site, an NS4A/NS4B junction cleavage site, an NS4B/NS5A junction cleavage site, an NS5A/NS5B junction cleavage site, and variants thereof cleavable by the viral protease.

13 . The composition of claim 1 , wherein the protease cleavage site is cleaved by a protease upon activation of the CFP, in a cell expressing Fc receptor γ-chain.

14 . (canceled)

15 . (canceled)

16 . The composition of claim 1 , wherein the recombinant polynucleic acid further comprises a sequence encoding an additional fusion protein, comprising a phosphotyrosine binding (PTB) domain connected to a protease.

17 . (canceled)

18 . (canceled)

19 . The composition of claim 16 , wherein the additional fusion protein is a soluble cytosolic fusion protein.

20 . The composition of claim 16 , wherein the sequence encoding the additional fusion protein is separated from the sequence encoding the CFP by an auto-cleavable sequence.

21 . The composition of claim 16 , wherein the additional fusion protein is intracellularly tethered to a cell membrane when expressed in a cell.

22 . The composition of claim 21 , wherein the second additional fusion protein is intracellularly tethered to the cell membrane:

(i) via a transmembrane domain, or dimerization domain that dimerizes with Fc receptor γ-chain,

(ii) via a dimerization domain that comprises a leucine zipper domain, a helix-loop-helix domain, or both; or

(iii) via an anchor, wherein the anchor is a glycolipid anchor.

23 . The composition of claim 16 , wherein the sequence encoding the additional fusion protein further comprises a sequence encoding a dimerization domain that dimerizes with a domain of a cell surface receptor to promote association of the protease and the cell surface receptor.

24 - 32 . (canceled)

33 . The composition of claim 16 , wherein the second additional fusion protein further comprises a degron, wherein degradation activity of the degron is inhibited by binding of the PTB domain of the fusion protein to a phosphorylated tyrosine residue, wherein the phosphorylated tyrosine residue is on an endogenous receptor of a cell that is not constitutively phosphorylated at the tyrosine residue.

34 . (canceled)

35 . (canceled)

36 . The composition of claim 33 , wherein the endogenous receptor is phosphorylated at the tyrosine residue in cells expressing the CFP that are bound to a diseased cell expressing an antigen recognized by the antigen binding domain of the CFP.

37 - 39 . (canceled)

40 . The composition of claim 1 , wherein the antigen binding domain is a CD5 binding domain, a HER2 binding domain, a GPC3 binding domain, or a TROP2 binding domain.

41 - 45 . (canceled)

46 . The composition of claim 1 , wherein the transmembrane domain of the CFP is a transmembrane domain from CD16a, CD64, CD68 or CD89.

47 - 59 . (canceled)

60 . The composition of claim 1 , wherein the recombinant polynucleic acid is an mRNA.

61 - 66 . (canceled)

67 . The composition of claim 1 , wherein the composition further comprises an inhibitor of the protease.

68 . The composition of claim 67 , wherein the inhibitor of the protease is selected from the group consisting of: asunaprevir (ASV), danoprevir (DPV), simeprevir (SPV), grazoprevir (GPV), and any combination thereof.

69 - 82 . (canceled)

83 . A pharmaceutical composition comprising the composition of claim 16 , wherein the recombinant polynucleic acid is mRNA, and a nanoparticle delivery vehicle encapsulating the mRNA.

84 - 87 . (canceled)

88 . A method of treating a cancer in a human subject in need thereof, comprising administering to the human subject the pharmaceutical composition of claim 83 .

89 - 92 . (canceled)

Assignments (2)
CHANGE OF NAME Recorded Oct 15, 2025
From: MYELOID THERAPEUTICS, INC.
To: CREATE MEDICINES, INC.
Reel/Frame 073098/0011 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 17, 2023
From: GETTS, DANIEL; WANG, YUXIAO
To: MYELOID THERAPEUTICS, INC.
Reel/Frame 065251/0947 →