COMPOSITIONS AND METHODS OF USE OF IL-10 AGENTS IN CONJUNCTION WITH CHIMERIC ANTIGEN RECEPTOR CELL THERAPY
The present invention relates to methods of modulating the activity of CAR-T cells in the treatment of diseases, disorders and conditions by the administration of an IL-10 agent. The invention further provides engineered CAR-T cells to express additional therapeutically effective agents. The present invention further provides improved pharmaceutical and therapeutic compostions and methods relating to the use of CAR-T cell therapies in the treatment of disease in mammalian subjects.
1 . A method of treating a mammalian subject suffering from a neoplastic disease the method comprising:
a. obtaining a sample of T-cells derived from the patient;
b. transducing a fraction of T-cells in the sample with a vector, the vector comprising a nucleic acid sequence encoding a chimeric antigen receptor (CAR) the nucleic acid sequence being in operable association with one or more control elements to effect transcription and translation of the nucleic acid sequence encoding a chimeric antigen receptor (CAR) in a T-cell, so as to generate a population of T-cells expressing the CAR;
c. isolating the T-cells expressing the CAR (CAR-T cells);
d. culturing the CAR-T cells ex vivo in the presence of an IL-10 agent; and
e. administering the CAR-T cells from step (d) to the mammalian subject.
2 . The method of claim 1 , further comprising the step:
administering to the subject a therapeutically effective amount of a pharmaceutical formulation comprising an IL-10 agent.
3 . The method of claim 2 wherein the the IL-10 agent of step (d) and the IL-10 agent of the pharmaceutical formulation of step (f) are the same IL-10 agent.
4 . The method of claim 2 wherein the IL-10 agent of step (d) and the IL-10 agent of the pharmaceutical formulation of step (f) are different IL-10 agents.
5 . The method of claim 4 wherein the first IL-10 agent of step (d) is rhIL-10 and the pharmaceutical formulation of IL-10 agent of step (f) comprises a PEGylated IL-10 agent.
6 . The method of claim 5 wherein the pharmaceutical formulation comprising an IL-10 agent comprises a mono-PEGylated IL-10 agent.
7 . The method of claim 5 wherein the pharmaceutical formulation comprising an IL-10 agent comprises a mixture of a mono-PEGylated IL-10 agent and a diPEGylated IL-10 agent.
8 . The method of claim 2 wherein the administering of a pharmaceutical formulation comprising the IL-10 agent is sufficient to maintain a serum trough concentration of the IL-10 agent in the subject of at least 0.01 ng/ml over a period of at least 72 hours.
9 . The method of claim 2 wherein the administering of a pharmaceutical formulation comprising the IL-10 agent is sufficient to maintain a serum trough concentration of the IL-10 agent in the subject of at least 0.05 ng/ml over a period of at least 72 hours.
10 . The method of claim 2 wherein the administering of a pharmaceutical formulation comprising the IL-10 agent is sufficient to maintain a serum trough concentration of the IL-10 agent in the subject of at least 0.1 ng/ml over a period of at least 72 hours.
11 . The method of claim 2 wherein the administering of a pharmaceutical formulation comprising the IL-10 agent is sufficient to maintain a serum trough concentration of the IL-10 agent in the subject of at least 0.5 ng/ml over a period of at least 72 hours.
12 . The method of claim 1 wherein the IL-10 agent is an IL-10 variant derived from hIL-10.
13 . The method of claim 1 wherein the antigen recognition domain of the CAR is a polypeptide that specifically binds to HER2, MUC1, telomerase, PSA, CEA, VEGF, VEGF-R2, T1, CD19, CD20, CD22, ROR1, mesothelin, CD33/IL3Ra, c-Met, PSMA, Glycolipid F77, FAP, EGFRvIII, GD-2, NY-ESO-1 TCR, MAGE A3 TCR, 5T4, WT1, KG2D ligand, folate receptor (FRa), platelet-derived growth factor receptor A, or Wnt1 antigens.
14 . The method of claim 1 wherein the antigen recognition domain of the CAR is selected from the group consisting of an anti-CD19 scFv, an anti-PSA scFv, an anti-CD19 scFv, an anti-HER2 scFv, an anti-CEA scFv, an anti-EGFR scFv, an anti-MUC1 scFv, an anti-HER2-neu scFv, an anti-VEGF-R2 scFv, an anti-T1 scFv, an anti-CD22 scFv, an anti-ROR1 scFv, an anti-mesothelin scFv, an anti-CD33/IL3Ra scFv, an anti-c-Met scFv, an anti-PSMA scFv, an anti-Glycolipid F77 scFv, an anti-FAP scFv, an anti-EGFRvIII scFv, an anti-GD-2 scFv, an anti-NY-ESO-1 scFv, an anti-MAGE scFv, an anti-A3 scFv, an anti-5T4 scFv, an anti-WT1 scFv, or an anti-Wnt1 scFv.
15 . The method of claim 1 wherein intracellular signaling domain of the CAR is a polypeptide comprising an amino acid sequence derived from the cytoplasmic domain of CD27, CD28, CD137 CD278, CD134, FcεR1γ and β chains, MB1 (Igα) chain, B29 (Igβ) chain, the human CD3 zeta chain, CD3, a syk family tyrosine kinase, a src family tyrosine kinase, CD2, CD5 or CD28.
16 . The method of claim 1 wherein intracellular signaling domain of the CAR comprises an amino acid sequence derived from the cytoplasmic domain of CD28, CD137 (4-1BB), CD134 (OX40), Dap10, CD27, CD2, CD5, ICAM-1, LFA-1 (CD11a/CD18), Lck, TNFR-I, TNFR-II, Fas, CD30, and CD40.
17 . The method of claim 1 , the method further comprising the administration to the subject of one or more supplemental agents.
18 . The method of claim 17 wherein the one or more supplemental agents is selected from the group consisting of chemotherapeutic agents, immune checkpoint modulators, IL-2 agents, IL-7 agents, IL-12 agents, IL-15 agents and IL-18 agents.
19 . The method of claim 17 wherein the one or more supplemental agents is one or more chemotherapeutic agents.
20 . The method of claim 17 wherein the one or more supplemental agents is one or more immune checkpoint modulators selected from the group consisting of PD1 modulators, PDL1 modulators, CTLA4 modulators, LAG-3 modulators, TIM-3 modulators, ICOS modulators, OX40 modulators, cd-27 modulators, CD-137 modulators, HVEM modulators, CD28 modulators, CD226 modulators, GITR modulators, BTLA modulators, A2A modulators, IDO modulators and VISTA modulators.
21 . The method of claim 20 wherein the immune checkpoint modulator is an antibody.
22 - 66 . (canceled)
67 . A recombinant vector comprising nucleic acid sequences encoding an IL-10 agent, a CAR, and a cytokine the nucleic acid sequences operably linked to an expression control sequence.
68 . The recombinant vector of claim 67 wherein the antigen recognition domain of the CAR is a polypeptide that specifically binds to HER2, MUC1, telomerase, PSA, CEA, VEGF, VEGF-R2, T1, CD19, CD20, CD22, ROR1, mesothelin, CD33/IL3Ra, c-Met, PSMA, Glycolipid F77, FAP, EGFRvIII, GD-2, NY-ESO-1 TCR, MAGE A3 TCR, 5T4, WT1, KG2D ligand, folate receptor (FRa), platelet-derived growth factor receptor A, or Wnt1 antigens.
69 . The recombinant vector of claim 67 wherein the antigen recognition domain of the CAR is selected from the group consisting of an anti-CD19 scFv, an anti-PSA scFv, an anti-CD19 scFv, an anti-HER2 scFv, an anti-CEA scFv, an anti-EGFR scFv, an anti-MUC1 scFv, an anti-HER2-neu scFv, an anti-VEGF-R2 scFv, an anti-T1 scFv, an anti-CD22 scFv, an anti-ROR1 scFv, an anti-mesothelin scFv, an anti-CD33/IL3Ra scFv, an anti-c-Met scFv, an anti-PSMA scFv, an anti-Glycolipid F77 scFv, an anti-FAP scFv, an anti-EGFRvIII scFv, an anti-GD-2 scFv, an anti-NY-ESO-1 scFv, an anti-MAGE scFv, an anti-A3 scFv, an anti-5T4 scFv, an anti-WT1 scFv, or an anti-Wnt1 scFv.
70 . The recombinant vector of claim 67 wherein intracellular signaling domain of the CAR comprises an amino acid sequence derived from the cytoplasmic domain of CD27, CD28, CD137 CD278, CD134, FcεR1γ and β chains, MB1 (Igα) chain, B29 (Igβ) chain, the human CD3 zeta chain, CD3, a syk family tyrosine kinase, a src family tyrosine kinase, CD2, CD5 or CD28.
71 . The recombinant vector of claim 67 wherein the intracellular signaling domain of the further comprises a polypeptide comprising an amino acid sequence derived from one or more co-stimulatory domains derived from of the intracellular signaling domains of CD28, CD137 (4-1BB), CD134 (OX40), Dap10, CD27, CD2, CD5, ICAM-1, LFA-1 (CD11a/CD18), Lck, TNFR-I, TNFR-II, Fas, CD30, and CD40.
72 . The recombinant vector of claim 67 wherein the cytokine is selected from the group consisting of IL-7, IL-12, IL-15, and IL18, and variants thereof.
73 . The vector of claim 67 wherein said vector is a viral vector.
74 . The vector of claim 73 wherein the viral vector is a lentiviral vector.
75 . A recombinantly modified T-cell transfected with a vector of claim 67 .
76 - 85 . (canceled)