NK CELL-BASED THERAPY
Disclosed herein are methods of cancer treatment comprising administration of a natural killer (NK) cell or cell line in combination with an IL-6 antagonist, such as an antibody to IL-6 or its receptor, especially for treatment of cancer expressing IL-6 receptors and in which checkpoint inhibitory receptors, such as PDL-1 and/or PDL-2 are expressed/upregulated during disease.
1 - 20 . (canceled)
21 . A method of treating cancer comprising administering to a patient an effective amount of a composition comprising an NK cell and an IL-6 receptor (IL-6R) antagonist.
22 . The method of claim 21 , wherein the NK cell and the IL-6R antagonist do not interact to induce antibody-dependent cell-mediated cytotoxicity (ADCC).
23 . The method of claim 21 , wherein the IL-6R antagonist is an antibody that binds IL-6R.
24 . The method of claim 21 , wherein the cancer expresses IL-6R.
25 . The method of claim 21 , wherein the cancer expresses PDL-1, PDL-2, or a combination thereof.
26 . The method of claim 21 , comprising administering to the patient an effective amount of the NK cell pre-bound with the IL-6R antagonist.
27 . The method of claim 21 , wherein the IL-6R antagonist is an IL-6R antibody selected from the group consisting of tocilizumab, sarilumab, PM-1 and AUK12-20.
28 . The method of claim 21 , wherein the cancer is a blood cancer.
29 . The method of claim 28 , wherein the blood cancer is selected from the group consisting of acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), chronic myeloid leukemia (CML), hairy cell leukemia, T-cell prolymphocytic leukemia, large granular lymphocytic leukemia, Hodgkin's lymphoma, non-Hodgkin's lymphoma, including T-cell lymphomas and B-cell lymphomas, asymptomatic myeloma, smoldering multiple myeloma (SMM), multiple myeloma (MM), and light chain myeloma.
30 . The method of claim 21 , wherein the NK cell is KHYG-1.
31 . A method of treating a cancer selected from (i) a IL-6 receptor (IL-6R) expressing multiple myeloma and (ii) a IL-6R expressing leukemia, in a human patient, comprising administering to the patient an effective amount of a composition comprising an NK cell and an antibody that neutralizes IL-6R.
32 . The method of claim 31 , wherein the NK cell and the IL-6R antibody do not interact to induce antibody-dependent cell-mediated cytotoxicity (ADCC).
33 . The method of claim 31 , wherein the antibody is selected from the group consisting of tocilizumab, sarilumab, PM-1 and AUK12-20.
34 . The method of claim 31 , wherein the NK cell is KHYG-1.
35 . A method of treating a cancer comprising administering to a patient an effective amount of (a) an NK cell and (b) an IL-6 receptor (IL-6R) antagonist.
36 . The method of claim 35 , wherein the NK cell and the IL-6R antagonist do not interact to induce antibody-dependent cell-mediated cytotoxicity (ADCC).
37 . The method of claim 35 , wherein the NK cell and the IL-6R antagonist are administered separately.
38 . The method of claim 35 , wherein the patient is pretreated with the IL-6R antagonist before administration of the NK cell.
39 . The method of claim 35 , wherein the IL-6R antagonist is an IL-6R antibody selected from the group consisting of tocilizumab, sarilumab, PM-1 and AUK12-20.
40 . The method of claim 35 , wherein the cancer is a blood cancer selected from the group consisting of acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), chronic myeloid leukemia (CML), hairy cell leukemia, T-cell prolymphocytic leukemia, large granular lymphocytic leukemia, Hodgkin's lymphoma, non-Hodgkin's lymphoma, including T-cell lymphomas and B-cell lymphomas, asymptomatic myeloma, smoldering multiple myeloma (SMM), multiple myeloma (MM), and light chain myeloma.