1 . A method for expanding tumor infiltrating lymphocytes (TILs) into a therapeutic population of TILs comprising: (a) obtaining a first population of TILs from a tumor resected from a subject by processing a tumor sample obtained from the subject into multiple tumor fragments; (b) performing a priming first expansion by culturing the first population of TILs in a cell culture medium comprising IL-2, OKT-3, and antigen presenting cells (APCs) to produce a second population of TILs, wherein the priming first expansion is performed in a container comprising a first gas-permeable surface area, wherein the priming first expansion is performed for first period of about 1 to 7 days to obtain the second population of TILs, wherein the second population of TILs is greater in number than the first population of TILs; (c) performing a rapid second expansion by supplementing the cell culture medium of the second population of TILs with IL-2, OKT-3, and APCs, to produce a third population of TILs, wherein the number of APCs added in the rapid second expansion is at least twice the number of APCs added in step (b), wherein the rapid second expansion is performed for a second period of about 1 to 11 days to obtain the third population of TILs, wherein the third population of TILs is a therapeutic population of TILs, wherein the rapid second expansion is performed in a container comprising a second gas-permeable surface area; (d) harvesting the therapeutic population of TILs obtained from step (c); (e) engineering the TILs to express orthogonal IL-2Rβ; and (f) transferring the harvested and engineered TIL population to an infusion bag.
2 . A method for expanding tumor infiltrating lymphocytes (TILs) into a therapeutic population of TILs comprising: (a) obtaining a first population of TILs from a tumor resected from a subject by processing a tumor sample obtained from the subject into multiple tumor fragments; (b) performing a priming first expansion by culturing the first population of TILs in a cell culture medium comprising IL-2, OKT-3, and optionally comprising antigen presenting cells (APCs), to produce a second population of TILs, wherein the priming first expansion is performed for a first period of about 1 to 7 days to obtain the second population of TILs, wherein the second population of TILs is greater in number than the first population of TILs; (c) performing a rapid second expansion by contacting the second population of TILs with a cell culture medium comprising orthogonal IL-2, OKT-3, and APCs, to produce a third population of TILs, wherein the rapid second expansion is performed for a second period of about 1 to 11 days to obtain the third population of TILs, wherein the third population of TILs is a therapeutic population of TILs; (d) engineering the TILs to express orthogonal IL-2Rβ; and (e) harvesting the therapeutic population of TILs obtained from step (d).
3 . The method of claim 2 , wherein in step (b) the cell culture medium further comprises antigen-presenting cells (APCs), and wherein the number of APCs in the culture medium in step (d) is greater than the number of APCs in the culture medium in step (b).
4 . A method for expanding tumor infiltrating lymphocytes (TILs) into a therapeutic population of TILs comprising: (a) performing a priming first expansion by culturing a first population of TILs, said first population of TILs obtainable by processing a tumor sample from a tumor resected from a subject into multiple tumor fragments, in a cell culture medium comprising IL-2, OKT-3, and antigen presenting cells (APCs) to produce a second population of TILs, wherein the priming first expansion is performed in a container comprising a first gas-permeable surface area, wherein the priming first expansion is performed for first period of about 1 to 7 days to obtain the second population of TILs, wherein the second population of TILs is greater in number than the first population of TILs; (b) performing a rapid second expansion by contacting the second population of TILs to a cell culture medium of the second population of TILs with additional IL-2, OKT-3, and APCs, to produce a third population of TILs, wherein the number of APCs in the rapid second expansion is at least twice the number of APCs in step (a), wherein the rapid second expansion is performed for a second period of about 1 to 11 days to obtain the third population of TILs, wherein the third population of TILs is a therapeutic population of TILs, wherein the rapid second expansion is performed in a container comprising a second gas-permeable surface area; (c) harvesting the therapeutic population of TILs obtained from step (b); and, (d) engineering the TILs produced in step (c) to express orthogonal IL-2Rβ.
5 . A method for expanding tumor infiltrating lymphocytes (TILs) into a therapeutic population of TILs comprising: (a) performing a priming first expansion by culturing a first population of TILs in a cell culture medium comprising IL-2, OKT-3, and optionally comprising antigen presenting cells (APCs), to produce a second population of TILs, wherein the priming first expansion is performed for a first period of about 1 to 7 days to obtain the second population of TILs, wherein the second population of TILs is greater in number than the first population of TILs; (b) performing a rapid second expansion by contacting the second population of TILs with a cell culture medium comprising IL-2, OKT-3, and APCs, to produce a third population of TILs, wherein the rapid second expansion is performed for a second period of about 1 to 11 days to obtain the third population of TILs, wherein the third population of TILs is a therapeutic population of TILs; (c) harvesting the therapeutic population of TILs obtained from step (b); and, (d) engineering the TILs produced in step (c) to express orthogonal IL-2Rβ.
6 . The method of claim 5 , wherein in step (a) the cell culture medium further comprises antigen-presenting cells (APCs), and wherein the number of APCs in the culture medium in step (c) is greater than the number of APCs in the culture medium in step (b).
7 .- 8 . (canceled)
9 . The method of claim 1 , wherein the ratio of the number of APCs in the rapid second expansion to the number of APCs in the priming first expansion is selected from a range of from about 2:1 to about 5:1.
10 - 11 . (canceled)
12 . The method of claim 1 , wherein the number of APCs in the priming first expansion is selected from the range of about 1.0×10 6 APCs/cm 2 to about 4.5×10 6 APCs/cm 2 , and wherein the number of APCs in the rapid second expansion is selected from the range of about 2.5×10 6 APCs/cm 2 to about 7.5×10 6 APCs/cm 2 .
13 .- 14 . (canceled)
15 . The method of claim 1 , wherein the number of APCs in the priming first expansion is selected from the range of about 1×10 8 APCs to about 3.5×10 8 APCs, and wherein the number of APCs in the rapid second expansion is selected from the range of about 3.5×10 8 APCs to about 1×10 9 APCs.
16 .- 18 . (canceled)
19 . The method of claim 1 , wherein the ratio of the number of TILs in the second population of TILs to the number of TILs in the first population of TILs is about 1.5:1 to about 100:1.
20 .- 65 . (canceled)
66 . The method of claim 1 , wherein after 2 to 3 days in the step of the rapid second expansion, the cell culture medium is supplemented with additional IL-2.
67 . The method of claim 1 , further comprising cryopreserving the harvested TIL population in the step of harvesting the therapeutic population of TILs using a cryopreservation process.
68 .- 69 . (canceled)
70 . The method according to claim 1 , wherein the antigen-presenting cells are peripheral blood mononuclear cells (PBMCs).
71 . The method according to claim 70 , wherein the PBMCs are irradiated and allogeneic.
72 . The method according to claim 1 , wherein in the step of the priming first expansion the cell culture medium comprises peripheral blood mononuclear cells (PBMCs), and wherein the total number of PBMCs added to the cell culture medium in the step of the priming first expansion is about 2.5×10 8 .
73 . The method according to claim 1 , wherein in the step of the rapid second expansion the antigen-presenting cells (APCs) in the cell culture medium are peripheral blood mononuclear cells (PBMCs), and wherein the total number of PBMCs added to the cell culture medium in the step of the rapid second expansion is about 5×10 8 .
74 . The method according to claim 1 , wherein the antigen-presenting cells are artificial antigen-presenting cells.
75 .- 81 . (canceled)
82 . The method according to claim 1 , wherein the IL-2 concentration is about 10,000 IU/mL to about 5,000 IU/mL.
83 . The method according to claim 1 , wherein the IL-2 concentration is about 6,000 IU/mL.
84 . (canceled)
85 . The method according to claim 67 , wherein the cryopreservation media comprises dimethlysulfoxide (DMSO).
86 .- 87 . (canceled)
88 . The method according to claim 1 , wherein the first period in the step of the priming first expansion is performed within a period of 5 days, 6 days, or 7 days.
89 . The method according to claim 1 , wherein the second period in the step of the rapid second expansion is performed within a period of 7 days, 8 days, or 9 days.
90 . (canceled)
91 . The method according to claim 1 , wherein steps of the priming first expansion through the harvesting of the therapeutic population of TILs are performed within a period of about 14 days to about 16 days.
92 .- 95 . (canceled)
96 . The method according to claim 1 , further comprising the step of cryopreserving the harvested therapeutic population of TILs using a cryopreservation process, wherein steps of the priming first expansion through the harvesting of the therapeutic population of TILs and cryopreservation are performed in 16 days or less.
97 . The method according to claim 1 , wherein the therapeutic population of TILs harvested in the step of harvesting of the therapeutic population of TILs comprises sufficient TILs for a therapeutically effective dosage of the TILs.
98 . The method according to claim 97 , wherein the number of TILs sufficient for a therapeutically effective dosage is from about 2.3×10 10 to about 13.7×10 10 .
99 .- 101 . (canceled)
102 . The method according to claim 1 , wherein the therapeutic population of TILs from the step of the harvesting of the therapeutic population of TILs are infused into a patient.
103 . A method for treating a subject with cancer, the method comprising administering expanded tumor infiltrating lymphocytes (TILs) comprising: (a) obtaining a first population of TILs from a tumor resected from a subject by processing a tumor sample obtained from the subject into multiple tumor fragments; (b) performing a priming first expansion by culturing the first population of TILs in a cell culture medium comprising IL-2, OKT-3, and antigen presenting cells (APCs) to produce a second population of TILs, wherein the priming first expansion is performed in a container comprising a first gas-permeable surface area, wherein the priming first expansion is performed for about 1 to 7 days to obtain the second population of TILs; (c) performing a rapid second expansion by supplementing the cell culture medium of the second population of TILs with additional IL-2, OKT-3, and APCs, to produce a third population of TILs, wherein the number of APCs added to the rapid second expansion is at least twice the number of APCs added in step (b), wherein the rapid second expansion is performed for about 1 to 11 days to obtain the third population of TILs, wherein the third population of TILs is a therapeutic population of TILs, wherein the rapid second expansion is performed in a container comprising a second gas-permeable surface area; (d) harvesting the therapeutic population of TILs obtained from step (c); (e) engineering the TILs produced in step (d) to express orthogonal IL-2Rβ; (f) transferring the harvested TIL population from step (e) to an infusion bag; (g) administering a therapeutically effective dosage of the TILs from step (f) to the subject; and (h) administering a therapeutically effective dosage to the subject of an IL-2 ortholog capable of binding to said expressed orthogonal IL-2Rβ.
104 .- 212 . (canceled)
213 . The method of claim 1 , wherein the engineering to express orthogonal IL-2Rβ is performed between steps (b) and (c).
214 . The method of claim 1 , wherein the engineering to express orthogonal IL-2Rβ is performed between steps (c) and (d).
215 . The method of claim 213 , wherein orthogonal IL-2 is substituted for IL-2 in step (c).
216 .- 225 . (canceled)
