CPC C12M 41/48 (2013.01) [A61K 39/0008 (2013.01); A61K 40/19 (2025.01); A61K 40/24 (2025.01); A61K 40/4524 (2025.01); C12M 23/16 (2013.01); C12M 23/28 (2013.01); C12M 27/00 (2013.01); C12M 29/04 (2013.01); C12M 33/00 (2013.01); C12M 35/08 (2013.01); C12M 41/14 (2013.01); C12N 5/0639 (2013.01); C12N 2501/22 (2013.01); C12N 2501/2306 (2013.01); C12N 2501/25 (2013.01)] | 17 Claims |
1. A system for producing an immunotherapeutic product, the system comprising:
a first module configured for processing cellular material associated with a disease of a patient, the first module comprising a fluid inlet port and a separate fluid outlet port;
a second module configured for generating immune cells, the second module comprising a cell culture chamber, a fluid inlet port, and a separate fluid outlet port disposed on opposite sides of the cell culture chamber, the separate fluid outlet port positioned at a height above the fluid inlet port, wherein the cell culture chamber comprises a monocyte-binding substrate, and wherein the fluid inlet port and the separate fluid outlet port are fluidically coupled to the cell culture chamber and configured to provide flow of a liquid culture medium across the monocyte-binding substrate from the fluid inlet port to the separate fluid outlet port that minimizes mechanical detachment of cells from the monocyte-binding substrate; and
a third module separately coupled to and in fluidic communication with each of the first and second modules, the third module comprising a first inlet port for fluidic communication with the first module and a separate second inlet port for fluidic communication with the second module such that the third module separately receives a flow of processed cellular material from the first module and separately receives a flow of immune cells from the second module, wherein the third module is configured to co-culture the processed cellular material and the immune cells to produce an immunotherapeutic product.
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