Marrow Infiltrating Lymphocytes (MILS) as a Source of T-Cells for Chimeric Antigen Receptor (CAR) Thereapy
US-2018200367-A1 · Jul 19, 2018 · US
US11478548B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11478548-B2 |
| Application number | US-201615742684-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 8, 2016 |
| Priority date | Jul 8, 2015 |
| Publication date | Oct 25, 2022 |
| Grant date | Oct 25, 2022 |
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In some embodiments, marrow-infiltrating lymphocytes (“MILs”) comprising a chimeric antigen receptor (“CAR”) are provided. In some aspects, the embodiments relate to a method for making a recombinant MIL, comprising obtaining bone marrow comprising MILs; and transfecting, transforming, or transducing the MILs with a nucleic acid encoding a chimeric antigen receptor. In some aspects, the embodiments relate to a method for treating a condition in a subject, comprising administering to the subject a MIL comprising a CAR.
Opening claim text (preview).
What is claimed is: 1. A marrow infiltrating lymphocyte (“MIL”), comprising a chimeric antigen receptor (“CAR”), wherein: the CAR comprises a scFV antigen-binding domain that can bind to an extracellular domain of CD19 or CD38; and a transmembrane domain of CD19 or CD8, and an intracellular domain selected from the group consisting of 4-1BB, CD3ζ, and a combination thereof and wherein the MIL is autologous MIL isolated from a cancer patient. 2. The MIL of claim 1 , wherein the MIL is CD3+, CD4+, CD8+, or a combination thereof. 3. The MIL of claim 1 , wherein the MIL is CD45RO+, CD62L+, or CXCR4+. 4. The MIL of claim 1 , wherein the MIL is 4-1BB+. 5. The MIL of claim 1 , wherein the MIL is interferon γ+ and/or is CD138+. 6. The MIL of claim 1 , wherein the MIL is CD33+. 7. The MIL of claim 1 , wherein the MIL is CD34-. 8. A method of inhibiting the growth of a neoplastic cell that expresses CD19 or CD38 in a subject, comprising administering to the subject the CD19 or CD38 binding MIL of claim 1 .
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