Methods of engineering immune cells for enhanced potency and persistence and uses of engineered cells in immunotherapy
US-2024335536-A1 · Oct 10, 2024 · US
US11807675B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11807675-B2 |
| Application number | US-201415027148-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 3, 2014 |
| Priority date | Oct 3, 2013 |
| Publication date | Nov 7, 2023 |
| Grant date | Nov 7, 2023 |
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The present invention relates to, in part, artificial antigen presenting cells that are useful in treating disease (including cancers) and have uses, for example, directly in vivo and/or in the expansion of a patients cells for re-introduction ex vivo.
Opening claim text (preview).
What is claimed is: 1. A microparticle or nanoparticle artificial antigen presenting cell for stimulation and expansion of NKT cells, comprising: (a) a paramagnetic iron dextran bead; and, on the surface of the bead, (b) a population of CD1d antigen presenting complexes that activate T cell receptors (TCRs) of natural killer T (NKT) cells, wherein the CD1d antigen presenting complexes present an NKT cell antigen selected from the group consisting of α-C-GalCer, GSL-1, and iGB3; (c) a population of NKT cell costimulatory ligands which specifically bind to CD44; (d) a population of NKT cell costimulatory ligands which specifically bind to CD161; (e) a population of binding NKT cell costimulatory ligands which specifically bind to CD28 and a population of NKT cell costimulatory ligands which specifically bind to CD40, wherein the NKT cell costimulatory ligands are antibodies or antigen-binding fragments thereof, wherein the CD1d antigen is a fusion protein with an immunoglobulin sequence, wherein the ratio of CD1d-Ig to anti-CD28 is 10:1, wherein the microparticle or nanoparticle artificial antigen presenting cell has a size of 150 nm or 200 nm. 2. A microparticle or nanoparticle artificial antigen presenting cell for stimualation and expansion of NKT cells, consisting essentially of: (a) a paramagnetic iron dextran bead; and, on the surface of the bead, (b) a population of CD1d antigen presenting complexes that activate T cell receptors (TCRs) of natural killer T (NKT) cells, wherein the CD1d antigen presenting complexes present an NKT cell antigen selected from the group consisting of a-C-GalCer, GSL-1, and iGB3; (c) a population of NKT cell costimulatory ligands which specifically bind to CD44; (d) a population of NKT cell costimulatory ligands which specifically bind to CD161; (e) a population of binding NKT cell costimulatory ligands which specifically bind to CD28 and a population of NKT cell costimulatory ligands which specifically bind to CD40, wherein the NKT cell costimulatory ligands are antibodies or antigen-binding fragments thereof, wherein the CD1d antigen is a fusion protein with an immunoglobulin sequence, wherein the ratio of CD 1 d-Ig to NKT cell costimulatory CD28-binding ligand is 10:1, wherein the microparticle or nanoparticle artificial antigen presenting cell has a size of 150 nm or 200 nm. 3. The microparticle or nanoparticle artificial antigen presenting cell of claim 1 , wherein the CD1d antigen presenting complexes are fused with an immunoglobulin heavy chain sequence, or fragment thereof, thereby providing a dimeric CD1d ligand. 4. The microparticle or nanoparticle artificial antigen presenting cell of claim 2 , wherein the CD1d antigen presenting complexes are fused with an immunoglobulin heavy chain sequence, or fragment thereof, thereby providing a dimeric CD1d ligand. 5. The microparticle or nanoparticle artificial antigen presenting cell of claim 1 , wherein the NKT cells are Type I and/or Type II NKT cells. 6. The microparticle or nanoparticle artificial antigen presenting cell of claim 2 , wherein the NKT cells are Type I and/or Type II NKT cells. 7. The microparticle or nanoparticle artificial antigen presenting cell of claim 1 , wherein the NKT cells are CD4+, CD8+, or CD4+CD8+, CD4−CD8−. 8. The microparticle or nanoparticle artificial antigen presenting cell of claim 2 , wherein the NKT cells are CD4+, CD8+, or CD4+CD8+, CD4−CD8−. 9. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and the microparticle or nanoparticle artificial antigen presenting cell of claim 1 . 10. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and the microparticle or nanoparticle artificial antigen presenting cell of claim 2 .
Melan-A/MART · CPC title
Natural-killer [NK] cells; Natural-killer T [NKT] cells · CPC title
T-cells, e.g. tumour infiltrating lymphocytes [TIL] or regulatory T [Treg] cells; Lymphokine-activated killer [LAK] cells · CPC title
Skin; melanoma · CPC title
Blood cells, e.g. leukemia or lymphoma · CPC title
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