Chimeric receptor with NKG2D specificity for use in cell therapy against cancer and infectious disease
The invention provides a chimeric receptor comprising NKG2D, DAP10 and CD3 zeta. Also disclosed is a composition comprising this chimeric receptor and methods for making and using it to enhance the cytotoxicity and antitumor capacity of NK cells. The invention also encompasses methods for use of NKG2D-DAP10-CD3 zeta polypeptides, vectors and cells in methods for treating cancer and other proliferative disorders, as well as infectious diseases.
1. A method of producing a population of natural killer (NK) cells for use in treating cancer, said method comprising:
obtaining a peripheral blood sample comprising a mixed population of mononuclear cells comprising NK cells and T cells,
culturing said mixed population of mononuclear cells under culture conditions resulting in the enhanced expansion of NK cells, and
introducing into the NK cells a nucleic acid encoding a chimeric receptor, the chimeric receptor comprising:
i) an extracellular receptor domain, wherein said extracellular receptor domain comprises a fragment of NKG2D that binds one or more of MICA, MICB, ULBP1, ULBP2, ULBP3, ULBP4, ULBP5, and ULBP6, and
ii) a CD3 zeta cytoplasmic domain.
2. The method of claim 1 , wherein the culture conditions comprise culturing said mixed population of mononuclear cells with K562 myeloid leukemia cells, wherein said K562 myeloid leukemia cells are genetically modified to express membrane bound interleukin 15.
3. The method of claim 1 , further comprising removing T cells from the mixed population of mononuclear cells using beads coupled to an anti-CD3 antibody.
4. The method of claim 1 , wherein the nucleic acid is introduced into said NK cells by transduction.
5. The method of claim 1 , wherein the nucleic acid is introduced into said NK cells by electroporation.
6. The method of claim 1 , wherein the chimeric receptor comprises the fragment of NKG2D, the CD3 zeta cytoplasmic domain and a DNAX-activating protein 10 (DAP10) polypeptide.
7. The method of claim 6 , wherein the CD3 zeta cytoplasmic domain comprises the amino acid sequence of SEQ ID NO: 10 and the DAP10 polypeptide comprises the amino acid sequence of SEQ ID NO: 14.
8. The method of claim 6 , wherein the nucleic acid sequences encoding each of the fragment of NKG2D, the CD3 zeta cytoplasmic domain and the DAP10 polypeptide are in frame with one another.
9. The method of claim 1 , wherein the expanded population of NK cells has enhanced cytotoxicity as compared to NK cells stimulated with Interleukin-2.
10. A method of producing a population of immune cells for use in treating cancer, said method comprising:
obtaining a peripheral blood sample comprising mononuclear cells;
culturing said mononuclear cells under culture conditions resulting in the expansion of natural killer (NK) and T cells; and
introducing into the NK cells and into the T cells a nucleic acid encoding a chimeric receptor comprising:
i) an extracellular receptor domain, wherein said extracellular receptor domain comprises a fragment of NKG2D that binds one or more of MICA, MICB, ULBP1, ULBP2, ULBP3, ULBP4, ULBP5, and ULBP6, and
ii) a CD3 zeta cytoplasmic domain.
11. The method of claim 10 , wherein the chimeric receptor comprises the fragment of NKG2D, the CD3 zeta cytoplasmic domain and a DNAX-activating protein 10 (DAP10) polypeptide.
12. The method of claim 10 , wherein said population of immune cells is for use in allogeneic cancer therapy.
13. A method of producing a population of immune cells for use in treating cancer, said method comprising:
culturing a population of mononuclear cells comprising natural killer (NK) cells and T cells resulting in the resulting in the expansion of NK and T cells, and
introducing into the NK cells and the T cells a nucleic acid encoding a chimeric receptor comprising:
an extracellular receptor domain, wherein said extracellular receptor domain comprises a fragment of NKG2D that binds one or more of MICA, MICB, ULBP1, ULBP2, ULBP3, ULBP4, ULBP5, and ULBP6, and
a CD3 zeta cytoplasmic domain,
wherein upon binding of one or more of MICA, MICB, ULBP1, ULBP2, ULBP3, ULBP4, ULBP5, and ULBP6 to the extracellular receptor domain, the NK cells exhibit one or more of enhanced cytotoxicity and anti-tumor capacity against target cells, triggered signal transduction, triggered secretion of cytokines and chemokines, increased target cell apoptosis, and sustained cytotoxicity against target cells.
14. The method of claim 13 , wherein the CD3zeta cytoplasmic domain is at least 95% identical to SEQ ID NO: 10.
15. The method of claim 1 , wherein the population of NK cells is for use in allogeneic cancer therapy.
16. The method of claim 1 , wherein the CD3 zeta cytoplasmic domain is at least 95% identical to SEQ ID NO: 10.
17. The method of claim 10 , wherein the CD3 zeta cytoplasmic domain is at least 95% identical to SEQ ID NO: 10.
18. The method of claim 10 , wherein the nucleic acid is introduced into the NK cells and the T cells by transduction.
19. The method of claim 13 , wherein the nucleic acid is introduced into the NK cells and the T cells by transduction.