Modified rapid expansion methods(“modified-REM”) for in vitro propagation of T lymphocytes
View Patent ↗The present invention provides a modified rapid expansion method (termed “low-PBMC-REM” or “modified-REM”), for quickly generating large numbers of T lymphocytes, including cytolytic and helper T lymphocytes, without using the large excesses of peripheral blood mononuclear cells (PBMC) or EBV-transformed lymphoblastoid cells (LCL) characteristic of high-PBMC-REM. Clonal expansions of greater than 500-fold can be achieved within a single stimulation cycle of about 8-14 days.
1. A method for expanding an initial cloned T lymphocyte population in culture medium in vitro, comprising the steps of:
adding an initial cloned T lymphocyte population to a culture medium in vitro; adding to the culture medium a non-dividing mammalian coil line expressing at least one T-cell-stimulatory component, wherein said cell line is not an EBV-transformed lymphoblastoid cell line (LCL); and
incubating the culture, thereby expanding the cloned T lymphocyte population.
2. The expansion method of claim 1 , wherein said T-cell-stimulatory component is selected from the group consisting of an Fc-γ receptor, a cell adhesion-accessory molecule and a cytokine.
3. The expansion method of claim 1 , further comprising the step of adding anti-CD3 monoclonalantibody to the culture medeium wherein the concentration of anti-CD3 monoclonal antibody is at least 1.0 ng/ml.
4. The expansion method of claim 1 , further comprising the step of adding IL-2 to the culture medium, wherein the concentration of IL-2 is at least 10 units/ml.
5. The expansion method of claim 1 , wherein said mammalian cell line comprises at least one cell type that is present at a frequency at least three times that found in human peripheral blood mononuclear cells (human PBMCs).
6. The expansion method of claim 1 , wherein said T-cell-stimulatory component is selected from the group consisting of an Fc-γ receptor and a cell adhesion-accessory molecule.
7. The expansion method of claim 1 , wherein said T-cell-stimulatory component is selected from the group consisting of a cell adhesion-accessory molecule and a cytokine.
8. The expansion method of claim 1 , wherein said T-cell-stimulatory component is selected from the group consisting of an Fc-γ receptor a cytokine.
9. The expansion method of claim 1 , wherein said mammalian cell line expresses a cell adhesion-accessory molecule.
10. The expansion method of claim 9 , wherein said cell adhesion-accessory molecule is selected from the group consisting of Class II MHC, Class I MHC, ICAM 1, ICAM 2, ICAM 3, CD58, CD72, CD 80, CD86, fibronectin, ligand to CD27, and hyaluronate.
11. The expansion method of claim 1 , wherein said mammalian cell line expresses a cytokine.
12. The expansion method of claim 1 , wherein said T-cell-stimulatory component is a molecule that binds to CD21.
13. The expansion method of claim 11 , wherein said cytokine is selected from the group consisting of IL-1, IL-2, IL-4, IL-6, IL-7, IL-12and IL-15.
14. The expansion method of claim 1 , further comprising the step of adding a soluble T-cell-stimulatory factor to the culture medium.
15. The expansion method of claim 14 , wherein said soluble T-cell-stimulatory factor is selected from the group consisting of a cytokine, an antibody specific for a T cell surface component, and an antibody specific for a component capable of binding to a T cell surface component.
16. The expansion method of claim 14 , wherein said soluble T-cell-stimulatory factor is a cytokine selected from the group consisting of IL-1, IL-2, IL-4, IL-6, IL-7, IL-12 and IL-15.
17. The expansion method of claim 14 , wherein said soluble T-cell-stimulatory factor is an antibody specific for a T cell surface component, and wherein said T cell surface component is selected from the group consisting of CD4, CD8, CD11a, CD2CD5, CD49d, CD27, CD28 and CD44.
18. The expansion method of claim 14 , wherein said soluble T-cell-stimulatory factor is an antibody specific for a component capable of binding to a T cell surface component, and wherein said T cell surface component is selected from the group consisting of CD4, CD8, CD11a, CD2, CD5, CD49d, CD27, CD28 and CD44.
19. The expansion method of claim 14 , wherein said soluble T-cell-stimulatory factor is a molecule that binds to CD21.
20. The expansion method of claim 19 , wherein said molecule that binds to CD21 is an anti-CD21 antibody.
21. The expansion method of claim 1 , further comprising the step of adding to the culture a multiplicity of peripheral blood mononuclear cells (PBMCs).
22. The expansion method of claim 21 , wherein the ratio of PBMCs to initial T cells to be expanded is less than 40:1.
23. The expansion method of claim 21 , wherein the ratio of PBMCs to initial T cells to be expanded is less than 10:1.
24. The expansion method of claim 21 , wherein the ratio of PBMCs to initial T cells to be expanded is less than 3:1.
25. The expansion method of claim 1 , further comprising the step of adding to the culture a multiplicity of EBV-transformed lymphoblastoid cells (LCLs).
26. The expansion method of claim 25 , wherein the ratio of LCLs to initial T cells to be expanded is less than 10:1.
27. The expansion method of claim 1 , wherein the initial T lymphocyte population comprises at least one human CD8+antigen-specific cytotoxic T lymphocyte (CTL).
28. The expansion method of claim 1 , wherein the initial T lymphocyte population comprises at least one human CD4+antigen-specific helper T lymphocyte.
29. The method of claim 1 , wherein the cell line is the K562 cell line.
30. A method for expanding an initial cloned T lymphocyte population in culture medium in vitro, comprising the steps of:
adding an initial cloned T lymphocyte population to a culture medium in vitro;
adding to the culture a multiplicity of BBV-transformed lymphoblastoid cells (LCLs), an anti-CD3 antibody and an CD21 antibody; and a multiplicity of peripheral blood mononuclear cells (PBMCs), wherein the ratio of PBMCs to initial T cells to be expanded is less than 40:1; and
incubating the culture, thereby expanding the cloned T lymphocyte population.
31. The method of claim 1 wherein the cells of the cloned T lympbocyte population comprise T cell receptor complexes, and wherein the method further comprises specifically stimulating said T-cell receptor complexes.