Cancer immunotherapy with a viral antigen-defined, immunomodulator-secreting cell vaccine
View Patent ↗A human cell line, which lacks major histocompatibility class I (MHC-I) antigens and major histocompatibility class II (MHC-II) antigens and which has been modified to comprise and express (i) a nucleotide sequence encoding an immunomodulator and (ii) a nucleotide sequence encoding a viral antigen, and a method of inducing or stimulating an immune response in a human to a viral-associated disease or cancer comprising administering to the human (i) the aforementioned human cell line in an amount sufficient to induce or stimulate an immune response to the viral associated disease or cancer, (ii) a human cell line, which lacks MHC-I and MHC-11 antigens and which has been modified to comprise and express a nucleotide sequence encoding an immunomodulator, and a human cell line, which lacks MHC-I and MHC-II antigens and which has been modified to comprise and express a nucleotide sequence encoding an antigen of EBV, simultaneously or sequentially in either order, by the same or different routes, in amounts sufficient to induce or stimulate an immune response to the viral-associated disease or cancer, or (iii) an immunomodulator and a human cell line, which lacks MHC-I and MHC-II antigens and which has been modified to comprise and express a nucleotide sequence encoding an antigen of EBV, simultaneously or sequentially in either order, by the same or different routes, in amounts sufficient to induce or stimulate an immune response to the viral associated disease or cancer.
1. An isolated human cell line K562, which lacks major histocompatibility class I (MHC-I) antigens and major histocompatibility class II (MHC-II) antigens and which has been modified to comprise and express (i) a gene encoding an immunomodulator selected from the group consisting of macrophage colony factor (M-CSF), granulocyte colony stimulating factor (G-CSF), granulacyte-macrophage colony stimulating factor (GM-CSF) and (ii) a gene encoding an antigen of Epstein-Barr virus (EBV).
2. The human cell line of claim 1 , wherein the antigen of EBV is Epstein-Barr nuclear antigen-1 (EBNA1), latent membrane protein 1 (LMP1), or latent membrane protein 2 (LMP2).
3. The human cell line of claim 1 , wherein the immunomodulator is GM-CSF and the antigen of EBV is LMP2.
4. A composition comprising the isolated human cell line K562 of claim 1 and a pharmaceutical accepted carrier or diluent.
5. A method of inducing or stimulating an immune response in a human to an EBV-associated cancer, which method comprises administering to the human the human cell line of claim 1 in an amount sufficient to induce or stimulate an immune response to the EBV-associated cancer, whereupon an immune response to the EBV-associated cancer is induced or stimulated.
6. The method of claim 5 , wherein the human has or is at risk for Hodgkin's lymphoma.
7. The method of claim 5 , wherein the human has or is at risk for nasopharyngeal carcinoma.
8. The method of claim 5 , wherein the human has or is at risk for gastric carcinoma, Burkitt's lymphoma, T-cell lymphoma, B-cell lymphoma, parotid carcinoma, breast carcinoma, and leiomyosarcoma.
9. The method of claim 5 , which further comprises quantifying the human's immune response to the antigen of EBV encoded by the human cell line before and after administration of the human cell line to the human and comparing the immune responses before and after administration, whereupon the immune response of the human to the antigen of EBV is characterized.
10. The method of claim 9 , which further comprises adjusting the amount of the human cell line administered to the human and/or the frequency of administration of the human cell line as necessary in view of the human's immune response to the antigen of EBV, whereupon the treatment of the human is adjusted.
11. A method of inducing or stimulating an immune response in a human to an EBV-associated cancer, which method comprises administering to the human the human cell line of claim 3 in an amount sufficient to induce or stimulate an immune response to the EBV-associated cancer, whereupon an immune response to the EBV-associated cancer is induced or stimulated.
12. The method of claim 11 , wherein the human has or is at risk for Hodgkin's lymphoma.
13. The method of claim 11 , wherein the human has or is at risk for nasopharyngeal carcinoma.
14. The method of claim 11 , wherein the human has or is at risk for gastric carcinoma, Burkitt's lymphoma, T-cell lymphoma, B-cell lymphoma, parotid carcinoma, breast carcinoma, and leiomyosarcoma.
15. A method of inducing or stimulating an immune response in a human to an EBV-associated cancer, which method comprises administering to the human the composition of claim 14 in an amount sufficient to induce or stimulate an immune response to the EBV-associated cancer, whereupon an immune response to the EBV-associated cancer is induced or stimulated.
16. The method of claim 15 , wherein the human has or is at risk for Hodgkin's lymphoma.
17. The method of claim 15 , wherein the human has or is at risk for nasopharyngeal carcinoma.
18. The method of claim 15 , wherein the human has or is at risk for gastric carcinoma, Burkitt's lymphoma, T-cell lymphoma, B-cell lymphoma, parotid carcinoma, breast carcinoma, and leiomyosarcoma.