WT1 HLA class II—binding peptides and compositions and methods comprising same
This invention provides WT1 peptides and methods of treating, reducing the incidence of, and inducing immune responses against a WT1-expressing cancer, comprising same.
1. A method of treating a subject with a WT1-expressing cancer, the method comprising administering to said subject a vaccine comprising (a) an isolated WT1 peptide consisting of the amino acid sequence RSDELVRHHNMHQRNMTKL (SEQ ID No: 2) or PGCNKRYFKLSHLQMHSRKHTG (SEQ ID No: 4) and (b) an adjuvant or a carrier, thereby treating a subject with a WT1-expressing cancer.
2. The method of claim 1 , wherein said WT1-expressing cancer is a leukemia, a desmoplastic small round cell tumor, a gastric cancer, a colon cancer, a lung cancer, a breast cancer, a germ cell tumor, an ovarian cancer, a uterine cancer, a thyroid cancer, a liver cancer, a renal cancer, a kaposi's sarcoma, a sarcoma, or a hepatocellular carcinoma.
3. The method of claim 1 , wherein said WT1-expressing cancer is a Wilms' tumor, an acute myelogenous leukemia (AML), a myelodysplastic syndrome (MDS), or a non-small cell lung cancer (NSCLC).
4. The method of claim 1 , said vaccine comprising (a) an antigen-presenting cell and (b) the peptide sequence of SEQ ID NO: 2 or SEQ ID NO: 4.
5. The method of claim 4 , wherein said WT1-expressing cancer is a leukemia, a desmoplastic small round cell tumor, a gastric cancer, a colon cancer, a lung cancer, a breast cancer, a germ cell tumor, an ovarian cancer, a uterine cancer, a thyroid cancer, a liver cancer, a renal cancer, a kaposi's sarcoma, a sarcoma, or a hepatocellular carcinoma.
6. The method of claim 4 , wherein said WT1-expressing cancer is a Wilms' tumor, an acute myelogenous leukemia (AML), a myelodysplastic syndrome (MDS), or a non-small cell lung cancer (NSCLC).
7. The method of claim 1 , wherein said adjuvant is QS21, Freund's incomplete adjuvant, aluminum phosphate, aluminum hydroxide, BCG, alum, a growth factor, a cytokine, a chemokine, an interleukin, Montanide ISA 51, or GM-CSF.
8. The method of claim 1 wherein the vaccine further comprises an antigen presenting cell.
9. A method of reducing an incidence of a WT1-expressing cancer, or its relapse, in a subject, the method comprising administering to said subject a vaccine comprising (a) an isolated WT1 peptide consisting of the amino acid sequence RSDELVRHHNMHQRNMTKL (SEQ ID No: 2) or PGCNKRYFKLSHLQMHSRKHTG (SEQ ID No: 4) and (b) an adjuvant or a carrier, thereby reducing an incidence of a WT1-expressing cancer, or its relapse, in a subject.
10. The method of claim 9 , wherein said WT1-expressing cancer is a leukemia, a desmoplastic small round cell tumor, a gastric cancer, a colon cancer, a lung cancer, a breast cancer, a germ cell tumor, an ovarian cancer, a uterine cancer, a thyroid cancer, a liver cancer, a renal cancer, a kaposi's sarcoma, a sarcoma, or a hepatocellular carcinoma.
11. The method of claim 9 , wherein said WT1-expressing cancer is a Wilms' tumor, an acute myelogenous leukemia (AML), a myelodysplastic syndrome (MDS), or a non-small cell lung cancer (NSCLC).
12. The method of claim 9 , said vaccine comprising (a) an antigen-presenting cell and (b) the peptide sequence of SEQ ID NO: 2 or SEQ ID NO: 4.
13. The method of claim 12 , wherein said WT1-expressing cancer is a leukemia, a desmoplastic small round cell tumor, a gastric cancer, a colon cancer, a lung cancer, a breast cancer, a germ cell tumor, an ovarian cancer, a uterine cancer, a thyroid cancer, a liver cancer, a renal cancer, a kaposi's sarcoma, a sarcoma, or a hepatocellular carcinoma.
14. The method of claim 12 , wherein said WT1-expressing cancer is a Wilms' tumor, an acute myelogenous leukemia (AML), a myelodysplastic syndrome (MDS), or a non-small cell lung cancer (NSCLC).
15. The method of claim 9 , wherein said adjuvant is QS21, Freund's incomplete adjuvant, aluminum phosphate, aluminum hydroxide, BCG, alum, a growth factor, a cytokine, a chemokine, an interleukin, Montanide ISA 51, or GM-CSF.
16. The method of claim 9 wherein the vaccine further comprises an antigen presenting cell.
17. A method of inducing the formation and proliferation of CTL specific for a WT1-expressing cancer, the method comprising administering to said subject a vaccine comprising (a) an isolated WT1 peptide consisting of the amino acid sequence RSDELVRHHNMHQRNMTKL (SEQ ID No: 2) or PGCNKRYFKLSHLQMHSRKHTG (SEQ ID No: 4) and (b) an adjuvant or a carrier, thereby inducing the formation and proliferation of CTL specific for a WT1-expressing cancer.
18. The method of claim 17 , wherein said WT1-expressing cancer is a leukemia, a desmoplastic small round cell tumor, a gastric cancer, a colon cancer, a lung cancer, a breast cancer, a germ cell tumor, an ovarian cancer, a uterine cancer, a thyroid cancer, a liver cancer, a renal cancer, a kaposi's sarcoma, a sarcoma, or a hepatocellular carcinoma.
19. The method of claim 17 , wherein said WT1-expressing cancer is a Wilms' tumor, an acute myelogenous leukemia (AML), a myelodysplastic syndrome (MDS), or a non-small cell lung cancer (NSCLC).
20. The method of claim 17 , wherein said adjuvant is QS21, Freund's incomplete adjuvant, aluminum phosphate, aluminum hydroxide, BCG, alum, a growth factor, a cytokine, a chemokine, an interleukin, Montanide ISA 51, or GM-CSF.
21. The method of claim 17 wherein the vaccine further comprises an antigen presenting cell.