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Last Updated: April 23, 2024

Claims for Patent: 9,937,250


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Summary for Patent: 9,937,250
Title:Immunogenic tumor associated stromal cell antigen peptides and methods of their use
Abstract: Immunogenic peptides from tumor associated stromal cell antigens, including combinations of such peptides, are disclosed herein. In some examples the peptides are useful for methods of eliciting an immune response. In additional examples the peptides are useful for methods of treating cancer. Methods for decreasing vascularization of a tumor using a Protein Delta Homolog 1 (DLK1) protein or a nucleic acid encoding the protein are also disclosed.
Inventor(s): Storkus; Walter J. (Pittsburgh, PA), Bose; Anamika (Kolkata, IN), Taylor; Jennifer Lynn (McDonald, PA), Zhao; Xi (Pittsburgh, PA), Lowe; Devin B. (Pittsburgh, PA)
Assignee: University of Pittsburgh--Of the Commonwealth System of Higher Education (Pittsburgh, PA)
Application Number:15/133,038
Patent Claims:1. A method for eliciting an immune response to a tumor in a subject, comprising administering to a subject a therapeutically effective amount of a composition comprising a plurality of polypeptides, wherein each polypeptide in the plurality is at most twelve amino acids in length, wherein the plurality of polypeptides comprises: (a) a Protein Delta Homolog 1 (DLK1) polypeptide comprising the amino acid sequence set forth as ILGVLTSLV (SEQ ID NO: 2) (b) a Neuropilin 1 (NRP1) polypeptide comprising the amino acid sequence set forth as GX.sub.4LGMVSGL (SEQ ID NO: 7), wherein X.sub.4 is a leucine (L) or a methionine (M); (c) a Tumor Endothelial Marker 1 (TEM1) polypeptide comprising the amino acid sequence set forth as LLVPTCVFXSV (SEQ ID NO: 9), wherein X.sub.5 is a leucine (L) or a valine (V); (d) an Ephrin Type A receptor 2 (EphA2) polypeptide comprising the amino acid sequence set forth as TLADFDPRV (SEQ ID NO: 10); (e) a Hemogolobin Subunit B (HBB) polypeptide comprising the amino acid sequence set forth as RLLVVYPWX.sub.3 (SEQ ID NO: 4), wherein X.sub.3 is a threonine (T) or a valine (V); and (f) a Regulator of G-Protein Signaling 5 (RGS5) polypeptide comprising the amino acid sequence set forth as LX.sub.6ALPHSCL (SEQ ID NO: 11) wherein X.sub.6 is a leucine (L) or an alanine (A), thereby eliciting the immune response to the tumor in the subject, wherein the tumor expresses DLK1, NRP, TEM1, EphA2, HBB, and RGS5.

2. The method of claim 1, further comprising administering to the subject a therapeutically effective amount of dasatinib, bevacizumab, sunitinib, axitinib, an HSP90 inhibitor, or gemcitabine/fludarabine.

3. The method of claim 1, wherein the immune response decreases growth of the tumor in the subject.

4. The method of claim 1, wherein the immune response decreases vascularization of the tumor.

5. The method of claim 1, wherein the tumor is a melanoma.

6. The method of claim 5, wherein the melanoma is a superficial spreading melanoma, a nodular melanoma, an acral lentiginous melanoma, a lentigo maligna, a clear cell sarcoma, a mucosal melanoma or a uveal melanoma.

7. The method of claim 5, wherein the plurality of polypeptides comprises: (a) a Protein Delta Homolog 1 (DLK1) polypeptide comprising the amino acid sequence set forth as ILGVLTSLV (SEQ ID NO: 2) (b) a Neuropilin 1 (NRP1) polypeptide comprising the amino acid sequence set forth as GX.sub.4LGMVSGL (SEQ ID NO: 7), wherein X.sub.4 is a methionine (M); and (c) a Tumor Endothelial Marker 1 (TEM1) polypeptide comprising the amino acid sequence set forth as LLVPTCVFX.sub.5V (SEQ ID NO: 9), wherein X.sub.5 is a leucine (L); (d) an Ephrin Type A receptor 2 (EphA2) polypeptide comprising the amino acid sequence set forth as TLADFDPRV (SEQ ID NO: 10); (e) a Hemoglobin Subunit B (HBB) polypeptide comprising the amino acid sequence set forth as RLLVVYPWX.sub.3 (SEQ ID NO: 4), wherein X.sub.3 is a threonine (T); and (f) a Regulator of G-Protein Signaling 5 (RGS5) polypeptide comprising the amino acid sequence set forth as aLX.sub.6ALPHSCL (SEQ ID NO: 11) wherein X.sub.6 is an alanine (A).

8. The method of claim 7, further comprising administering to the subject a therapeutically effective amount of dasatinib.

9. The method of claim 1, wherein the tumor is a colorectal cancer.

10. The method of claim 1, wherein the plurality of polypeptides comprises: (a) a Protein Delta Homolog 1 (DLK1) polypeptide comprising the amino acid sequence set forth as ILGVLTSLV (SEQ ID NO: 2); (b) a Neuropilin 1 (NRP1) polypeptide comprising the amino acid sequence set forth as GX.sub.4LGMVSGL (SEQ ID NO: 7), wherein X.sub.4 is a methionine (M); (c) a Tumor Endothelial Marker 1 (TEM1) polypeptide comprising the amino acid sequence set forth as LLVPTCVFX.sub.5V (SEQ ID NO: 9), wherein X.sub.5 is a leucine (L); (d) an Ephrin Type A receptor 2 (EphA2) polypeptide comprising the amino acid sequence set forth as TLADFDPRV (SEQ ID NO: 10); (e) a Hemogolobin Subunit B (HBB) polypeptide comprising the amino acid sequence set forth as RLLVVYPWX.sub.3 (SEQ ID NO: 4), wherein X.sub.3 is a threonine (T); and (f) a Regulator of G-Protein Signaling 5 (RGS5) polypeptide comprising the amino acid sequence set forth as aLX.sub.6ALPHSCL (SEQ ID NO: 11) wherein X.sub.6 is an alanine (A).

11. The method of claim 10, wherein the tumor is a melanoma, and wherein the method further comprises administering to the subject a therapeutically effective amount of dasatinib.

12. The method of claim 1, wherein the tumor is a melanoma, lung cancer or a breast cancer.

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