Multivalent breast cancer vaccine
Compositions and methods for immunization against human breast cancer are disclosed. In one embodiment the multivalent antigenic composition is provided comprising immunogenic polypeptides selected from the group consisting of human α-lactalbumin, αS1 casein, β-casein and κ-casein.
1. A method of preventing or treating breast cancer expressing human α-lactalbumin, human αS1 casein, human β-casein or human κ-casein in a non-lactating human female of a non-child bearing age in whom the genes encoding human α-lactalbumin, human αS1 casein, human β-casein and human κ-casein are not expressed by normal breast tissue, said method comprising administering to said non-lactating human female a multivalent antigenic composition comprising:
(i) human α-lactalbumin or a polypeptide comprising a 15 amino acid fragment thereof;
(ii) human αS1 casein or a polypeptide comprising a 15 amino acid fragment thereof;
(iii) human β-casein or a polypeptide comprising a 15 amino acid fragment thereof; and
(iv) of human κ-casein or a polypeptide comprising a 15 amino acid fragment thereof,
wherein the multivalent antigenic composition is administered in an amount effective to elicit a T-cell-mediated anti-tumor immune response against said breast cancer.
2. The method of claim 1 , wherein the multivalent antigenic composition comprises
human α-lactalbumin.
3. The method of claim 2 , wherein said method further comprises administering chemotherapy and/or radiotherapy to the non-lactating human female.
4. The method of claim 1 , wherein each of said polypeptides present in the composition are linked to one another.
5. The method of claim 1 wherein said multivalent antigenic composition comprises
human α-lactalbumin and
αS1 casein.
6. The method of claim 1 wherein the composition comprises
human α-lactalbumin,
human αS1 casein, human β-casein and human κ-casein.
7. The method of claim 1 wherein one of said polypeptides is covalently linked to an immune-enhancing cytokine selected from the group consisting of granulocyte-macrophage colony stimulating factor, interleukin-2 and interleukin-4.