Telomerase reverse transcriptase fusion protein, nucleotides encoding it, and uses thereof
View Patent ↗Polynucleotides encoding telomerase reverse transcriptase (TERT) fusion proteins are provided, the TERT fusion proteins comprising a TERT protein, or functional variant thereof, fused to a substantial portion of the B subunit of heat labile enterotoxin (LTB). TERT variants useful in TERT-LTB fusion proteins of the invention comprise mutations that function to eliminate telomerase catalytic activity. The polynucleotides of the present invention can elicit an immune response in a mammal, which, in preferred embodiments, is stronger than the immune response elicited by a wild-type TERT. TERT expression is commonly associated with the development of human carcinomas. The present invention provides compositions and methods to elicit or enhance immunity to the protein product expressed by the TERT tumor-associated antigen, wherein aberrant TERT expression is associated with a carcinoma or its development. This invention specifically provides adenoviral vector and plasmid constructs carrying polynucleotides encoding TERT fusion proteins and TERT variants and discloses their use in vaccines and pharmaceutical compositions for preventing and treating cancer.
1. An isolated nucleic acid molecule comprising a sequence of nucleotides that encodes a human telomerase reverse transcriptase (hTERT) fusion protein, wherein the hTERT fusion protein comprises a hTERT protein fused to an Escherichia coli heat-labile enterotoxin B-subunit (LTB) peptide, wherein the sequence of nucleotides comprises the sequence of SEQ ID NO:5 or SEQ ID NO:1, and wherein the fusion protein is capable of producing an immune response.
2. A recombinant vector comprising the nucleic acid molecule of claim 1 .
3. The recombinant vector of claim 2 , wherein the vector is a plasmid vector or an adenovirus vector.
4. A host cell comprising the recombinant vector of claim 3 .
5. The vector of claim 3 , wherein the recombinant vector is an adenoviral vector that is selected from the group consisting of: an adenovirus type 5 (Ad5)vector, and an adenovirus type 5 (Ad6) vector.