Chimeric HIV Env proteins comprising CD4 mini-proteins or CD4 mimetics that are capable of inducing neutralizing antibody responses against cryptic Env epitopes
View Patent ↗Env-CD4 complexes and hybrids are disclosed that expose cryptic epitopes that are important in virus neutralization. Methods of diagnosis, treatment and prevention using the polynucleotides and polypeptides are also provided.
1. A polynucleotide encoding a hybrid human immunodeficiency virus (HIV) envelope (Env)-CD4 protein, wherein the hybrid HIV Env-CD4 protein comprises:
(1) an HIV Env polypeptide which comprises a CD4-binding site and a deletion region from which one or more variable (V) regions are deleted; and
(2) a CD4 mini-protein or a CD4-mimetic inserted into the deletion region,
wherein the CD4 mini-protein or CD4-mimetic maintains the structural conformation of a CDR2-like loop; and
wherein the insertion of the CD4 mini-protein or the CD4 mimetic leads to exposure of a cryptic HIV envelope epitope in or near the CD4-binding site or in or near the chemokine receptor-binding site.
2. The polynucleotide of claim 1 , wherein the deletion region comprises a deletion in V1 and/or V2.
3. The polynucleotide of claim 1 , further comprising one or more linker sequences.
4. The polynucleotide of claim 3 , wherein the one or more linker sequences flank the CD4 mini-protein or the CD4 mimetic.
5. The polynucleotide of claim 1 , wherein the CD4 mini-protein comprises an amino acid sequence selected from the group consisting of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3 and SEQ ID NO:4.
6. The polynucleotide of claim 1 , wherein the HIV Env polypeptide comprises gp140.
7. A composition comprising the polynucleotide of claim 1 .
8. The composition of claim 7 , further comprising an adjuvant.
9. An isolated cell comprising the polynucleotide of claim 1 , wherein said polynucleotide sequence is operably linked to control elements compatible with expression in the selected cell.
10. The isolated cell of claim 9 , wherein the cell is selected from the group consisting of a mammalian cell, an insect cell, a bacterial cell, a yeast cell and a plant cell.
11. The isolated cell of claim 9 , wherein the cell is selected from the group consisting of an antigen presenting cell, a lymphoid cell, a primary cell, an immortalized cell and a tumor-derived cell.
12. A vector for use in a mammalian subject, wherein said vector comprises a polynucleotide of claim 1 , and wherein said polynucleotide sequence is operably linked to control elements compatible with expression in the subject.
13. A method of inducing an immune response in a subject comprising, administering to the subject a composition of claim 7 in an amount sufficient to induce an immune response in the subject.
14. A method of inducing an immune response in a subject, comprising introducing a vector of claim 12 into said subject under conditions that are compatible with expression of said polynucleotide in said subject.
15. The method of claim 14 , wherein said vector is a nonviral vector.
16. The method of claim 14 , wherein said vector is delivered using a particulate carrier.
17. The method of claim 16 , wherein said vector is coated on a gold or tungsten particle and said coated particle is delivered to said subject using a gene gun.
18. The method of claim 14 , wherein said vector is encapsulated in a liposome preparation.
19. The method of claim 14 , wherein said vector is a recombinant viral vector.
20. The method of claim 19 , wherein said viral vector is selected from the group consisting of a retroviral vector, an alphaviral vector, an adenoviral vector, an adeno-associated viral vector, a pox viral vector and an avipoxviral vector.
21. The method of claim 14 , wherein said subject is a mammal.
22. The method of claim 21 , wherein said mammal is a human.
23. The polynucleotide of claim 1 wherein the CD4 mini-protein is inserted into the deletion region.
24. The polynucleotide of claim 1 wherein the CD4 mimetic is inserted into the deletion region.