Interleukin-2 fusion proteins and uses thereof
The present invention generally relates to fusion proteins of immunoglobulins and interleukin-2 (IL-2). In addition, the present invention relates to polynucleotides encoding such fusion proteins, and vectors and host cells comprising such polynucleotides. The invention further relates to methods for producing the fusion proteins of the invention, and to methods of using them in the treatment of disease.
1. A method for selectively activating regulatory T cells in an autoimmune disease, said method comprising: administering to a patient an effective amount of a pharmaceutical composition comprising a fusion protein comprising (i) a human IgG1 immunoglobulin molecule comprising a modification reducing binding affinity of the immunoglobulin molecule to an Fc receptor as compared to a corresponding immunoglobulin molecule without said modification, and (ii) two identical human interleukin-2 (IL-2) molecules to a patient, wherein said immunoglobulin molecule comprises the heavy chain variable region sequence of SEQ ID NO: 9 and the light chain variable region sequence of SEQ ID NO: 11, and wherein said immunoglobulin molecule comprises the amino acid substitutions L234A, L235A and P329G (EU numbering) in the immunoglobulin heavy chains, and wherein the autoimmune disease is selected from the group consisting of type 1 diabetes, systemic lupus erythematosus, ulcerative colitis, Crohn's disease and multiple sclerosis.
2. The method of claim 1 , wherein said immunoglobulin molecule is not capable of specific binding to an antigen.
3. The method of claim 1 , wherein said Fc receptor is a human Fcγ receptor.
4. The method of claim 1 , wherein said IL-2 molecules comprise the sequence of SEQ ID NO: 1 or SEQ ID NO: 3.
5. The method of claim 1 , wherein said IL-2 molecules comprise the sequence of SEQ ID NO: 3.
6. The method of claim 1 , wherein said IL-2 molecules are each fused at their N-terminal amino acid to the C-terminal amino acid of one of the immunoglobulin heavy chains of said immunoglobulin molecule.
7. The method of claim 6 , wherein said IL-2 molecules are each fused at their N-terminal amino acid to the C-terminal amino acid of one of the immunoglobulin heavy chains of said immunoglobulin molecule through a peptide linker.
8. The method of claim 1 , wherein said fusion protein is administered at a concentration of about 1 ng/mL or less, particularly about 0.1 ng/mL or less.
9. The method of claim 1 , wherein said fusion protein is administered at a dose of about 20 μg/kg body weight or less.
10. The method of claim 9 , wherein said dose is less than or equal to about 12 μg/kg body weight.