Molecules with extended half-lives, compositions and uses thereof
View Patent ↗The present invention provides molecules, including IgGs, non-IgG immunoglobulins, proteins and non-protein agents, that have increased in vivo half-lives due to the presence of an IgG constant domain, or a portion thereof that binds the FcRn, having one or more amino acid modifications that increase the affinity of the constant domain or fragment for FcRn. Such proteins and molecules with increased half-lives have the advantage that smaller amounts and or less frequent dosing is required in the therapeutic, prophylactic or diagnostic use of such molecules.
1. A nucleic acid comprising a nucleotide sequence encoding a modified IgG constant domain, wherein the modified IgG constant domain comprises a human IgG constant domain in which there are one or more amino acid substitutions relative to the corresponding wild-type human IgG at one or more of amino acid residues 251-256, 285-290, 308-314, 385-389 or 428-436 relative to a wild-type human IgG constant domain, numbered according to the EU numbering index of Kabat, wherein the modified IgG constant domain has a higher affinity for FcRn than the wild-type human IgG constant domain, and wherein the modified IgG constant domain has an increased half-life compared to the half-life of the wild-type human IgG constant domain.
2. A nucleic acid comprising a nucleotide sequence encoding a modified IgG constant domain, wherein the modified IgG constant domain comprises a human IgG constant domain in which there are amino acid substitutions relative to the corresponding wild-type human IgG at amino acid residues 252, 254, and 256, numbered according to the EU numbering index of Kabat, wherein the modified IgG constant domain has a higher affinity for FcRn than the wild-type human IgG constant domain, and wherein the modified IgG constant domain has an increased half-life compared to the half-life of the wild-type human IgG constant domain.
3. A nucleic acid comprising a nucleotide sequence encoding a modified IgG constant domain, wherein the modified IgG constant domain comprises a human IgG constant domain in which there is an amino acid substitution relative to the corresponding wild-type human IgG at amino acid residue 428, numbered according to the EU numbering index of Kabat, wherein the modified IgG constant domain has a higher affinity for FcRn than the wild-type human IgG constant domain, and wherein the modified IgG constant domain has an increased half-life compared to the half-life of the wild-type human IgG constant domain.
4. The nucleic acid of claim 1 , wherein the modified IgG constant domain comprises a human IgG constant domain in which there are one or more amino acid substitutions relative to the corresponding wild-type human IgG at one or more of amino acid residues 252, 254, or 256, numbered according to the EU index of Kabat, and wherein the amino acid substitutions is:
a tyrosine, a phenylalanine, serine, tryptophan or threonine amino acid substitution at amino acid residue 252;
a threonine amino acid substitution at amino acid residue 254; or
a serine, arginine, glutamine, glutamic acid or aspartic acid amino acid substitution at amino residue 256.
5. The nucleic acid of claim 1 , wherein the modified IgG constant domain comprises a human IgG constant domain in which there are one or more amino acid substitutions relative to the corresponding wild-type human IgG at one or more of amino acid residues 433, 434 or 436, numbered according to the EU index of Kabat, and wherein the amino acid substitutions is:
an arginine, serine, isoleucine, proline, or glutamine amino acid substitution at amino acid residue 433;
a histidine, phenylalanine or tyrosine amino acid substitution at amino acid residue 434; or
a histidine, asparagine, arginine, threonine, lysine or methionine amino acid residue 436.
6. The nucleic acid of claim 1 , wherein the modified IgG constant domain comprises a human IgG constant domain in which there are one or more amino acid substitutions relative to the corresponding wild-type human IgG at amino acid residues 433, 434 and 436, numbered according to the EU index of Kabat, and wherein the substitution at amino acid residue 433 is a substitution with a lysine, the substitution at amino acid residue 434 is substitution with a phenylalanine, and the substitution at amino acid residue 436 is a substitution with a histidine.
7. The nucleic acid of claim 2 , wherein the substitution at amino acid residue 252 is a substitution with a tyrosine, the substitution at amino acid residue 254 is a substitution with a threonine, and the substitution at amino acid residue 256 is a substitution with a glutamic acid.
8. The nucleic acid of claim 3 , wherein the substitution at amino acid residue 428 is a substitution with threonine, leucine, phenylalanine or serine.
9. The nucleic acid of claim 1 , wherein the modified human IgG constant domain has a higher affinity for FcRn than the wild-type human IgG constant domain at pH 6.0 than at pH 7.4.
10. The nucleic acid of claim 2 , wherein the modified human IgG constant domain has a higher affinity for FcRn than the wild-type human IgG constant domain at pH 6.0 than at pH 7.4.
11. The nucleic acid of claim 3 , wherein the modified human IgG constant domain has a higher affinity for FcRn than the wild-type human IgG constant domain at pH 6.0 than at pH 7.4.
12. The nucleic acid of claim 1 , wherein the human IgG constant domain is the constant domain of IgG 1 , IgG 2 , IgG 3 or IgG 4 .
13. The nucleic acid of claim 2 , wherein the human IgG constant domain is the constant domain of IgG 1 , IgG 2 , IgG 3 or IgG 4 .
14. The nucleic acid of claim 3 , wherein the human IgG constant domain is the constant domain of IgG 1 , IgG 2 , IgG 3 or IgG 4 .
15. A vector comprising the nucleic acid of claim 1 .
16. A vector comprising the nucleic acid of claim 2 .
17. A vector comprising the nucleic acid of claim 3 .
18. A host cell comprising the nucleic acid of claim 1 .
19. A host cell comprising the nucleic acid of claim 2 .
20. A host cell comprising the nucleic acid of claim 3 .