US2024018259A1PendingUtilityA1

Antibody fc variants

Assignee: ROCHE GLYCART AGPriority: Mar 29, 2011Filed: Sep 11, 2023Published: Jan 18, 2024
Est. expiryMar 29, 2031(~4.7 yrs left)· nominal 20-yr term from priority
C07K 16/2896A61P 7/02C07K 2317/734C07K 2317/71C07K 2317/52A61P 3/10A61K 39/395C07K 16/00C07K 16/2854C07K 16/2887C07K 2317/732C07K 2319/30C07K 2317/92Y10S435/81A61P 25/00A61P 29/00A61P 35/00C07K 16/28C07K 2317/56C07K 2317/73
84
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

The invention relates to engineered nolyneptides comprising Fc variants and their uses. More specifically, Fc variants are described exhibiting reduced effector function. These variantg cause a benefit for a patient suffering from a disease which could be treated with an antibody for which it is desirable to reduce the effector function elicited by antibodies.

Claims

exact text as granted — not AI-modified
1 . A polypeptide comprising an Fc variant of a wild-type human IgG Fc region, said Fc variant comprising an amino acid substitution at position Pro329 and at least one further amino acid substitution, wherein the residues are numbered according to the EU index of Kabat, and wherein said polypeptide exhibits a reduced affinity to the human FcγRIDA and/or FcγRIIA and/or FcγRI compared to a polypeptide comprising the wildtype IgG Fc rogion, and wherein the ADCC induced by said polypeptide is reduced to at least 20% of the ADCC induced by the polypeptide comprising a wild-type human IgG Fc region. 
     
     
         2 . The polypeptide according to  claim 1 , wherein Pro329 of a wild-type human Fc region is substituted with glycine or arginine or an amino acid residue large enough to destroy the proline sandwich within the Fe/Fcγreceptor interface. 
     
     
         3 . The polypeptide according to any one of  claim 1  or  2 , wherein said at least one further amino acid substitution is S228P, E233P, L234A, L235A, L235E, N297A, N297D, or P331S. 
     
     
         4 . The polypeptide according to any one of  claims 1 - 3 , wherein said at least one further amino acid substitution is L234A and L235A of the human IgGI Fc region or S228P and 1235E of the human IgG4 Fc region. 
     
     
         5 . The polypeptide according to any one of  claims 1 - 4 , wherein the affinity to at least one further receptor of the group comprising the human receptors FcγI, FcγIIA, and C1q is reduced compared to the polypeptide comprising a wild-type human IgG Fc region. 
     
     
         6 . The polypeptide according to any one of  claims 1 - 5 , wherein the polypeptide comprises a human IgGI or IgG4 Fc region. 
     
     
         7 . The polypeptide according to any one of  claims 1 - 6 , wherein the polypeptide is an antibody or an Fc fusion protein. 
     
     
         8 . The polypeptide according to any one of  claims 1 - 7 , wherein thrombocyte aggregation induced by the polypeptide is reduced compared to the thrombocyte aggregation induced by a polypeptide comprising a wild-type human IgG Fc region. 
     
     
         9 . The polypeptide according to any one of  claims 1 - 8 , wherein CDC induced by the polypeptide is strongly reduced compared to the CDC induced by a polypeptide comprising a wild-type human IgG Fc region. 
     
     
         10 . The polypeptide according to any one of  claims 1 - 9  for use as a medicament. 
     
     
         11 . The polypeptide according to any one of  claims 1 - 10 , wherein the polypeptide is an anti-CD9 antibody, which is characterized in that the polypeptide comprising the wildtype Fc region comprises as heavy chain variable region SEQ ID NO:9 and as variable light chain region SEQ ID NO:8. 
     
     
         12 . The polypeptide according to any one of  claims 1 - 11 , for use in treating a disease wherein it is favorable that an effector function of the polypeptide is strongly reduced compared to the effector function induced by a polypeptide comprising a wild-type human IgG Fc region. 
     
     
         13 . Use of the polypeptide according to any one of  claims 1 - 12  in the manufacture of a medicament for the treatment of a disease, wherein it is favorable that the effector function of the polypeptide comprising an Fc variant of a wild-type human IgG Fc region is strongly reduced compared to the effector function induced by a polypeptide comprising a wild-type human IgG Fc region. 
     
     
         14 . A method of treating an individual having a disease, wherein it is favorable that the effector function of the polypeptide comprising an Fc variant of a wild-type human IgG Fc region is strongly reduced compared to the effector function induced by a polypeptide comprising a wildtype human Fc polypeptide, comprising administering to an individual an effective amount of the polypeptide according to any one of  claims 1 - 12 . 
     
     
         15 . Use of a polypeptide comprising an Fc variant of a wild-type human IgG Fc region, said polypeptide having Pro329 of the human IgG Fc region substituted with glycine, wherein the residues are numbered according to the EU index of Kabat, wherein said polypeptide exhibits a reduced affinity to the human FcγRIIIA and FcγRIA for down-modulation of ADCC to at least 20% of the ADCC induced by the polypeptide comprising the wildtype human IgG Fc region, and/or for down-modulation of ADCP. 
     
     
         16 . Use of a polypeptide according to  claim 15 , wherein the Fc variant comprises at least two further amino acid substitution at L234A and L235A of the human IgGI Fc region or S228P and L235B of the human IgG4 Fc region. 
     
     
         17 . The use according to  claims 15 - 16 , wherein thrombocyte aggregation induced by the polypeptide is reduced compared to the thrombocyte aggregation induced by a polypeptide comprising a wildtype human Fc region, wherein the polypeptide is a platelet activating antibody. 
     
     
         18 . A method of treating an individual having a disease with a polypeptide, said polypeptide having Pro329 of the human IgG Fc region substituted with Gly, wherein the residues are numbered according to the EU index of Kabat, wherein said polypeptide is characterized by a strongly reduced binding to FcγRIIIA and FcγRIIA compared to a polypeptide comprising a wildtype human IgG Fc region, comprising administering to the individual an effective amount of said polypeptide. 
     
     
         19 . The method according to  claim 18 , wherein said polypeptide comprises at least two further amino acid substitution at L234A and L235A of the human IgG1 Fc region or S228P and L235E of the human IgG4 Fc region.

Join the waitlist — get patent alerts

Track US2024018259A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.