Antibodies with engineered CH2 domains, compositions thereof and methods of using the same

US11098107B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11098107-B2
Application numberUS-201716309821-A
CountryUS
Kind codeB2
Filing dateJun 14, 2017
Priority dateJun 15, 2016
Publication dateAug 24, 2021
Grant dateAug 24, 2021

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present disclosure relates to antibodies and antibody conjugates having one or more site-specific mutations in the CH2 domain of the heavy chain. The antibody variants disclosed herein can have improved characteristics (e.g., thermal stability, antibody yields, antibody titers, cell-killing) relative to a parent or wild type antibody, including aglycosylated parent or wild type antibodies. Pharmaceutical compositions, diagnostic compositions and kits comprising the same, as well as methods of using these compositions and kits for therapeutic and diagnostic purposes, are also described.

First claim

Opening claim text (preview).

What is claimed: 1. An antibody of the IgG class with amino acid substitutions in the CH2 domain of the heavy chain comprising: V262E, V264S, and V303R; V262E, V264S, and V305R; V262E, V303R, and V305R; or V262E, V264S, V303R and V305R. 2. The antibody of claim 1 , further comprising an amino acid substitution at position F241 and/or F243 of the CH2 domain. 3. The antibody of claim 1 , wherein the antibody is aglycosylated. 4. The antibody of claim 1 , further comprising one or more non-natural amino acid residues, wherein the one or more non-natural amino acid residues comprises a moiety selected from the group consisting of amino, carboxy, acetyl, hydrazine hydrazido, semicarbazido, sulfanyl, azido, alkynyl, and tetrazine. 5. The antibody of claim 1 , wherein the antibody is a bi-specific antibody. 6. The antibody of claim 1 , that is of the IgG1 subclass. 7. The antibody of claim 1 , that is of the IgG2 subclass. 8. The antibody of claim 1 that is of the IgG4 subclass. 9. The antibody of claim 1 that is in a form selected from the group consisting of Fc, and full-length antibody. 10. The antibody of claim 4 , wherein at least one non-natural amino acid is para-azido phenylalanine or para-azido methyl phenylalanine. 11. The antibody of claim 4 comprising two or more non-natural amino acid residues. 12. The antibody of claim 11 , wherein a second non-natural amino acid residue is para-azido phenylalanine or para-azido methyl phenylalanine. 13. The antibody of claim 11 , wherein at least one non-natural amino acid residue comprises a tetrazine moiety and at least second non-natural amino acid residue comprises an azide moiety. 14. An antibody conjugate comprising the antibody of claim 4 linked to one or more therapeutic moieties or labeling moieties by one or more non-natural amino acid residues. 15. The antibody conjugate of claim 14 , wherein at least one of said therapeutic moieties or labeling moieties is linked to said antibody via a residue of a non-natural amino acid comprising an azide moiety. 16. The antibody conjugate of claim 14 , wherein at least one of said therapeutic moieties or labeling moieties is linked to said antibody via a residue of the non-natural amino acid comprising a tetrazine moiety. 17. The antibody conjugate of claim 14 , wherein at least one of said therapeutic moieties or labeling moieties is linked to said antibody via a residue of the non-natural amino acid comprising an azide moiety and at least one of said therapeutic moieties or labeling moieties is linked to said antibody via a residue of the non-natural amino acid comprising a tetrazine moiety. 18. The antibody conjugate of claim 14 , wherein said antibody is linked to said one or more therapeutic moieties or labeling moieties via one or more linkers. 19. A composition comprising the antibody of claim 1 , wherein said antibody is substantially pure. 20. A composition comprising the antibody of claim 1 wherein said antibody is at least 95% by mass of the total antibody mass of said composition. 21. A kit comprising an antibody of claim 1 , and instructions for use of the antibody. 22. A kit comprising an antibody conjugate of claim 14 , and instructions for use of the antibody. 23. A polynucleotide encoding an antibody of claim 1 . 24. A vector comprising the polynucleotide of claim 23 . 25. A host cell comprising the vector of claim 24 .

Assignees

Inventors

Classifications

  • C07K16/00Primary

    Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies · CPC title

  • C07K16/18Primary

    against material from animals or humans · CPC title

  • characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin · CPC title

  • Antineoplastic agents · CPC title

  • expressing industrially exogenous proteins, e.g. for pharmaceutical use, human insulin, blood factors, immunoglobulins, pseudoparticles · CPC title

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What does patent US11098107B2 cover?
The present disclosure relates to antibodies and antibody conjugates having one or more site-specific mutations in the CH2 domain of the heavy chain. The antibody variants disclosed herein can have improved characteristics (e.g., thermal stability, antibody yields, antibody titers, cell-killing) relative to a parent or wild type antibody, including aglycosylated parent or wild type antibodies. …
Who is the assignee on this patent?
Sutro Biopharma Inc
What technology area does this patent fall under?
Primary CPC classification C07K16/00. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 24 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).