Construction and characterization of multimeric IL-15-based molecules with CD3 binding domains

US10865230B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10865230-B2
Application numberUS-201715606552-A
CountryUS
Kind codeB2
Filing dateMay 26, 2017
Priority dateMay 27, 2016
Publication dateDec 15, 2020
Grant dateDec 15, 2020

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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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Abstract

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The invention features soluble fusion protein complexes comprising at least two soluble fusion proteins. For example, the first fusion protein is an anti-CD3 antibody covalently linked to an interleukin-15 (IL-15) polypeptide or functional fragment thereof. The second fusion protein comprises a binding domain that recognizes disease antigens, wherein this domain is covalently linked to a soluble interleukin-15 receptor alpha (IL-15Rα) polypeptide or a functional fragment thereof. One or both of the first and second fusion proteins further includes an immunoglobulin Fc domain or a functional fragment thereof, and the IL-15 domain of first fusion protein binds to the soluble IL-15Rα domain of the second fusion protein to form a soluble fusion protein complex. The invention further provides methods for making and using the complexes of the invention.

First claim

Opening claim text (preview).

What is claimed is: 1. An isolated soluble fusion protein complex comprising at least two soluble fusion proteins, wherein the first fusion protein comprises (a) a first binding domain covalently linked to (b) a interleukin-15 (IL-15) polypeptide domain; and the second fusion protein comprises (c) a second binding domain covalently linked to (d) a soluble IL-15 receptor alpha sushi-binding domain (IL-15RαSu) fused to an immunoglobulin Fc domain, wherein the first binding domain comprises an anti-CD3 antibody and the second binding domain comprises a means for binding an antigen on a tumor cell, and wherein the IL-15 domain of the first fusion protein binds to the soluble IL-15RαSu domain of the second fusion protein to form a soluble fusion protein complex, and wherein the first fusion protein comprises the amino acid sequence set forth in SEQ ID NO: 2. 2. The soluble fusion protein complex of claim 1 , wherein the IL-15 polypeptide is an IL-15 variant comprising an N72D mutation (IL-15N72D). 3. The soluble fusion protein complex of claim 1 , wherein the anti-CD3 antibody comprises an immunoglobulin light chain variable domain covalently linked to an immunoglobulin heavy chain variable domain by a polypeptide linker sequence. 4. The soluble fusion protein of claim 1 , wherein the means for binding an antigen on a tumor cell binds an antigen on a tumor cell and comprises an anti-CD20 antibody. 5. The soluble fusion protein complex of claim 4 , wherein the anti-CD20 antibody comprises an immunoglobulin light chain variable domain covalently linked to an immunoglobulin heavy chain variable domain by a polypeptide linker sequence. 6. The soluble fusion protein complex of claim 4 , wherein the second fusion protein comprises the amino acid sequence set forth in SEQ ID NO: 4. 7. A soluble fusion protein complex comprising a first soluble fusion protein complex of claim 1 covalently linked to a second soluble fusion protein complex of claim 1 . 8. The soluble fusion protein complex of claim 7 , wherein the first soluble fusion protein complex is covalently linked to the second soluble fusion protein complex by a disulfide bond linking the Fc domain of the first soluble fusion protein complex to the Fc domain of the second soluble fusion protein complex. 9. A nucleic acid sequence encoding the first fusion protein of claim 1 , wherein said nucleic acid sequence comprises the sequence set forth in SEQ ID NO: 1. 10. The nucleic acid sequence of claim 9 , wherein the nucleic acid sequence further comprises a promoter, translation initiation signal, and leader sequence operably linked to the sequence encoding the fusion protein. 11. The soluble fusion protein complex of claim 1 , wherein a nucleic acid sequence encoding the second fusion protein comprises the sequence set forth in SEQ ID NO: 3. 12. The soluble fusion protein complex claim 11 , wherein the nucleic acid sequence further comprises a promoter, translation initiation signal, and leader sequence operably linked to the sequence encoding the fusion protein. 13. The soluble fusion protein complex of claim 1 , wherein the antigen-specific binding domain recognizes disease antigens. 14. The soluble fusion protein complex of claim 13 , wherein the disease antigens are associated with neoplasia, infectious disease or autoimmune disease. 15. The soluble fusion protein complex of claim 1 , wherein the second binding domain comprises a tumor cell antigen-specific binding domain.

Assignees

Inventors

Classifications

  • Non-immunoglobulin-derived peptide or protein having an immunoglobulin constant or Fc region, or a fragment thereof, attached thereto · CPC title

  • containing a signal sequence · CPC title

  • Single chain antibody (scFv) · CPC title

  • multispecific · CPC title

  • against CD20 · CPC title

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What does patent US10865230B2 cover?
The invention features soluble fusion protein complexes comprising at least two soluble fusion proteins. For example, the first fusion protein is an anti-CD3 antibody covalently linked to an interleukin-15 (IL-15) polypeptide or functional fragment thereof. The second fusion protein comprises a binding domain that recognizes disease antigens, wherein this domain is covalently linked to a solubl…
Who is the assignee on this patent?
Altor Bioscience Corp, Altor Bioscience Llc
What technology area does this patent fall under?
Primary CPC classification C07K14/5443. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 15 2020 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 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).