IP Library › Granted Patent US 12,252,543
Granted Patent B2
US 12,252,543 · App. 16/173,150 · Granted Mar 18, 2025

Multispecific NK engager protein

Inventors: Laurent Gauthier (Marseilles, FR); Nadia Anceriz (Aubagne, FR); Ariane Morel (Marseilles, FR); Benjamin Rossi (Marseilles, FR)
Assignee: INNATE PHARMA
C07K16/2896A61K39/4613A61K39/464412C07K16/2803C07K16/2809C07K16/283C07K16/2866C07K16/2887A61K2239/48C07K2317/31C07K2317/522C07K2317/524C07K2317/526C07K2317/565C07K2317/622C07K2317/71C07K2317/732C07K2317/75C07K2317/92C07K2319/30
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,252,543
App. No.
16/173,150
Granted
Mar 18, 2025
Kind
B2
Abstract

Multispecific proteins that bind and specifically redirect NK cells to lyse a target cell of interest are provided without non-specific activation of NK cells in absence of target cells. The proteins have utility in the treatment of disease, notably cancer or infectious disease.

Claims (154)

1. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein comprising:

(a) a first antigen binding domain (ABD) which:

(i) monovalently binds to a human NKp46 polypeptide having the amino acid sequence of SEQ ID NO: 1; and

(ii) comprises a first immunoglobulin heavy chain variable region (VH1) and a first immunoglobulin light chain variable region (VL1);

(b) a second ABD which:

(i) binds to a first antigen of interest other than an internalizing cytokine receptor alpha chain or B-cell maturation antigen (BCMA); and

(ii) comprises a second immunoglobulin heavy chain variable region (VH2) and a second immunoglobulin light chain variable region (VL2); and

(c) a dimeric human Fc polypeptide capable of binding to CD16A,

or a vector or vectors containing the nucleic acid or nucleic acids.

2. An isolated cell which comprises a nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein according to claim 1 .

3. A method of producing a multispecific antigen binding protein comprising culturing an isolated cell according to claim 2 .

4. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the first antigen of interest is expressed by a solid tumor.

5. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the first antigen of interest is expressed by a hematological cancer.

6. A nucleic acid or nucleic acids encoding a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the antigen of interest is expressed by an infectious agent.

7. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein:

(i) the dimeric human Fc polypeptide is modified to enhance CD16A binding relative to the corresponding wild-type Fc polypeptide;

(ii) the dimeric human Fc polypeptide is capable of binding to human neonatal Fc receptor (FcRn);

(iii) the multispecific protein binds to the first antigen of interest monovalently;

(iv) the multispecific antigen binding protein mediates lysis of target cells by a combination of NKp46 signaling and CD16A-mediated antibody-dependent cell-mediated cytotoxicity (ADCC);

(v) the multispecific antigen binding protein mediates NKp46-signaling-mediated lysis and CD16-mediated lysis resulting in a synergistic enhancement in the lysis of target cells;

(vi) the multispecific antigen binding protein mediates lysis of target cells by a combination of NKp46-signaling, CD137-signaling and CD16A-mediated ADCC;

(vii) the second ABD comprises a monovalent or bivalent antibody or antibody fragment comprising the VH2 and the VL2;

(viii) (ix) the spacing between the first ABD and the second ABD is less than 80 angstroms;

(ix) the spacing between the first ABD and the second ABD is about 55 angstroms;

(x) the multispecific antigen binding protein is a heterodimeric, or heterotrimeric protein;

(xi) the multispecific antigen binding protein comprises at least one polypeptide chain that comprises an ABD bound to the dimeric human Fc polypeptide by a flexible linker;

(xii) the multispecific antigen binding protein comprises at least one polypeptide chain that comprises an ABD bound to the dimeric human Fc polypeptide by a flexible polypeptide linker;

(xiii)

(xiii-1) the multispecific antigen binding protein comprises: a first polypeptide comprising an immunoglobulin heavy chain variable region (VH) and an immunoglobulin light chain variable region (VL) separated by a polypeptide linker; and a second polypeptide comprising a VH and a VL separated by a polypeptide linker;

(xiii-2) the multispecific antigen binding protein comprises:

a first polypeptide comprising the VH1 and the VL1 separated by a polypeptide linker; and a second polypeptide comprising the VH2 and the VL2 separated by a polypeptide linker;

(xiii-3) the multispecific antigen binding protein comprises: a first polypeptide comprising the VH1 and the VL2; and a second polypeptide comprising the VH2 and the VL1;

(xiii-4) the first ABD comprises a Fab comprising the VH1 and the VL1 or comprises the VH1 and the VL1 separated by a linker, optionally by a polypeptide linker;

(xiii-5) the second ABD comprises a Fab comprising the VH2 and the VL2 or comprises the VH2 and VL2 separated by a linker, optionally by a linker comprising a linear or cyclic peptide;

(xiii-6) the first ABD comprises a Fab comprising the VH1 and the VL1 or comprises the VH1 and the VL1 separated by a linker; and the second ABD comprises a Fab comprising the VH2 and the VL2 or comprises the VH2 and the VL2 separated by a linker;

(xiii-7) the first ABD comprises a Fab comprising the VH1 and the VL1; and the second ABD comprises the VH2 and the VL2 separated by a linker; or

(xiii-8) the first ABD comprises the VH1 and the VL1 separated by a linker; and the second ABD comprises a Fab comprising the VH2 and the VL2;

(xiv) the multispecific antigen binding protein further comprises a third ABD which binds to a second antigen of interest, wherein the second antigen of interest is same as or different from the first antigen of interest and is different from said human NKp46 polypeptide;

(xv) the first antigen of interest comprises a cell surface polypeptide which is, when bound by a full-length IgG1 antibody,

(xv-1) capable of undergoing intracellular internalization or

(xv-2) not capable of undergoing intracellular internalization;

(xvi) the multispecific protein does not substantially increase or induce intracellular internalization of the first antigen of interest on target cells;

(xvii) the multispecific antigen binding protein upregulates CD137 expression on NK cells;

(xviii) the multispecific antigen binding protein elicits the expression of CD137 on the surface of NKp46 + CD16 + NK cells; or

(xix) any combination of the foregoing.

8. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the dimeric human Fc polypeptide is capable of binding to human FcRn.

9. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 8 , wherein the dimeric human Fc polypeptide comprises one or more amino acid modifications that increase binding affinity for CD16A.

10. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the multispecific antigen binding protein comprises a first (central) polypeptide chain comprising one variable domain that, together with a complementary variable domain comprised in a second polypeptide chain, forms an antigen binding domain specific for one antigen of interest, and the first (central) polypeptide chain further comprises a second variable domain that is paired with a complementary variable domain to form an antigen binding domain specific for another antigen of interest, wherein the variable domain that is complementary to the second variable domain is comprised in the central polypeptide or in a third polypeptide chain.

11. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the multispecific antigen binding protein is a hetero-multimeric protein comprising at least:

(a) a first polypeptide chain comprising at least:

(a-1) first variable domain (V1);

(a-2) a first human constant domain (C1) fused to the V1; and

(a-3) a first human Fc domain (Fc1);

(b) a second polypeptide chain comprising at least:

(b-1) a second variable domain (V2);

(b-2) a second human constant domain (C2) fused to the V2; and

(b-3) a second human Fc domain (Fc2),

wherein:

(i) the V1 and the V2 are a VH and a VL, respectively, or are a VL and a VH, respectively; and

(ii) the C1 and the C2 are a CH1 domain and a Cκ domain, respectively, or a Cκ domain and a CH1 domain, respectively,

and wherein the first and second polypeptide chains undergo CH1-Cκ dimerization and are bound to one another by disulfide bonds formed between the C1 and the C2, and by non-covalent bonds between the CH3 domain of the Fc1 and the CH3 domain of the Fc2.

12. A nucleic acid or nucleic acids encoding a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the protein is an isolated heterodimeric polypeptide comprising:

(a) a first polypeptide chain comprising, from N- to C-terminus;

(a-1) a second variable domain (V1-2);

(a-2) a third variable domain (V1-3);

(a-3) a Fc domain or portion thereof;

(a-4) a first variable domain (V1-1); and

(a-5) a first CH1 or Cκ constant region; and

(b) a second polypeptide chain comprising, from N- to C-terminus:

(b-1) a first variable domain (V2-1);

(b-2) a second CH1 or Cκ constant region; and

(b-3) an Fc domain or portion thereof,

wherein the second CH1 or Cκ constant region is selected to be complementary to the first CH1 or Cκ constant region, such that the first and second polypeptides form a CH1-Cκ heterodimer in which: the V1-1 and the V2-1 together form an antigen binding domain; and the V1-2 and the V1-3 together form an antigen binding domain.

13. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the protein is an isolated heterodimeric polypeptide comprising:

(a) a first polypeptide chain comprising, from N- to C-terminus:

(a-1) a first variable domain (V1-1);

(a-2) a first constant domain (C1);

(a-3) a first human Fc domain (Fc1);

(a-4) a second variable domain (V1-2); and

(a-5) a third variable domain (V1-3); and

(b) a second polypeptide chain comprising, from N- to C-terminus:

(b-1) a first variable domain (V2-1);

(b-2) a second constant domain (C2); and

(b-3) a second human Fc domain (Fc2),

wherein:

(i) the C1 and the C2 are a CH1 domain and a Cκ domain, respectively, or a Cκ domain and a CH1 domain, respectively;

(ii) the first and second polypeptide chains form a CH1-Cκ heterodimer;

(iii) the V1-1 and the V2-1 form an ABD; and

(iv) the V1-2 and the V1-3 form an ABD.

14. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the protein is a heterodimer and comprises:

(a) a first polypeptide having a domain arrangement:

V a-1 -(CH1 or CK) a -human Fc domain-V a-2 -V b-2 ,

and

(b) a second polypeptide chain having a domain arrangement:

V b-1 -(CH1 or CK) b -human Fc domain,

wherein one of the V a-1 and the V b-1 is a VL and the other is a VH, one of the V a-2 and the V b-2 is a VL, and the other is a VH;

wherein the (CH1 or CK) b dimerizes with the (CH1 or CK) a , and the V b-1 forms an ABD together with the V a-1 , and wherein the V a-2 and the V b-2 together form an ABD.

15. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 14 , wherein the V a-2 and the V b-2 together form the first ABD.

16. A nucleic acid or nucleic acids encoding a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the protein is a heterodimer and comprises a domain arrangement:

wherein:

(a) one of the V a-1 and the V b-1 is a VH and the other is a VL; and

(b) one of the V a-2 and the V b-2 is a VH and the other is a VL,

such that:

(i) the V a-1 and the V b-1 form an ABD which binds to said human NKp46 polypeptide, and the V a-2 and the V b-2 form an ABD which binds to an antigen of interest; or

(ii) the V a-1 and the V b-1 form an ABD which binds to an antigen of interest, and the V a-2 and the V b-2 form an ABD which binds to said human NKp46 polypeptide.

17. A nucleic acid or nucleic acids encoding a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the protein is a heterotrimer comprising a domain arrangement:

wherein: (a) one of the V a-1 and the V b-1 is a VH and the other is a VL such that the V a-1 and the V b-1 form an ABD; and

(b) one of the V a-2 and the V b-2 is a VH and the other is a VL such that the V a-2 and the V b-2 form an ABD,

wherein the chain 1 and the chain 2 associate by CH3-CH3 dimerization and the chain 1 and the chain 3 associate by CH1-C K dimerization.

18. A nucleic acid or nucleic acids encoding a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 17 , wherein the chain 2 comprises a domain arrangement:

V b-2 -V a-2 -(C K or CH1)-(hinge or linker)-CH2-CH3.

19. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the multispecific antigen binding protein comprises a polypeptide comprising:

(a) a CH1 or C K domain;

(b) a hinge domain; and

(c) a CH2 or Fc domain,

where in the CH1 or C K domain is separated from the CH2 or Fc domain by the hinge domain, optionally wherein the hinge domain:

(i) comprises a cysteine residue capable of forming an interchain disulfide bond;

(ii) is modified to delete or substitute a cysteine residue; or

(iii) is derived from an IgM isotype antibody.

20. A nucleic acid or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the first ABD binds to the D2 domain of said human NKp46 polypeptide.

21. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein:

(a) the VH1 comprises HCDR1, 2, and 3; and

(b) the VL1 comprises LCDR1, 2, and 3,

and wherein:

(i) the amino acid sequences of the HCDR1, 2, and 3 are respectively identical to those of the heavy chain variable region of SEQ ID NO: 3, and the amino acid sequences of the LCDR1, 2, and 3 are respectively identical to those of the light chain variable region of SEQ ID NO: 4;

(ii) the amino acid sequences of the HCDR1, 2, and 3 are respectively identical to those of the heavy chain variable region of SEQ ID NO: 5, and the amino acid sequences of the LCDR1, 2, and 3 are respectively identical to those of the light chain variable region of SEQ ID NO: 6;

(iii) the amino acid sequences of the HCDR1, 2, and 3 are respectively identical to those of the heavy chain variable region of SEQ ID NO: 7, and the amino acid sequences of the LCDR1, 2, and 3 are respectively identical to those of the light chain variable region of SEQ ID NO: 8;

(iv) the amino acid sequences of the HCDR1, 2, and 3 are respectively identical to those of the heavy chain variable region of SEQ ID NO: 9, and the amino acid sequences of the LCDR1, 2, and 3 are respectively identical to those of the light chain variable region of SEQ ID NO: 10;

(v) the amino acid sequences of the HCDR1, 2, and 3 are respectively identical to those of the heavy chain variable region of SEQ ID NO: 11, and the amino acid sequences of the LCDR1, 2, and 3 are respectively identical to those of the light chain variable region of SEQ ID NO: 12; or

(vi) the amino acid sequences of the HCDR1, 2, and 3 are respectively identical to those of the heavy chain variable region of SEQ ID NO: 13, and the amino acid sequences of the LCDR1, 2, and 3 are respectively identical to those of the light chain variable region of SEQ ID NO: 14.

22. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein:

(i) at least one of the ABDs comprises framework residues from a human framework region and/or is humanized;

(ii) the first antigen of interest is a cell surface polypeptide capable of undergoing intracellular internalization when bound by a full-length IgG1 antibody; and/or

(iii) the multispecific antigen binding protein does not substantially increase or induce intracellular internalization of the first antigen of interest on target cells.

23. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 1 , wherein the multispecific antigen binding protein is an isolated heterodimeric polypeptide comprising Format 13 as shown in FIG. 2 D .

24. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids according to claim 14 , wherein: (i) the VH1 comprises the HCDR1, 2, and 3 amino acid sequences according to Kabat of SEQ ID NOS: 15, 18 and 21, respectively; and (ii) the VL1 comprises the LCDR1, 2, and 3 amino acid sequences according to Kabat of SEQ ID NOS: 24, 27 and 28, respectively.

25. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein or a vector or vectors containing the nucleic acid or nucleic acids, wherein the multispecific antigen binding protein comprises:

(a) a first antigen binding domain (ABD) which:

(i) binds to a human NKp46 polypeptide having the amino acid sequence of SEQ ID NO: 1; and

(ii) comprises a first immunoglobulin heavy chain variable region (VH1) comprising HCDR1, 2, and 3 and a first immunoglobulin light chain variable region (VL1) comprising LCDR1, 2, and 3;

(b) a second ABD which binds to a first antigen of interest other than an internalizing cytokine receptor alpha chain or B-cell maturation antigen (BCMA),

or a vector or vectors containing the nucleic acid or nucleic acids, wherein:

(i) the amino acid sequences of the HCDR1, 2, and 3 are respectively identical to those of the heavy chain variable region of SEQ ID NO: 3, and the amino acid sequences of the LCDR1, 2, and 3 are respectively identical to those of the light chain variable region of SEQ ID NO: 4;

(ii) the amino acid sequences of the HCDR1, 2, and 3 are respectively identical to those of the heavy chain variable region of SEQ ID NO: 5, and the amino acid sequences of the LCDR1, 2, and 3 are respectively identical to those of the light chain variable region of SEQ ID NO: 6;

(iii) the amino acid sequences of the HCDR1, 2, and 3 are respectively identical to those of the heavy chain variable region of SEQ ID NO: 7, and the amino acid sequences of the LCDR1, 2, and 3 are respectively identical to those of the light chain variable region of SEQ ID NO: 8;

(iv) the amino acid sequences of the HCDR1, 2, and 3 are respectively identical to those of the heavy chain variable region of SEQ ID NO: 9, and the amino acid sequences of the LCDR1, 2, and 3 are respectively identical to those of the light chain variable region of SEQ ID NO: 10;

(v) the amino acid sequences of the HCDR1, 2, and 3 are respectively identical to those of the heavy chain variable region of SEQ ID NO: 11, and the amino acid sequences of the LCDR1, 2, and 3 are respectively identical to those of the light chain variable region of SEQ ID NO: 12; or

(vi) the amino acid sequences of the HCDR1, 2, and 3 are respectively identical to those of the heavy chain variable region of SEQ ID NO: 13, and the amino acid sequences of the LCDR1, 2, and 3 are respectively identical to those of the light chain variable region of SEQ ID NO: 14.

26. A nucleic acid which encodes or nucleic acids which separately or in combination encode a multispecific antigen binding protein according to claim 25 , wherein the multispecific antigen binding protein further comprises a dimeric Fc polypeptide capable of binding to CD16A, optionally wherein:

(i) the dimeric Fc polypeptide is a dimeric human Fc polypeptide, optionally comprising one or more amino acid modifications that increase binding affinity for CD16A relative to the corresponding wild-type Fc polypeptide;

(ii) the first antigen of interest is expressed by a cancer cell, optionally by a hematological cancer or a solid tumor;

(iii) the multispecific antigen binding protein binds to said human NKp46 polypeptide monovalently;

(iv) the multispecific antigen binding protein binds to the first antigen of interest monovalently or bivalently; and/or

(v) the dimeric Fc polypeptide is capable of binding to human FcRn.

Continuity (4)
Division 15190337 · Jun 23, 2016
Continuation In Part PCTEP2015064063 · Jun 23, 2015
Provisional Application 62271459 · Dec 28, 2015
Related Publication 20190055315A1 · Feb 21, 2019
References Cited (133)
US 5229275A · Goroff · 1993 [cited by applicant]
US 5565332A · Hoogenboom et al. · 1996 [cited by applicant]
US 5567610A · Borrebaeck et al. · 1996 [cited by applicant]
US 5573905A · Lerner et al. · 1996 [cited by applicant]
US 6162963A · Kucherlapati et al. · 2000 [cited by applicant]
US 6737056B1 · Presta · 2004 [cited by applicant]
US 6821505B2 · Ward · 2004 [cited by applicant]
US 7122637B2 · Presta · 2006 [cited by applicant]
US 7183387B1 · Presta · 2007 [cited by applicant]
US 7332581B2 · Presta · 2008 [cited by applicant]
US 7355742B2 · Presta · 2008 [cited by applicant]
US 7355008B2 · Stavenhagen et al. · 2008 [cited by applicant]
US 7371826B2 · Presta · 2008 [cited by applicant]
US 7416727B2 · Presta · 2008 [cited by applicant]
US 7425619B2 · Koenig et al. · 2008 [cited by applicant]
US 7521542B2 · Johnson et al. · 2009 [cited by applicant]
US 7632497B2 · Stavenhagen · 2009 [cited by applicant]
US 7825085B2 · Mandelboim · 2010 [cited by examiner]
US 9539251B2 · Sampath · 2017 [cited by examiner]
US 10113003B2 · Gauthier · 2018 [cited by examiner]
US 10519234B2 · Gauthier · 2019 [cited by examiner]
US 11001629B2 · Gauthier · 2021 [cited by examiner]
US 11267897B2 · Gauthier · 2022 [cited by examiner]
US 20020161201A1 · Filpula et al. · 2002 [cited by applicant]
US 20040242851A1 · Zhu · 2004 [cited by applicant]
US 20050136050A1 · Kufer et al. · 2005 [cited by applicant]
US 20050238646A1 · Ledbetter et al. · 2005 [cited by applicant]
US 20060074225A1 · Chamberlain et al. · 2006 [cited by applicant]
US 20060275254A1 · Kim et al. · 2006 [cited by applicant]
US 20090155275A1 · Wu et al. · 2009 [cited by applicant]
US 20100316645A1 · Imhof-Jung et al. · 2010 [cited by applicant]
US 20120201746A1 · Liu et al. · 2012 [cited by applicant]
EP 1176195 · 2002 [cited by applicant]
WO WO1992011018 · 1992 [cited by applicant]
WO WO1999954342 · 1999 [cited by applicant]
WO WO2000042072 · 2000 [cited by applicant]
WO WO2003035835 · 2003 [cited by applicant]
WO WO2004063351 · 2004 [cited by applicant]
WO WO2004099249 · 2004 [cited by applicant]
WO 2005000086 · 2005 [cited by applicant]
WO WO2005040219 · 2005 [cited by applicant]
WO WO2005047327 · 2005 [cited by applicant]
WO 2005061547 · 2005 [cited by applicant]
WO 2005105858 · 2005 [cited by applicant]
WO WO2005110474 · 2005 [cited by applicant]
WO WO2005115452 · 2005 [cited by applicant]
WO WO2006031994 · 2006 [cited by applicant]
WO WO2006053301 · 2006 [cited by applicant]
WO WO2006064136 · 2006 [cited by applicant]
WO WO2006088494 · 2006 [cited by applicant]
WO WO2006133148 · 2006 [cited by applicant]
WO WO2007021841 · 2007 [cited by applicant]
WO WO2007024249 · 2007 [cited by applicant]
WO WO2007073499 · 2007 [cited by applicant]
WO WO2007106707 · 2007 [cited by applicant]
WO WO2008002933 · 2008 [cited by applicant]
WO WO2008105886 · 2008 [cited by applicant]
WO WO2008119353 · 2008 [cited by applicant]
WO WO2009089004 · 2009 [cited by applicant]
WO WO2010032269 · 2010 [cited by applicant]
WO WO2011063348 · 2011 [cited by applicant]
WO WO2011066501 · 2011 [cited by applicant]
WO WO2011069104 · 2011 [cited by applicant]
WO WO2011109400 · 2011 [cited by applicant]
WO WO2011131746 · 2011 [cited by applicant]
WO WO2011133886 · 2011 [cited by applicant]
WO WO2012089814 · 2012 [cited by applicant]
WO WO2014044686 · 2014 [cited by applicant]
WO 2015197593 · 2015 [cited by applicant]
WO 2015197598 · 2015 [cited by applicant]
WO 2016207273 · 2016 [cited by applicant]
WO 2016207278 · 2016 [cited by applicant]
Khan and Salunke (J. Immunol, 2014, 192: 5398-5405) (Year: 2014). [cited by examiner]
Gauthier et al (Cell, Jun. 2019, 177: 1701-1713) (Year: 2019). [cited by examiner]
Germain et al (Prot. Eng. Design Select. 2008, 21(11): 665-672) (Year: 2008). [cited by examiner]
Vyas et al (Trends Molec. Med. Feb. 2014, 20(2): 72-82) (Year: 2014). [cited by examiner]
Testa et al (Biomarker Research, 2014, 2: 4, pp. 1-11) (Year: 2014). [cited by examiner]
Lin et al (Blood, 2008, 12(3): 699-707) (Year: 2008). [cited by examiner]
Baeuerle PA, et al. “Bispecific T-cell engaging antibodies for cancer therapy,” Cancer Res. Jun. 15, 2009;69(12):4941-4. [cited by applicant]
Bolzhauser, Markus: “Immuntherapie der kindlichen ALL: Einfluss eines bispezifischen CD19*NKp46-Antikörpers auf die zytotoxische Aktivität von NK-Zellen gegenüber CD19 + ALL-Blasten pädiatrischer Patienten”, Inaugural-D… [cited by applicant]
Chames P, et al. “Bispecific antibodies for cancer therapy: the light at the end of the tunnel?” MAbs. Nov.-Dec. 2009;1(6):539-47. [cited by applicant]
Germain C, et al. “Redirecting NK cells mediated tumor cell lysis by a new recombinant bifunctional protein,” Protein Eng Des Sel. Nov. 2008;21(11):665-72. [cited by applicant]
Hollander, Nurit. “Bispecific antibodies for cancer therapy,” Immunotherapy. Mar. 2009;1(2):211-22. [cited by applicant]
Jackman J, et al. “Development of a two-part strategy to identify a therapeutic human bispecific antibody that inhibits IgE receptor signaling,” J Biol Chem. Jul. 2, 2010;285(27):20850-9. [cited by applicant]
Kellner C, et al. “Heterodimeric bispecific antibody-derivatives against CD19 and CD16 induce effective antibody-dependent cellular cytotoxicity against B-lymphoid tumor cells,” Cancer Lett. Apr. 28, 2011;303(2):128-39. [cited by applicant]
Kufer P, et al. “A revival of bispecific antibodies,” Trends Biotechnol. May 2004;22(5):238-44. [cited by applicant]
Low SC, et al. “Inhibitors of the FcRn:IgG protein-protein interaction,” AAPS J. Sep. 2009;11(3):432-4. [cited by applicant]
Müller KM, et al. “The first constant domain (C(H)1 and C(L)) of an antibody used as heterodimerization domain for bispecific miniantibodies,” FEBS Lett. Jan. 30, 1998;422(2):259-64. [cited by applicant]
Rozan C, et al. “Single-domain antibody-based and linker-free bispecific antibodies targeting FcγRIII induce potent antitumor activity without recruiting regulatory T cells,” Mol Cancer Ther. Aug. 2013;12(8):1481-91. [cited by applicant]
Communication from the International Searching Authority received in PCT/EP2016/064537 dated Sep. 7, 2016. [cited by applicant]
Torres and Casadevall, “The immunoglobulin constant region contributes to affinity and specificity,” Trends Immunol. Feb. 2008;29(2):91-7. [cited by applicant]
Weiner GJ. “Rituximab: mechanism of action,” Semin Hematol. Apr. 2010;47(2):115-23. [cited by applicant]
Vyas M, et al. “Natural ligands and antibody-based fusion proteins: harnessing the immune system against cancer,” Trends Mol Med. Feb. 2014;20(2):72-82. [cited by applicant]
Weidle UH, et al. “The intriguing options of multispecific antibody formats for treatment of cancer,” Cancer Genomics Proteomics. Jan.-Feb. 2013;10(1):1-18. [cited by applicant]
Kim HR, et al. “Anti-cancer activity and mechanistic features of a NK cell activating molecule,” Cancer Immunol Immunother. Oct. 2009;58(10):1691-700. [cited by applicant]
Holmes TD, et al. “A human NK cell activation/inhibition threshold allows small changes in the target cell surface phenotype to dramatically alter susceptibility to NK cells,” J Immunol. Feb. 1, 2011;186(3):1538-45. [cited by applicant]
Altschul SF, et al., “Basic local alignment search tool,” J Mol Biol. Oct. 5, 1990;215(3):403-10. [cited by applicant]
Armour KL, et al., “Recombinant human lgG molecules lacking Fcγ receptor I binding and monocyte triggering activities,” Eur J immunol. Aug. 1999;29(8):2613-24. [cited by applicant]
Barb AW, et al. “NMR analysis demonstrates immunoglobulin G N-glycans are accessible and dynamic,” Nat Chem Biol. Mar. 2011;7(3):147-53. [cited by applicant]
Brando C, et al., “Receptors and lytic mediators regulating anti-tumor activity by the leukemic killer T cell line TALL-104,” J Leukocyte Biol. Aug. 2005;78(2):359-71. [cited by applicant]
Chothia c, et al., “Canonical structures for the hypervariable regions of immunoglobulins.” J. Mol Biol. Aug. 20, 1987, 196(4):901-17. [cited by applicant]
Chung S., et al. “Quantitative evaluation of fucose reducing effects in a humanized antibody on Fcγ receptor binding and antibody-dependent cell-mediated cytotoxicity activities,” MAbs. May-Jun. 2012;4(3):326-40. [cited by applicant]
Devereux J, et al., A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. Jan. 11, 1984;12(1 Pt 1):387-95. [cited by applicant]
El-Sherbiny YM, et al., “The requirement for DNAM-1, NKG2D, and NKp46 in the natural killer cell-mediated killing of myeloma cells,” Cancer Res. Sep. 15, 2007;67(18):8444-9. [cited by applicant]
Feige et al. (Molecular Cell, 34:569-579, 2009). [cited by applicant]
Gebauer M, et al., “Engineered protein scaffolds as next-generation antibody therapeutics,” Curr Opin Chem Biol, Jun. 2009;13(3):245-55. Epub Jun. 6, 2009. [cited by applicant]
Griffiths AD, et al., “Human anti-self antibodies with high specificity from phage display libraries,” EMBO J. Feb. 1993;12(2):725-34. [cited by applicant]
Holliger et al., “Engineered antibody fragments and the rise of single domains,” Nat Biotechnol. Sep. 2005;23(9);1126-36. [cited by applicant]
Idusogie EE, et al., “Mapping of the C1q binding site on rituxan, a chimeric antibody with a human IgG1 Fc,” J Immunol. Apr. 15, 2000;164(8):4178-84. [cited by applicant]
Ill CR, et al., “Design and construction of hybrid immunoglobulin domain with properties of both heavy and light chain variable regions,” Protein Eng. Aug. 1997;10(8):949-57. [cited by applicant]
Jakobovitz A, et al., “Germ-line transmission and expression of a human-derived yeast artificial chromosome,” Nature. Mar. 18, 1993;362(6417):255-8. [cited by applicant]
Jaron-Mendelson M, et al., “Dimerization of NKp46 receptor is essential for NKp46-mediated lysis: characterization of the dimerization site by epitope mapping,” J Immunol. Jun. 15, 2012;188(12):6165-74. [cited by applicant]
Jones PT, et al., “Replacing the complementarity-determining regions in a human antibody with those from a mouse,” Nature. May39-Jun. 4, 1986;321(6069):522-525. [cited by applicant]
Kabat EA, et al. “Identical V region amino acid sequences and segments of sequences in antibodies of different specificities. Relative contributions of VH and VL genes, minigenes, and complementarity-determining regions… [cited by applicant]
McCafferty J, et al., “Phage antibodies: filamentous phage displaying antibody variable domains,” Nature. Dec. 1990;348(6301):552-53. [cited by applicant]
McDonagh CF, et al., “Antitumor activity of a novel bispecific antibody that targets the ErbB2/ErbB3 oncogenic unit and inhibits heregulin-induced activation of ErbB3,” Mol. Cancer Ther. Mar. 2012;11(3):582-93. [cited by applicant]
Müller R., “Determination of affinity and specificity of anti-hapten antibodies by competitive radioimmunoassay,” Methods Enzymol. 1983;92:589-601. [cited by applicant]
Nolte EN, et al., “Increased surveillance of cells in mitosis by human NK cells suggests a novel strategy for limiting tumor growth and viral replication,” Blood. Jan. 15, 2007;109(2):670-3. [cited by applicant]
Pessino A, et al., “Molecular cloning of NKp46: a novel member of the immunoglobulin superfamily involved in triggering of natural cytotoxicity,” J Exp Med. Sep. 7, 1998;188(5):953-60. [cited by applicant]
Plückthun, A. “Antibodies from [cited by applicant]
Presta, L. G., et al., Engineering therapeutic antibodies for improved function. (2002): 487-490. [cited by applicant]
Schleinitz N, et al., “Expression of the CD85j (leukocyte Ig-like receptor 1, Ig-like transcript 2) receptor for class I major histocompatibility complex molecules in idiopathic inflammatory myopathies,” Arthritis & Rhe… [cited by applicant]
Shields RL, et al., “High resolution mapping of the binding site on human IgG1 for Fc gamma RI, Fc gamma RII, Fc gamma RIII, and FcRn and design of IgG1 variants with improved binding to the Fc gamma R.” J Biol Chem. Ma… [cited by applicant]
Shields RL, et al., “Lack of fucose on human lgG1 N-linked oligosaccharide improves binding to human FcyRIII and antibody-dependent cellular toxicity,” J Biol Chem. Jul. 26, 2002;277(30):26733-40. Epub May 1, 2002. [cited by applicant]
Sivori S, et al., “NKp46 is the major triggering receptor involved in the natural cytotoxicity of fresh or cultured human NK cells. Correlation between surface density of NKp46 and natural cytotoxicity against autologou… [cited by applicant]
Umaña P, et al., “Engineered glycoforms of an antineuroblastoma IgG1 with optimized antibody-dependent cellular cytotoxic activity,” Nat Biotechnol. Feb. 1999;17(2):176. [cited by applicant]
Verhoeyen et al,. “Reshaping human antibodies: grafting an antilysozyme activity,” Science. Mar. 25, 1988;239(4847):1534-6. [cited by applicant]
Ward ES, et al., “Binding activities of a repertoire of single immunoglobulin variable domains secreted from [cited by applicant]
Winter, C. C., et al., “Natural Killer Cells Protocols (edited by Campbell KS and Colonna M).” (2000): 219-238. [cited by applicant]
Ying T. et al., “Soluble monomeric IgG1 Fc.” J Biol Chem. Jun. 1, 2012;287(23):19399-408. [cited by applicant]
Shields, R L et al. “High resolution mapping of the binding site on human IgG1 for Fc gamma RI, Fc gamma RII, Fc gamma RIII, and FcRn and design of lgG1 variants with improved binding to the Fc gamma R.” The Journal of … [cited by applicant]
Bruhns, Pierre, and Friederike Jönsson. “Mouse and human FcR effector functions.” Immunological reviews vol. 268,1 (2015): 25-51. doi:10.1111/imr.12350. [cited by applicant]
Bryceson, Yenan T et al. “Synergy among receptors on resting NK cells for the activation of natural cytotoxicity and cytokine secretion.” Blood vol. 107,1 (2006): 159-66. doi:10.1182/blood-2005-04-1351. [cited by applicant]