Lipocalin muteins with binding affinity for LAG-3

Patent metadata

Field	Value
Publication number	US-11773147-B2
Application number	US-202117499640-A
Country	US
Kind code	B2
Filing date	Oct 12, 2021
Priority date	Jan 18, 2017
Publication date	Oct 3, 2023
Grant date	Oct 3, 2023

Abstract

The present disclosure provides human tear lipocalin muteins that specifically bind to LAG-3, which can be used in pharmaceutical applications, for example, as anti-cancer agents and/or immune modulators for the treatment or prevention of human diseases such as cancer, infectious diseases, and autoimmune diseases. The present disclosure further shows the human lipocalin muteins can inhibit the binding of LAG-3 to MHC class II on cells overexpressing MHC class II. The present disclosure also concerns methods of making LAG-3 binding lipocalin muteins described herein as well as compositions comprising such lipocalin muteins. The present disclosure further relates to nucleic acid molecules encoding such lipocalin muteins and to methods for generation of such lipocalin muteins and nucleic acid molecules. In addition, the application discloses therapeutic and/or diagnostic uses of these lipocalin muteins as well as compositions comprising one or more of such lipocalin muteins.

First claim

The invention claimed is:

1. A lipocalin mutein that is capable of binding lymphocyte-activation protein 3 (LAG-3), wherein the mutein has at least 85% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 20-28,
wherein the amino acid sequence of the mutein comprises the following amino acid mutations in comparison with the linear polypeptide sequence of mature human tear lipocalin (SEQ ID NO: 1): Ser 14→Pro; Asp 25→Ser; Phe 28→Asp; Lys 52→Arg; Met 55→Val; Ser 58→Asp; Ala 66→Asn; Ala 79→Glu; Ala 86→Asp; Cys 101→Phe; Leu 105→Gly; Lys 108→Thr; Lys 114→Ala; Lys 121→Thr, and
wherein the amino acid sequence of the mutein further comprises at least one of the following mutated amino acid residues in comparison with the linear polypeptide sequence of mature human tear lipocalin (SEQ ID NO: 1): Arg 26→Ser, Asp, Glu, or Ala; Met 31→Leu; Asn 32→Thr; His 84→Tyr or Leu; His 106→Glu, Lys, or Pro; Val 110→Asn; Gly 112→Val or Leu; Val 113→Ala or Leu.

2. The lipocalin mutein of claim 1 , wherein
(i) the mutein is capable of binding LAG-3 with an affinity measured by K d of about 250 nM or lower, about 50 nM or lower, about 3 nM or lower, about 0.1 nM or lower, or about 0.05 nM or lower;
(ii) the mutein binds LAG-3 with an EC 50 value of about 320 nM or lower, about 10 nM or lower, or about 0.2 nM or lower;
(iii) the mutein is cross-reactive with both human LAG-3 and cynomolgus LAG-3; or
(iv) the mutein is capable of interfering with the binding of human LAG-3 to major histocompatibility complex (MHC) class II.

3. The lipocalin mutein of claim 1 , wherein the amino acid sequence of the mutein comprises at least 20 of the following mutated amino acid residues in comparison with the linear polypeptide sequence of mature human tear lipocalin (SEQ ID NO: 1): Ser 14→Pro; Asp 25→Ser; Arg 26→Ser, Asp, Glu, Ala, or Gly; Phe 28→Asp; Met 31→Leu; Asn 32→Met or Thr; Lys 52→Arg; Met 55→Val; Ser 58→Asp; Ala 66→Asn; Ala 79→Glu; His 84→Tyr or Leu; Ala 86→Asp; Cys 101→Phe; Leu 105→Gly; His 106→Gln, Glu, Lys, or Pro; Lys 108→Thr; Val 110→Gly or Asn; Gly 112→Met, Val or Leu; Val 113→Ala or Leu; Lys 114→Ala; Lys 121→Thr.

4. The lipocalin mutein of claim 1 , wherein the amino acid sequence of the mutein comprises one of the following sets of amino acid mutations in comparison with the linear polypeptide sequence of mature human tear lipocalin (SEQ ID NO: 1):
(a) Ser 14→Pro; Asp 25→Ser; Arg 26→Asp; Phe 28→Asp; Asn 32→Thr; Lys 52→Arg; Met 55→Val; Ser 58→Asp; Ala 66→Asn; Ala 79→Glu; His 84→Tyr; Ala 86→Asp; Cys 101→Phe; Leu 105→Gly; Lys 108→Thr; Val 110→Gly; Gly 112→Met; Lys 114→Ala; and Lys 121→Thr;
(b) Ser 14→Pro; Asp 25→Ser; Arg 26→Glu; Phe 28→Asp; Met 31→Leu; Asn 32→Thr; Lys 52→Arg; Met 55→Val; Ser 58→Asp; Ala 66→Asn; Ala 79→Glu; His 84→Tyr; Ala 86→Asp; Cys 101→Phe; Leu 105→Gly; His 106→Gln; Lys 108→Thr; Val 110→Gly; Gly 112→Met; Lys 114→Ala; and Lys 121→Thr;
(c) Ser 14→Pro; Asp 25→Ser; Arg 26→Glu; Phe 28→Asp; Asn 32→Thr; Lys 52→Arg; Met 55→Val; Ser 58→Asp; Ala 66→Asn; Ala 79→Glu; His 84→Tyr; Ala 86→Asp; Cys 101→Phe; Leu 105→Gly; His 106→Glu; Lys 108→Thr; Val 110→Gly; Gly 112→Val; Lys 114→Ala; and Lys 121→Thr;
(d) Ser 14→Pro; Asp 25→Ser; Arg 26→Asp; Phe 28→Asp; Asn 32→Thr; Lys 52→Arg; Met 55→Val; Ser 58→Asp; Ala 66→Asn; Ala 79→Glu; His 84→Tyr; Ala 86→Asp; Cys 101→Phe; Leu 105→Gly; His 106→Gln; Lys 108→Thr; Val 110→Gly; Gly 112→Leu; Lys 114→Ala; and Lys 121→Thr;
(e) Ser 14→Pro; Asp 25→Ser; Arg 26→Ser; Phe 28→Asp; Asn 32→Thr; Lys 52→Arg; Met 55→Val; Ser 58→Asp; Ala 66→Asn; Ala 79→Glu; His 84→Tyr; Ala 86→Asp; Cys 101→Phe; Leu 105→Gly; His 106→Gln; Lys 108→Thr; Val 110→Gly; Gly 112→Met; Lys 114→Ala; and Lys 121→Thr;
(f) Ser 14→Pro; Asp 25→Ser; Arg 26→Ala; Phe 28→Asp; Asn 32→Thr; Lys 52→Arg; Met 55→Val; Ser 58→Asp; Ala 66→Asn; Ala 79→Glu; His 84→Tyr; Ala 86→Asp; Cys 101→Phe; Leu 105→Gly; His 106→Lys; Lys 108→Thr; Val 110→Gly; Gly 112→Met; Lys 114→Ala; and Lys 121→Thr;
(g) Ser 14→Pro; Asp 25→Ser; Phe 28→Asp; Asn 32→Thr; Lys 52→Arg; Met 55→Val; Ser 58→Asp; Ala 66→Asn; Ala 79→Glu; Ala 86→Asp; Cys 101→Phe; Leu 105→Gly; His 106→Gln; Lys 108→Thr; Val 110→Asn; Gly 112→Met; Val 113→Ala; Lys 114→Ala; and Lys 121→Thr;
(h) Ser 14→Pro; Asp 25→Ser; Arg 26→Gly; Phe 28→Asp; Met 31→Leu; Asn 32→Thr; Lys 52→Arg; Met 55→Val; Ser 58→Asp; Ala 66→Asn; Ala 79→Glu; His 84→Tyr; Ala 86→Asp; Cys 101→Phe; Leu 105→Gly; His 106→Pro; Lys 108→Thr; Val 110→Gly; Gly 112→Met; Lys 114→Ala; and Lys 121→Thr; or
(i) Ser 14→Pro; Asp 25→Ser; Arg 26→Asp; Phe 28→Asp; Asn 32→Thr; Lys 52→Arg; Met 55→Val; Ser 58→Asp; Ala 66→Asn; Ala 79→Glu; His 84→Leu; Ala 86→Asp; Cys 101→Phe; Leu 105→Gly; His 106→Gln; Lys 108→Thr; Val 110→Gly; Gly 112→Met; Val 113→Leu; Lys 114→Ala; and Lys 121→Thr.

5. The lipocalin mutein of claim 1 , wherein the amino acid sequence of the mutein comprises cysteine residues at the sequence positions 61 and 153 of the linear polypeptide sequence of mature human tear lipocalin (SEQ ID NO: 1).

6. The lipocalin mutein of claim 1 , wherein the mutein comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 20-28 or a functional fragment thereof.

7. The lipocalin mutein claim 1 , wherein the mutein has at least 90%, at least 95%, at least 97.5% or at least 99% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 20-28.

8. The lipocalin mutein of claim 1 , wherein the mutein is conjugated to a compound selected from the group consisting of an organic molecule, an enzyme label, a radioactive label, a colored label, a fluorescent label, a chromogenic label, a luminescent label, a hapten, digoxigenin, biotin, a cytostatic agent, a toxin, a metal complex, a metal, colloidal gold, and a compound that extends the serum half-life of the mutein.

9. The lipocalin mutein of claim 8 , wherein the compound that extends the serum half-life is selected from the group consisting of a polyalkylene glycol molecule, a polyethylene (PEG) glycol molecule, hydroxyethyl starch, an Fc part of an immunoglobulin, a C H 3 domain of an immunoglobulin, a C H 4 domain of an immunoglobulin, an albumin binding peptide, and an albumin binding protein.

10. The lipocalin mutein of claim 1 , wherein the mutein is fused at its N-terminus and/or its C-terminus to a fusion partner that is an antibody, an antibody fragment, a protein, a protein domain, or a peptide.

11. A nucleic acid molecule comprising a nucleotide sequence encoding the lipocalin mutein of claim 1 .

12. A host cell containing a nucleic acid molecule of claim 11 .

13. A method of producing a lipocalin mutein of claim 1 , wherein the mutein is produced starting from the nucleic acid coding for the mutein or fragment thereof.

14. A method of binding or detecting LAG-3 in a subject, comprising applying one or more lipocalin muteins of claim 1 or one or more compositions comprising such muteins.

15. A method of stimulating an immune response in a subject, comprising applying one or more lipocalin muteins of claim 1 or one or more compositions comprising such muteins.

16. A method of inducing T lymphocyte proliferation in a subject, comprising applying one or more lipocalin muteins of claim 1 or one or more compositions comprising such muteins.

17. A method of interfering with the binding of human LAG-3 to MHC class II in a subject, comprising applying one or more lipocalin muteins of claim 1 or one or more compositions comprising such muteins.

18. A pharmaceutical composition comprising the lipocalin mutein of claim 1 and a pharmaceutically acceptable excipient.

19. An i

Assignees

• Pieris Pharmaceuticals Gmbh

Inventors

• Rothe Christine
• Olwill Shane
• Allersdorfer Andrea
• Eichner Timo
• Bel Aiba Rachida Siham
• Pavlidou Marina

Classifications

• C07K14/47 Primary

  from mammals · CPC title

• G01N33/6872

  Intracellular protein regulatory factors and their receptors, e.g. including ion channels · CPC title

• A61K38/00

  Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title

• C07K2318/20

  Antigen-binding scaffold molecules wherein the scaffold is not an immunoglobulin variable region or antibody mimetics · CPC title

• G01N2333/70503

  Immunoglobulin superfamily, e.g. VCAMs, PECAM, LFA-3 · CPC title