TSLP Binding Proteins

Patent metadata

Field	Value
Publication number	US-2016264658-A1
Application number	US-201615064745-A
Country	US
Kind code	A1
Filing date	Mar 9, 2016
Priority date	Mar 11, 2015
Publication date	Sep 15, 2016
Grant date	—

Abstract

The present disclosure relates to TSLP binding proteins, such as anti-TSLP single variable domains, polynucleotides encoding such TSLP binding proteins, pharmaceutical compositions and kits comprising said TSLP binding proteins and methods of manufacture. The present invention also concerns the use of such TSLP binding proteins in the treatment of diseases associated TSLP signaling, such as asthma.

First claim

1 . A TSLP binding protein that comprises an amino acid sequence selected from the group consisting of:
a. CDR1, CDR2, and CDR3 of SEQ ID NO: 9 or a variant thereof, wherein the CDR variant has between 1 and 3 amino acid modifications; and b. an amino acid sequence at least 90% identical to the sequence of SEQ ID NO: 9;
wherein the TSLP binding protein has an IC50 of less than or equal to 5 nM.

2 . The TSLP binding protein according to claim 1 , wherein in a variant of CDR1, the residue corresponding to residue 28 in SEQ ID NO:9 is Pro, the residue corresponding to residue 30 in SEQ ID NO:9 is Arg, the residue corresponding to residue 31 in SEQ ID NO:9 is Asn, the residue corresponding to residue 32 in SEQ ID NO: 9 is Trp, and the residue corresponding to residue 34 in SEQ ID NO:9 is Asp; in a variant of CDR2, the residue corresponding to residue 50 in SEQ ID NO:9 is Gly, the residue corresponding to residue 53 in SEQ ID NO:9 is His, and the residue corresponding to residue 55 in SEQ ID NO:9 is Gln; and in a variant of CDR3 the residue corresponding to residue 91 in SEQ ID NO:9 is Ile, Leu, Val or Phe, the residue corresponding to residue 92 in SEQ ID NO:9 is Gly or Ala, the residue corresponding to residue 93 in SEQ ID NO:9 is Glu, Phe, Asp or Ser, and the residue corresponding to residue 94 in SEQ ID NO:9 is Asp.

3 . The TSLP binding protein according to claim 2 , wherein in a variant of CDR2, the residue corresponding to residue 46 in SEQ ID NO:9 is Leu.

4 . The TSLP binding protein according to claim 2 , wherein CDR3 consists of the sequence X 1 GlnX 2 X 3 X 4 AspProX 5 Thr, wherein X 1 represents Lys, Trp, Val, Met or Ile, X 2 represents Val, Leu, Ile or Phe, X 3 represents Gly or Ala, X 4 represents Glu, Phe, Asp or Ser, and X 5 represents Val or Thr.

5 . The TSLP binding protein according to claim 2 , wherein the TSLP binding protein exhibits less than or equal to a 5-fold difference in IC50 using human and cynomolgus TSLP, and wherein the residue corresponding to residue 91 in SEQ ID NO:9 is Ile, Leu or Val.

6 . The TSLP binding protein according to claim 5 , wherein CDR3 consists of the sequence X 1 GlnX 2 X 3 X 4 AspProX 5 Thr, wherein X 1 represents Lys, Trp, Val or Met, X 2 represents Val, Leu or Ile, X 3 represents Gly or Ala, X 4 represents Glu, Phe, Asp or Ser, and X 5 represents Val or Thr.

7 . The TSLP binding protein according to claim 1 that comprises CDR1, CDR2, and CDR3 of SEQ ID NO: 9.

8 . The TSLP binding protein according to claim 7 , wherein CDR1 consists of the sequence defined as SEQ ID NO: 1, CDR2 consists of the sequence defined as SEQ ID NO: 4, and CDR3 consists of the sequence defined as SEQ ID NO:7.

9 . The TSLP binding protein according to claim 7 , wherein CDR1 consists of the sequence defined as SEQ ID NO: 1, CDR2 consists of the sequence defined as SEQ ID NO: 5 and CDR3 consists of the sequence defined as SEQ ID NO:7.

10 . The TSLP binding protein according to any preceding claim, wherein the TSLP binding protein binds to full length human TSLP with a dissociation constant (KD) of less than 2 nM.

11 . The TSLP binding protein as according to claim 1 , wherein the TSLP binding protein competes for binding to full-length human TSLP with a single variable domain of SEQ ID NO:9.

12 . The TSLP binding protein according to claim 1 , wherein the TSLP binding protein exhibits no significant binding to IL-7.

13 . The TSLP binding protein according to claim 1 , wherein the TSLP binding protein is a single variable domain.

14 . The TSLP binding protein according to claim 13 , wherein the single variable domain is a Vκ single variable domain.

15 . The TSLP binding protein according to claim 14 , wherein the Vκ single variable domain has a C-terminus ending in RT.

16 . The TSLP binding protein according to claim 14 , wherein the Vκ single variable domain has a C-terminus that does not end in R.

17 . The TSLP binding protein according to claim 14 , wherein the residue corresponding to residue 27 in SEQ ID NO:9 is Arg, the residue corresponding to residue 29 in SEQ ID NO: 9 is Ile, the residue corresponding to residue 89 in SEQ ID NO:9 is Val, and the residue corresponding to residue 96 in SEQ ID NO: 9 is Val.

18 . The TSLP binding protein according to claim 14 , wherein the residue corresponding to residue 49 in SEQ ID NO:9 is Trp.

19 . The TSLP binding protein according to claim 14 , wherein the residue corresponding to residue 36 in SEQ ID NO:9 is Tyr, the residue corresponding to residue 38 in SEQ ID NO:9 is Gln, the residue corresponding to residue 44 in SEQ ID NO:9 is Pro, the residue corresponding to residue 67 in SEQ ID NO:9 is Ser, the residue corresponding to residue 87 in SEQ ID NO:9 is Tyr, the residue corresponding to residue 98 in SEQ ID NO:9 is Phe, and the residue corresponding to residue 100 in SEQ ID NO:9 is Gln.

20 . The TSLP binding protein that consists of the amino acid sequence of SEQ ID NO.9.

21 . An isolated nucleic acid encoding the TSLP binding protein as defined in claim 1 .

22 . An isolated nucleic acid molecule according to claim 21 , wherein the nucleic acid molecule is selected from the group consisting of: SEQ ID NO:10 and SEQ ID NO:11.

23 . A vector comprising the nucleic acid molecule as defined in claim 21 or claim 22 .

24 . A host cell comprising a nucleic acid as defined in claim 21 or 22 or a vector as defined in claim 23 .

25 . A method of producing a TSLP binding protein as defined in claim 1 , the method comprising the steps of: maintaining a host cell as defined in claim 24 under conditions suitable for expression of said nucleic acid or vector, whereby a TSLP binding protein is produced.

26 . A method of treating a disease associated with TSLP signaling in a patient in need thereof comprising administering to the patient a therapeutically effective amount of the TSLP binding protein as claimed in claim 1

27 . The method of treatment according to claim 26 , wherein the patient is human.

28 . The method of treatment according to claim 27 , wherein the disease associated with TSLP signaling is selected from the group consisting of: asthma, idiopathic pulmonary fibrosis, atopic dermatitis, allergic conjunctivitis, allergic rhinitis, Netherton syndrome, eosinophilic esophagitis (EoE), food allergy, allergic diarrhoea, eosinophilic gastroenteritis, allergic bronchopulmonary aspergillosis (ABPA), allergic fungal sinusitis, cancer, rheumatoid arthritis, COPD, systemic sclerosis, keloids, ulcerative colitis, chronic rhinosinusitis (CRS), nasal polyposis, chronic eosinophilic pneumonia, eosinophilic bronchitis, coeliac disease, Churg-Strauss syndrome, eosinophilic myalgia syndrome, hypereosinophilic syndrome, eosinophilic granulomatosis with polyangiitis, and inflammatory bowel disease.

29 . The method of treatment according to claim 28 , wherein the disease associated with TSLP signaling is selected from the group consisting of: asthma, idiopathic pulmonary fibrosis, atopic dermatitis, allergic conjunctivitis, allergic rhinitis, Netherton syndrome, eosinophilic esophagitis (EoE), food allergy, allergic diarrhoea, eosinophilic gastroenteritis, allergic bronchopulmonary aspergillosis (ABPA), allergic fungal sinusitis, cancer, rheumatoid arthritis, COPD, systemic sclerosis, keloids, ulcerative colitis, chronic rhinosinusitis (CRS) and nas

Assignees

• Glaxosmithkline Ip Dev Ltd

Inventors

• Ahmed Farheen
• Bartholomew Michelle Anne
• Della Cristina Pietro
• Dimech Caroline
• Morley Peter
• Shah Rachana Shailesh
• Tilling Paula

Classifications

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P7/00

  Drugs for disorders of the blood or the extracellular fluid · CPC title

• A61P37/08

  Antiallergic agents (antiasthmatic agents A61P11/06; ophthalmic antiallergics A61P27/14) · CPC title

• A61P37/00

  Drugs for immunological or allergic disorders · CPC title

• A61P25/04

  Centrally acting analgesics, e.g. opioids · CPC title