IP Library Granted Patent US 11,926,651
Granted Patent B2
US 11,926,651 · App. 16/335,022 · Granted Mar 12, 2024

Polypeptide construct comprising fragments of allergens

Inventors: Monika Hochradl (Vienna, AT); Frank Stolz (Vienna, AT); Angela Neubauer (Vienna, AT); Rainer Henning (Vienna, AT); Elijahu Babaev (Vienna, AT)
Assignee: WORG PHARMACEUTICALS (ZHEJIANG) CO., LTD.
C07K14/415A61K39/36A61P37/08C07K14/005C12N5/10C12N15/00C12N15/64C12N15/66A61K2039/575A61K2039/6075C07K2319/00C07K2319/21C12N2511/00C12N2523/00C12N2730/10122C12N2730/10134
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Quick Facts
Patent No.
US 11,926,651
App. No.
16/335,022
Granted
Mar 12, 2024
Kind
B2
Abstract

The present invention relates to a polypeptide construct comprising at least two fragments of an allergen from the Amb a 1 family of allergens from Ambrosia atermisiifolia or variants of said at least two fragments, wherein each of the at least two fragments consist of 20 to 50 amino acid residues and wherein at least one fragment is derived from amino acid residues 1 to 50 of the mature allergen and at least one fragment is derived from amino acid residues 240 and ending at the C-terminal end of the mature allergen.

Claims (34)

1. A polypeptide construct comprising at least a first and a second fragment of a mature allergen derived from an allergen of the Amb a 1 family of Ambrosia artemisiifolia , wherein the first and second fragments are not located adjacent to each other in the mature allergen, wherein each of the first and second fragments consists of up to 50 amino acid residues, wherein

a. the first fragment is derived from the N-terminus of the mature allergen, wherein:

the first fragment comprises a sequence selected from the group consisting of AEDLQEILPVNETRRLTTSGAYNIIDGX 1 (SEQ ID No. 2); AEDLQQILPSANETRSLTTX 2 GTYNIIDGX 1 (SEQ ID No. 3); AEGVGEILPSVNETRSLQAX 2 EAYNIIDKX 1 (SEQ ID No. 4); and AEDVEEFLPSANETRRSLKAX 2 EAHNIIDKX 1 (SEQ ID No. 5);

wherein X 1 is cysteine, serine or no amino acid residue and X 2 is cysteine or serine, and

b. the second fragment is derived from the C-terminus of the mature allergen, wherein:

the second fragment comprises a sequence selected from the group consisting of

X 3 RX 4 GFX 5 QVVNNNYX 6 X 7 WGX 8 YAX 9 GGSX 10 X 11 PTIL (SEQ ID No. 6);

X 12 DPVLTPX 13 QX 14 AGMIPAEPGEX 15 X 16 X 17 X 18 LTSSAGVLS X 19 (SEQ ID No. 7);

X 20 RHGFFQVVNNNYDKWGSYAIGGSASPTIL (SEQ ID No. 8); X 21 RFGFFQVVNNNYDRWGTYAIGGSSAPTIL (SEQ ID No. 9); VDPVLTPEQSAGMIPAEPGESALSLTSSAGVLSX 22 (SEQ ID No. 10); and

SDPVLTPVQSAGMIPAEPGEAAIKLTSSAGVLSX 23 (SEQ ID No. 11),

wherein X 3 is cysteine, serine, leucine or no amino acid residue, X 4 is histidine or phenylalanine, X 5 is phenylalanine or valine, X 6 is aspartic acid or glutamic acid, X 7 is arginine or lysine, X 8 is threonine or serine, X 9 is isoleucine or leucine, X 10 is serine or alanine and X 11 is glycine, serine or alanine, X 12 is serine or valine, X 13 is valine or glutamic acid, X 14 is serine, lysine or asparagine, X 15 is alanine or serine, X 16 is valine or alanine, X 17 is leucine or isoleucine, X 18 is serine, lysine or arginine and X 19 is cysteine, serine or no amino acid residue, X 20 and X 21 are independently cysteine, leucine, serine or no amino acid residue, X 22 and X 23 are independently cysteine, serine or no amino acid residue,

wherein the first and second fragments are fused or conjugated to a carrier protein, wherein at least one of the first or second fragments is fused to the N-terminus of the carrier protein and at least one of the first or second fragments is fused to the C-terminus of the carrier protein.

2. The polypeptide construct according to claim 1 , wherein the allergen of the Amb a 1 family is selected from the group consisting of Amb a 1.0101, Amb a 1.0201, Amb a 1.0202, Amb a 1.0301, Amb a 1.0302, Amb a 1.0303, Amb a 1.0304, Amb a 1.0305, Amb a 1.0401, Amb a 1.0402, Amb a 1.0501 and Amb a 1.0502.

3. The polypeptide construct according to claim 2 , wherein the allergen of the Amb a 1 family is Amb a 1.0101, Amb a 1.0201, Amb a 1.0305 or Amb a 1.0401.

4. The polypeptide construct according to claim 1 , wherein the first fragment comprises amino acid residues 1 to 20-40 of the mature allergen according to SEQ ID No. 1.

5. The polypeptide construct according to claim 1 , wherein the first and second fragments consist of 25 to 45 amino acid residues.

6. The polypeptide construct according to claim 1 , wherein the polypeptide construct comprises the second fragment comprising X 3 RX 4 GFX 5 QVVNNNYX 6 X 7 WGX 8 YAX 9 GGSX 10 X 11 PTIL (SEQ ID No. 6).

7. The polypeptide construct according to claim 1 , wherein the polypeptide construct comprises the second fragment comprising X 12 DPVLTPX 13 QX 14 AGMIPAEPGEX 15 X 16 X 18 LTSSAGVLSX 19 (SEQ ID No. 7).

8. The polypeptide construct according to claim 1 , wherein the second fragment comprises X 20 RHGFFQVVNNNYDKWGSYAIGGSASPTIL (SEQ ID No. 8), X 21 RFGFFQVVNNNYDRWGTYAIGGSSAPTIL (SEQ ID No. 9), VDPVLTPEQSAGMIPAEPGESALSLTSSAGVLSX 22 (SEQ ID No. 10) or SDPVLTPVQSAGMIPAEPGEAAIKLTSSAGVLSX 23 (SEQ ID No. 11).

9. The polypeptide construct according to claim 1 , wherein the carrier protein is a viral protein or a fragment thereof consisting of 50 to 300 amino acid residues.

10. The polypeptide construct according to claim 9 , wherein the viral protein is a capsid protein.

11. The polypeptide construct according to claim 9 , wherein the viral protein is derived from a virus of the hepadnaviridae family.

12. The polypeptide construct according to claim 11 , wherein the virus of the hepadnaviridae family is a Hepatitis B virus.

13. The polypeptide construct according to claim 12 , wherein the viral protein of the Hepatitis B virus is PreS, PreS1 or PreS2.

14. The polypeptide construct according to claim 1 , wherein the first and second fragments are fused to the N-terminus and/or C-terminus of the carrier protein.

15. The polypeptide construct according to claim 1 for the use in the treatment of a ragweed pollen allergy.

16. A nucleic acid molecule encoding a polypeptide construct as defined in claim 1 , wherein the first and second fragments are fused to a carrier protein.

17. A vector comprising a nucleic acid molecule according to claim 16 .

18. The vector according to claim 17 , wherein said vector is an expression vector.

19. The vector according to claim 17 , wherein said vector is a bacterial, fungal, insect, viral or mammalian vector.

20. A host cell comprising a nucleic acid molecule according to claim 16 .

21. An immunogenic formulation for treatment of a ragweed pollen allergy comprising at least one polypeptide construct according to claim 1 .

22. The immunogenic formulation according to claim 21 , wherein said formulation comprises 10 ng to 1 g of said polypeptide.

23. The immunogenic formulation according to claim 21 , wherein said formulation further comprises at least one adjuvant, pharmaceutical acceptable excipient and/or preservative.

Assignments (3)
CHANGE OF NAME Recorded Jul 14, 2023
From: WORG PHARMACEUTICALS (HANGZHOU) CO., LTD.
To: WORG PHARMACEUTICALS (ZHEJIANG) CO., LTD.
Reel/Frame 064260/0606 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2022
From: HOCHRADL, MONIKA
To: BIOMAY AG
Reel/Frame 059229/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 9, 2020
From: BIOMAY AG
To: WORG PHARMACEUTICALS (HANGZHOU) CO., LTD.
Reel/Frame 054318/0838 →
Priority Claims (1)
EP 16189774 · Sep 20, 2016 · regional
Continuity (1)
Related Publication 20190248844A1 · Aug 15, 2019