Modular antigen transportation molecules and uses thereof in animals

Patent metadata

Field	Value
Publication number	US-10898568-B2
Application number	US-201615276922-A
Country	US
Kind code	B2
Filing date	Sep 27, 2016
Priority date	Sep 30, 2015
Publication date	Jan 26, 2021
Grant date	Jan 26, 2021

Abstract

The present invention relates to (isolated) recombinant proteins, also referred to as improved MAT (iMAT) molecules, comprising at least one translocation module, at least one targeting module and at least one antigen module, wherein at least one cysteine residue is substituted with a different amino acid residue. Such iMAT molecules are useful specifically as vaccines, e.g. for therapy and/or prevention of allergies and/or infectious diseases and/or prevention of transmission of infectious diseases in animals, more preferably ruminants, pigs, dogs and/or cats, but excluding equines. The present invention further relates to nucleic acids encoding such iMAT molecules, corresponding vectors and primary cells or cell lines.

First claim

The invention claimed is:

1. A method of prophylactically and/or therapeutically treating one or more allergic diseases in a dog or a cat, comprising administering an effective amount of an improved modular antigen transportation (iMAT) molecule, wherein said iMAT molecule comprises:
(i) at least one first module, wherein said at least one first module comprises an amino acid sequence allowing the translocation of the iMAT molecule from the extracellular space into the interior of cells, wherein said at least one first module is selected from the group consisting of:
(a) the amino acid sequence of HIV-tat, VP22, Antennapedia, or a partial sequence thereof;

(ii) at least one second module, wherein said at least one second module comprises an amino acid sequence allowing species-specific intracellular targeting of the iMAT molecule to the cell organelles which are involved in the processing of antigens and/or the loading of major histocompatibility complex (MHC) molecules with antigens, preferably processed antigens, wherein said at least one second module is selected from the group consisting of:
(a) the invariant chain selected from the canine and/or feline species' or a partial sequence thereof; and

(iii) at least one third module, wherein said at least one third module is an antigen module having an amino acid sequence of at least one epitope of at least one allergen eliciting an immune response in dogs and/or cats in response to allergens derived from fleas and/or mites, wherein the antigen module determines the specificity of an immune response modulated by such iMAT molecule, characterized in that in the entire iMAT molecule all cysteine residues are substituted with a different amino acid residue.

2. A method of prophylactically and/or therapeutically treating one or more allergic diseases in a cat or a dog comprising administering an effective amount of an improved MAT (iMAT) molecule, wherein said iMAT molecule comprises:
(i) at least one first module, wherein said at least one first module comprises an amino acid sequence allowing the translocation of the iMAT molecule from the extracellular space into the interior of cells, wherein said at least one first module is selected from the group consisting of:
(a) the amino acid sequence of HIV-tat, VP22, Antennapedia, or a partial sequence thereof,

(ii) at least one second module, wherein said at least one second module comprises an amino acid sequence allowing species-specific intracellular targeting of the iMAT molecule to the cell organelles which are involved in the processing of antigens and/or the loading of major histocompatibility complex (MHC) molecules with antigens, wherein said at least one second module is selected from the group consisting of:
the invariant chain selected from the canine and/or feline species' or a partial sequence thereof; and

(iii) at least one third module, wherein said at least one third module is an antigen module having an amino acid sequence of at least one epitope of at least one allergen eliciting an allergic disease in cats or dogs, wherein the allergic disease is selected from the group consisting of: allergies to flea bites, allergies to mite derived allergens, food allergies, atopic dermatitis, atopic dermatitis caused by flea bites, allergic asthma, allergic airway inflammation and/or obstruction; characterized in that in the entire iMAT molecule all cysteine residues are substituted with a different amino acid residue.

3. The method of claim 1 or claim 2 , wherein the modules of the iMAT molecule are covalently linked to each other, and wherein no additional spacer module(s) between two or more adjacent modules of said first, second and/or third modules are present at all.

4. The method of claim 1 or claim 2 , wherein said at least one antigen module comprises Der f 15 allergen according to SEQ ID NO: 11, 18, and/or Cte f1 allergen according to SEQ ID NO: 13 and/or 20.

5. The method of claim 1 or claim 2 , wherein said iMAT molecule further comprises at least one His-tag module, wherein the at least one His-tag module is present N-terminally and/or C-terminally.

6. The method of claim 1 or claim 2 , wherein said at least one first module consists of SEQ ID NO: 1.

7. The method of claim 1 or claim 2 , wherein said at least one third module consists of an amino acid sequence selected from the group consisting of SEQ ID NOs: 7 to 23.

8. The method of claim 1 or claim 2 , wherein said iMAT molecule consists of an amino acid sequence selected from the group consisting of SEQ ID NOS: 24 to 83.

9. The method of claim 1 or claim 2 , wherein said iMAT molecule, comprises:
(i) said at least one first module, wherein said at least one module consists of SEQ ID NO: 1;
(ii) said at least one second module, wherein said second module is selected from a group consisting of SEQ ID NOs: 4 or 5; and
(iii) said at least one third module, wherein said at least one third module is selected from a group consisting of SEQ ID NOs: 14 to 23.

10. The method of claim 1 or claim 2 , wherein said iMAT molecule, comprises:
(i) said at least one first module, wherein said at least one module consists of SEQ ID NO: 1;
(ii) said at least one second module, wherein said second module is selected from a group consisting of SEQ ID NOs: 4 or 5; and
(iii) said at least one third module, wherein said at least one third module is an antigen module having an amino acid sequence of at least one epitope, selected from the group consisting of: SEQ ID NO: 7, 8, 9, 10, 11, 12, 13, 84, 85, 86, 87, and 88.

11. The method of claim 1 or claim 2 , wherein said iMAT molecule, comprises:
(i) said at least one first module, wherein said at least one module consists of SEQ ID NO: 1;
(ii) said at least one second module, wherein said second module is selected from a group consisting of SEQ ID NOs: 4 or 5; and
(iii) said at least one third module, wherein said at least one third module is an antigen module having an amino acid sequence of at least one epitope, selected from the group consisting of two or more antigens selected from the group consisting of: SEQ ID NO: 10, 11, 84, 85, 86, 87, and 88, or any combination of two or more antigens selected from the group consisting of: SEQ ID NO: 7, 8, 9, 10, 11, and 12, or any combination of two or more antigens selected from the group consisting of: SEQ ID NO: 7, 8, 10, and 11.

12. The method of claim 1 or claim 2 , wherein said iMAT molecule further comprises at least one His-tag module, wherein the at least one His-tag module is present N-terminally after one methionine residue.

13. The method of claim 1 or claim 2 , wherein said amino acid sequence of said at least one first module is selected from the group consisting of the amino acid sequence of HIV-tat or a partial sequence thereof.

14. The method of claim 1 or 2 , wherein said amino acid sequence of said at least one first module is selected from the group consisting of the amino acid sequence having at least 95% sequence identity with the amino acid sequence set forth in SEQ ID NO: 1.

15. The method of claim 1 or claim 2 , wherein said amino acid sequence of said at least one second module is selected from the group consisting of the sequence according to SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, and fragments thereof.

16. The method of claim 1 or claim 2 , wherein said amino acid sequence of at least one allergen of said at least one third module is selected from the group consisting of the amino acid sequence for Der f 1, Der f 2, Der f 23, Der f 18/Der f 18p, Der f 15, Zen 1, Cte f1, and f

Assignees

• Boehringer Ingelheim Vetmedica Gmbh

Inventors

• Rose Horst
• Reiche Dania Birte
• Tammen Harald

Classifications

• C07K7/06

  having 5 to 11 amino acids · CPC title

• A61K2039/622

  non-covalent binding · CPC title

• A61K39/385

  Haptens or antigens, bound to carriers · CPC title

• C07K2319/10

  containing a tag for extracellular membrane crossing, e.g. TAT or VP22 · CPC title

• A61K2039/55505

  Inorganic adjuvants · CPC title