CA2331274C - Hybrid protein for inhibiting the degranulation of mastocytes and the use thereof - Google Patents

Abstract

The invention relates to a hybrid protein comprising or comprised of (i) a known protein which binds to mastocytes and/or basophils in a known manner and/or is absorbed thereby, and of (ii) protease which splits one or more proteins of the secretory apparatus of the mastocytes and/or basophils.

Description

Hybrid Protein for Inhibiting the Degranulation of Mastocytes and the Use Thereof Background of the Invention Allergic reactions of the immediate type are characterized in that the patients concerned have formed antibodies of the IgE type against allergens (for example pollen, house dust, mites, animal hair). These antibodies circulate not only in the blood but are also bound to cells present in the tissue exhibiting in the plasma membrane a specific receptor for a portion of the IgE molecule, the Fc fragment (Fishman & Lorberboum-Galski 1997; Hamawy 1997).
Cells with IgE receptors are mastocytes and basophils exclusively. These cells are the cells effecting the allergic reaction of the immediate type. They store vesicles containing vasoactive amines and prostaglandins and leukotrienes (derivatives of the arachidonic acid).
The release of these substances resulting in the degranulation of the mastocytes, occurs through a specific and an unspecific mechanism. Once cells are mechanically destroyed, e.g., by a scratch on the skin, histamine is unspecifically released. At the wound the skin turns red.
Nettles (edemas) are formed and the skin itches (triple response). Substances releasing histamine specifically are effective in relatively low concentrations and trigger the following cascade of responses (signal cascade): activation of phospholipase C -formation of the second messengers "diacylglycerol" and "IP3" - mobilization of calcium from cellular depots - fusion of the granula with the cell membrane - exocytosis of the granula without cytolysis -exchange of sodium against the positively charged histamine of the complex with heparin and a basic protein - release of the histamine from the granula matrix. Provided there is a contact between the mastocytes of an allergic person and an allergen, the IgE
molecules on the cell surface bind this allergen. Once allergen molecules are bound in sufficient amounts aggregation of the receptors in the plasma membrane occurs. The aggregation is the specific stimulus for the induction of the above described signal cascade in the interior of the cell. The substances released induce the allergic syinptoms (conjunctivitis, rhinitis, asthma, laryngeal edema, urticaria, blood pressure drop up to a pronounced anaphylactic shock).
Peptides contained in the toxin of the bee such as the mast cell degranulating peptide (MCD) also effect a degranulation of the mastocytes. Additionally, some pharmaceuticals cause a specific release of histamine as an undesired effect. The release of histamine in humans is described for muscle relaxing agents, dextrans, acetylsalicylic acid (aspirin), morphine, antibiotics, contrast media in radiography, foreign sera etc.

If the fiision of the vesicles with the plasma membrane is sticcessfiilly inhibited, then there is no release of the amines and arachidonic acid derivatives. Consequently, no allergic reactions are induced. Several proteins (fusion proteins) are involved in the secretion process and the release, respectively, which proteins may be bound to membranes of secretory vesicles and./or to the plasma membrane. Likewise they may appear in the cytosol.
Representatives of these proteins are SNAP 25, synaptobrevin (VA,MP), syntaxine and its isoforms, respectively.
These proteins form a complex (fusion complex) fixating the secretory vesicles to the inner side of the plasma membrane. The fixation anticipates the fusion of the vesicles with the plasma membrane, said fusion being induced by the influx of Ca++ trig~ered by IgE. By inactivation of one of these proteins, for example by proteolytic cleavage, the formation of the complex is inhibited.

It is known that the fiision proteins mentioned are the target molecules (substrates) of the lic"ht chains of the neurotoxins produced by the bacillus Clostridium botiilinzinz in the nerve cells (Ahnert-Hilger & Bigalke, 1995; Bigalke and Shoer, 2000). At present seven different types of botulinum toxins are known (A, B, Cl, D, E, F, and G). The synaptobrevin mentioned additionally is a target molecule for TeNT (Link et al., 1993) produced by Clostridiurn tetani, and also for a protease from 1Veisseria gonorrhoeae (Binscheck et al., 1995).
The toxins, apart from the latter, consist of at least two functional domains. The C terminal portion of the protein (heavy chain) is responsible for its binding to the nerve cell whilst the N terminus (light chain) is characterized by the above described highly specific proteolytic activity. The toxins bind to nerve cells via their heavy chain and reach the cytosol via a receptor-mediated endocytosis and subsequent translocation, where they cleave one or more of the fitsion proteins mentioned which, in turn, are constitutive for the fiision complex.
After the cleavage of the respective protein the secretion of acetylcholin and other transmitters, respectively, from the nerve cells is inhibited (Binscheck and Wellhoner, 1997).

The inhibition of the release of transmitters has been therapeutically used in the past for the treatment of dystonic motor disturbances and for the suppression of excessive parasympathic activities (Benecke and Kessler, 1995). For the clostridial neurotoxins biological substrates other than the fiision proteins are not known. The heavy chains have a high affinity for peripheric nerve cells such that the light chains connected to them reach only these cells and become effective only in these cells - althoulgh other cell types, such as mastocytes and basophils, in which secretion processes occur possess the above mentioned substrates, they do not possess a mechanism for the uptake of the protease, however (Marxen et al., 1989).
Description of the Invention One embodiment of the present invention relates a hybrid protein, comprising or consisting of (i) a protein known per se, said protein binding to mastocytes and/or basophils and/or being taken up by these cells in a manner known per se, (ii) a protease known per se, said protease cleaving one or several proteins of the secretion apparatus of the mastocytes and/or basophils.

A further embodiment of the present invention relates to a hybrid protein comprising or consisting of (i) a protein binding to mastocytes and/or basophils and/or being taken up by these cells, wherein the protein (i) is selected from the group consisting of:
IgE;
IgE fragment, in particular IgE Fc fragment;
antibody against IgE receptor of mastocytes and/or basophils; fragment of the antibody against IgE receptor of mastocytes and/or basophils, in particular Fab fragment; antibody against mastocyte-specific potassium channel; and inactive but binding MCD peptide; and (ii) a protease, in particular a protease known per se, cleaving one or several proteins of the secretion apparatus of the mastocytes and/or basophils.

Still a further embodiment of the present invention relates to a hybrid protein comprising or consisting of (i) a protein, in particular a protein known per se, said protein binding to mastocytes and/or basophils and/or being taken up by these cells, in particular in a manner known per se; and (ii) a protease, said protease cleaving one or several proteins of the secretion apparatus of the mastocytes and/or basophils, wherein the protease (ii) is selected from the group consisting of:
light chain of a Clostridium botulinum toxin, in particular the toxins of type A, B, C 1, D, E, F, and G;

catalytically active fragment of the light chain of a Clostridiuni botulinaim toxin, in particular a toxin of type A, B, C l, D, E, F, and G;
light chain of the tetanus toxin (TeNT);
catalytically active fragment of the light chain of the tetanus toxin;
IgA protease of Neisseria gonorrhoeae; and catalytic domain of the IgA protease of Neisseria gonorrhoeae.

The hybrid protein of the present invention may be characterized in that the protein (i) and the protease (ii) are selected from the previous groups of proteins and proteases, respectively.

The hybrid protein of the present invention may additionally be characterized in that the N-terminal portion of the heavy chain of the respective toxin (HN fragment) or a fragment thereof may be part of the hybrid protein, in addition to the light chain of a Clostridium botulinum toxin or of the tetanus toxin.

Finally, one embodiment of the present invention relates to the use of the present hybrid protein to inhibit the granulation of mastocytes.

If mastocytes would be killed there existed the danger that an allergic shock would be induced once the dying mastocytes release the stored endogenous amines. Additionally, the drop of the number of mastocytes would stimulate the de novo synthesis of these cells which, in turn, would be available again for allergic reactions. The hybrid protein of the present invention is thus fundamentally different from the IgE-Fc/pseudomonas exotoxin conjugate inhibiting protein synthesis by its ADP ribosylation activity and thus effecting cell death (Fishman &
Lorberboum-Galski, 1997). Quite conversely, the hybrid protein of the present invention does not serve to kill mastocytes. Rather, the cell remain vital after having been subjected to the hybrid protein of the present invention and lost no more than their capacity to release vasocontrictive amines.

A stimulation of the de novo synthesis does not occur. When therapeutically used, conceivable toxic side effects to be expected with a conjugate based on the complete cytotoxic pseudomonas toxin or a comparable cytotoxin are avoided.

Subject-matter of the invention may thus be a conjugate (hybrid protein) consisting of (i) a protein or peptide (transport protein/peptide) exhibiting a high affinity to mastocytes/basophils and (ii) a specific protease, which conjugate blocks the degranulation and the secretory mechanism, respectively, of the cells. The conjugate is useful for the therapy/prophylaxis of allergic reactions of the immediate type.

(i) Preferred highly affinic mastocyte-binding components of the conjugates are immunoglobulins of type E (IgE) and its fragments (e.g. the Fc-fragment), respectively. Additionally, antibodies against specific surface molecules of mastocytes/basophils are used, which antibodies selectively bind to the plasma membrane of these cells. Above all, antibodies against the IgE receptor fulfill this purpose. Furthermore, inactive but binding mutants of the mast cell degranulating peptide are to be used as transport peptides/proteins in the hybrid protein.
These transport peptides/proteins are useful to channel a protease into the cells.
This protease cleaves proteins in the fusion complex of mastocytes in a highly specific manner, which proteins initiate the degranulation mechanism of the cells.

(ii) Useful as a highly specific protease is a metalloprotease, e.g., the light chain of botulinum toxin of type A, B, C1, D, E, F, or G (BoNT/X) and of the tetanus toxin (TeNT) or the IgA protease of Neisseria gonorrhoeae. These proteases cleave the synaptosomal associated protein (MR 25,000) (SNAP 25), synaptobrevin or syntaxin.
If only one of these proteins/peptides is cleaved, the degranulation of the mastocytes is inhibited. As a result, no secretion of histamine, prostaglandins, and leukotrienes will occur, and allergic symptoms cannot occur any nlore.

In the present invention the non-toxic light chains of the toxins can be attached to transport proteins exclusively binding to mastocytes and basophils, respectively, and thus, can be taken up only by these cells, wherein the light chains - as if carried along as a passenger - reach the cells. They cannot invade in nerve cells and cells of other type of the organism such that the effect is limited to mastocytes and basophils. If one of the substrates is proteolytically destroyed, no allergic symptoms occur subsequent to the contact of these IgE-loaded cells with an allergen or with one of the above mentioned pharmaceuticals.

Useful as proteins specifically binding to mastocytes are 1) immunoglobulins of type E and their fragments of type Fc;
2) antibodies against the IgE receptor;
3) the mast cell degranulating peptide; and 4) an antibody against the mastocyte-specific potassium channel.

In regard of the protein listed reference is made to the following publications:
- IgE Helman (1995) - IgE-Fc fragment Helman (1995) - Antibody against IgE receptor of mastocytes/basophils, antibodies against mastocyte-specific potassium channel, Fab fragment of the antibody: these are standard procedures described in:
Liddel & Weeks (1995) - MCD peptides Gmachel & Krell (1995) - Inactive but binding mutant The mutated peptide is prepared according to standard procedures:
Nichol D.S.T. (1995) - Light chains of the various botulinum toxins of type A-G:
Binz et al. (1990) - Light chain of tetanus toxin Eisel et al. (1989) - IgA protease Bruscheck et al. (1995) The connection of both components (transport protein and protease) occurs via different routes. First, the light chain of the toxin is chromatographically purified.
The light chain is entirely non-toxic because, after its separation from the heavy chain, the neurotropic transport protein, it cannot reach the nerve cells and an extracellular substrate does not exist. The light chain is then chemically bound to one of the four mastocyte-binding proteins to form a conjugate which, in turn, is taken up in the cytosol of mastocytes. The light chain cleaves its substrate there, which cleavage inhibits the secretion of histamine and other substances. A
second way to prepare the conjugate is to fuse the gene for the light chain and the gene for one of the four mastocyte-binding proteins such that a hybrid protein is expressed in suitable host cells. This biotechnologically produced hybrid protein should block the secretory process from mastocytes in analogy to the conjugate prepared from two protein components. The preparation of hybrid proteins is a procedure known per se, in particular in the field of tumor therapy (Vogel, 1987; Magerstadt, 1991). In this therapeutic concept an antibody against surface proteins of the tumor cells are attached to a cytotoxic protein, e.g., ricin, diphtheria toxin, to kill cancer cells. The novel aspect in the method of the present invention is the use of specific proteases and proteolytic domains, respectively, in hybrid proteins for the inhibition of the degranulation of mastocytes and, thus, for an anti-allergic therapy.
These hybrid proteins were not only useftll to avoid heavily impairing allergic symptoms (hey fever, asthma, and neurodermitis). They could be administered also prophylactically to avoid allergic reactions during therapies with life-saving pharmaceuticals.
Moreover, they could avoid allergic symptoms occurrinj in the course of desensitization.

Example 1: Synthesis of a hybrid protein from IgE and the light chain of BoNT/A

The purified botulinum toxin (5.0 mg) of type A was applied, after equilibration in 15 m1til sodium tetraborate and 30 mM phosphate pH 8.4, to a QAE Sephadex column (1.0 x 3.0 cm), equilibrated with the same buffer. The column was subsequently washed with 10 ml 120 mitil dithioerythrol, 2 M urea and 1 mM EDTA and incubated over night. Thereafter, the light chain was eluted from the column by means of 10 mM borate buffer and dialyzed acainst 20 mM phosphate pH 7Ø

Immunoarlobulin E (rat) was purchased. 10 mg of the immuno-lobulin were cleaved with 50 g papain in I ml phosphate buffer (4 C over night). The Fc fragment -%vas purified over a gel Tm filtration column (Sephacryl S200). 3.0 mg of the purified Fc fragment were incubated with 3.0 mg of a purified light chain of botulinum toxin with 10 m1V1 dithiobis-succinimidylpropionate (bifiinetional agent) in 2 ml Na-phosphate, pH 7.0, over a period of 16 hours. The hybrid protein thus synthesized was purified via gel filtration (Sephacryl S200) and analyzed for its purity via SDS gel electrophoresis.

The inhibition of the degranulation of the mastocytes is examined in two experimental approaches. In the first approach isola*ed mastocytes of the rat are incubated with the hybrid molecule. Thereafter the release of histamine is stimulated. The stimulation occurs with specific histamine liberators such as the MCD peptide and concanavalin A (the latter being an experimentally utilized substance) and by a direct increase of the intracellular calcium concentration, respectively. The latter is achieved by an injection of calcium into distinct mastocytes. Thus, one short-circuits the above described signal cascade as the increase of the calcium concentration is the step during the secretion process which is followed by the fusion of the vesicles. The degranulation of the mastocyte reflecting the release of histamine is followed in the phase-contrast microscope. Subsequently it is possible to quantify released histamine by means of a measurement of the fluorescence. Finally, the enlargement of the mastocyte caused by the incorporation of vesicle membranes into the plasma membrane during degranulation can be determined electrophysiologically. In the cells treated with hybrid protein there will, in contrast to control cells, occur (1) no morphological change, (2) no enhancement of the fluorescence in the supernatant of the cell, and (3) no enlargement of the cell. Thereby it is possible to prove that the release of histamine is blocked by the hybrid protein.

In the second experimental approach the hybrid protein is injected into living rats. The rats are killed after several days and their mastocytes conventionally isolated. The degranulation and release of histamine, respectively, is determined as described above. In this approach it is examined whether the conjugate is able to reach the compartment also in the living animal, in which compartment the mastocytes are located in, and whether the conjugate inactivates the mastocyte in the living animal.

Example 2: Production of a recombinant hybrid protein by operably linking the gene encoding the light chain of Clostridium botulinum type A to the gene encoding immunoglobulin E and one of its fragments (Fc fragment), respectively The gene encoding the light chain of botulinum toxin type A is isolated by means of suitable primers via PCR (polymerase chain reaction). A culture of Clostridiurn bottclinum type A is prepared from which the DNA is prepared. From the published sequence of the toxin gene (Binz et al.) a pair of primers is derived and the gene for the light sub-unit amplified via PCR.
Thereafter this gene is cloned into a commercial expression vector pQE
according to the recipe of the producer.

The gene encoding the Fc fragment of the human immunoglobulin E (Helman L.) was isolated via PCR from a commercial cDNA library and fused in the vector construct with the gene light chain of botulinum toxin type A.

With this construct competent M15 cells (E. coli) are transformed. As in this expression system the inserted genes are equipped with a "his tag" the recombinant protein is purified through a Ni affinity column. The process of highly purifying the protein is followed by a gel filtration through Sephacryl S300.

The measurement of the biological activity was performed again on isolated mastocytes in vitro.

Example 3: Preparation of a recombinant hybrid protein by operably linking the gene encoding the light sub-unit of the tetanus toxin with a mutated gene encoding the mast cell degranulating peptide (MCD) The "sequence for the "mast cell degranulating peptide", a 22mer, is known (Gmachl and Kreil). Based thereon a corresponding oligonucleotide is synthesized.

In order to isolate the sequence of the light sub-unit of the tetanus toxin a culture of C. tetani was prepared and DNA recovered therefrom. From the known nucleic acid sequence of the tetanus toxin a primer for PCR and hence the gene for the light sub-unit of the toxin was obtained.

As described in Example 1, both nucleic acid sequences were fused in an expression vector pQU and subsequently expressed in E. coli. The hybrid protein which, in turn, was equipped with a his-tag was purified through affinity chromatography and subsequent gel filtration. The purified gene encoding the mast cell degranulating peptide is chemically synthesized including a point mutation in the active domain of the peptide. The gene is operably linked to the gene encoding the light chain of the tetanus toxin. The hybrid protein is expressed in E.
coli and purified. The thus produced hybrid protein is tested in vitro in the mastocyte degranulation assay.

Example 4: Preparation of a recombinant hybrid protein by linking the gene encoding the Fc fragment of IgE to the gene encoding the IgA protease The gene encoding the Fc fragment of IgE was isolated as described in Example 1.

The gene encoding the IgA protease from N. gonorrhoeae is known. Primers were derived therefrom, and the gene encoding the specific protease was recovered by means of PCR from a nucleic acid preparation obtained from N. gonorrhoeae.

Both nucleic acids were integrated into a commercial vector following the recipe giving by the producer and the hybrid protein purified by affinity chromatography (see Example 2).

The inhibitory activity is again proven in vitro on isolated mastocytes (see above).

Example 5: Preparation of a hybrid protein consisting of the Fab fragment of an antibody against the IgE receptor and the light chain of botulinum toxin type B

A monoclonal antibody against the IgE receptor on mastocytes was purchased and chromatographically re-purified. 0.5 mg of the antibody were conjugated to 0.4 g of the purified light chain of botulinum toxin F. The light sub-unit was isolated by cleavage of the neurotoxin and subsequent purification through ion exchange chromatography, once the preparation of the neurotoxin had been performed according to the procedure in Example 1.
Both proteins (light sub-unit of toxin type F and monoclonal antibody) were linked to each other by using a bifunctional agent. The isolated proteins were incubated with 10 mM
maleimidobenzoyl-N-hydroxy-succinimidester for this purpose. The hybrid protein was subsequently purified from non-conjugated proteins by gel filtration over Sephacryl S300.
Again isolated mastocytes were used to demonstrate that the hybrid protein synthesized inhibited the secretion of histamine.

Reference to further patents:
Patent No. 4902495 IgE Fc directed delivery systems Novel Agent Controlling Cell Activitv PCT application WO 94/21300 References:

1) Ahnert-Hillger G., Bigalke H. (1995) Molecular aspects of tetanus and botulinum neurotoxin poisoninc,.
Progress in Neurobiology 46: 83-96 2) Benecke R., Kessler K.R. (1995) Botulinumtoxin A
Akt. Neurol 22: 209-213 3) Bigalke, H. and Shoer, L.F. (2000) Clostridial Toxins, Handbook of Experimental Pharmacology and Toxicology, Ed.
Just &
Aktories, Springer Verlag, pp. 407-443 4) Binscheck T., Bartels F., Bergel H., Bigalke H., Yamasaki S., Hayashi T., Niemann H., Polner J. (1995) IgA protease from Neisseria gonorrhoeae inhibits exocytosis in bovine chromaffin cells like tetanus toxin.
J. biol. Chem. 270: 1770-1774 5) Binscheck T., Wellhoner H.H. (1997) Tetanus and botulinum toxins - zinc proteases - synaptotagmin - exocytosis.
In: Toxins and signal transduction (Eds.: Gutman Y., Lazarovici P.) 1: 457-487 6) Binz, T., Kurazono, H., M., Frevert, J., Wernars K. & Niemann, H. (1990) The complete sequence of botulinum toxin A and comparison with other clostridial neurotoxins J. Biol. Chem. 265: 9153-9158 7) Cardoso, F. & Jancovic, J. (1995) Clinical use of botulinum neurotoxins Current Topics Microbiol. Immunol. 195: 123-141 8) Fishman, A. , L'orberboum-Galski, H. (1997) Targeted elimination of cells expressing the high-affinity receptor for IgE
(Fc epsilon RI) by a Pseudomonas exotoxin-based chimeric protein Eur. J. Immunol., 27: 486-494 9) Gmachl, M. & Kreil, G. (1995) The precursors of the bee venom constituents apamin and MCE peptide are encoded by two genes in tandem which share the same 3'-exon J.Biol.Chem 270 (21): 12704-12708 10) Helman, L. (1995) Characterization of four novel epsilon chain mRNA and a comparative analysis of genes for immunoglobulin E in rodents and man Eur. J. Immunol. 23 (1): 159-167 11) Liddel & Weeks (1995) Antikorp er-Techniken Spektrum Akademischer Verlag Heidelberg 12) Link E., Edelmann L., Chou J., Binz T., Yamasaki S., Eisel U., Baumert M., Sudhof T.C., Niemann H. & Jahn R. (1992) Tetanus toxin action: Inhibition of neurotransmitter release linked to synaptobrevin proteolysis.
Biochem. Biophys. Res. Comm. 189: 18423-26 13) Magerstadt, M. (1991) Antibody conjugates and malignant diseases CRC Press 14) Hamawy M.M. (Ed.) (1997) IgE Receptor (FceRI) Function In: Mast Cells and Basophils Springer Verlag 15) Marxen P., Fuhrmann U., Bigalke H. (1989) Gangliosides mediate inhibitory effects of tetanus and botulinum A neurotoxins on exocytosis in chromaffin cells Toxicon 27: 849-859 16) Nichols D.S. T. (1995) Gentechnische Methoden Spektrum Akademischer Verlag 17) Vogel, C.-W. (Ed.) (1987) Immunoconjugates: Antibody conjugates in radio-immagining anth therapy of cancer Oxford UP Inc.

Claims (12)

Claims

1. A hybrid protein comprising:

(i) a protein known per se, said protein binding to mastocytes or basophils or being taken up by the mastocytes or basophils in a manner known per se, (ii) a protease known per se, said protease cleaving one or several proteins of the secretion apparatus of the mastocytes or basophils.

2. A hybrid protein comprising:

(i) a protein binding to mastocytes or basophils or being taken up by the mastocytes or basophils, wherein the protein is selected from the group consisting of IgE;
IgE fragment;

antibody against IgE receptor of mastocytes or basophils;

fragment of the antibody against IgE receptor of mastocytes or basophils;
antibody against mastocyte-specific potassium channel; and inactive but binding mast cell degranulating peptide; and (ii) a protease, cleaving one or several proteins of the secretion apparatus of the mastocytes or basophils.

3. The hybrid protein of claim 2, wherein the IgE fragment is an IgE Fc fragment.

4. The hybrid protein of claim 2, wherein the fragment of the antibody against IgE
receptor is an Fab fragment.

5. The hybrid protein of claim 2, wherein the protease is a protease known per se.

6. A hybrid protein comprising:

(i) a protein binding to mastocytes or basophils or being taken up by the mastocytes or basophils; and (ii) a protease, said protease cleaving one or several proteins of the secretion apparatus of the mastocytes or basophils, wherein the protease is selected from the group consisting of:

light chain of a Clostridium botulinum toxin;

catalytically active fragment of the light chain of a Clostridium botulinum toxin;

light chain of the tetanus toxin (TeNT);

catalytically active fragment of the light chain of the tetanus toxin;
IgA protease of Neisseria gonorrhoeae; and catalytic domain of the IgA protease of Neisseria gonorrhoeae.

7. The hybrid protein of claim 6, wherein the Clostridium botulinum toxin is selected from a group consisting of types A, B, C1, D, E, F, and G.

8. The hybrid protein of claim 6, wherein the protein is a protein known per se.

9. The hybrid protein of claim 6, wherein the protein is taken up by the mastocytes or basophils in a manner known per se.

10. The hybrid protein of any one of claims 2 to 9, characterized in that the protein is selected from the group according to claim 2 and the protease is selected from the group according to claim 6.

11. The hybrid protein of claim 10, characterized in that the N-terminal portion of the heavy chain of the respective toxin (H N fragment) or a fragment thereof is part of the hybrid protein, in addition to the light chain of a Clostridium botulinum toxin or of the tetanus toxin.

12. Use of a hybrid protein of any one of claims 1 to 11 for inhibiting the degranulation of mastocytes.