Patent Application
20110293567
The present invention relates to the field of cancer therapy. Specifically, a chemotaxis fusion-receptor that directs bacteria towards tumors is disclosed. Further encompassed by the present invention is a bacterial cell that comprises at least one chemotaxis fusion-receptor and, preferably, a killing module for the destruction of tumor cells.
Cancer constitutes the fourth leading cause of death in Western countries. As the average age in the Western population steadily rises, so do cancer-related deaths indicating that cancer will be one of the most common causes of death in the 21st century. The aggressive cancer cell phenotype is the result of a variety of genetic and epigenetic alterations leading to deregulation of intracellular signaling pathways. This leads to uncontrolled proliferation of the affected cells and, thus, to the formation of a tumor. Malignant tumors have three characteristics: (i) they infiltrate healthy tissues, (ii) they destroy the surrounding tissue, and (iii) they form metastases in other parts of the body.
As long as the cancer has not formed metastases, it can be treated by surgery or radiotherapy. Both methods, however, are not suited for the systemic treatment of cancer that has already formed metastases. In most of these cases chemotherapy is the only available option for systemic cancer treatment. Traditional chemotherapeutic agents are cytotoxic substances that target preferably rapidly dividing cells. Unfortunately cancer cells are not the only cells which display high proliferation rates. Many cells of the body, such as cells of the immune system, have high proliferation rates, too. Thus, classical chemotherapy usually causes severe side effects that sometimes necessitate the cessation of treatment. Furthermore, cancer cells are often resistant against one or more of the applied pharmaceuticals or develop resistances during the course of treatment.
In recent years systemic cancer treatments have become available which target cancer cells with higher specificity. Imatinib, for example, targets cancer cells that are characterized by an abnormal tyrosine kinase, which is formed by the fusion of the bcr and abl gene. Because this fusion gene is only present in cancer cells, normal cells are considerably less affected by this treatment as compared to traditional chemotherapy. However, Imatinib can only be used for the treatment of cancers with the bcr-abl fusion gene. Thus, a higher specificity of the novel cancer treatments often means that their efficacy is limited to a restricted number of cancers. For this reason, there is a continuing need for the development of novel cancer therapies that enable the treatment of cancer more generally.
The development of safe and effective cancer therapies has been hampered by the difficulties in targeting cancer cells (i) specifically and (ii) completely. One of the reasons for these deficiencies is the fact that non-living substances generally do not actively accumulate close to the cancer cells. As the vascular system in tumor tissue is often poorly developed, blood flow in tumors is often disorganized and variable. This creates heterogenous microenvironments within the tumor, because passive spreading by diffusion is very inefficient. Medicaments often do not reach poorly supplied regions of the tumor. Bacteria, in contrast, have mechanisms to actively accumulate in tumor tissues. The main mechanisms are specific chemotaxis, preferred growth in tumor tissue and hypoxic germination. Facultative anaerobes from the genera Salmonella and Escherichia have been shown to accumulate in tumors by chemotaxis. Due to this specific accumulation in tumors it has been tried to use bacteria for cancer therapy. In order to make bacteria toxic towards cancer cells, several methods have been used. Bacteria have been engineered to produce bioactive molecules or to transfer the genes encoding such molecules into cancer cells. Furthermore, bacteria have been equipped with genes encoding for pro-drug activating enzymes. For a review of bacterial cancer treatments see St Jean A T, 2008, Curr. Opin. Biotechnol. 19: 511-517.
Bacteria are attracted to certain substances (“attractants”), such as carbon sources or amino acids, while they avoid other substances (“repellents”), e.g. weak organic acids. This phenomenon is known as bacterial chemotaxis. Normally, bacteria swim for an average period of 1 second in a straight line, then change their direction (“tumble”) in a random fashion and swim again in a straight line. This is called “random walk”. When moving in a concentration gradient of an attractant towards the higher concentration, the interval between the tumbling movements increases so that the movement along the gradient is stabilized. Since bacteria are too small to sense a gradient along their cells, the spatial signal of a concentration gradient is intracellularly transformed into a temporal signal. The key components for the sensing of concentration gradients are methyl-accepting chemotaxis proteins (MCPs). The periplasmic domain of these proteins contains several methylation sites. An increasing methylation of the MCP leads to an increasing duration of the intervals between the tumbling movements. The methylation state of the MCP is determined by the interplay of two enzymes, a permanently active methyltransferase and a methylase. The binding of an attractant to the receptor leads to a lower affinity of the methylase for the MCP so that the balance of methylation and demethylation is shifted towards methylation. Conversely, the binding of a repellent to a suitable receptor indirectly increases the activity of the methylase so that the MCP is demethylated. This favours tumbling movements of the bacterial cell. Different MCPs act on the same target proteins, i.e. CheA and CheY. Thus, the signals different chemotaxis receptors can be integrated to produce a response of the bacterial cell. For the structure and function of chemotaxis receptors see Mowbray and Sandgren (1998) Structural Biology 124: 257-275.
The previous attempts to use bacteria in cancer treatments have focussed on means to increase the ability of the bacteria to kill cancer cells. Regarding the delivery of the bacteria to the cancer cells the state of the art relies on the innate capabilities of the bacterial strains used in the experiments. This severely limits the possibilities of this therapeutical approach. Those bacteria that accumulate best in tumors are not necessarily also the best candidates for killing of cancer cells. The ability to equip almost any bacterial strain with the ability to accumulate close to cancer cells is clearly desirable. In addition to this, as long as the naturally occurring chemotaxis systems of bacteria are used, the specificity and sensitivity of these systems cannot be influenced.
The technical problem is solved by the embodiments characterized in the claims and below.
The present invention relates to a chemotaxis fusion-receptor comprising
A “chemotaxis fusion-receptor” as referred to in the present application is a methyl-accepting chemotaxis protein that comprises two components which originate from at least two different proteins. The signal transduction component comprises two transmembrane domains and the cytoplasmic domain. These domains originate, preferably, from a bacterial chemotaxis receptor. They are functionally linked to a periplasmic domain comprising a ligand binding site, so that the binding of a ligand activates the cytoplasmatic domain. The periplasmic domain is located between the two transmembrane domains. The ligand binding site originates from a different protein, preferably, from a receptor, i.e. an antibody or protein listed in table 1.
The cytoplasmic domains at the N-termini of naturally occurring methyl-accepting chemotaxis proteins (MCPs) are highly conserved among those proteins. The ligand binding sites in the periplasmic domains, in contrast, are highly variable. Thus, MCPs couple various different signal inputs to the same output, i.e. a positive or negative chemotaxis. As the signal transduction of an MCP functions equally well with different ligand binding sites in the periplasmic domain, it is possible to replace the naturally occurring binding site of an MCP by a selected ligand binding site from another protein. Such a chemotaxis fusion-receptor enables the construction of bacterial cells which display positive or negative chemotaxis for a ligand which is not recognized by naturally occurring bacterial chemotaxis receptors. Bacterial chemotaxis systems with customized specificities can be found in the examples.
In a preferred embodiment of the present invention the chemotaxis fusion-receptor comprises elements from the chemotaxis receptor Tar of Escherichia coli and the LuxQ-protein of Vibrio harveyi.
The aspartate receptor Tar (SEQ iD NO. 1) is a 60 kDa protein with about 2500 copies per cell. The smallest units of the receptor are dimers, but the major species in the membrane are tetramers. There is no evidence that tar can form heterodimers with other MCP (methyl-accepting chemotaxis protein). The receptor has a very high helical content of about 80%. The following description of its structure is that of the tar receptor from E. coli. The N-terminal cytoplasmic segment is very small (residues 1-6) and can be altered greatly without effecting the function very much. The periplasmic region (residues 31-188) is responsible for ligand binding. In this part the sequence is very low conserved, because of the need of binding different chemoeffectors. In the absence of a ligand the periplasmic part is a symmetric dimer, where each subunit is built up by an antiparallel four-helix bundle. The tar receptor has two transmembrane regions flanking the periplamsic domain: residues 7-30 (TM1) and residues 189-212 (TM2). Both transmembrane segments have a clear helix pattern. The cytoplasmic region, responsible for signal transduction, has a size of about 37 kDa including residues 213-553 of the protein. It is the most conserved part, with sequence identity of ˜70% between Tar and Tsr. Also it is the least understood domain. Residues 213-259 are referred to as the linker region and its integrity is crucially important for receptor function (Mowbray and Sandgren (1998) Journal of Structural Biology, 124: 257-275). LuxQ (SEQ iD NO. 2) is a transmembrane receptor with similar structure to that of Tar. It is part of the quorum-sensing system of Vibrio harveyi. LuxQ binds the complex of LuxP and Autoinducer-2 (AI-2). AI-2 is produced by LuxS, 159 amino acids long and with a molecular weight of 17.6 kDa. In the natural quorum-sensing system binding of AI-2 results in gene regulation. LuxP is 365 amino acids in length and has a molecular weight of 41-kDa. Its signal sequence is proteolytically removed upon translocation into the periplasm, yielding mature LuxP. LuxQ is 594 amino acids long with a molecular weight of 67 kDa. It has, similar to Tar, two transmembrane Domains flanking the periplasmic domain (residues 39-280). The cytoplasmic domain (residues 299-859) is responsible for signal transduction, and not important for the chemotaxis fusion receptor.
The N-terminal sequence of the chemotaxis fusion-receptor comprises the amino acid residues 1 to 298 of SEQ ID. NO. 2, i.e. transmembrane domain 1, the periplasmic domain and transmembrane domain 2 of LuxQ. The periplasmic domain is, preferably, exchanged completely or partially against the ligand binding domain of a receptor able to bind a ligand. At the carboxy-terminus the sequence of the chemotaxis fusion-receptor comprises the amino acid residues 225 to 564 of Seq ID NO. 1, i.e. the cytoplasmic domain of the chemotaxis-receptor Tar of Escherichia coli.
In another preferred embodiment of the present invention the N-terminal sequence of the chemotaxisfusion receptor comprises the amino acid residues 1 to 280 of SEQ ID. NO. 2, i.e transmembrane domain 1 and the periplasmic domain of LuxQ. The periplasmic domain is, preferably, exchanged completely or partially against the ligand binding domain of a receptor able to bind a ligand. At the carboxy-terminus the sequence of the chemotaxis fusion-receptor comprises the amino acid residues 200 to 564 of Seq ID NO. 1, i.e. transmembrane domain 2 and the cytoplasmic domain of Tar.
In another preferred embodiment of the present invention the first transmembrane domain and the periplasmic domain of the chemotaxis fusion-receptor are exchanged for the ligand binding domain of a receptor able to bind a ligand. Also preferably, said exchange also includes the second transmembrane domain. This embodiment is preferred for receptors able to bind a ligand which are structurally similar to Tat or LuxQ, i.e. comprise at the N-terminus a first transmembrane domain, a periplasmic domain and a second transmembrane domain or at least a periplasmic domain and a transmembrane domain.
Suitable ligands for the binding site are chemical compounds, preferably proteins or small molecules, that are secreted by cancer cells. Preferred ligands are secreted either exclusively by cancer cells or are secreted by the cancer cells in an increased or decreased amount compared to a corresponding non-cancer cell (normal cell). More preferred are ligands that are secreted by cancer cells in higher amounts than by normal cells. Even more preferred are ligands that are exclusively secreted by cancer cells. The most preferred ligands are those given in table 1.
Preferred receptors able to bind a ligand are given in table 1.
Advantageously, the chemotaxis fusion-receptor of the present invention enables a flexible use of bacterial host cells in cancer therapy. A broad range of bacterial host cells capable of chemotaxis can be equipped with the chemotaxis fusion-receptor of the present invention by well established genetic methods. Furthermore, it is possible to select the ligand of the chemotaxis system at will. This enables the construction of bacteria that recognize specific types of cancer cells only depending on the chosen ligand. While the currently used bacteria are only reported to target solid tumors, the present invention enables the construction of chemotaxis fusion-receptors for the targeting of leukaemia. The combination of more than one chemotaxis fusion-receptor enables the integration of signals from more than one ligand thus further increasing the flexibility of the system.
The present invention further relates to a polynucleotide comprising at least one nucleic acid encoding the chemotaxis fusion-receptor of the present invention.
The polynucleotide of the present invention shall be provided, preferably, either as an isolated polynucleotide (i.e. isolated from its natural context) or in genetically modified form. The polynucleotide, preferably, is DNA including cDNA or RNA. The term encompasses single as well as double stranded polynucleotides. Moreover, comprised are also chemically modified polynucleotides including naturally occurring modified polynucleotides such as glycosylated or methylated polynucleotides or artificial modified one such as biotinylated polynucleotides.
Moreover, the present invention relates to a vector comprising the polynucleotide of the present invention.
The term “vector”, preferably, encompasses phage, plasmid or vectors as well artificial chromosomes, such as bacterial chromosomes. Moreover, the term also relates to targeting constructs which allow for random or site-directed integration of the targeting construct into genomic DNA. Such target constructs, preferably, comprise DNA of sufficient length for either homologous or heterologous recombination as described in detail below. The vector encompassing the polynucleotides of the present invention, preferably, further comprises selectable markers for propagation and/or selection in a host. The vector may be incorporated into a host cell by various techniques well known in the art. For example, a plasmid vector can be introduced in a precipitate such as a calcium phosphate precipitate or rubidium chloride precipitate, or in a complex with a charged lipid or in carbon-based clusters, such as fullerens. Alternatively, a plasmid vector may be introduced by heat shock or electroporation techniques. Should the vector be a virus, it may be packaged in vitro using an appropriate packaging cell line prior to application to host cells. Retroviral vectors may be replication competent or replication defective. In the latter case, viral propagation generally will occur only in complementing host/cells.
More preferably, the vector of the invention the polynucleotide is operatively linked to expression control sequences allowing expression in prokaryotic cells or isolated fractions thereof. Expression of said polynucleotide comprises transcription of the polynucleotide, preferably into a translatable mRNA. Possible regulatory elements permitting expression in prokaryotic host cells comprise, e.g., the lac, trp or tac promoter in E. coli. Moreover, inducible expression control sequences may be used in an expression vector encompassed by the present invention. Such inducible vectors may comprise tet or lac operator sequences or sequences inducible by heat shock or other environmental factors. Suitable expression control sequences are well known in the art. Beside elements which are responsible for the initiation of transcription such regulatory elements may also comprise transcription termination signals. In this context, suitable expression vectors are known in the art. Preferred expression vectors are given in Seleem et al. (2008), Gene 421: 95-98 and Shkoporov et al. (2008) Biotechnol. Lett. 30: 1983-1988. Preferably, said vector is an expression vector and a gene transfer or targeting vector. Methods which are well known to those skilled in the art can be used to construct recombinant viral vectors; see, for example, the techniques described in Sambrook, Molecular Cloning A Laboratory Manual, Cold Spring Harbor Laboratory (1989) N.Y. and Ausubel, Current Protocols in Molecular Biology, Green Publishing Associates and Wiley Interscience, N.Y. (1994).
The present invention further relates to a bacterial host cell comprising the chemotaxis fusion-receptor of the present invention, the polynucleotide of the present invention, or the vector of the present invention.
A “bacterial host cell” as referred to in the present application is, preferably, a bacterial cell which is capable of surviving in an animal organism without causing systemic infection. To limit the pathogenic potential of such a bacterial host cell it is envisaged to limit its ability to proliferate in the animal body, e.g. by deleting genes that are required for iron uptake. A further criterion for the suitability of a bacterial host cell according to the invention is the possibility to functionally integrate the above described chemotaxis fusion-receptor so that the chemotaxis fusion-receptor can elicit positive or negative chemotaxis upon binding of the ligand. Preferred bacteria to be used as host cells according to the present invention belong to the genera Clostridium, Bifidobacterium, Salmonella and Escherichia. Especially preferred are S. thyphimurium, E. coli, C. novyi and C. acetobutylicum.
The present invention further relates to a bacterial host cell comprising at least two chemotaxis fusion-receptors. In many cases cancer cells can not be identified by the secretion of unique compounds, i.e. compounds that are only secreted by cancer cells and not by normal cells. Thus, it is not possible to use a single compound as a target for bacterial chemotaxis in order to direct the bacterial host cells to the cancer cells. However, compounds that are secreted by many or even all cell types of the animal body may be secreted by cancer cells in different amounts. Hence, cancer cells show different secretion profiles of these compounds as compared to normal cells. As described in the introduction it is possible to integrate the signals from different compounds. The combination of at least two chemotaxis fusion-receptors specific for different ligands in one bacterial host cell increases its specificity for cancer cells, because it enables the differentiation between cells with quantitatively but not qualitatively different secretion profiles.
Preferably, the expression level of a receptor in a bacterial host cell can be used to achieve a different sensitivity of the cell for the respective ligand. For example, a bacterial host cell expressing high amounts of a chemotaxis fusion-receptor according to the present invention is capable of responding to lower levels of the ligand than a bacterial host cell expressing a lower amount of the chemotaxis fusion-receptor of the present invention. Also preferably, the affinity of the receptor for the ligand is changed by directed or undirected evolution. Further preferred, is the addition of specificity to the sensing by combining receptors for attracting ligands (i.e. ligands which elicit positive chemotaxis) and repelling ligands (i.e. ligands which elicit negative chemotaxis) in the same bacterial host cell.
The term “cancer” as referred to in the present application refers to cancer of haematopoietic origin or solid cancers. Preferably it refers to leukaemia, lymphoma, breast cancer, gastric cancers, colon cancer, lung cancer, cancers of the skin, brain tumors, cancers of the oesophagus, kidney cancer, liver cancer, osteosarcoma, prostrate cancer, cervix carcinoma. Most preferably the term “cancer” refers to melanoma, lung cancer and oral submucous fibrosis.
Furthermore, the present invention, preferably, relates to a bacterial host cell comprising at least one chemotaxis fusion-receptor and at least one gene which enables the bacterial host cell to kill cancer cells. Said bacterial host cell, preferably, kills the cancer cell by inducing apoptosis or necrosis.
In a preferred embodiment of the present invention the killing module comprises a gene which encodes at least one physiologically active molecule to induce a physiological response in the cancer cells. Preferred physiologically active molecules that induce biological responses in cancer cells are TNFα, interleukin-2, molecules inhibiting hypoxia inducible factor 1α, endostatin, and thrombospondin 1. More preferred is a killing module which enables the bacterial host cell to produce a bacteriocin. The anti-cancer properties of bacteriocins are discussed by Comut et al. (2008) Am. J. Oncol. 31: 399-404. Most preferred is a killing module which enables the bacterial host cell to produce a colicin. Colicins are peptides produced by the enterobacterium Escherichia coli. They are lethal for other bacteria. Interestingly, colicins are toxic for cancer cells as well (Smarda J et al., 2001 Folia Microbiol. (Praha) 47: 11-13). To be effective the colicins have to be taken up by the target cell. Most colicins have either nuclease activity or form pores in the bacterial cell membrane. The nuclease activity degrades the genome of the target cell. Colicins that form pores in the cell membrane make it permeable for inorganic ions and, thus, destroy the electrochemical gradient across the membrane. The target cell dies because ATP-production stops. Colicins are potentially lethal for the bacterial host cell, too. Thus, the killing module preferably comprises additionally an immunity gene against the colicin under the control of a constitutive promoter. Furthermore, the killing module comprises, preferably, a lysis gene that induces lysis of the bacterial host cell to liberate the produced colicins. Especially preferred killing modules comprise the colicins E9, a colicin with nuclease activity, or the colicin E1, a pore-forming colicin.
It is further envisaged to equip the bacterial host with a killing module that enables the transfer of genes encoding physiologically active proteins into the cancer cells. This process is known as bactofection (Palffy R et al., 2006, Gene Ther. 13: 101-105).
Furthermore, a preferred killing module in the context of the present invention comprises at least one gene encoding at least one pro-drug activating enzyme. If the expression of such an enzyme occurs preferably close to the cancer cells, the activation of the pro-drug happens at a higher rate close to the cancer cells so that the effective concentration of the active drug is high at the cancer cells and comparatively low at other places. Thus, a maximal therapeutic effect on the cancer cells is combined with little undesired side effects of the drug. A preferred pro-drug activating enzyme is cytosine deaminase which converts the pro-drug 5-fluorocytosine into the chemotherapeutic 5-fluorouracil.
All of the above described killing modules are, preferably, under the control of promoters that ensure that the killing module is only activated after the bacteria have reached the cancer cells. Thus, in a preferred embodiment of the present invention the killing module is controlled by a promoter which is specifically activated in the tumor-environment. A preferred promoter is the promoter controlling the formiate dehydrogenase gene in E. coli. It is active under hypoxic conditions. Such conditions are frequently encountered in tumor tissue.
In another preferred embodiment of the present invention the promoter is PLuxR from Vibrio harveyi. In this case the bacterial host cell comprises a further gene encoding a modified LuxR-protein. In the modified LuxR-protein the ligand binding domain of the original LuxR-protein is exchanged for a binding domain recognizing a compound produced by a HI tumor cell. Preferred binding domains are derived from the antibodies, receptors and proteins given in table 1, third column. However, since the LuxR-protein is located intracellularly, a modified LuxR-protein can only be used, if the chosen ligand is able to permeate the bacterial cell membrane.
In yet another preferred embodiment of the present invention the promoter controlling the expression of the killing module is controlled by an external stimulus. Preferred promoters that are controlled by external stimuli react to non-toxic small molecules or radiation. Especially preferred are the PBAD-promoter of E. coli which is induced by L-arabinose or the radiation-induced recA-promoter sequence. Furthermore, the use of a system comprising the rtTA-protein or the tTA-protein in combination with the tetO-operator is envisaged by the present invention for the expression control of the killing module.
In another preferred embodiment of the present invention any of the above described bacterial host cells is used for the manufacture of a pharmaceutical composition for treating cancer in patient.
The term “pharmaceutical composition” as used in the present patent application comprises the bacterial host cell of the present invention and, preferably, one or more pharmaceutically acceptable carrier(s). The pharmaceutical compositions are, preferably, administered systemically. Preferred routes of administration are intravenous or parenteral administration.
Moreover, the bacterial host cells can be administered in combination with other drugs either in a common pharmaceutical composition or as separated pharmaceutical compositions wherein said separated pharmaceutical compositions may be provided in form of a kit of parts.
The bacterial host cells are, preferably, administered in conventional dosage forms prepared by combining the drugs with standard pharmaceutical carriers according to conventional procedures. These procedures may involve mixing, suspending or dissolving the ingredients as appropriate to the desired preparation. It will be appreciated that the form and character of the pharmaceutically acceptable carrier or diluent is dictated by the amount of active ingredient with which it is to be combined, the route of administration and other well-known variables.
The carrier(s) must be acceptable in the sense of being compatible with the other ingredients of the formulation and being not deleterious to the recipient thereof. The pharmaceutical carrier employed may be, for example a liquid. Exemplary of liquid carriers are phosphate buffered saline solution, syrup, oil, water, emulsions, various types of wetting agents and the like. Similarly, the carrier or diluent may include time delay material well known to the art, such as glyceryl mono-stearate or glyceryl distearate alone or with a wax. Said suitable carriers comprise those mentioned above and others well known in the art, see, e.g., Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, Pa.
The diluent(s) is/are selected so as not to affect the biological activity of the bacterial host cell. Examples of such diluents are physiological saline, Ringer's solutions, dextrose solution, and Hank's solution. In addition, the pharmaceutical composition or formulation may also include other carriers, adjuvants, or nontoxic, nontherapeutic, nonimmunogenic stabilizers and the like.
A therapeutically effective dose refers to an amount of the compounds to be used in a pharmaceutical composition of the present invention which prevents, ameliorates or treats the symptoms accompanying a disease or condition referred to in this specification. Therapeutic efficacy and toxicity of such compounds can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., ED50 (the dose therapeutically effective in 50% of the population) and LD50 (the dose lethal to 50% of the population). The dose ratio between therapeutic and toxic effects is the therapeutic index, and it can be expressed as the ratio, LD50/ED50.
The dosage regimen will be determined by the attending physician and other clinical factors; preferably in accordance with any one of the above described methods. As is well known in the medical arts, dosages for any one patient depends upon many factors, including the patient's size, body surface area, age, the particular compound to be administered, sex, time and route of administration, general health, and other drugs being administered concurrently. Progress can be monitored by periodic assessment.
The pharmaceutical compositions and formulations referred to herein are administered at least once in order to treat or ameliorate or prevent a disease or condition recited in this specification. However, the said pharmaceutical compositions may be administered more than one time, for example from one to four times daily up to a non-limited number of days. Dosage recommendations shall be indicated in the prescribers or users instructions in order to anticipate dose adjustments depending on the considered recipient.
The term “treating” refers to ameliorating the diseases or disorders referred to herein or the symptoms accompanied therewith to a significant extent. Said treating as used herein also includes an entire restoration of the health with respect to the diseases or disorders referred to herein. It is to be understood that treating as used in accordance with the present invention may not be effective in all subjects to be treated. However, the term shall require that a statistically significant portion of subjects suffering from a disease or disorder referred to herein can be successfully treated. Whether a portion is statistically significant can be determined without further ado by the person skilled in the art using various well known statistic evaluation tools, e.g., determination of confidence intervals, p-value determination, Student's t-test, Mann-Whitney test etc. Preferred confidence intervals are at least 90%, at least 95%, at least 97%, at least 98% or at least 99%. The p-values are, preferably, 0.1, 0.05, 0.01, 0.005, or 0.0001. Preferably, the treatment shall be effective for at least 60%, at least 70%, at least 80%, or at least 90% of the subjects of a given cohort or population.
A “subject” as referred to herein is, preferably, an animal. More preferably, it is a mammal. Even more preferably it is a cat, dog, mouse, rat, guinea pig, pig, horse or sheep. Most preferably, the patient is a human. Preferably, the patient to be treated with one of the pharmaceutical compositions described above is suffering from cancer or suspected to suffer from cancer.
The present invention, finally, relates to a method for treating cancer in a subject comprising the step of administering any of the above described bacterial host cells or compositions to a subject suffering from cancer in a therapeutically active amount.
All the references cited in this specification are herewith incorporated by reference with respect to their entire disclosure content and the disclosure content specifically mentioned in the specification.
The following Examples are given to illustrate the invention. They shall not be construed as to limit the scope of the invention.
LuxS (SEQ ID NO. 3) was amplified from the V. harveyi genome and cloned into pTrc99α (SEQ ID NO. 5) with NcoI/BamHI. Restriction sites were introduced into the gene via the PCR primers. Subsequently the construct was cloned into E. coli DH5α. LuxS expression is controlled via an IPTG-inducible promoter.
First LuxQ and Tar parts for each Fusion receptor were amplified. LuxQ was taken from V. harveyi genome, Tar from pDK48 (SEQ ID NO. 6). Reverse Primers of LuxQ and forward primers of Tar were complementary, thus making it possible to fuse both parts together in a second PCR. Afterwards the Fusion constructs were cloned into pDK48 with NcoI/NdeI. AI-2 binding to LuxQ also requires LuxP (SEQ ID NO. 4) wherefore this was also amplified from V. harveyi. First it was cloned into native pDK48 with SalI/NotI and later on pDK48 containing the Fusion receptors at the same sites. It was necessary to first produce the Fusion constructs, because of conflicting restriction sites. Subsequently the constructs were transformed into E. coli MG1655 and HCB33 which could be used to the test the constructs in swarm assays. Since those two strains also contain other chemotaxis receptors swarm assays needed to be performed on minimal medium where cells do not grow so well. Therefore UU1250, a knock-out strain for chemotaxis receptors, was also used for swarm assay. Yet there was a conflict with antibiotic resistance. UU1250 have Kanamycin resistance encoded on the genome which is also on pDK48. Therefore the Fusion constructs were cloned into pBAD33 (SEQ ID NO. 7; Chloramphenicol resistance) with BamHI/PstI and then transformed into UU1250. Expression of the Fusion receptor is controllable via an arabinose-inducible promoter, both on pDK48 and pBAD33.
The sender activity test was performed to measure the efficiency of the AHL production of the sender cells. Therefore TB-media with the appropriated antibiotic was inoculated from with 2 μl/ml of an overnight culture. For 7 hours every hour the OD of the medium was measured and 5 ml of the culture were spin down to produce supernatant. The sterile filtered supernatant, still containing the AHL, was stored at 4° C. The supernatant of every hour was then added in different ratios to a constant amount of AHL inducible cells which produce GFP after induction. The OD and GFP intensities were measured at 37° C. in the Tecan Microplate Reader every half an hour for about 12 hours. The same test was carried out with amplifier cells. To calculate the produced amount of AHL by sender or amplifier cells as reference the test were performed also with different AHL concentration (0 M-100 nM) instead of AHL producing cells.
As shown in
To measure the killing efficiency and which amount of cells or colicins are needed to reach any killing activity a colicin activity test was carried out. Therefore bacteria containing the colicin plasmid (TOP10 or MG1655) and GFP producing cells (reference promoter, TOP10) were inoculated in TB-media with appropriated antibiotics at 37° C. for 4 to 6 hours and the optical density of the two strains was adapted. The colicin cells themselves, their produced supernatant or the supernatant of the lysed colicin cells were added in different ratios to a constant amount of GFP producing cells. The total volume was kept constant and the missing amount added with TB-media without antibiotics. The colicin production was induced by several concentrations (0 M-100 nM) of N-Acyl-Homoserin-Lactone (AHL). The OD and GFP intensities were measured at 37° C. in the Tecan Microplate Reader every half an hour for about 12 hours.
As a negative control the similar test was carried out with cells, containing the same plasmid without the colicin gene on it.
The two bar diagrams in
| Number | Date | Country | Kind |
|---|---|---|---|
| 08167775.9 | Oct 2008 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2009/064047 | 10/26/2009 | WO | 00 | 8/5/2011 |
