Patent Application
20150147290
The content of the following submission on ASCII text file is incorporated herein by reference in its entirety: a computer readable form (CRF) of the Sequence Listing (file name: 720622000201SeqList.txt, date recorded: Oct. 27, 2014, size: 23 KB).
This invention relates to the area of biological and medical technologies, in particular, this invention relates to the use of recombinant human G-CSF (rhG-CSF) dimer in the treatment of neutropenia.
Human granulocyte colony-stimulating factor (G-CSF) is a glycoprotein having 204 amino acids with 30 amino-acid signal peptides. Mature G-CSF protein, having 18-20 kDa in molecular weight, is composed of 174 amino acids without signal peptides and secreted out of the cells. Human cells mainly responsible for such secretion are monocytes, fibroblasts, and endothelial cells.
There are three main biological functions for G-CSF in an living organism, namely: 1. acting on neutrophil precursor cells and myeloid stem cells to drive the differentiation, proliferation, and maturation of neutrophils; 2. activating mature neutrophils to participate in immune response; and 3. synergizing with other hematopoietic growth factors such as stem cell factor, Flt-3 ligand, and GM-CSF to perform hematopoietic functions.
G-CSF receptor (G-CSFR) is proven to exist in bone marrow hematopoietic stem cell Sca+Lin−Th1low, precursor cell CD34+, committed granulocyte precursor cell, and mature neutrophil. Human G-CSFR is a single-chain specific receptor having a high affinity to G-CSF and is composed of 812 amino acids.
Tamada et al. obtained the crystalline structure of the G-CSF:G-CSFR complex and the stoichiometry of G-CSF:G-CSFR complex was shown as a 2:2 ratio by the 2.8 angstrom diffraction analysis (PNAS, 2008, Vol. 103: 3135-3140). In other words, each complex has two G-CSF molecules and two G-CSFR molecules. Each G-CSF molecule binds to one receptor to form a G-CSF-receptor complex and when two G-CSF-receptor complexes are brought to close proximity, a 2:2 dimer is formed as a result of this interaction. Under this circumstance, the carboxyl terminal of the G-CSF receptor is then able to activate the downstream signal molecules JAK2 (Janus tyrosine kinases). Consequently, JAK2 actives STAT3 to switch on the transcriptional genes to stimulate the cell proliferation.
Neutropenia is characterized by a neutrophil count in the peripheral blood of lower than 1.8×109/L for an adult and 1.5×109/L for a child. Neutropenia is often a precursor of infection: the lower the neutrophil count is, the higher the risk of infection is.
The guideline used to classify neutropenia is shown as below:
The frequency and severity of infection caused by neutropenia are also influenced by other factors, such as: the integrity of the mucosa and skin, immunoglobulin, lymphocytes, monocytes, the function and level of the complement system, etc.
According to the cause of neutropenia, the common clinical neutropenia can be divided into the following categories: disorder of hematopoietic system generation that are caused by secondary factors such as drugs, radiation, chemical reagents and infection; changes of in vivo distribution and circulation, increased utilization and turnover. The severity of chemotherapy-induced neutropenia in tumor patients generally depends on the dosage of chemotherapy, and the repeated use of chemotherapy may have a cumulative effect on neutropenia. A main clinical consequence of neutropenia is infected complication. Most of the infections in those patients are mainly caused by aerobic bacteria, including Gram-negative bacteria (Escherichia coli, Klebsiella pheumoniae and Pseudomonas aeruginosa), Gram-positive bacteria (Staphylococci, α-hemolytic Streptococci, and Straphylococcus aureus) and fungi.
Cytotoxic-chemotherapy is still one of the major treatments of cancer. The biggest disadvantage of chemotherapy treatment is that this treatment would indiscriminately kill healthy cells with rapid proliferation and differentiation together with tumor cells. The toxicity caused by chemotherapy is mainly expressed in the hematopoietic system that is neutropenia which is clinically known as chemotherapy-induced neutropenia.
Neutropenia may delay the next treatment cycle, which directly impacts on the therapeutic effects of chemotherapy. A severe neutropenia, i.e. the absolute neutrophil count (ANC) is lower than 0.5×109/L, can cause infection in patient, organ failure and even threaten the life of the patient. Recombinant human granulocyte colony-stimulating factor (rhG-CSF) has been widely used in chemotherapy-induced and/or radiotherapy-induced neutropenia as a standard supportive therapy for chemotherapy-treated cancer patients.
There are two main categories of rhG-CSF used for therapy available in the market. The first category comprises recombinant proteins expressed by E. coli comprising 175 amino acids with 19 kD in molecular weight and the amino terminus thereof is methionine (Filgrastim); recombinant proteins produced by the mammalian cell CHO comprising 174 amino acids and modified by glycosylation. This category of rhG-CSF is short-acting and requires multiple injections daily or weekly. The second category comprises Filgrastim with pegylation (20 kD-PEG) modification on the N terminal of the protein molecule thereof. The molecular weight of the modified Pegfilgrastim is doubled, which reduces the renal excretion rate, increases the half-life of Filgrastim from 3.5 hours to 15-80 hours and facilitates the clinical use. The rhG-CSF used in both categories is G-CSF monomer.
However, the short-acting Filgrastim and the long-acting Pegfilgrastim currently used in clinical application still cannot meet the needs of patients. In 2008, Sierra et. al. compared the effects of Filgrastim and the Pegfilgrastim in the treatment of neutropenia in chemotherapy-treated acute leukemia patients (BMC Cancer 2008, 8:195). The study was designed as a randomized double-blind clinical trial. Patients with acute myeloid leukemia were treated with chemotherapy Induction I, receiving a chemotherapeutic agent of Idarubicin 12 mg/M2 from Day 1 to Day 3, and a chemotherapeutic agent of Cytarabine 100 mg/M2 from Day 1 to Day 7, twice per day. The patients were randomly divided into two groups at Days 6-8. One group was treated with Filgrastim 5 μg/kg/day (n=41) while the other group was treated with Pegfilgrastim 6.0 mg/week (n=42). The results showed that, after completion of chemotherapy, all patients suffered from severe neutropenia that lasted around three weeks starting from 3-4 days upon the use of rhG-CSF therapy. Moreover, there was no significant difference in the efficacy of two groups receiving two different rhG-CSF treatments. This suggested that the mere extension of half-life seems to be sufficient to obtain a satisfactory therapeutic effect.
Therefore, there is an urgent need in the art to develop more effective drugs for treating neutropenia, in order to effectively reduce the severity of the neutropenia and/or shorten the time of severe neutropenia.
In the light of the foregoing background, it is an object of the present invention to provide an alternate drug for the treatment of neutropenia with improved efficacy and the use thereof.
Accordingly, the present invention, in one aspect, provides a use of human granulocyte colony-stimulating factor (G-CSF) dimer in the manufacture of a drug for treating neutropenia.
In an exemplary embodiment of the present invention, the neutropenia comprises a condition in which neutropenia induced by chemotherapy and/or radiotherapy.
In another exemplary embodiment, the neutropenia is severe neutropenia.
In another implementation, the human G-CSF (hG-CSG) dimer is shown as formula (I):
M1-L-M2 (I)
wherein
M1 is a first human G-CSF monomer;
M2 is a second human G-CSF monomer; and
L is a linker connecting the first monomer and the second monomer and disposed there between.
The G-CSF dimer retains the biological activity of a G-CSF monomer and has a serum half-life of at least twice of the half-life of either the first or the second monomer.
In an exemplary embodiment of the present invention, the linker L is selected from the group consisting of:
i). a short peptide (or a connecting peptide) comprising 3 to 50 (or 5 to 50) amino acids; and
ii). a polypeptide of formula (II):
—Z—Y—Z— (II)
wherein
Y is a carrier protein;
Z is null, or a short peptide(s) comprising 1 to 30 amino acids.
“—” is a chemical bond or a covalent bond.
In another exemplary embodiment, the first monomer and the second monomer are of the same entity.
In another exemplary embodiment, the first monomer and the second monomer are of the different entities.
In an exemplary embodiment, the biological activity includes:
(a). acting on neutrophil precursor cells and myeloid stem cells to drive the differentiation, proliferation, and maturation of neutrophils; and
(b). activating mature neutrophils to participate in immune response.
In another exemplary embodiment, the carrier protein is albumin or Fc fragment of human IgG.
In another exemplary embodiment, at least the first to the fourth amino acids of the hinge region are missing in the Fc fragment of human IgG and at least two cysteine residues are retained in the Fc fragment.
In another exemplary embodiment, the carrier protein is formed by the connection of two Fc fragments of IgG via disulfide bonds. In another exemplary embodiment, there are 2-3 disulfide bonds between the two Fc fragments.
In another exemplary embodiment, the “—” is a peptide bond.
In one exemplary embodiment, the serum half-life of the G-CSF dimer is at least three, five, or ten times of the half-life of the first and/or the second monomer.
In another exemplary embodiment, the G-CSF dimer is formed by two monomers in which the monomer comprises an amino acid sequence selected from a group consisting of SEQ ID NO: 2-6.
In another aspect of the present invention, a G-CSF dimer of formula (I) is provided:
M1-L-M2 (I)
wherein
M1 is a first G-CSF monomer;
M2 is a second G-CSF monomer; and
L is a linker connecting the first monomer and the second monomer and disposed there between.
Also, the G-CSF dimer retains the biological activity of G-CSF monomer and has a serum half-life of at least twice of the half-life of either the first or the second monomer.
In another exemplary embodiment, the carrier protein is albumin or Fc fragment of human IgG.
In another exemplary embodiment, a method of preparing the (i-CSF dimer comprises the following steps of:
a). transforming mammalian cells with an expression vector comprising a DNA sequence encoding G-CSF-Fc complex;
b). culturing the transformed mammalian cells for expressing an expression product comprising the G-CSF-Fc complex, the G-CSF dimer and the polymer thereof; and
c). isolating and purifying the G-CSF dimer.
In the third aspect of the present invention, a pharmaceutical composition is provided, comprising a human G-CSF dimer as described in the second aspect of the present invention and a pharmaceutically acceptable carrier.
In another exemplary embodiment, said pharmaceutical composition basically does not comprise any human G-CSF monomer. In a preferred exemplary embodiment, a weight ratio of human G-CSF dimer to human G-CSF monomer is ≧20:1; in an even preferred embodiment, the weight ratio thereof is ≧30:1; and in the most preferred embodiment, the weight ratio thereof is ≧50:1.
It is clear for a skilled person in the art that, the technical features mentioned above and discussed in the examples below of the present invention could combine with each other to result in a new or even better technical solution. Hence this invention should not be construed as limited to the embodiments set forth herein.
An amino acid sequence of the G-CSF dimer is shown in SEQ ID NO:1, in which the amino acid residues 1-174 represent a G-CSF monomer, the amino acid residues 175-190 represent a linker, and the amino acid residues 191-364 represent another G-CSF monomer.
An amino acid sequence of a G-CSF monomer with Fc fragment to form a G-CSF dimer is shown in SEQ ID NO: 2, in which the amino acid residues 1-174 represent a G-CSF monomer, the amino acid residues 175-190 represent a linker, and the amino acid residues 191-418 represent an Fc fragment of human IgG2. A G-CSF dimer is formed by the coupling of the Fc fragments present in the two G-CSF monomers.
An amino acid sequence of a G-CSF monomer with Fc fragment to form a G-CSF dimer is shown in SEQ ID NO: 3, in which the amino acid residues 1-174 represent a G-CSF monomer, the amino acid residues 175-180 represent a linker, and the amino acid residues 191-408 represent an Fc fragment of human IgG2. A G-CSF dimer is formed by the coupling of the Fc fragments present in the two G-CSF monomers.
An amino acid sequence of a G-CSF monomer with Fc fragment to form a G-CSF dimer is shown in SEQ Ill NO: 4, in which the amino acid residues 1-228 represent an Fc fragment of human IgG2, the amino acid residues 229-244 represent a linker, and the amino acid residues 245-418 represent a G-CSF monomer. A G-CSF dimer is formed by the coupling of the Fc fragments present in the two G-CSF monomers.
An amino acid sequence of a G-CSF monomer with Fc fragment to form a G-CSF dimer is shown in SEQ ID NO: 5, in which the amino acid residues 1-228 represent an Fe fragment of human IgG2, the amino acid residues 229-234 represent a linker, and the amino acid residues 235-418 represent a G-CSF monomer. A G-CSF dimer is formed by the coupling of the Fc fragments present in the two G-CSF monomers.
Upon an extensive and thorough research, the inventors have, for the first time ever, accidentally discovered that on comparing with G-CSF monomer, rhG-CSF dimer can generate a stronger receptor activation signal to accelerate the differentiation and proliferation of hone marrow neutrophils. Meanwhile, the properties of the pharmacokinetics and pharmacodynamics of G-CSF dimer are better than that of the rhG-CSF monomer. Therefore, the G-CSF dimer can effectively reduce the extent of the severe neutropenia and shorten the time of severe neutropenia for cancer patients upon receiving chemotherapy. The present invention was made based on the above understanding.
G-CSF Dimer
The first embodiment of the present invention is a G-CSF dimer represented by the aforesaid formula (I) and the structural illustration thereof is shown in
In one preferred embodiment, G-CSF can be disposed at the C-terminal or N-terminal of the carrier protein.
As used herein, “linker” can refer to a short peptide for connecting the two G-CSF monomers and being disposed therebetween. There is no special restriction on the length of the linker. A linker is usually 5-50 amino acid residues in length; in general, a linker does not affect or significantly affect the proper fold and spatial conformation formed by the configuration of the two G-CSF monomers. Examples of linker include but not limited to:
In a further preferred embodiment, the linker comprises amino acid sequence selected from a group consisting of:
(a). an amino acid sequence with 3-16 amino acid residues formed by hydrophobic amino acids glycine (Gly) or proline (Pro), such as Gly-Pro-Gly-Pro-Gly-Pro;
(b). an amino acid sequence encoded by multiple cloning sites. Such sequence usually contains 5-20 amino acid residues; in a preferred embodiment, such sequence contains 10-20 amino acid residues;
(c). an amino acid sequence comprising protein(s) not from G-CSF monomer, such as an amino acid sequence of IgG or albumin;
(d). an amino acid sequence comprising any combination of (a), (b), and (c) above.
In one preferred embodiment, the linker has the sequence of GSGGGSGGGGSGGGGS (i.e. 175-190 amino acid residues of SEQ ID NO:1). In another preferred embodiment, the linker has the sequence of ASTKGP (i.e. 175-180 amino acid residues of SEQ ID NO:3).
In a further preferred embodiment, an amino acid sequence not affecting the biological activity of G-CSF monomer can be added to the N-terminal or C-terminal of the fusion protein. In a preferred embodiment, such appended amino acid sequence is beneficial to expression (e.g. signal peptide), purification (e.g. 6×His sequence, the cleavage site of Saccharomyces cerevisiae α-factor signal peptide (Glu-Lys-Arg)), or enhancement of biological activity of the fusion protein.
Preparation Method
The encoding of the DNA sequence of the G-CSF dimer or fusion protein of the present invention can be entirely synthesized artificially. Alternatively, the encoded DNA sequences of the first G-CSF monomer and/or the second G-CSF monomer can be obtained by PCR amplification or synthesis and then joined together to form the encoded DNA sequence of the G-CSF dimer or fusion protein of the present invention.
In order to enhance the expression volume of the host cells, modification can be performed on the encoded sequence of G-CSF dimer. For example, codon bias of host cells can be used to eliminate sequences that are not beneficial to gene transcription and translation. In a preferred embodiment, codon bias of yeast cells or mammalian cells can be used together with DNA software for detecting genes of G-CSF dimer, in order to eliminate sequences that are not beneficial to gene transcription and translation. In one preferred embodiment, the eliminated sequences can be intron cutting site, transcription terminating sequence, etc.
After the encoded DNA sequence of the novel fusion protein of the present invention is obtained, it is first inserted into an appropriate expression carrier, followed by an appropriate host cell. Finally, the transformed host cell is cultivated and purified to obtain the novel fusion protein of the present invention.
As used herein and in the claims, “carrier” refers to plasmid, cosmid, expression vehicle, cloning vector, virus vector, etc.
In this invention, carrier known in the art, such as those available in the market, can be used. For example, with the use of carrier obtained from the market, encoded nucleotide sequence of the novel fusion protein of the present invention is operationally connected to the expressing and controlling sequence to form the protein-expressing carrier.
As used herein and in the claims, “operationally connected” refers to a scenario that some parts of a linear DNA sequence can affect the biological activity of other parts of the same linear DNA sequence. For instance, if signal DNA is used as the expression of a precursor and participates in secretion of polypeptides, the signal DNA (secretion leader sequence) is “operationally connected” to the polypeptides. If a promoter controls sequence transcription, the promoter is “operationally connected” to the encoded sequence. If a ribosome binding site is situated at a position where translation thereof is made possible, the ribosome binding site is “operationally connected” to the encoded sequence. In general, “operationally connected” means that the residues of concern are in proximity; for secretion leader sequence, “operationally connected” refers to proximity within the reading frame.
As used herein and in the claims, “host cells” refers to both prokaryotic cells and eukaryotic cells. Prokaryotic host cells commonly used include E. coli, B. subtilis, etc.
Eukaryotic host cells commonly used include yeast cells, insect cells, mammalian cells, etc. In a preferred embodiment, the host cells used are eukaryotic cells; in another preferred embodiment, the host cells used are mammalian cells.
After the transformed host cells are obtained, they can be cultivated under an environment suitable to express the fusion protein of the present invention for expressing the fusion protein. The expressed fusion protein is then separated.
Pharmaceutical Composition and Method of Administration Thereof
Since the G-CSF dimer of the present invention can generate a stronger receptor activation signal and has an excellent serum half-life, the G-CSF dimer and a pharmaceutical composition comprising the G-CSF dimer as the main active ingredient can be used for treating neutropenia. In a preferred embodiment, the neutropenia comprises a condition in which neutropenia is induced by chemotherapy and/or radiotherapy.
The pharmaceutical composition of the present invention comprises a safe and effective amount of the G-CSF dimer of the present invention and a pharmaceutically acceptable excipient or carrier. “Safe and effective amount” refers to an amount of a compound sufficient to substantially improve the condition of the patient in need thereof without causing serious side-effects. In general, the pharmaceutical composition comprises 0.001-1,000 mg of G-CSF dimer of the present invention per dose; in a preferred embodiment, the pharmaceutical composition comprises 0.05-300 mg of G-CSF dimer of the present invention per dose; in a further preferred embodiment, the pharmaceutical composition comprises 0.5-200 mg of G-CSF dimer of the present invention per dose.
The compound of the present invention and its pharmaceutically acceptable salts can be manufactured into different formulations, which comprises a safe and effective amount of the G-CSF dimer of the present invention or its pharmaceutically acceptable salts and a pharmaceutically acceptable excipient or carrier. “Safe and effective amount” refers to an amount of a compound sufficient to substantially improve the condition of the patient in need thereof without causing serious side-effects. The safe and effective amount of a compound is determined according to the age, condition, course of treatment, etc. of the patient in treatment.
“Pharmaceutically acceptable excipient or carrier” refers to solid or liquid filling or gelatin materials with one or different kinds of compatibility which are suitable to be used in human with sufficient purity and sufficiently low toxicity. “Compatibility” refers to the ability of each ingredient of the composition to mutually blend with the compound of the present invention and the mutual blending ability there between, without substantially decreasing the clinical efficacy of the compound. Some of the examples of pharmaceutically acceptable excipient or carrier include cellulose and its derivatives (e.g. sodium carboxymethylcellulose, sodium ethylcellulose, cellulose acetate, etc), gelatin, speckstone, solid lubricating agent (e.g. stearic acid, magnesium stearate), calcium sulphate, plant oil (e.g. pea oil, sesame oil, peanut oil, olive oil, etc.), polyols (e.g. propylene glycol, glycerol, mannitol, sorbitol, etc.), emulsifier (e.g. Tween®), wetting agent (e.g sodium lauryl sulfate), colorant, flavoring agent, stabilizer, anti-oxidant, antiseptic, pyrogen-free water, etc.
Route of administration of the G-CSF dimer of the present invention comprises oral administration, rectal administration, parenteral administration (intravenous, intramuscular, or subcutaneous), and partial administration.
Solid form for oral administration comprises capsules, tablets, pills, powder, and granules. In these solid forms, active compound is mixed with at least one of the conventionally inert excipients (or carriers), such as sodium citrate, dicalcium phosphate, or any of the following ingredients: (a) filing or bulking agent, e.g. starch, lactose, sucrose, glucose, mannitol, and silicic acid; (b) adhesion agent, e.g. carboxymethylcellulose, alginate, gelatin, polyvinyl pyrrolidone, sucrose, and acacia; (c) humectants, e.g. glycerol; (d) disintegrating agent, e.g. agar, calcium carbonate, potato starch or cassava starch, alginic acid, compounded silicate, and sodium carbonate; (e) buffering agent, e.g. paraffin wax; (f) absorption accelerating agent, e.g. quaternary amine compound; (g) wetting agent, e.g. cetanol and glycerin monostearate; (h) absorbent, e.g. bolus alba; and (i). lubricating agent, e.g. speckstone, calcium stearate, sodium stearate, solid polyethylene glycol, sodium lauryl sulfate, or any mixture thereof. Capsules, tablets, and pills can also comprise buffering agent.
Solid forms such as tablets, sugar pill, capsules, pills, and granules can be prepared with coating and core-shell materials, such as casing and other materials known in the art. These materials comprise opacifying agent and the active compound or compound in such composition can be released in a delayed fashion that the release is done in certain part of the alimentary canal. Embedding component such as polymer materials and wax materials can be used. If desired, active compounds can be mixed with one or more of the above-described excipients to formulate a micro capsule form.
Liquid forms for oral administration comprise pharmaceutically acceptable emulsion, solution, suspension, syrup, or tincture. Apart from active compounds, liquid forms also comprise inert diluents conventionally used in the art such as water or other solvent, solublilizing agent and emulsifier such as ethanol, isopropanol, carbonate acetate, ethyl acetate, propan-2-ol, 1,3-butan-2-ol, dimethylfomamide, and oil, in particular cotton oil, peanut oil, castor oil, olive oil, maize embryo oil, and sesame oil or any mixture thereof.
Apart from the inert diluents, the compound can also comprise additives, such as wetting agent, emulsifying agent, suspending agent, sweetening agent, correctives, and spices.
Apart from active compounds, suspension can also comprise suspending agent, such as ethoxyl isostearic alcohol, polyoxyethylene sorbitol, sorbitan, microcrystalline cellulose, aluminium methoxide, agar, or any mixture thereof.
Compounds used for parenteral administration can also comprise physiologically acceptable sterile water or anhydrous solution, dispersion solution, suspension, or emulsion, and sterile powder that can be re-dissolved into sterile injectable solution or dispersion solution. Appropriate hydrated or anhydrous carriers, diluting agent, solvent, or excipient comprises water, ethanol, polyols, and their appropriate mixtures thereof.
Forms of the G-CSF dimer of the present invention used for partial administration comprise ointment, powder, patch, sprayer, and inhalant. Under sterile conditions, active components can be mixed with physiologically acceptable carrier and any antiseptic, buffering agent, or may be propellant if desired.
The G-CSF dimer of the present invention can be solely administrated or be administrated in conjunction with any pharmaceutically acceptable compounds. Usually, the G-CSF dimer of the present invention is not administrated associated with a G-CSF monomer.
On using the pharmaceutical composition, a safe and effective of the amount of the G-CSF dimer of the present invention is administrated to a mammal (e.g. human) in use thereof in which the dosage administrated is a pharmaceutically acceptable effective administration dosage. For a human of 60kg, the administration dosage is usually 0.01-300 mg; in a preferred embodiment, the administration dosage is 0.5-100 mg. In determination of the actual dosage, factors known in the art such as administration route, patients' condition, etc. have to be considered, which is clear to a skilled person in the art.
There arc many advantages of the G-CSF dimer of the present invention which include but not limited to:
1. A stronger receptor activation signal;
2. A longer in vivo biological half-life.
3. A substantial clinical efficacy in the treatment of neutropenia in animal models, which is better than other present products.
The following exemplary embodiments further describe the present invention. Although the description referred to particular embodiments, it will be clear to one skilled in the art that the present invention may be practiced with variation of these specific details. Hence this invention should not be construed as limited to the embodiments set forth herein. Further, for the embodiments in which details of the experimental methods are not described, such methods are carried out according to conventional conditions such as those described in Sambrook et al. Molecular Cloning: A Laboratory Manual (New York: Cold Spring Harbor Laboratory Press, 1989), or suggested by the manufacturers.
The G-CSF dimer with the structure described in
Rats received a single subcutaneous injection of G-CSF dimer (which is formed by two G-CSF monomers of SEQ ID NO: 2) with a dose of 100 μg/kg. The pharmacokinetic parameters (n=6) were calculated and listed in Table 1 below. The half-life of G-CSF monomer in rats is about 2 hours.
ICR mice, female, 20-22 grams, were randomly divided into four groups with 6-8 mice per group. The injection volume is 0.1 ml/10 g of body weight, and each test group were given equal molar dosage of the G-CSF molecule (i.e. 1 mole of G-CSF dimer comprises 2 moles of G-CSF monomer). In other words, the mice were injected subcutaneously once with an equal volume of the carrier (control group), G-CSF-Peg 40 μg/kg, rhG-CSF 40 μg/kg and G-CSF-D 100 μg/kg.
G-CSF-Peg monomer is Neulasta (Amgen, Pegylated Filgrastim).
G-CSF monomer is injectable rhG-CSF (GenSci).
G-CSF-D is a G-CSF dimer formed by two G-CSF monomers with an amino acid sequence as shown in SEQ ID NO:5.
After drug administration, blood samples (40 μL) were collected from orbital venous plexus at corresponding time points, and the blood count was detected and classified.
The result is shown in
It is worth noting that, at an equal molar dosage of the G-CSF molecule, the ANC increasing of G-CSF-D group was the highest. In particular, at the 48th hour after drug administration, the average value of neutrophil of the G-CSF-D group, the G-CSF-Peg group and the G-CSF monomer group was 22.14×109/L, 7.04×109/L and 3.61×109/L respectively, which means, the neutrophil count of the G-CSF-D group was 3.1 times of that of the G-CSF-Peg group, and 6.1 times of that of the G-CSF monomer group. Efficacy comparison result was: G-CSF-D>G-CSF-Peg>G-CSF, showing that G-CSF dimer has a better therapeutic effect. In other words, the increase of neutrophil in mice injected with G-CSF dimer was not only significantly higher than the group injected with G-CSF monomer, but also significantly higher than the group injected with G-CSF-Peg monomer which had a longer half-life. The result showed that G-CSF dimer has better biologic activities than G-CSF monomer in animals at equal molar dosage of G-CSF.
ICR mice, half male and half female, 24-26 grams, were randomly divided into groups with 10 mice per group. All animals were intravenously injected a dose of 150 mg/kg 5-FU for modeling. 24 hours later, animals of the control group were injected with the carrier; those of the G-CSF-D (dimer) group were injected with 1500 μg/kg rhG-CSF dimer (which was formed by two G-CSF monomers with amino acid sequence shown in SEQ ID NO:3); and those of the G-CSF-Peg monomer group were injected with 300 μg/kg Neulasta. The animals of the test groups were given at equal molar dosage of the G-CSF molecule (i.e. 1 mole of G-CSF dimer comprises 2 moles of G-CSF monomer) by subcutaneous injection. Each group was administrated once on Day 1, 3, 5 and 7 with an injection dosage of 0.1 ml/10 g body weight. Peripheral blood samples were collected on Day 0, 2, 4, 6 and 8, and the white blood cell count was detected and classified.
The result was shown in
The result indicated that in the treatment of mice model with 5-Fu induced neutropenia, G-CSF dimer (G-CSF-D) had a significantly better therapeutic effect comparing to G-CSF monomer (G-CSF-Peg).
24 healthy cynomolgus monkeys, half male and half female, were intravenously injected a dose of 60 mg/kg cyclophosphamide (lot: 2008040921, Jiangsu Hengrui Medicine Co., Ltd.) twice (Day 0 and Day 1) to induce a decrease of white blood cells and neutrophils. The cynomolgus monkeys were randomly divided into three groups, half male and half female. Starting from Day 5, the test groups were separately subcutaneously injected with G-CSF dimer (60 μg/kg, which is equal to 0.67 μM/kg) (G-CSF-D is a dimer formed by two G-CSF monomers with an amino acid sequence shown in SEQ ID NO:2) once; or with G-CSF-Peg monomer (60 μg/kg, which is equal to 3.2 μM/kg) once; or with G-CSF monomer (10 μg/kg/day, which is equal to 0.53 μM/kg) for 5 continuous days with a total dose of 50 μg/kg, which is equal to 2.65 μM/kg. The injection volume was 0.2 mL/kg. Blood samples were collected at different time points, and the effect of F627 with different dose on the neutrophil count in peripheral blood of cynomolgus monkeys was observed.
The result was shown in
The result indicated that in the treatment of cynomolgus monkeys model with cyclophosphamide-induced neutropenia, G-CSF dimer (G-CSF-D) had a better therapeutic effect than G-CSF monomer and G-CSF-Peg, which can effectively prevent the occurrence of neutropenia induced by chemotherapy agent, and can reduce the severity of neutropenia and/or shorten the time of severe neutropenia.
a. Construction of a Cell Line Expressing G-CSF Dimer
The full length cDNA sequence of the G-CSF-Fc complexes (as shown in SEQ ID NO: 7) was synthesized. cDNA sequence of human G-CSF monomer was connected with cDNA sequence of Fc fragment of IgG2. cDNA sequences containing Hind III site, and expression elements required by mammalian cell such as Kozak sequence and signal peptide were introduced at the 5′ end. cDNA sequence containing EcoRI site was introduced at the 3′ end. The full length G-CSF dimer cDNA sequence was cloned into pUC19 plasmid to obtain pG-CSF-Fc, transformed E. coli TG1. The plasmid was digested with Hind III and EcoRI, an approximately 1400 bp G-CSF-IgG2Fc fragment was harvested and connected with pcDNA3 (Invitrogen) expression plasmid which was also digested with Hind III and EcoRI, and an expression plasmid pEX-G-CSF-Fc was then constructed. pEX-G-CSF-Fc was linearized, purified and transfected into CHO cells by electroporation. The transfected cells were selected in selecting media. The expression levels of individual clones were measured by ELISA. The cell lines with the higher protein expression levels were selected and cells thereof were frozen to generate cell bank.
The first G-CSF monomer synthesized using SEQ ID NO: 7 had a structure of “G-CSF-linker-IgG2Fc”, and the amino acid sequence thereof was shown in SEQ ID NO: 6.
The expression plasmids were constructed in similar methods, resulting in the second, third and fourth G-CSF monomers (Table 1) with different structures. G-CSF dimers with different structures were obtained by similar expression methods.
b. Production of rhG-CSF Dimer Protein Cells
One vial of cells (˜1×107 cells/mL) from the cell bank was thawed and seeded in 10 mL basal medium in a 10 cm Petri dish, and incubated at 37° C., 5% CO2 for approximately 24 hours.
The seeding expansion: The culture volume was expanded from 10 mL to 30-40 mL. When the cell density reached 1.0-1.5×106 cells/mL with viability ≧90%, the culture volume was expanded to 300-400 mL progressively and then the culture was moved to shaking flasks and incubated at 120 rpm, 37° C., 5% CO2.
Culture expansion in bioreactor (3 L-10 L): When the cell density in the seeding expansion reached 1.0-3.0×106 cells/mL with viability ≧90%, the 300-400 mL seeding expanded culture was transferred to a 3-10 L bioreactor containing basal medium, with the culture control conditions at pH of 6.8, dissolved oxygen at approximately 50% and stirring speed at 65-100 rpm.
Culture expansion in bioreactor (30-100 L): When the cell density in the 3.0-10 L bioreactor reached 1.0-3.0×106 cells/ml with viability ≧90%, the culture was transferred to 30-100 L bioreactor with the culture control conditions at pH of 6.8, dissolved oxygen at approximately 50% and stirring speed at 65-100 rpm. The culture was fed for 12 to 48 hours before controlling the glucose level (<1 g/L) with the addition of fed-batch medium.
c. Separation and Purification of Recombinant Human G-CSF Dimer Protein
After the culture expansion in bioreactor, cell supernatant was harvested which contained G-CSF-Fc complex, G-CSF dimer, G-CSF-Fc multi-mers, and metabolites. After being harvested from the bioreactor culture, the cell culture supernatant was obtained by filtration and purified by a series of chromatography methods; for example, using a rProtein A Sepharose FF (GE Healthcare, cat #17-1279-04), eluted with 50 mM critic acid/sodium citrate and 0.2M NaCl at pH 3.7-3.8, resulting in >90% pure G-CSF dimer. Additional chromatography steps were performed using Capto Adhere column with elution buffer of 50 mM NaAc/HAC and 0.2 M NaCl at pH 4.5-5.0, followed by SP Sepharose FF (GE Heathcare Cat #17-0729-04) and balanced with equilibrium buffer of 10 mM PR (pH 6.0±0.1). Elution buffer used was 10 mM PR and 0.2M NaCl (pH 7.2±0.1). Additional processes involved viral activation at low pH, filtration, resulting in G-CSF dimer.
The purity of the G-CSF dimer was >95% (analyzed by reverse phase HPLC), with estimated molecular weight of 47±5 kD (analyzed by reduced SDS-PAGE analysis). The G-CSF dimer was glycosylated with oligosaccharide of 2-10% of the total molecular weight. The isoelectric point of the protein was between pH 5.8 to pH 6.8. The maximum UV absorbing wavelength was at 280 nM. The G-CSF dimer can activate STAT3 in M-NSF-60 cells and stimulate the proliferation of M-NSF-60 cells in vitro (the ED50 thereof was between 0.1-10 ng/mL)
The purification result of G-CSF dimer (comprising two G-CSF monomers with sequence shown in SEQ ID NO: 6) was shown in
Moreover, the results showed that, if the Fc fragment of the carrier protein contained four cysteine at the N-terminal, for example, ERKCCVECPPC(SEQ ID NO.: 2, amino acid residues 191-201), the formation of normally paired G-CSF dimer may be effected, indicating that it would be better for two Fc fragments to be connected with each other via 2-3 disulfide bonds.
Healthy subjects were randomly divided into four dosage groups of 30, 60, 120, 240 μg/kg respectively receiving a single dose of 30, 60, 120, 240 μg/kg of G-CSF dimer (comprising two G-CSF monomers with sequence shown in SEQ ID NO: 6). Blood samples were collected at the 0.5, 1st, 2nd 4th, 8th, 16th 24th, 36th, 48th, 72nd, 96th hour, Day 6 (120 hours), 7, 9, 11, 13, and 15 after administration. Serum was separated and stored below −70° C. The blood concentrations of G-CSF-D were measured by ELISA (ELISA, Quantikine human G-CSF ELISA kit, R&D System, Inc. Minneapolis, Minn., Cat: PDCS50). The pharmacokinetic parameters were calculated using the standard non-compartmental analytical procedures (Software WinNonlin v 5.2, Pharsight Corporation, USA). The results were shown in Table 2.
All references mentioned in the present invention are cited herein by reference. Although the description referred to particular embodiments, it will be clear to one skilled in the art that the present invention may be practiced with variation of these specific details. Hence this invention should not be construed as limited to the embodiments set forth herein.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201010268290.X | Aug 2010 | CN | national |
This application is a continuation of U.S. patent application Ser. No. 13/819,716, which is a U.S. National Phase Application of PCT/CN2011/079143 having an international filing date of Aug. 31, 2011, which claims priority to Chinese Application No. 201010268290.X, filed on Aug. 31, 2010.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 13819716 | Feb 2013 | US |
| Child | 14526382 | US |
