US20190177408A1 - Antibody for binding to interleukin 4 receptor - Google Patents

Antibody for binding to interleukin 4 receptor Download PDF

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Publication number
US20190177408A1
US20190177408A1 US16/307,930 US201716307930A US2019177408A1 US 20190177408 A1 US20190177408 A1 US 20190177408A1 US 201716307930 A US201716307930 A US 201716307930A US 2019177408 A1 US2019177408 A1 US 2019177408A1
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seq
set forth
variable region
chain variable
light chain
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Wei Zheng
Wubin PAN
Xin Yang
Yang Chen
Limin Zhang
Jie Jiang
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Connect Biopharma Hongkong Ltd
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Suzhou Connect Biopharmaceuticals Ltd
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Definitions

  • the present invention relates to the field of biopharmaceutics. Particularly, the present invention relates to an antibody that is capable of binding to interleukin 4 (IL-4) receptor (IL-4R) and uses thereof.
  • IL-4 interleukin 4 receptor
  • Interleukin-4 is a cytokine produced primarily by activated T cells, monocytes, basophils, mast cells, and eosinophils.
  • IL-4 is involved in a variety of biological processes, and its biological effects known in the art include stimulating the proliferation of activated B cells and T cells and the differentiation of CD4+ T cells into type II helper T cells.
  • IL-4 has multiple effects in mediating immune responses to diseases such as allergic diseases, autoimmune diseases, infectious diseases and tumors, and has therapeutic effects on tumors, autoimmune diseases and infectious diseases and the like. Meanwhile, IL-4 can also regulate immune response to vaccine. Therefore, IL-4 has always been one hot area for research attracting extensive attentions.
  • IL-13 is also a cytokine produced by activated T cells, which has different functions in different types of cells, such as monocytes, B cells, mast cells and keratinocytes.
  • IL-13 can inhibit the release of inflammatory cytokines and chemokines from monocytes, induce the proliferation and differentiation of B cells, and promote the synthesis of IgE, IL-13 and IL-4 share many common properties in terms of biological functions, including inhibiting the release of inflammatory mediators from monocytes, inducing dendritic-like development of macrophages, promoting the expression of CD23 on the surface of monocytes and stimulating the synthesis of immunoglobulins by B cells.
  • IL-13 also has its own biological features, mainly including: promoting the differentiation of human monocytes and changes of antigens on cell surface; inducing the proliferation and differentiation of B cells, and promoting the secretion of antibodies from B cells; regulating the synthesis of IgE, thereby being associated with allergic reactions in the body; inhibiting the growth of tumor cells; inhibiting the replication of HIV; and the like.
  • IL-4R The biological activity of IL-4 is mediated by a specific IL-4 receptor on cell surface (IL-4R, which is called “hIL-4R” in human).
  • Human IL-4R is a heterodimer formed by two polypeptide chains, in which the alpha chain (hIL-4R ⁇ , UniProtKB: P24394) has a high affinity for IL-4.
  • IL-13R ⁇ chain the cell surface receptor alpha chain of IL-13
  • IL-4R ⁇ chain Since the IL-4R ⁇ chain in the IL-4R complex plays a leading role in binding to IL-4 and other cytokines are involved, the IL-4R ⁇ chain is currently being studied as a major target. What's more, human monoclonal antibodies against the IL-4R ⁇ chain have been clinically proven to be effective in relieving and treating conditions such as asthma, eczema, atopic dermatitis and the like.
  • Human interleukin-4 receptor is known to produce a soluble form of protein (shIL-4R ⁇ , SEQ ID NO: 94) that inhibits cell proliferation mediated by IL-4 and IL-5 up-regulation mediated by T cells.
  • shIL-4R ⁇ soluble form of protein
  • Two forms of the receptor are associated with allergic reaction, which manifests as diseases like allergic rhinitis, sinusitis, asthma, eczema and so on. Therefore, blocking antibodies that target the protein can help treat and relieve said diseases.
  • Asthma is a chronic airway inflammatory disease, in which many inflammatory cells, such as eosnophils, mast cells and lymphocytes are involved, and its specific pathogenesis is still unclear. Since cytokines such as IL-4 play an important role in the occurrence and development of bronchial asthma, the development of antibodies specific for IL-4 is one of the effective ways to treat asthma. Inhibition of IL-4/IL-4R ⁇ can have an effective immunomodulatory effect on asthma.
  • Allergic rhinitis has a pathogenesis much in common with that of asthma, and it and asthma both belong to type I allergy. Meanwhile, studies have found that IL-4, IL-17 and IgE play an important role in the pathogenesis of allergic rhinitis. So far, drug therapy is the focus of AR treatment, in which intranasal corticosteroids and antihistamines are at the core position.
  • Atopic dermatitis also known as heterotopic dermatitis or hereditary allergic dermatitis, is a common dermatological disease that is mostly seen in children and adolescents, and is often complicated with certain hereditary allergic diseases such as allergic rhinitis, asthma and the like.
  • the involvement of immunological factors such as IL-4 and IL-13 are one of the main pathogenesis.
  • Eosinophilic esophagitis is a chronic immune inflammatory disease characterized by infiltration of eosinophils (EOS) in all layers of esophagus. The onset of EoE is associated with dysfunction of Th2 cells.
  • EOS eosinophils
  • protocols with high specificity such as novel biological agent anti-IL-5 (such as mepolizumab) have become hotspots in research.
  • immune-modulating therapy has achieved results in animal models, explorations are still needed in human clinical trials.
  • Medicaments such as PGD2 inhibitors, anti-TNF- ⁇ , and anti-IL-13 are under investigation at present.
  • the present invention provides an antibody specific for IL-4R through antibody screening and optimization, and the antibody can serve as a blocking agent for the binding of IL-4 to IL-4R, and can be used for treating inflammation or allergic diseases by binding to IL-4R.
  • the antibody of the present invention has a serine at position 31 (31Ser) of the light chain variable region comprised therein, and with reference to the numbering of amino acid residues of the sequence as set forth in SEQ ID NO: 93, the antibody has an aspartic acid at position 103 (103Asp), and a tyrosine at position 104 (104Tyr) of the heavy chain variable region comprised therein.
  • the 31Ser is located in CDR1 of the light chain variable region of the present antibody correspondingly
  • the 103Asp and 104Tyr are located in the CDR3 of the heavy chain variable region of the present antibody correspondingly.
  • the light chain variable region of the present antibody comprises CDR1 as set forth in SEQ ID NO: 2
  • the heavy variable region of the antibody comprises CDR3 as set forth in SEQ ID NO: 19.
  • the light chain variable region of the present antibody comprises a combination of CDR1, CDR2, and CDR3 selected from the group consisting of:
  • the present invention antibody comprises a light chain variable region selected from the amino acid sequences shown in the following sequences: SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 44, SEQ ID NO: 45, SEQ ID NO: 46, SEQ ID NO: 47, SEQ ID NO: 49, SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 54, SEQ ID NO: 55 and SEQ ID NO: 57, and the antibody comprises a heavy chain variable region selected from the amino acid sequences shown in the following sequences: SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 61, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 74, SEQ ID NO: 75, SEQ ID NO: 76, SEQ ID NO: 77, SEQ ID NO: 78, SEQ ID NO: 79, SEQ ID NO
  • the present antibody comprises a combination of a light chain variable region and a heavy chain variable region selected from the group consisting of:
  • the present invention provides an antibody that can bind to Interleukin 4 (IL-4) receptor (IL-4R).
  • the antibody comprises a light chain variable region (VL), and the light chain variable region comprises a combination of CDR1, CDR2 and CDR3 selected from the group consisting of:
  • the light chain variable region of the present antibody preferably comprises a combination of FR1, FR2, FR3 and FR4 selected from the group consisting of:
  • the heavy chain variable region of the antibody comprises a combination of FR1, FR2, FR3 and FR4 selected from the group consisting of:
  • the light chain variable region or the heavy chain variable region of present antibody comprises the above domain components in an order of FR1-CDR1-FR2-CDR2-FR3-CDR3-FR4, or comprises the above domain components in an order of (X)n-FR1-(X)n-CDR1-(X)n-FR2-(X)n-CDR2-(X)n-FR3-(X)n-CDR3-(X)n-FR4-(X)n, in which, X is any amino acid residue, and n is zero or an integer greater than zero.
  • the antibody provided by the present invention comprises a light chain variable region selected from the amino acid sequences shown in the following sequences:
  • the antibody provided by the present invention comprises a combination of a light chain variable region and a heavy chain variable region selected from the group consisting of:
  • the antibody provided by the present invention is capable of binding to IL-4R and functions as an antagonist of IL-4R.
  • the antibody is capable of binding to IL-4R ⁇ , preferably to mammal IL-4R ⁇ , more preferably to human IL-4R ⁇ , even more preferably to human soluble IL-4R ⁇ .
  • Binding affinity of the antibody provided by the present invention to IL-4R ⁇ can be determined by method Biacore or ELISA.
  • the antibody is determined to bind IL-4R ⁇ with an affinity of less than 100 nM, less than 10 nM, less than 1 nM, less than 0.5 nM, and even less than 0.1 nM.
  • the ratio of the expression level of the antibody provided by the present invention to that of reference antibody is 0.1-3:1, preferably 0.3-3:1, more preferably 0.4-3:1, still preferably 0.5-3:1, still more preferably 0.6-3:1, further preferably 0.7-3:1, further more preferably 1-3:1.
  • the antibody provided by the present invention can be a monoclonal antibody, fully or partially humanized antibody or chimeric antibody.
  • the antibody is an immunoglobulin, preferably IgA, IgD, IgE, IgG or IgM, more preferably IgG1, IgG2, IgG3 or IgG4 subtype, further more preferably IgG2 or IgG4 subtype.
  • the invention provides a fusion protein or conjugate comprising the antibody of the present invention.
  • the fusion protein or conjugate may further comprises cell surface receptor, active protein or active polypeptide, small molecule compound such as amino acid and saccharide, small molecule polymer or other parts chemically modifying the antibody, etc., bound to the present antibody by chemical or physical means.
  • the present invention provides a nucleic acid sequence that can encode the heavy chain variable region and/or light chain variable region of the antibody provided by the present invention.
  • the nucleic acid sequence can encode the heavy chain and/or light chain of the antibody provided by the present invention.
  • the present invention also provides a vector comprising the nucleic acid sequence provided by the present invention.
  • the vector may be an eukaryotic expression vector, a prokaryotic expression vector, an artificial chromosome, a phage vector or the like.
  • the vector or nucleic acid sequence as described above can be used to transform or transfect host cells for purposes of preservation or antibody expression, and the like. Accordingly, the invention also provides a host cell transformed or transfected with the nucleic acid sequence or the vector.
  • the host cell can be any prokaryotic or eukaryotic cell, such as a bacterial or insect, fungal, plant or animal cell.
  • the antibody provided by the present invention can be obtained through any method known in the art.
  • the heavy chain variable region and/or the light chain variable region of the antibody, or the heavy and/or light chain of the antibody can be obtained from the nucleic acid sequence provided by the present invention firstly, and then assembled into the antibody with any other domain of the antibody; or, the host cell provided by the present invention is cultured under conditions that the host cell is allowed to express the heavy chain variable region and/or the light chain variable region of the antibody or the heavy and/or light chain of the antibody for assembly into the antibody.
  • the method further includes a step of recovering the produced antibody.
  • the antibody, fusion protein or conjugate, nucleic acid sequence, vector or host cell provided by the present invention or antibody produced by the method as described above may be contained in a pharmaceutical composition, and more particularly, in a pharmaceutical preparation for various purposes as actually needed. Therefore, in a further aspect, the present invention also provides a pharmaceutical composition comprising the antibody, fusion protein or conjugate, nucleic acid sequence, vector, host cell of the present invention and/or antibody produced by the method as described above.
  • the pharmaceutical composition can be a pharmaceutical preparation.
  • the pharmaceutical preparation is, for example, an injection.
  • the pharmaceutical composition or pharmaceutical preparation may further comprises a pharmaceutically acceptable carrier or excipient, depending on the particular dosage form.
  • At least one of the following medicaments may also be contained: antiasthmatics such as albuterol etc., antihistamines such as loratadine etc., Immunosuppressive agents such as tacrolimus and pimecrolimus etc., M receptor blockers such as ipratropium bromide etc., leukotriene receptor blockers such as montelukast etc., phosphodiesterase inhibitors such as theophylline etc., non-steroidal anti-inflammatory drugs such as 5-aminosalicylic acid etc., hormones such as beclomethasone and budesonide etc., that is to say the antibody, fusion protein or conjugate, nucleic acid sequence, vector, host cell provided by the preset invention or antibody produced by the present method as described above may be used in combination with other medicaments as required.
  • antiasthmatics such as albuterol etc.
  • antihistamines such as loratadine etc.
  • Immunosuppressive agents such as tacrolimus and
  • the present invention also provides use of the antibody, fusion protein or conjugate, nucleic acid sequence, vector, host cell or antibody produced by the method for manufacturing a medicament for the prevention, treatment or amelioration of inflammation or allergic disease.
  • the inflammation or allergic disease includes autoimmune disease, such as allergic dermatitis, asthma, eosinophilic esophagitis, eczema, allergic rhinitis, nasal polyp, rheumatoid arthritis and the like.
  • autoimmune disease such as allergic dermatitis, asthma, eosinophilic esophagitis, eczema, allergic rhinitis, nasal polyp, rheumatoid arthritis and the like.
  • the present invention provides a method of preventing, treating or ameliorating inflammation or allergic disease, and the method includes administering to a subject in need thereof the antibody, fusion protein or conjugate, nucleic acid sequence, vector, host cell provided by the present invention and/or antibody produced by the present method.
  • the subject is a mammal, more preferably, the subject is a human.
  • the inflammation or allergic disease includes autoimmune disease, such as allergic dermatitis, asthma, eosinophilic esophagitis, eczema, allergic rhinitis, nasal polyp, rheumatoid arthritis and the like.
  • autoimmune disease such as allergic dermatitis, asthma, eosinophilic esophagitis, eczema, allergic rhinitis, nasal polyp, rheumatoid arthritis and the like.
  • medicaments can be used in combination to prevent, treat or ameliorate inflammation or allergic disease, for example, the method further includes administering to a subject in need thereof at least one medicament selected from the group consisting of: antiasthmatics such as albuterol etc., antihistamines such as loratadine etc., Immunosuppressive agents such as tacrolimus and pimecrolimus etc., M receptor blockers such as ipratropium bromide etc., leukotriene receptor blockers such as montelukast etc., phosphodiesterase inhibitors such as theophylline etc., non-steroidal anti-inflammatory drugs such as 5-aminosalicylic acid, etc., hormones such as beclomethasone and budesonide etc.
  • antiasthmatics such as albuterol etc.
  • antihistamines such as loratadine etc.
  • Immunosuppressive agents such as tacrolimus and pimecrolimus etc.
  • M receptor blockers such as ipra
  • the medicament is administered simultaneously or sequentially with the antibody, fusion protein or conjugate, nucleic acid sequence, vector, host cell provided by the present invention and/or antibody produced by the present method.
  • the present invention also provides a kit, and the kit comprises the antibody, fusion protein or conjugate, nucleic acid sequence, vector, host cell provided by the present invention and/or antibody produced by the present method.
  • FIG. 1 shows the pharmacokinetic curves of the antibodies of the present invention in mouse.
  • FIG. 2 shows the pharmacokinetic curves of the antibodies of the present invention in macaca fascicularis.
  • FIG. 3 includes panels 3A-3C which show the specific binding of the antibodies of the present invention with TF-1 cells expressing IL-4R ⁇ , as determined by FACS, in which panel 3A shows the fluorescence signal without the addition of antibody L1012H1031 of the present invention; panel 3B shows the fluorescence signal with the addition of antibody L1012H1031 of the present invention; and panel 3C shows the signal superposition of panels 3A and 3B for comparison.
  • FIG. 4 includes panels 4A-4D which show that the specific binding of the antibodies of the present invention with TF-1 cells expressing IL-4R ⁇ is blocked by sIL-4R ⁇ present in the system, as determined by FACS, in which panel 4A shows the fluorescence signal without the addition of antibody L1012H1031 of the present invention; panel 4B shows the fluorescence signal with the addition of antibody L1012H1031 of the present invention; panel 4C shows the fluorescence signal with the addition of antibody L1012H1031 of the present invention and sIL-4R ⁇ ; and panel 4D shows the signal superposition of panels 4A-4C for comparison.
  • FIG. 5 includes panels 5A-5B which show the effect of the antibodies of the present invention on the inhibition of TARC and MDC release, as determined by ELISA, in which panel 5A shows the result that antibody L1020H1031 of the present invention inhibits TARC release, and panel 5B shows the result that antibody L1020H1031 of the present invention inhibits MDC release.
  • Example 1 Preparation of the Antibodies of the Present Invention and Determination of Expression Levels by Non-Reduced SDS-PAGE Gel Electrophoresis
  • the sequence coding for the light chain variable region of the antibody was inserted into vector pFUSE2ss-CLIg-hK (Invivogen, Catalog Number: pfuse2ss-hclk) using EcoRI and BsiWI restriction sites to construct a light chain expression vector.
  • the sequence coding for the heavy chain variable region of the antibody was inserted into vector pFUSEss-CHIg-hG2 (Invivogen, Catalog Number: pfusess-hchg2) or vector pFUSEss-CHlg-hG4 (Invivogen, Catalog Number: pfusess-hchg4) using EcoRI and NheI restriction sites to construct a heavy chain expression vector.
  • Expi293 cells The culture and transfection of Expi293 cells were performed in accordance with the handbook of Expi293TM Expression System Kit from Invitrogen (Catalog Number: A14635). The density of the cells was adjusted to 2 ⁇ 10 6 cells/ml for transfection, and 0.6 ⁇ g of the light chain expression vector as described above and 0.4 ⁇ g of the heavy chain expression vector as described above were added to each ml of cell culture, and the supernatant of the culture was collected four days later.
  • the culture supernatant was subjected to non-reduced SDS-PAGE gel electrophoresis in accordance with the protocol described in Appendix 8, the Third edition of the “Molecular Cloning: A Laboratory Manual”.
  • control antibody 1 was constructed according to U.S. Pat. No. 7,186,809, which comprises a light chain variable region as set forth in SEQ ID NO: 10 of U.S. Pat. No. 7,186,809 and a heavy chain variable region as set forth in SEQ ID NO: 12 of U.S. Pat. No. 7,186,809, the same below)
  • control antibody 2 was constructed according to U.S. Pat. No.
  • 7,638,606 which comprises a light chain variable region as set forth in SEQ ID NO: 6 of U.S. Pat. No. 7,638,606 and a variable region as set forth in SEQ ID NO: 42 of U.S. Pat. No. 7,638,606, the same below). See Tables 2a-2c below for the results.
  • hIL-4 (Invivogen, Catalog Number: rhil-4) solution: hIL-4 was dissolved in 100 ⁇ l of PBS containing 0.1% BSA (Beyotime, Catalog Number: ST023) to obtain a solution with a concentration of 100 ⁇ g/ml, and the dissolved hIL-4 was dispensed into 1.5 ml (Nunc) centrifuge tubes in a volume of 5 ⁇ l per tube, and then the tubes were stored in a refrigerator at ⁇ 20° C.
  • BSA Beyotime, Catalog Number: ST023
  • WST-1 Beyotime, Catalog Number: 00036
  • C0036-2 electron coupling agent
  • TF-1 cells (ATCC: CRL2003TM) frozen in liquid nitrogen were taken out, shaken in a 37° C. water bath to dissolve quickly.
  • the dissolved cell suspension was transferred to a 15 ml centrifuge tube, and then 1640 medium was added therein to 10 ml.
  • the tube was centrifuged at 800 rpm for 5 min, the supernatant therein was aspirated, and cell pellets were retained and washed once again.
  • 10 ml of 1640 medium containing 10% FBS and 2 ng/ml GM-CSF (Sino Biological, Catalog Number: 10015-H01H) was added to the tube, and a cell density of 1 ⁇ 10 5 -1 ⁇ 10 6 cells/ml was obtained.
  • the suspension was transferred to a T75 cell culture flask (Nunc), and the cells were statically cultured in an incubator (Thermo) at 37 CC, 5% CO 2 . Every 2-3 days, the cell suspension was taken out, centrifuged at 800 rpm for 5 min, and the cells were resuspended in 10 ml of medium. Subsequently, 1 ⁇ 10 6 cells were counted and transferred into a new T75 cell culture flask, and the medium was supplemented thereto to 10 ml. The cells were continuously passaged for 2-3 times to reach a good state (the cells were bright and had a slightly irregular shape when suspended individually) for proliferation blocking experiment.
  • Expi293 cells were transfected with plasmids carrying different groups of genes of the antibodies, and 200 ⁇ l of the cell culture supernatant was taken out 4 days after transfection, and then centrifuged at 800 rpm for 5 min. The supernatant was filtered through a 0.22 ⁇ m pore size filter and used for proliferation blocking experiment.
  • the well-grown cells in the T75 cell flask were taken out and transferred into a 15 ml centrifuge tube, which was then centrifuged at 800 rpm for 5 min. The supernatant was discarded and the cell pellets were resuspended with 10 ml PBS, centrifuged at 800 rpm for 5 min. The supernatant was discarded and the cell pellets were resuspended in 10 ml of 1640 medium (without GM-CSF) containing 10% FBS, centrifuged at 800 rpm for 5 min. The supernatant was discarded and the cell pellets were resuspended in 5 ml of 1640 medium (without GM-CSF) containing 10% FBS.
  • the cells were counted and adjusted to a cell density of 5 ⁇ 10 5 cells/ml through supplementing the medium.
  • the cell suspension was added to a 96-well plate at a volume of 80 ⁇ l per well (wells in the outer ring were left free of cells to prevent volatilization).
  • 10 ⁇ l of purified antibody with different concentrations or 10 ⁇ l of the corresponding cell culture supernatant was added to the cells in the 96-well plate (in 3 replicate wells).
  • the hIL-4 was then diluted to 50 ng/ml with 1640 medium containing 10% FBS, and was added to the corresponding wells in the 96-well plate in a volume of 10 ⁇ l per well, so that the final cell density was 4 ⁇ 10 5 cells/ml, the concentration of hIL-4 was 5 ng/ml, and the volume in each well of the 96-well plate was 100 ⁇ l.
  • a negative control group (in 3 replicate wells) was set, in which no hIL-4 or the antibody was added, and only the same number of cells and the same volume of the culture medium were added.
  • a positive control group in 3 replicate wells
  • a positive control group with addition of the same concentration of hIL-4 and the same volume of the medium was set, and no antibody was added in this group.
  • 200 ⁇ l of PBS was added to each well in the outer ring of the 96-well cell plate to prevent the volatilization of liquid in the inner ring.
  • the 96-well cell plate was placed in a 5% CO 2 incubator at 37° C. for static culture.
  • 96-well cell plates were statically cultured for 72 hours in the 5% CO 2 incubator, 10 ⁇ l of the WST-1 solution was added to the cells in each well.
  • the 96-well cell plate was placed in a 5% CO2 incubator at 37° C. for further static culture. 24 h later, the 96-well plate was placed in flexstation 3 (Molecular Devices) and the values of OD450-OD650 were read.
  • inhibitory rate (OD value of supernatant of the transfected cells—OD value of the positive control group)/(OD value of the negative control group—OD value of the positive control group) ⁇ 100%.
  • the measured OD450-OD650 data were input into prisms software, in which the value of the negative control group was set to the lowest one, the value of the positive control group was set to the highest one, and the logarithm of the antibody concentration was taken. Then the curve of the antibody concentration logarithm to the OD450-OD650 value was fitted by prism5 software.
  • the calculated 1050s are shown in Table 4 below.
  • sIL-4R ⁇ (PEPRO TECH, Catalog Number: 200-04R) solution: the sIL-4R ⁇ was taken and 1 ml ddH2O was added therein, mixed up and down, and then a solution of 100 ⁇ g/ml was obtained. The solution was stored in a refrigerator at ⁇ 20° C. after being subpacked.
  • Sample to be tested For each antibody of the present invention, 10 ⁇ l and 2 ⁇ l of the culture supernatant of Expi293 cells expressing the antibody after transient transfection (the medium was Expi293 Expression Medium, Invitrogen, Catalog Number: A1435102; suspension culture was performed for 4 days at 100 rpm in a 8% CO2 incubator) were respectively added to 990 ⁇ l and 998 ⁇ l of PBS to prepare antibody samples to be tested of 1:100 and 1:500 dilutions.
  • the medium was Expi293 Expression Medium, Invitrogen, Catalog Number: A1435102; suspension culture was performed for 4 days at 100 rpm in a 8% CO2 incubator
  • Control sample As negative control samples, the culture supernatant of normal cells (untransfected Expi293 cells; the medium was Expi293 Expression Medium, Invitrogen, Catalog Number: A1435102; suspension culture was performed for 4 days at 100 rpm in a 8% CO2 incubator) were also diluted at 1:100 and 1:500.
  • the 96-well ELISA plate was incubated for 2 hours in a refrigerator at 4° C., Then the PBS containing 2% BSA was discarded and the plate was washed 3 times with PBST. Diluted antibodies to be tested were sequentially added to the corresponding wells, while the normal cell culture supernatants, as negative control samples, were added too. Three duplicate wells were made for each sample with a volume of 100 ⁇ l per well. The ELISA plate was wrapped with preservative film (or covered) and incubated for 1 h at 10° C. in a constant temperature incubator. Subsequently, the 96-well ELISA plate was taken out, and the solution therein was discarded.
  • TMB solution (Solarbio, Catalog Number: PR1200) was added to the 96-well ELISA plate row by row with a volume of 100 ⁇ l per well.
  • the 96-well ELISA plate was placed at room temperature for 5 minutes, and 2 M H2SO4 solution was added in immediately to terminate the reaction.
  • the 96-well ELISA plate was placed in flexstation 3 (Molecular Devices), the values of OD450 were read, and the data were collected, calculated and analyzed. Results were expressed relative to the affinity of control antibody 1. See Tables 5a-5c below for the results.
  • affinities of the antibodies of the present invention for sIL-4R ⁇ (antibodies whose affinities are equal to or slightly lower than that of control antibody 1) Number of the antibody OD 450/OD450 Control antibody 1 L1010H1000 1 L1021H1029 1 L1011H1000 0.9 L1008H1000 0.9 L1021H1031 0.9 L1024H1031 0.9 L1007H1000 0.8 L1020H1016 0.8 L1000H1029 0.8 L1000H1001 0.7
  • mice 6-8 week-old SPF Balb/c mice were selected and injected subcutaneously with antibodies (the antibodies of the present invention or control antibody 2) in a dose of 5 mg/kg (weight of the mouse).
  • Blood samples were collected at the time points before administration (0 h) and at 2, 8, 24, 48, 72, 120, 168, 216, 264, 336 h after administration.
  • the animals were anesthetized by inhaling isoflurane, blood samples were taken from the orbital venous plexus, and the sampling volume for each animal was about 0.1 ml; 336 h after administration, the animals were anesthetized by inhaling isoflurane and then euthanized after taking blood in the inferior vena cava.
  • sIL-4R ⁇ (PEPRO TECH, Catalog Number: 200-04R) solution: sIL-4R ⁇ was taken and 1 ml ddH2O was added therein, mixed up and down, and then a solution of 100 ⁇ g/ml was obtained. The solution was stored in a refrigerator at ⁇ 20° C. after being subpacked.
  • Sample to be tested 1 ⁇ l of serum collected at different time points was added to 999 ⁇ l of PBS containing 1% BSA to prepare a serum sample to be tested of 1:1000 dilution.
  • Standard sample The antibody to be tested was diluted to 0.1 ⁇ g/ml with PBS containing 1% BSA and 0.1% normal animal serum (Beyotime, Catalog Number: ST023). Afterwards, 200, 400, 600, 800, 900, 950, 990 and 1000 ⁇ l of PBS containing 1% BSA and 0.1% normal animal serum were respectively added to 800, 600, 400, 200, 100, 50, 10 and 0 ⁇ l of 0.1 ⁇ g/ml antibodies to be tested, and thus standard samples of the antibodies of the present invention were prepared with a final concentration of 80, 60, 40, 20, 10, 5, 1, or 0 ng/ml respectively. 2. Detection by ELISA
  • sIL-4R ⁇ solution 250 ⁇ l of 100 ⁇ g/ml sIL-4R ⁇ solution was added to 9.75 ml of PBS, mixed up and down, and then an antigen coating buffer of 2.5 ⁇ g/ml was obtained.
  • the prepared antigen coating buffer was added to a 96-well ELISA plate (Corning) with a volume of 100 ⁇ l per well.
  • the 96-well ELISA plate was incubated overnight in a refrigerator at 4° C. after being wrapped with preservative film (or covered). On the next day, the 96-well ELISA plate was taken out and the solution therein was discarded, and PBS containing 2% BSA was added thereto with a volume of 300 ⁇ l per well.
  • the 96-well ELISA plate was incubated for 2 hours in a refrigerator at 4° C. after being wrapped with preservative film (or covered). Then the 96-well ELISA plate was taken out and the solution therein was discarded, and the plate was washed 3 times with PBST. The diluted standard antibodies and the sera to be detected were sequentially added to the corresponding wells, and three duplicate wells were made for each sample with a volume of 100 ⁇ l per well. The ELISA plate was wrapped with preservative film (or covered) and incubated for 1 h at room temperature. Subsequently, the solution in the 96-well ELISA plate was discarded and then the plate was washed with PBST for 3 times.
  • TMB solution (Solarbio, Catalog Number: PR1200) was added to the 96-well ELISA plate row by row with a volume of 100 ⁇ l per well.
  • the 96-well ELISA plate was placed at room temperature for 5 minutes, and 2 M H2SO4 solution was added in immediately to terminate the reaction.
  • the 96-well ELISA plate was then placed in flexstation 3 (Molecular Devices), the values of OD450 were read, the data were collected and the results were calculated with Winnonlin software.
  • the pharmacokinetic results were shown in FIG. 1 and Table 6 below.
  • 3-5 year-old macaca fascicularises each weighting 2-5 Kg were selected and injected subcutaneously with antibodies (the antibodies of the present invention or control antibody 2) in a dose of 5 mg/kg (weight of the macaca fascicularis ).
  • the antibody or control antibody 2 to be administered was accurately extracted with a disposable aseptic injector, and multi-point injections were made subcutaneously on the inner side of the thigh of the animal, and the injection volume per point was not more than 2 ml.
  • TF-1 cells (ATCC: CRL-2003TM) frozen in liquid nitrogen were taken out, shaken in a 37° C. water bath gently to dissolve quickly. The dissolved cell suspension was transferred to a 15 ml centrifuge tube, and then 1640 medium (Hyclone, Catalog Number: SH30809.01B) was added therein to 10 ml. The tube was centrifuged at 800 rpm for 5 min, the supernatant therein was aspirated off, and the cell pellets were retained and washed once again.
  • 1640 medium Hyclone, Catalog Number: SH30809.01B
  • the cell density was adjusted to 1 ⁇ 10 5 -1 ⁇ 10 6 cells/ml with 1640 medium containing 10% FBS (Hyclone, Catalog Number: SV30184.02) and 2 ng/ml GM-CSF (Sino Biological, Catalog Number: 10015-H01H).
  • the suspension was transferred to a T75 cell culture flask (Nunc), and the cells were statically cultured in an incubator (Thermo) at 37° C., 5% CO 2 . Every 2-3 days, the cell suspension was taken out, centrifuged at 800 rpm for 5 min, and the cells were resuspended in 10 ml of medium.
  • Tf-1 cells were taken and counted under a microscope. The cells were divided into three groups and placed into three 1.5 ml centrifuge tubes respectively. The number of cells for each group was 1 ⁇ 10 6 . The cells were centrifuged at 800 rpm for 5 min, and then resuspended in 1 ml of cold PBS containing 1% BSA for washing once again.
  • the cells were centrifuged at 800 rpm for 5 min, and 45 ⁇ l of cold PBS containing 1% BSA was added to each centrifuge tube to resuspend the cells, and then 5 ⁇ l (500 ⁇ g/ml) of the present antibody L1021H1031, L1020H1031 or L1012H1031 was added to the first centrifuge tube, and 5 ⁇ l of PBS was added to the second centrifuge tube as a negative control. The cells were allowed to stand on ice for 45 min and then centrifuged at 800 rpm for 5 min.
  • the cells were resuspended in 1 ml of cold PBS containing 1% BSA for washing once again, and centrifuged at 800 rpm for 5 min. 499 ⁇ l of cold PBS containing 1% BSA was added to each centrifuge tube to resuspend the cells, and then 1 ⁇ l of FITC-labeled goat anti-human IgG (H+L) (Beyotime, Catalog Number: A0556) was added thereto. After standing on ice for 45 min, the cells were centrifuged at 800 rpm for 5 min, and resuspended in 1 ml of cold PBS containing 1% BSA for washing once again. Thus, the cells to be detected were obtained.
  • H+L FITC-labeled goat anti-human IgG
  • hIL-4 Invivogen, Catalog Number: rhil-4
  • rhil-4 The hIL-4 (Invivogen, Catalog Number: rhil-4) solution was prepared as described in Example 2.
  • the TF-1 cells (ATCC: CRL-2003TM) were cultured as described in Example 6.
  • 10 ⁇ l (100 ⁇ g/ml) of sIL-4R ⁇ and 5 ⁇ l (500 ⁇ g/ml) of antibody L1021H1031, L1020H1031 or L1012H1031 of the present invention were uniformly mixed in a 1.5 ml centrifuge tube at a molar ratio of 2:1.
  • the mixture of 10 ⁇ l PBS and 5 ⁇ l of antibody L1021H1031, L1020H1031 or L1012H1031 of the present invention was served as a positive control and 15 ⁇ l PBS was served as a negative control.
  • the centrifuge tubes were placed in a 37° C. incubator for 1 h.
  • TF-1 cells were taken and then counted under a microscope.
  • the cells were divided into four groups and placed into four 1.5 ml centrifuge tubes respectively.
  • the number of cells for each group was 1 ⁇ 10 6 .
  • the cells were centrifuged at 800 rpm for 5 min, and then resuspended in 1 ml of cold PBS containing 1% BSA for washing once again. Subsequently, the cells were centrifuged at 800 rpm for 5 min, and 35 ⁇ l of cold PBS containing 1% BSA was added to each centrifuge tube to resuspend the cells, and then 15 ⁇ l of each of different antibody mixtures and the control prepared in step 3 was added to the tubes respectively.
  • the cells were centrifuged at 800 rpm for 5 min, and resuspended in 1 ml of cold PBS containing 1% BSA for washing once again, and centrifuged at 800 rpm for 5 min. 499 ⁇ l of cold PBS containing 1% BSA was added to each centrifuge tube to resuspend the cells, and then 1 ⁇ l of RTC-labeled goat anti-human IgG (H+L) (Beyotime, Catalog Number: A0556) was added thereto. After standing on ice for 45 min, the cells were centrifuged at 800 rpm for 5 min, and resuspended in 1 ml of cold PBS containing 1% BSA for washing once again. Thus, the cells to be detected were obtained.
  • An anti-human Fc (AHC) antibody (GE Healthcare) was coupled to a CM5 chip, and then the antibody of the present invention was captured by AHC respectively. Subsequently, different concentrations of human sIL-4R ⁇ were flowed through the surface of the chip on which the antibody of the present invention was captured. For capture and binding, the present antibody was diluted to 2 ⁇ g/ml and the antigen sIL-4R ⁇ was diluted to 0.39, 0.78, 1.56, 3.13, 6.25, 12.5, 25.0, 50.0 and 100.0 nM. The experimental method was then established in the Biacore T200 control software, after which the experimental program was run for detection. The results are shown in Table 8 below.
  • antibody L1020H1031 with a final concentration of 1000, 300, 100, 30 or 10 ng/ml was added to each well, following by the addition of IL-4 with a final concentration of 10 ng/ml (or IL-13 with a final concentration of 100 ng/ml) thereto.
  • Detection was carried out according to the method provided with Human TARC ELISA kit (Abcam, Catalog Number: ab183366) or Human MDC ELISA kit (Abcam, Catalog Number: ab179885) after 72 hours of culture.
  • the amino acid at position 103 in the sequence of the heavy chain H1031 (SEQ ID NO. 91) of the antibody (in CDR3) is Asp (103Asp), and the amino acid at position 104 is Tyr (104Tyr).
  • the present antibodies which have 103Asp and 104Tyr have a 2- to 4-fold higher area under the drug-time curve and an about 70% reduced clearance rate.
  • the expression levels of the antibodies of the present invention are also detected and compared, in order to investigate the possible effects of specific amino acids at specific positions on the expression of the antibodies.
  • Culture and transfection of Expi293 cells were conducted according to Example 1, and the collected culture supernatant was then passed through a 0.22 ⁇ m filter and then purified by GE MabSelect Sure (Catalog Number: 11003494) Protein A affinity chromatography column in the purification system GE AKTA purifier 10. The purified antibody was collected and concentrated using Amicon ultrafiltration concentrating tube (Catalog Number: UFC903096) and then quantified. The quantitative results are shown in Table 10 below.
  • the amino acid at position 31 in the sequence of the light chain L1012 (SEQ ID NO. 44), L1020 (SEQ ID NO, 55) or L1023 (SEQ ID NO. 51) of the antibody (in CDR1) is Ser (31Ser).
  • the present antibodies which have 31Ser have a 2- to 5-fold higher expression level.

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