Patent Grant
12325751
This application is a National Stage Application under 35 U.S.C. § 371 of International Application No. PCT/CN2020/094919, filed on Jun. 8, 2020, which claims priority to Chinese Application No. 201910495626.7, filed on Jun. 10, 2019, and Chinese Application No. 201910495614.4, filed on Jun. 10, 2019, the contents of which are incorporated herein by reference in their entirety.
The invention generally relates to a biomedical field, and more specifically, to an antibody that binds to CD25 and the application thereof.
Regulatory T cells (Treg) play a vital role in mediating immune homeostasis, and can promote the establishment and maintenance of peripheral tolerance. However, their role becomes more complex in the context of cancer. Because cancer cells express their own tumor-associated antigens, the presence of Treg that suppresses the response of effector cells can promote tumor progression. Therefore, the infiltration of Treg in established tumors is one of major obstacles for efficacy. Treg that uses inhibitory mechanisms is believed to make a significant contribution to the limitations and even failures of current therapies, especially immunotherapies that rely on inducing or enhancing anti-tumor responses (Onishi H et al., 2012 Anticanc. Res. 32, 997-1003). The tumor infiltration of Treg is also associated with several human cancers with poor prognosis (Shang B et al., 2015, Sci Rep. 5:15179). It has been proven that Treg cells contribute to the establishment and progression of tumors in mouse models and their absence leads to a delay in tumor progression. In humans, a high proportion of the infiltration of tumor Treg cells, more importantly, a lower ratio of effector T cells (Teff) to Treg cells, is associated with the poor prognosis of various human cancers (Shang et al., 2015).
CD25 is one of the potential molecular targets to achieve Treg depletion. CD25 is also known as interleukin-2 high affinity receptor alpha chain (IL-2Rα). CD25 is expressed at high levels on Treg, but CD25 is not present or expressed at low levels on Teff.
In the prior art, there are antibodies that bind to CD25 but do not block the binding of IL2 to CD25, such as MA251 (Rubin et al., 1985, Hybridoma 4(2)91-102, Tanaka et al., 1986, Microbiol. Immunol 30(4), 373-388), but they still exist defects such as insufficient CD25 binding activity, inhibition of PBMC activation, and general pharmacokinetic performance.
In the face of the patient's demand for medicines for disease treatment, especially demands for antibody drugs, there is still an urgent clinical need to provide an anti-CD25 antibody with higher binding activity.
In the full text of the present invention, various embodiments regarding VL (light chain variable region), VH (heavy chain variable region), LCDR (light chain complementarity determining region), HCDR (heavy chain complementarity determining region), LCDR1, LCDR2, LCDR3, HCDR1, HCDR2 and HCDR3 may be implemented individually or in any combination.
In an aspect of the present invention, the present invention relates to an antibody or antigen-binding fragment thereof including three heavy chain complementarity determining regions, wherein the HCDR1 amino acid sequence is represented by SEQ ID NO: 14, the HCDR2 amino acid sequence is represented by SEQ ID NO: 15, and the HCDR3 amino acid sequence is represented by SEQ ID NO: 16. Further, the antibody or antigen-binding fragment thereof further includes three light chain complementarity determining regions, wherein the LCDR1 amino acid sequence is represented by SEQ ID NO: 11, the LCDR2 amino acid sequence is represented by SEQ ID NO: 12, and the LCDR3 amino acid sequence is represented by SEQ ID NO: 13.
In an aspect of the present invention, the antibody or antigen-binding fragment thereof provided in the present invention includes a heavy chain variable region represented by SEQ ID NO: 4; preferably, further includes a light chain variable region represented by SEQ ID NO: 3.
In an aspect of the present invention, the present invention relates to an antibody or antigen-binding fragment thereof including three light chain complementarity determining regions, wherein the LCDR1 amino acid sequence is represented by SEQ ID NO: 5, the LCDR2 amino acid sequence is represented by SEQ ID NO: 6, and the LCDR3 amino acid sequence is represented by SEQ ID NO: 7; and/or three heavy chain complementarity determining regions, wherein the HCDR1 amino acid sequence is represented by SEQ ID NO: 8, the HCDR2 amino acid sequence is represented by SEQ ID NO: 9, and the HCDR3 amino acid sequence is represented by SEQ ID NO: 10.
In another aspect, the present invention relates to an antibody or antigen-binding fragment thereof including the light chain variable region of the amino acid sequence represented by SEQ ID NO: 1, and/or the heavy chain variable region of the amino acid sequence represented by SEQ ID NO: 2.
According to an aspect of the present invention, the sequence of the light chain constant region of the antibody or antigen-binding fragment thereof of anyone of the preceding aspects is SEQ ID NO: 20.
According to an aspect of the present invention, the sequence of the heavy chain constant region of the antibody or antigen-binding fragment thereof of any one of the preceding aspects is SEQ ID NO: 17.
Specifically, the antibody or antigen-binding fragment thereof provided in the present invention preferably includes the light chain variable region of the amino acid sequence represented by SEQ ID NO: 3, the heavy chain variable region of the amino acid sequence represented by SEQ ID NO: 4, the light chain constant region of the amino acid sequence represented by SEQ ID NO: 20 and the heavy chain constant region of the amino acid sequence represented by SEQ ID NO: 17.
Specifically, the antibody or antigen-binding fragment thereof provided in the present invention preferably includes the light chain variable region of the amino acid sequence represented by SEQ ID NO: 1, the heavy chain variable region of the amino acid sequence represented by SEQ ID NO: 2, the light chain constant region of the amino acid sequence represented by SEQ ID NO: 20 and the heavy chain constant region of the amino acid sequence represented by SEQ ID NO: 17.
According to an aspect of the present invention, the antibody or antigen-binding fragment thereof of the present invention binds to CD25, preferably to human CD25.
According to an aspect of the present invention, the present invention relates to the antibody or antigen-binding fragment thereof of any one of the preceding aspects including a monoclonal antibody, a polyclonal antibody, a chimeric antibody, a humanized antibody, a Fab fragment, a Fab′ fragment, a F(ab′)2 fragment, a Fv fragment, a scFv fragment, a dsFv fragment or the like.
According to an aspect of the present invention, the present invention relates to a nucleic acid encoding the antibody or antigen-binding fragment thereof of any one of the preceding aspects.
According to an aspect of the present invention, the present invention relates to a vector including the nucleic acid of the preceding aspect, or the vector can express the antibody or antigen-binding fragment thereof of anyone of the preceding aspects. Preferably, the vector may be a viral vector; preferably, the viral vector includes but is not limited to a lentiviral vector, an adenovirus vector, an adeno-associated viral vector, a retroviral vector, or the like; preferably, the vector may be a non-viral vector; preferably, the vector may be a mammalian cell expression vector; preferably, the expression vector may be a bacterial expression vector; and preferably, the expression vector may be a fungal expression vector.
According to an aspect of the present invention, the present invention relates to a cell that can express a cell of the antibody or antigen-binding fragment thereof of any one of the preceding aspects. Preferably the cell is a bacterial cell; preferably the bacterial cell is an E. coli cell and the like; preferably the cell is a fungal cell; preferably the fungal cell is a yeast cell; preferably the yeast cell is a Pichia pastoris cell and the like; preferably the cell is a mammalian cell; preferably the mammalian cell is a Chinese hamster ovary cell (CHO), a human embryonic kidney cell (293), a B cell, a T cell, a DC cell, a NK cell, or the like.
According to an aspect of the present invention, the present invention relates to a pharmaceutical composition including the antibody or antigen-binding fragment thereof, the nucleic acid, the vector or the cell of anyone of the preceding aspects, preferably the pharmaceutical composition further includes a pharmaceutically acceptable excipient, and the pharmaceutically acceptable vector preferably includes one or more of the following: a solvent, a dispersant, an additive, a plasticizer and the like which are pharmaceutically acceptable.
In some embodiments, the pharmaceutical composition may further include other therapeutic agents. In some embodiments, the other therapeutic agents include chemotherapeutic agents, immunotherapeutic agents, or hormonal therapeutic agents. The combined administration of the antibody or antigen-binding fragment thereof and the other therapeutic agents can enhance the therapeutic effect of the therapeutic agents.
In some embodiments, the “enhance the therapeutic effect” refers to enhancing the therapeutic effect of other therapeutic agents or therapies. The antibody or antigen-binding fragment provided in the present invention can be administered individually or in combination with other therapeutic agents or therapies. In some embodiments, the other therapeutic agents or therapies include chemotherapeutic agents, immunotherapeutic agents, hormonal therapeutic agents, radiation therapy and surgery.
According to an aspect of the present invention, there is provided a kit including the antibody or antigen-binding fragment thereof of the present invention, or including a nucleic acid encoding the antibody or antigen-binding fragment thereof.
According to an aspect of the present invention, the present invention relates to an application of the antibody or antigen-binding fragment thereof, the nucleic acid, the vector or the cell of any one of the preceding aspects in preparation of medicaments for treatment or prophylaxis of diseases.
According to an aspect of the present invention, the present invention relates to an application of the antibody or antigen-binding fragment thereof or the nucleic acid of any one of the preceding aspects in preparation of diagnostic or detection kits.
In an aspect of the present invention, there is provided a method of treating or preventing diseases including administering the antibody or antigen-binding fragment thereof, the nucleic acid, the vector, the cell or the pharmaceutical composition of the present invention to subjects in need.
In an aspect of the present invention, there is provided a method of diagnosis or detection including administering the antibody or antigen-binding fragment, the nucleic acid or the kits of the present invention to subjects or samples in need. Preferably, the method is a method of diagnosing or detecting diseases.
According to an aspect of the present invention, the present invention relates to use of the antibody or antigen-binding fragment thereof, the nucleic acid, the vector, the cell or the pharmaceutical composition of any one of the preceding aspects for the treatment or prophylaxis of diseases.
According to an aspect of the present invention, the present invention relates to use of the antibody or antigen-binding fragment thereof, the nucleic acid, or the kits of any one of the preceding aspects for detection or diagnosis. Preferably, the use is to diagnose or detect diseases.
According to an aspect of the present invention, the disease is a cancer.
According to an aspect of the present invention, the cancer includes gastric cancer, esophageal cancer, head-and-neck cancer, bladder cancer, cervical cancer, sarcoma, cytoma, lung cancer, colon cancer, ovarian cancer, renal cancer, colorectal cancer, pancreatic cancer, liver cancer, melanoma, breast cancer, myeloma, glioma, leukemia, lymphoma and the like.
According to an aspect of the present invention, the present invention relates to a method for preparing the antibody or antigen-binding fragment thereof of any one of the preceding aspects, which includes transfecting cells with the above vector, and expressing the antibody or antigen-binding fragment thereof by the transfected cells; or includes expressing the antibody or antigen-binding fragment thereof with the above cell.
According to an aspect of the present invention, the antibody or antigen-binding fragment thereof provided in the present invention has one or more of the following advantages: enhanced CD25 protein binding activity, enhanced CD25 protein affinity, enhanced CD25 expressing cell killing ability, reduced PBMC activation inhibition, enhanced in vivo tumor growth inhibition ability, enhanced in vivo tumor killing ability, enhanced ability to reduce the number of Treg cells, or enhanced ability to increase the number of effector T cells.
In order to more clearly explain the specific embodiments of the present invention or the technical solutions in the prior art, the drawings required for the specific embodiments or the description of the prior art will be briefly described below. Obviously, the drawings in the follow description are some embodiments of the present invention, and those of ordinary skill in the art can obtain other drawings based on these drawings without the exercise of inventive faculty.
The technical solutions of the present invention will be described clearly and completely below in connection with the drawings, and obviously, the described embodiments are part of the embodiments of the present invention, but not all the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those having ordinary skill in the art without the exercise of inventive faculty are within the scope of the present invention.
The technical features involved in the different embodiments described throughout the full text of the present invention can be implemented in combination with each other.
1.1 Immunization Scheme
The CD25 (Sino Biological, catalog NO. 10165-H08H) is emulsified with Freund's adjuvant to immunize fully human antibody transgenic mouse BoAn-hMab1 of Boan bio (prepared according to the method described in Chinese Patent CN103571872B). The first immunization uses Freund's complete adjuvant (Sigma, catalog number: F5881-10ML), the second immunization to the sixth immunization use Freund's incomplete adjuvant (Sigma, catalog number: F5506-10ML), total of 14 mice were immunized at this time. 7 mice with higher serum titers were selected for booster immunization, and the mice were sacrificed 3 days later to remove the spleen for subsequent experiments. The serum titers (62500-fold dilution) of the mice are shown in
1.2 Establishment of Phage Library
RNA is extracted from the spleen cells of the immunized mice in 1.1, and then reverse-transcribed into cDNA, the steps for establishing the phage library are performed referring to the method described in Carlos F. Barbas III, Phage display: A laboratory manual, the variable regions of the heavy and light chains are obtained from the cDNA by PCR method, and then scFv is obtained by overlapping extension PCR of the variable regions of the heavy chain and the light chain, scFv is ligated with plasmid pCOMB3× after digesting, and then the ligation product is electrotransfected into E. coli TG1 competent cells, add the phage to infect TG1 after being incubated, and the supernatant of the culture concentrated is the phage library of the present invention.
1.3 Phage Library Screening (Two Methods)
(1) Plate screening: the plate is coated with CD25 protein (Sino Biological, 10165-H08H) at 1 μg/well, and left overnight at 4° C., the plate is sealed with 2% BSA for 1 h the next day, and added to a phage library (2×1012) to incubate for 2 h, and the phage specifically bound to CD25 is eluted with elution buffer (add 4.2 ml of concentrated hydrochloric acid (Comeo) to 500 ml of ultrapure water and adjust pH to 2.2 with glycine powder (Biotopped, BG0617-500)) or 15 μg/mL MA251 after being washed 4-10 times.
(2) Magnetic bead screening: CD25-Fc protein (Sino Biological, 10165-H02H) is biotinylated according to the general steps, and bound to Thermo's magnetic beads (Invitrogen Dynabeads M-280 Streptavidin, 00355871) and then incubated with the phage library, and the phage specifically bound to CD25 is eluted with elution buffer (pH 2.2) or 15 μg/mL MA251 after being washed 4-10 times.
The screened phage clones express scFv, and detect the binding of scFv and CD25, and detect the blocking of scFv on IL2/CD25 binding, and select scFv that binds well to CD25 and does not block CD25 for subsequent construction.
ELISA detection of binding of scFv and CD25: Preparation of CBS buffer: 1.59 g of Na2CO3 (Sinopharm, 10019260) and 2.93 g of NaHCO3 are weighed, and the distilled water was added to 1 L to prepare CBS buffer. The CD25 (10165-H08H, Sino Biological) protein was diluted to 0.2 μg/mL with pH 9.6 CBS, coated with enzyme-labeled plate, 100 μL/well, and incubated overnight at 4° C.; 3% defatted milk powder was used for sealing at 37° C. for 1 h after washing the plate; 80 μL of PBST (PBS+0.05% Tween20) is added after washing the plate, and then 20 μL of scFv periplasm was added to incubate at 37° C. for 1 h. An anti-flag secondary antibody (Proteintech, catalog number: HRP-66008) was added after washing the plate to incubate at 37° C. for 1 h. 100 μL of TMB (Makewonder, catalog NO. 1001) substrate was added to each well for color development after washing the plate, 50 μL of 2M H2SO4 was added to each well to stop the color development after 10 mins, and OD450 was read with a microplate reader.
ELISA detection of blocking of scFv on CD25/IL2 binding: the CD25 (10165-H08H, Sino Biological) protein was diluted to 0.5 μg/mL with pH 9.6 CBS, and coated with enzyme-labeled plate, 100 μL/well, and incubated overnight at 4° C.; 3% defatted milk powder was used for sealing at 37° C. for 1 h after washing the plate. 50 μL of scFv periplasm was added to each well after washing the plate. Then, biotin-labeled IL2 protein (final concentration is 0.02 μg/mL) was added, 50 μL/well, and incubated at 37° C. for 1 h; STREP/HRP diluted with PBST was added after washing the plate, 100 μL/well, and incubated at 37° C. for 1 h. 100 μL of TMB is added to each well for color development after washing the plate, and 50 μL of 2M H2504 was added to each well to stop the color development after 10 mins, OD450 was read with a microplate reader.
Magnetic bead screened clones CD25Q2-BA3\BA9\BA125, CD25Q8-BT942, CD25Q11-BA402\BA406\BA410\BA415\BA422\BA428 and CD25Q14-BA443\BA448\BA458 and plate screened clones CD25Q11-CA35\CA36\CT848 and CD25Q14-CA705\CA707\CA721 were sent to Invitrogen Biotechnology Ltd for sequencing. The amino acid sequences of the light chain variable region and the heavy chain variable region of each clone are set forth in Table 1.
SLRSYLAWYQQKPGKAPKLLIYKASS
FDIWGQGTMVTVSS
SLRSYLAWYQQKPGKAPKLLIYKASS
FDIWGQGTMVTVSS (SEQ ID NO: 2)
IISGYLAWYQQKPGKAPKLLIYKASSL
GYSFANYWIVWVRQMPGKGLEWM
PYYSDYWGQGTLVTVSS
SISSWLAWYQQKPGKAPKLLIYKASS
GYSFTNYWIGWVRQMPGKGLEWM
GPYYFEYWGQGTLVTVSS
SVLYSSNNKNYLAWYQQKPGQPPKL
SGYDSNYWYFDLWGRGTLVTVSS
SISSYLAWYQQKPGKAPKLLIYKASTL
GYSFSNYWIAWVRQMPGKGLEWM
GPYYFEYWGQGTLVTVSS
SISSWLAWYQQKPGKAPKLLIYKASS
AFDLWGQGTMVTVSS
SISTWLAWYQQKPGKAPKLLIYKASS
GYSFTTYWIGWVRQMPGKGLEWM
PHWGDYWGQGTLVTVSS
SVLYSSNNKNYLAWYQQKPGQPPKL
GSGYDSNYWYFDLWGRGTLVTVSS
SISSWLAWYQQKPGKAPKLLIYKASS
GYSFTNYWIVWVRQMPGKGLEWM
PYYLEYWGQGTLVTVSS
SVSGYLAWYQQKPGKAPKLLIYKTSS
GYSFSNYWIGWVRQMPGKGLEWM
GPYYLDYWGQGTLVTVSS
SISSWLAWYQQKPGKAPKLLIYKASS
GYNFANYWIVWVRQMPGKGLEW
GPYYSDYVVGQGTLVTVSS
SISSWLAWYQQKPGKAPKLLIYKASS
GYSFSNYWIGWVRQMPGKGLEWM
GPYYLDYWGQGTLVTVSS
SIGSWLAWYQQKPGKAPKLLIFEASN
GYSFANYWIVWVRQMPGKGLEWM
PYYSDYWGQGTLVTVSS
SVSSWLAWYQQKPGKAPKLLIYKASS
GYSFSNYWIGWVRQMPGKGLEWM
GPYYLDYWGQGTLVTVSS
SVSSWLAWYQQKPGKAPKLLIYKASS
GYSFANYWIVWVRQMPGKGLEWM
PYYSDYWGQGTLVTVSS
SVSSWLAWYQQKPGKAPKLLIYKASS
AFDIWGQGTMVTVSS
SVLYSSNNKNYLAWYQQKPGQPPKL
RGDYSNFWYFDLWGRGTLVTVSS
SISSFLAWYQQKPGRAPELLIYKASTL
GYSFTNYWIAWVRQMPGKGLEWM
GPYYFEYWGQGTLVTVSS
The nucleotide sequence fragment encoding VH was finally inserted into the vector pCDNA3.4 (Life Technology) with the nucleotide sequence encoding the heavy chain constant region amino acid sequence SEQ ID NO: 17 of the antibody, the nucleotide sequence fragment encoding VL was inserted into the vector pCDNA3.4 (Life Technology) with the nucleotide sequence encoding the light chain constant region amino acid sequence (SEQ ID NO: 20) of the antibody, through variable region gene amplification (2*Phanta Max Master Mix, manufacturer: Vazyme, Item No.: P515-AA, Lot No.: TE211 GB), signal peptide and variable region overlap extension, homologous recombination (ClonExpress II One Step Cloning Kit, manufacturer: Vazyme, Item No.: C112-01, Lot No.: TE211 L8) and the like, performed by conventional molecular biology techniques. The linked vector is transfected into HEK293 cells and incubated in 37° C.\8% CO2\125 rpm shaker, and after transiently expressing 6-7 days, the supernatant was purified by Protein A affinity chromatography to obtain anti-CD25 antibody, and the antibody concentration was determined by UV280 binding extinction coefficient.
Production of control antibody: MA251 antibody is an anti-human CD25 antibody that does not block the binding of IL2 and CD25 in the prior art, has a high affinity for human CD25, and has a good performance of not blocking the binding of IL2 and CD25. The MA251 antibody is a classic antibody studying the binding of IL2 and CD25. The nucleotide sequence encoding the variable region of the MA251 antibody is synthesized by the complete gene and then inserted into the vector pCDNA3.4 and expressed by HEK293 cells, and the produced antibody is named CD25-MA251-IgG1 (the sequence of the heavy chain variable region is SEQ ID NO: 18, the sequence of the light chain variable region is SEQ ID NO: 19, the sequence of the light chain constant region is SEQ ID NO: 20, and the sequence of the heavy chain constant region is SEQ ID NO: 17).
3.1 ELISA Detection of Activity of Binding of Candidate Antibody and CD25 Protein
The CD25 protein (10165-H08H, Sino Biological) was diluted to different concentrations (0.08 μg/mL, 0.02 μg/mL, 0.005 μg/mL, 0.00125 μg/mL, 0.0003125 μg/mL, 0.000078125 μg/mL) with CBS, was coated with enzyme-labeled plate, 100 μL/well, and incubated overnight at 4° C.; 3% defatted milk powder was used for sealing at 37° C. for 1 h after washing the plate; 100 μL of candidate antibody that was diluted to 1 μL/mL with PBST (PBS+0.05% Tween20) was added to each well, and incubated at 37° C. for 1 h; then the goat anti-human IgG/HRP (KPL, catalog number: 5450-0009) was added and incubated at 37° C. for 1 h, and after color developing for 10 min, OD450 was read on a microplate reader to obtain EC50 by calculating. The results are shown in
As shown in Table 2, a EC50 value of the binding of the candidate antibody CD25Q2-BA9-IgG1 and antigen CD25 is 3.328, which is significantly lower than the EC50 value of the control group CD25-MA251-IgG1 that is 10.63, which indicates that the antigen binding capacity of the candidate antibody is significantly better than that of the control group CD25-MA251-IgG1.
As shown in Table 6, a EC50 value of the binding of the candidate antibody CD25Q2-BA9-IgG1 and antigen CD25 is 2.26, which is significantly lower than the EC50 value of the control group CD25-MA251-IgG1 that is 24.5, which indicates that the antigen binding capacity of the candidate antibody is significantly better than that of the control group CD25-MA251-IgG1.
It is predicted that the candidate antibodies CD25Q2-BA9-IgG1 and CD25Q8-BT942-IgG1 have a stronger targeting and binding effect on the Treg cells expressing CD25, have better killing effect, reduce inhibition of the Treg cells on the Teff cells, and have better pharmaceutical effects as compared with the control group CD25-MA251-IgG1.
3.2 Detection of Simulated Killing Activity of Candidate Antibody
FBS (Gibco, catalog number: 10091-148) and RPMI-1640 (Gibco, catalog number: 11875-093) were mixed according to 1:99 to prepare 1% FBS RPMI-1640, SU-DHL-1 target cells were collected, and was diluted to 1.2×106 cells/mL by using 1% FBS RPMI-1640, appropriate candidate antibody was taken and diluted to 25 μg/mL by using 1% FBS RPMI-1640, this concentration was used as an initial concentration; diluted 4 times in gradient in sequence to a total of 8 points for future use; effector cells Jurkat (G7011, Promega) were collected, and diluted to 2.4×106 cells/mL by using 1% FBS RPMI-1640, target cells were added in the white 96-well plate with 25 μL/well; the antibody diluted in gradient was added in the wells covered with target cells, with 25 μL/well; effector cells Jurkat were added with 25 μL/well, and the 96-well plate was placed into the cell incubator to culture 5 h; and the 96-well plate was removed and placed at room temperature to enable the temperature thereof to equilibrate to room temperature; Bio-Gl chromogenic solution (G7940, Promega) was added with 75 μL/well, reacting for 15 mins, Luminescense was read from a Tecan microplate reader to obtain a value. The results are shown in
As shown in Table 7, the EC50 value of simulated killing activity detection of the candidate antibody CD25Q2-BA9-IgG1 is 0.2356, which is lower than the EC50 value of the control group CD25-MA251-IgG1 that is 0.3606, which indicates that the killing ability of the candidate antibody to SU-DHL-1 is better than that of the control group CD25-MA251-IgG1.
The above results indicate that the candidate antibody CD25Q2-BA9-IgG1 has a good killing effect on cells expressing CD25, which predicts that the candidate antibody can reduce the Treg cells expressing CD25 and their inhibition on Teff cells, thereby having better pharmaceutical effects.
3.3 BiaCore Detection of Affinity of Antibody
Antibody binding kinetics uses BIAcore8K instrument based on surface plasmon resonance (SRP) technology to measure. Anti-human IgG antibody amino was coupled to a CMS biosensor chip by the GE anti Human IgG Fc amino coupling kit (GE, cat #BR-1008-39) to obtain approximately 1000 response units (RU). For kinetic measurements, the CD25 protein (Sino Biological, 10165-H08H) was diluted 2-fold continuously with HBS-EP+1×(GE, BR-1008-26) buffer, starting at 50 nM, being diluted 2-fold for 4 concentration gradients and setting 0 concentration. The antibody to be detected: 2 μg/ml, sample injection time 70 s, flow rate 5 μL/min, stable for 5 s; CD25 protein: binding for 60 s, flow rate 30 μL/min, dissociation for 450 s; regeneration: regeneration was performed for 30 s with 3M MgCl2 buffer, Startup 3 times. The association constant (ka) and dissociation constant (kd) were calculated using a simple one-to-one Languir binding model (BIAcore Evaluation Software version 3.2), and the equilibrium dissociation constant (KD) was calculated by the ratio kd/ka. The affinity data of each antibody is shown in Table 9.
As shown in Table 9, the equilibrium dissociation constant KD value of the candidate antibody CD25Q2-BA9-IgG1 is 8.43E-10, which is lower than the KD value of the control group CD25-MA251-IgG1 that is 5.19E-09, which indicates that the affinity of CD25 protein of the candidate antibody CD25Q2-BA9-IgG1 is better than that of the control group CD25-MA251-IgG1.
As shown in Table 9, the equilibrium dissociation constant KD value of the candidate antibody CD25Q8-BT942-IgG1 is 3.79E-09, which is lower than the KD value of the control group CD25-MA251-IgG1 that is 5.19E-09, which indicates that the affinity of CD25 protein of the candidate antibody CD25Q8-BT942-IgG1 is better than that of the control group CD25-MA251-IgG1.
The above results predict that the candidate antibodies CD25Q2-BA9-IgG1 and CD25Q8-BT942-IgG1 have a stronger targeting and binding effect on the Treg cells expressing CD25, have better killing effect, reduce inhibition of the Treg cells on the Teff cells, and have better pharmaceutical effects as compared with the control group CD25-MA251-IgG1.
3.4 Cell Blocking Activity of Candidate Antibody
The frozen PBMC (peripheral blood mononuclear cells, manufacturer: ALLCELLS, item no.: PB003F-C) were recovered and then co-cultured with 10 μg/mL of CD25 antibody on the 96-U bottom plate for 30 mins, no antibody was added to the control group, the control group was labeled as NoAb, and then IL2 (0.1 U/mL, 1 U/mL, 10 U/mL) was added to incubate for 10 mins (working medium: 1640+10% FBS, containing 2 mM L-glutamine and 10000 U/mL Pen-Strep), to prepare cell suspension: after the last washing, the supernatant was discarded and the sample was vortexed on pulse to completely dissociate the pellet; 200 μL Foxp3 fixation/permeabilization working solution was added to each well. It was incubated at 2-8° C. or room temperature in the dark for 30-60 minutes; the sample was centrifuged at 400-600 g for 5 minutes at room temperature, and the supernatant was discarded; 200 μL of 1× membrane breaking solution was added to each well, the sample was centrifuged at 400-600 g for 5 minutes at room temperature, the supernatant was discarded, and is washed twice; (BD Phosflow™ Perm Buffer III is preliminarily put at −20° C. to pre-cool) washed with PBS once, centrifuged and the supernatant being discarded; ice-cold Phosflow™ Perm Buffer III was added slowly while being vortexed, and incubated on ice for 30 minutes; the cells were washed twice with PBS, centrifuged at 250 g for 10 minutes to discard the supernatant; the cells were resuspend in PBS to 107 cells/mL, contained separately in 100 μL/well, the antibody staining fluorescently labeled was continued and the flow cytometry was performed; living cells were distinguished, and the CD3 positive T cells were further distinguished. The higher the percentage of phosphorylated signal transducers and transcription activator 5 (PSTAT5), the lower the blocking rate. The results are shown in
As shown in Table 10, the % PSTAT5 value of the candidate antibody CD25Q2-BA9-IgG1 is 26.09, which is significantly higher than the % PSTAT5 value of the control group CD25-MA251-IgG1 that is 18.52, which indicates that the candidate antibody is significantly better than the control group CD25-MA251-IgG1 in not blocking the binding of IL2 and PBMC. It indicates that the candidate antibody CD25Q2-BA9-IgG1 can inhibit the activation of PBMC less than the control group CD25-MA251-IgG1, which predicts that the candidate antibody CD25Q2-BA9-IgG1 can better achieve the PBMC immune effect and have better pharmaceutical effect/anti-tumor effect.
As shown in Table 10, the % PSTAT5 value of the candidate antibody CD25Q8-BT942-IgG1 is 16.46, and the % PSTAT5 value of CD25-MA251-IgG1 is 18.52, which indicates that the candidate antibody basically equivalent to the control group CD25-MA251-IgG1 in not blocking the binding of IL2 and PBMC. It predicts that the candidate antibody CD25Q8-BT942-IgG1 can well achieve the PBMC immune effect and have good pharmaceutical effect/anti-tumor effect.
4.1 PD Activity of CD25Q2-BA9-IgG1 in Healthy Rhesus Monkey
CD25Q2-BA9-IgG1 antibody was administered intravenously to 3 rhesus monkeys at a dose of 10 mg/kg, flow cytometer (Cytomics™ FC500) was used to detect the content of the Treg cells (CD3+CD4+CD25+FoxP3+) at different time points before and after the administration according to flow cytometry, and the detection time points were: (±1 minute) before and after the administration, 0.5 hours (±1 minute), 3 hours (±2 minutes), 6 hours (±5 minutes), 24 hours (±10 minutes), 48 hours (±20 minutes, 2 days), 96 hours (±30 minutes, 4 days), 168 hours (±1 hour, 7 days), 336 hours (±1 hour, 14 days) after the administration, the experimental results are shown in
As can be seen from
4.2 PK Activity of Candidate Antibody in Cynomolgus Monkey
There are two cynomolgus monkeys in each group, they were intravenously injected with different CD25 antibodies, and whole blood samples were taken out intravenously at (0 h) before the administration and 1 min, 30 min, 3 h, 6 h, 1 d, 2 d, 4 d, 7 d, 10 d, and 14 d after the administration, put in a blood sample collection tube, and coagulated naturally in the ice box, the blood sample was put in the centrifuge within 8 h after being taken out, centrifuged at 1000-3000 g for 10 mins, the serum was separated and put in the sample storage tube, and the cynomolgus monkeys were intravenously injected with different CD25 antibodies again on the 14th day, the whole blood samples were taken out intravenously at (0 h) before the administration and 1 min (14 d+1 m), 30 min (14 d+30 m), 3 h (14 d+3 h), 6 h (14 d+6 h), 1 d (15 d), 2 d (16 d), 4 d (18 d) and 7 d (21 d) after the administration, put in a blood sample collection tube, and coagulated naturally in the ice box, the blood sample were put in the centrifuge within 8 h after being taken out, centrifuged at 1000-3000 g for 10 mins, the serum was separated and put in the sample storage tube, the metabolism of antibodies in the cynomolgus monkeys was detected by ELISA, and the results are shown in
The results indicate: CD25Q2-BA9-IgG1 and CD25Q8-BT942-IgG1 have a higher bioavailability than that of the control antibody CD25-MA251-IgG1, and have good pharmacokinetic performance.
5.1 Efficacy Test of Candidate Antibody in B-hIL2Rα Humanized Mouse MC38 Colon Cancer Animal Model
B-hIL2Rα humanized mice (Biocytogen) were divided into 5 groups according to body weight, wherein 10 mice was in the G1 negative control group and 8 mice were in each of the G2-G4 treatment groups. Individual administration was performed from the day of grouping (10 mg/kg, I.P., BIW) (10 mg/kg, intraperitoneal injection, twice a week), the next day, the MC38 cells resuspended in PBS was inoculated subcutaneously on the right side of B-hIL2Rα humanized mice at a concentration of 5×105 cells/0.1 mL with 0.1 mL/mouse. The tumor volume and animal body weight were measured twice per week, and the measurement values were recorded, tumor volume (mm3)=0.5×long diameter×short diameter2. The results are shown in
As shown in
As shown in
5.2 FACS Detection of Infiltration Effect of Immune Cells on MC38 Tumor after Administration
After the 5th administration of the test mice (16 days after grouping) in 5.1, 4 mice were taken from the negative control group and 3 mice were taken from each treatment group, the mice were killed and the tumor was cut up, the digestive enzyme was added therein, incubated and digested for 40 minutes at 37° C., and resuspend as a single cell suspension after filtering and washing. 25 μL of sealing and death and life dye solution and 25 of cell suspension were added to each well of a 96-well round bottom plate, mixed well and incubated in the dark for 15 mins at 4° C.; 50 μL of surface dye was added to each well, mixed well and incubated in the dark for 30 mins at 4° C.; 150 μL of FACS solution was added to each well and washed twice, 4° C., 500 g, centrifuged for 5 mins, and the supernatant was discarded; 200 μL of the fixed solution resuspended cells were added to each well, fixed for 30 mins at room temperature after being mixed well; after fixation, centrifuged at 4° C., 1400 g for 5 mins, and the supernatant was discarded; 200 μL of membrane-penetrating solution was added to each well, centrifuged at 4° C., 1400 g for 5 mins, and the supernatant was discarded; 100 μL of intracellular dye solution was added to each well, room temperature, incubated in the dark for 30 mins; 150 μL of membrane-penetrating solution was added to each well and washed twice, 1400 g, centrifuged for 5 mins, and the supernatant was discarded; the cells were resuspend with 250 μL of PBS, and the content of CD8+ cells (Teff) in CD3, the content of CD25+Foxp3+ cells (Treg) in CD3 and the content of Foxp3+ cells (Treg) in CD4 were detected on machine. The results are shown in
As shown in
| Number | Date | Country | Kind |
|---|---|---|---|
| 201910495614.4 | Jun 2019 | CN | national |
| 201910495626.7 | Jun 2019 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2020/094919 | 6/8/2020 | WO |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2020/248938 | 12/17/2020 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 6521230 | Amlot et al. | Feb 2003 | B1 |
| 20040170626 | Schuurman et al. | Sep 2004 | A1 |
| 20080317746 | Bauerle et al. | Dec 2008 | A1 |
| 20200010554 | Goubier et al. | Jan 2020 | A1 |
| 20200140538 | Surh et al. | May 2020 | A1 |
| Number | Date | Country |
|---|---|---|
| 103571872 | Nov 2016 | CN |
| WO 2004045512 | Jun 2004 | WO |
| WO 2018167104 | Sep 2018 | WO |
| WO 2020248938 | Dec 2020 | WO |
| Entry |
|---|
| MacCallum et al. (1996). J. Mol. Biol. 262:732-745. |
| De Pascalis et al. (2002). Journal of Immunology. 169:3076-3084. |
| Casset et al. (2003). Biochemical and Biophysical Research Communications. 307:198-205. |
| Chen et al. (1999). J. Mol. biol. 293:865-881. |
| Wu et al. (1999). J. Mol. Biol. 294:151-162. |
| Rudikoff et al. (1982). PNAS. 79:1979-1983. |
| Extended European Search Report in European Appln. No. 20822215.8, dated May 31, 2022, 9 pages. |
| International Preliminary Report on Patentability in International Appln. No. PCT/CN2020/094919, dated Dec. 14, 2021, 12 pages (with English Translation). |
| International Search Report and Written Opinion in International Appln. No. PCT/CN2020/094919, dated Sep. 14, 2020, 10 pages (with English Translation). |
| Martin, “Humanized anti-CD25 antibody treatment with daclizumab in multiple sclerosis,” Neurodegenerative Dis, 2008 5(1):23-26. |
| Onishi et al., “Immunotherapy approaches targeting regulatory T-cells,” Anticancer Res, Mar. 2012, 32(3):997-1003. |
| Rubin et al., “A monoclonal antibody 7G7/B6, binds to an epitope on the human interleukin-2 (IL-2) receptor that is distinct from that recognized by IL-2 or anti-Tac,” Hybridoma, Jan. 1985, 4(2):91-102. |
| Shang et al., “Prognostic value of tumor-infiltrating FoxP3+ regulatory T cells in cancers: a systematic review and meta-analysis,” Scientific Reports, Oct. 2015, 5:15179, 9 pages. |
| Tanaka et al., “New monoclonal antibodies that define multiple epitopes and a human-specific marker on the interleukin 2 receptor molecules of primates,” Microbiology and Immunology, Apr. 1986, 30(4):373-388. |
| Walker et al., “Pharmacokinetic comparison of a diverse panel of non-targeting human antibodies as matched IgG1 and IgG2 isotypes in rodents and non-human primates,” PLoS One, May 2019, 14(5):e0217061, 24 pages. |
| Number | Date | Country | |
|---|---|---|---|
| 20220195055 A1 | Jun 2022 | US |
