Patent Application
20200347410
The present application claims the priority of CN201810053219.6 filed on Jan. 19, 2018, the entire contents of which are incorporated herein by reference.
The invention belongs to the field of immunotherapy, and in particular relates to a pair of plasmid vectors and an immune cell that target antigen-dependently regulates the expression of IL12.
IL12 is a kind of immune cell growth stimulating factor with multiple biological activities and a heterodimeric cytokine that can promote the proliferation of T helper cells 1 (Th1); induce NK cells and T cells to produce interferon gamma; improve the cytotoxicity of NK cells; and promote the formation of cytotoxic T cells. At present, IL12 is directly loaded to enhance the anti-tumor efficacy of a chimeric antigen receptor (CAR), however, IL12 will be systemically secreted with CAR-T by such manner, and the expression of IL12 will be out of control with the amplification of T cells, thereby causing serious toxic and side effects to the body.
U.S. Pat. No. 9,834,608 B2 (the patent is incorporated herein by reference in its entirety) disclosed a binding-triggered transcription switch polypeptide and an encoding nucleic acid and host cell thereof. The polypeptide is a chimeric Notch receptor polypeptide, including an extracellular domain, a Notch regulatory region and an intracellular domain, wherein the extracellular domain contains a first member of a specific binding pair, which specifically binds to a second member of the specific binding pair, the Notch regulatory region contains Lin 12-Notch repeat unit, S2 proteolytic cleavage site and the transmembrane domain comprising S3 proteolytic cleavage site, and the first member of the specific binding pair binds to the second member to induce cleavage at S2 and S3 proteolytic cleavage sites, thereby releasing the intracellular domain. The first member is selected from the group consisting of an antibody, an antibody-based recognition scaffold, a non-antibody-based recognition scaffold, an antigen, a ligand of a receptor, a receptor, a target for a non-antibody-based recognition scaffold, an extracellular matrix component, and an adhesion molecule. The intracellular domain contains a transcriptional activator, and the release of the intracellular domain causes the expression of an endogenous gene in cells induced by the transcriptional activator. Alternatively, the intracellular domain contains a transcription repressor, and the release of the intracellular domain inhibit the expression of an endogenous gene in cells by the transcription repressor.
However, the necessity for controlling the expression and local secretion of IL-12 in immune cells and caused beneficial effects are not mentioned in this US patent.
In the prior art, no immune cells can control expression and local secretion of IL-12. For resolving such technical problem, a pair of plasmid vectors and an immune cell that target antigen-dependently regulates the expression of IL12 through synNotch technology are provided in the present invention. In particular, in the present invention, a synthetic Notch (synNotch) receptor was used as a core in NK92 cells to construct two plasmid vectors for achieving local secretion of IL12. In one of the plasmid vectors, antiGPC3 scfv (SEQ ID NO: 2) is used as an extracellular segment to recognize the target antigen GPC3; the notch core (SEQ ID NO: 3) includes a transmembrane region and contains two enzyme cleavage sites; and GAL4VP64 (SEQ ID NO: 4) transcription factor is used as an intracellular segment. When the target antigen GPC3 is recognized, the cleavage site on the notch core will be recognized and hydrolyzed by the corresponding enzyme and the intracellular transcription factor GAL4VP64 will be released. Another plasmid vector carries the DNA recognition binding region GAL4UAS (SEQ ID NO: 5) of the GAL4 transcription factor and the corresponding minimal CMV promoter (SEQ ID NO: 6) that initiates the target gene IL12. When GAL4VP64 is hydrolyzed and cleaved, it will bind to the binding region GAL4UAS, thereby initiating the transcription of subsequent gene, expressing and secreting IL12 out of the cell.
The generation of toxicity can be reduced by the present invention, since the secretion and expression of IL12 can be induced only when exposed to a specific target antigen, thereby locally releasing IL12 near the tumor and enhancing the effects of CAR-T cells. Moreover, the used NK92 cell line will not substantially expand in vivo, thereby avoiding serious toxic and side effects caused by the uncontrolled expression of IL12 induced by T cell expansion in vivo. In addition, compared with NK cells, NK92 can be mass-produced, which is more suitable for industrial applications.
In one aspect, the present invention relates to a pair of plasmid vectors including a first vector and a second vector, wherein the first vector comprises a Notch core and further comprises encoding nucleic acid molecules for other extracellular segments and intracellular segments, and preferably, the intracellular segment comprises transcriptional activator; and the second vector comprises a nucleic acid molecule that specifically recognizes and binds to the intracellular segment in the first vector and a nucleic acid molecule encoding IL12.
In a preferred embodiment, the Notch core of the first vector has the nucleic acid sequence as shown in SEQ ID NO: 3.
According to the present invention, the intracellular segment of the first vector comprises a transcriptional activator, such as a tetracycline-controlled transcriptional activator (tTa), GAL4VP64 and ZFHD1-VP64, and the second vector comprises a DNA binding region corresponding to the transcriptional activator, for example, Tet, UAS and ZFRE. Preferably, the intracellular segment of the first vector comprises GAL4VP64 and the second vector comprises GAL4UAS. The intracellular segment of the first vector is a DNA-binding polypeptide, such as Zip(−)Gal4 DNA-binding polypeptide, or NLS VP64 Zip (+).
The extracellular segment in the first vector of the present invention is not particularly limited, as long as it can specifically bind to and pair with a target, for example, it may comprise an antigen or an antibody or fragment thereof of the antigen, a receptor or a ligand of the receptor, a non-antibody-based recognition scaffold or a target thereof, an adhesion molecule or an extracellular matrix thereof, Fc or a receptor thereof, a receptor or a co-receptor thereof, etc.
The antibodies of the present invention specifically bind to an antigen, including nobodies, single chain antibodies, bivalent antibodies, trivalent antibodies or mini antibodies. An antibody fragment refers to a part of an intact antibody, such as the antigen binding region or variable region of the intact antibody. The antibody fragment includes Fab, Fab′, F(ab′)2 and Fv fragment. Fv is the smallest antibody fragment that contains a complete antigen recognition and binding site. Single chain Fv (scFv) refers to the VH and VL domains of an antibody, these domains take the form of an single chain polypeptide. In some embodiments, the Fv polypeptide also comprises a linker between VH and VL. The extracellular segment preferably comprises an antibody, and more preferably comprises scFv.
The antibody of the present invention or a fragment thereof is specifically directed to an epitope on an antigen, especially an antigen associated with a cancer cell, including breast cancer, B-cell lymphoma, prostate cancer, Hodgkin lymphoma, ovarian cancer, and lung cancer (e.g., small cell lung cancer), mesothelioma, melanoma, acute and chronic lymphocytic leukemia, neuroblastoma, glioma, glioblastoma, medulloblastoma, colon cancer, gastric cancer, liver cancer, etc.
According to the present invention, the tumor antigens include one or more from prostate specific membrane antigen (PSMA), carcinoembryonic antigen (CEA), IL13Ralpha, HER-2, CD19, NY-ESO-1, HIV-1 Gag, Lewis Y, MART-1, Gp100, tyrosinase, WT-I, hTERT, mesothelin, EGFR, EGFRvIII, GPC3, EphA2, HER3, EpCAM, MUC1, MUC16, CLDN18.2, folate receptor, CLDN6, CD30, CD138, ASGPR1 CDH16, GD2, 5T4, 8H9, αvβ6 integrin, B cell maturation antigen (BCMA), B7-H3, B7-H6, CAIX, CA9, CD20, CD22, kappa light chain, CD33, CD38, CD44, CD44v6, CD44v7/8, CD70, CD123, CD171, CSPG4, EGP2, EGP40, ERBB3, ERBB4, ErbB3/4, FAP, FAR, FBP, embryonic AchR, GD2, GD3, HLA-AI MAGE A1, MAGE3, HLA-A2, IL11Ra, KDR, Lambda, MCSP, NCAM, NKG2D ligand, PRAME, PSCA, PSC1, ROR1, Sp17, SURVIVIN, TAG72, TEM1, TEM8, VEGRR2, HMW-MAA, VEGF receptor, and/or fibronectin, cytotactin or carcinoembryogenic variants of tumor necrosis region.
According to the present invention, the extracellular segment includes, but is not limited to, for example, anti-CD19 scFv, anti-mesothelin scFv, anti-GFP nanobody, anti-GPC3 scFv, etc., preferably, anti-GPC3 scFv (i.e., anti-GPC3 scFv).
According to the present invention, the Notch core includes a Notch transmembrane region and one or more cleavage sites.
According to the present invention, one or more epidermal growth factor (EGF) repeating units can optionally be added to the extracellular end of the Notch core. The EGF repeat unit can reduce the non-specific activation of the basic background.
According to the present invention, the first vector and the second vector optionally comprise elements, such as a signal sequence (for example, SEQ ID NO: 1), a linker, a promoter, a tag, and a reporter, wherein the tag includes one or more of blood coagulation HA, C-myc and Flag, and the like. The reporter includes one or more of green fluorescent protein (GFP), blue fluorescent protein (BFP) and mcherry, and the like.
According to the present invention, the first vector sequentially comprises the PGK promoter-signal sequence-myc tag-anti-GPC3 scFv-notch core-GAL4-linker-VP64, and the second vector sequentially comprises the GAL4UAS-CMV minimal promoter-IL12-PGK promoter-mcherry.
According to the present invention, the open reading frame of the first vector comprises a nucleotide sequence as shown in SEQ ID NO: 21, and the open reading frame of the second vector comprises a nucleotide as shown in SEQ ID NO: 22. The amino acid sequences encoded by the above nucleotide sequences are the elements of the vectors of the present invention and/or the polypeptides encoded by the vectors.
According to the invention, the function of a polypeptide variant generally won't be substantially affected by the substitution, deletion and/or addition of one or more amino acids, especially when the conservative regions of the polypeptide are known. Conservative substitutions (for example, one basic amino acid for another basic amino acid and one acidic amino acid for another acidic amino acid) are also readily conceived by a skilled person in the art. Therefore, in addition to the elements of the vector of the invention and/or the amino acid sequence of the polypeptide encoded by the vector, functional variants having at least 50%, preferably 70%, 75%, 80%, 85% or 90%, more preferably 95%, 96%, 97%, 98%, 99% identity with the elements of the vector of the invention and/or the amino acid sequence of the polypeptide encoded by the vector will fall within the protection scope. More over, nucleotide codons encoding the polypeptides may be degenerate, and therefore functional variants having at least 50%, preferably 70%, 75%, 80%, 85%, or 90% %, more preferably 95%, 96%, 97%, 98% or 99% identity with the elements of the vector of the invention and/or the nucleotide sequence of the vector also fall within the protection scope. Even more preferably, the anti-GPC3 scFv has at least 90% identity with the nucleotide sequence as shown in SEQ ID NO: 2.
In another aspect, the present invention also provides immune cells modified with the pair of plasmid vectors of the present invention. The immune cells are T cells or NK cells. Preferably, the immune cells are NK cells. The cells are transfected with any of the above pairs of the plasmid vectors. The NK cells are natural NK cells or immortalized NK cells, preferably, immortalized NK cells, more preferably, NK92 cell.
In another aspect, the present invention provides uses of any of the above pairs of the plasmid vectors or any of the above immune cells in the preparation of a medicament for local secretion of IL12 or regulating expression of IL12.
In yet another aspect, the present invention provides uses of any of the above pairs of plasmid vectors or any of the above immune cells in the preparation of a medicament for enhancing killing effects of CAR-T cells.
In a preferred embodiment, the tumor antigen specifically recognized by the extracellular segment of the first vector of the immune cell is the same as the tumor antigen recognized by the CAR-T cell.
In a preferred embodiment, both of the tumor antigen specifically recognized by the extracellular segment of the first vector of the immune cell and the tumor antigen recognized by the CAR-T cell are expressed on the same tumor.
In a preferred embodiment, both of the tumor antigen specifically recognized by the extracellular segment of the first vector of the immune cell and the tumor antigen recognized by the CAR-T cells are GPC3.
In a preferred embodiment, both of the tumor antigen specifically recognized by the extracellular segment of the first vector of the immune cell and the tumor antigen recognized by the CAR-T cells are expressed in liver cancer.
In a preferred embodiment, the first vector of the immune cells comprises the sequence as shown in SEQ ID NO: 21, and the second vector comprises the sequence as shown in SEQ ID NO: 22;
In a preferred embodiment, the CAR of the CAR-T cell has the sequence as shown in SEQ ID NO: 23, 24 or 25.
In a preferred embodiment, the ratio of the immune cells to CAR-T cells is 1:1˜4:1.
In a preferred embodiment, the immune cells can be administrated in multiple times within one administration cycle.
In yet another aspect, the present invention provides a composition of the immune cells and CAR-T cells as described.
In a preferred embodiment, the tumor antigen specifically recognized by the extracellular segment of the first vector of the immune cell is the same as the tumor antigen recognized by the CAR-T cell.
In a preferred embodiment, both of the tumor antigen specifically recognized by the extracellular segment of the first vector of the immune cell and the tumor antigen recognized by the CAR-T cell are expressed on the same tumor.
In a preferred embodiment, both of the tumor antigen specifically recognized by the extracellular segment of the first vector of the immune cell and the tumor antigen recognized by the CAR-T cell are GPC3.
In a preferred embodiment, both of the tumor antigen specifically recognized by the extracellular segment of the first vector of the immune cell and the tumor antigen recognized by the CAR-T cell are expressed in liver cancer.
In a preferred embodiment, the first vector of the immune cell comprises the sequence as shown in SEQ ID NO: 21, the second vector comprises the sequence as shown in SEQ ID NO: 22, and the CAR of the CAR-T cell comprises the sequence as shown in SEQ ID NO: 23, 24 or 25.
In a preferred embodiment, the ratio of the immune cells to the CAR-T cells is 1:1˜4:1.
In a final aspect, the present invention also relates to a combination of kits, including kit A of the immune cell and kit B containing the CAR-T cell as described above.
In a preferred embodiment, the tumor antigen specifically recognized by the extracellular domain of the first vector of the immune cell is the same as the tumor antigen recognized by the CAR-T cell.
In a preferred embodiment, both of the tumor antigen specifically recognized by the extracellular domain of the first vector of the immune cell and the tumor antigen recognized by the CAR-T cell are expressed on the same tumor.
In a preferred embodiment, both of the tumor antigen specifically recognized by the extracellular domain of the first vector of the immune cell and the tumor antigen recognized by the CAR-T cell are GPC3.
In a preferred embodiment, both of the tumor antigen specifically recognized by the extracellular domain of the first vector of the immune cell and the tumor antigen recognized by the CAR-T cell are expressed in liver cancer.
In a preferred embodiment, the first vector of the immune cell comprises the sequence as shown in SEQ ID NO: 21, the second vector comprises the sequence as shown in SEQ ID NO: 22, and the CAR of the CAR-T cell comprises the sequence as shown in SEQ ID NO: 23, 24 or 25.
In the present invention, it is demonstrated through experiments that uninfected NK92 cells secrete a low level of IL12, while the secretion of IL12 from pHRLSIN-antiGPC3-spNotch-GAL4VP64 and pHRLSIN-GAL4UAS-IL12-PGK-mcherry double-infected NK92 cells significantly increases, when co-incubated with cell lines highly expressing GPC3, respectively.
Therefore, the single-chain antibodies against GPC3 can regulate the expression of cytokine IL12 in NK92 cells and can locally release IL12.
In order to clearly describe the technical solution of the present invention, a brief introduction will be given below with reference to the drawings. These drawings are obviously only some specific embodiments described in this application. The invention includes, but is not limited to these drawings.
In order to further understand the present invention, the preferred solutions of the present invention will be described below in conjunction with embodiments. These descriptions are only illustrative of the features and advantages of the present invention, rather than limiting the protection scope of the present invention. If the conditions are not specified in the following examples, the experimental method is performed according to the conventional conditions, such as those described in Sambrook et al. “Molecular Cloning: Experimental Manual (1989)”, or the conditions recommended by the instructions from reagent companies.
The following detailed description shows in detail the embodiments disclosed herein. It should be understood that this description is not limited to the specific embodiments disclosed herein, which may vary. A skilled person in the art will understand that there may be many changes or variations for the contents disclosed in this specification, which are covered within the disclosed scope and principles. Unless otherwise stated, each embodiment can be arbitrarily combined with any other embodiment.
Certain embodiments disclosed herein include numerical ranges, and certain aspects of the invention can be described in terms of ranges. Unless otherwise stated, it should be understood that the numerical range or description in range is just for brevity and convenience, and should not be considered as a strict limitation on the scope of the present invention. Therefore, a description in range should be considered as specifically disclosing all possible sub-ranges and all possible specific numerical points within the range, as these sub-ranges and numerical points have been explicitly written herein. For example, the description of a range from 1 to 6 should be considered to specifically disclose subranges from 1 to 3, 1 to 4, 1 to 5, 2 to 4, 2 to 6, 3 to 6, etc., and specific numerical points within these ranges, such as 1, 2, 3, 4, 5, 6. Regardless of the scope of the value, the above principles are equally applicable. When a range is described, the endpoints of the range shall be included.
The term “receptor” is a type of special protein that exists in the cell membrane or intracellularly, and can combine with a special signaling molecule outside the cell to activate a series of biochemical reactions in the cell and cause the cell to produce corresponding effects to external stimuli. Biologically active substances that bind to a receptor are collectively called ligands.
The term “chimeric antigen receptor” or “CAR” refers to an engineered molecule that can be expressed by immune cells including but not limited to T cells. CAR is expressed in T cells and can redirect the T cells to induce killing effects on target cells with specificity determined by artificial receptors. The extracellular binding domain of CAR can be derived from murine, humanized or fully human monoclonal antibodies.
A chimeric antigen receptor usually comprises an extracellular antigen binding region. In some embodiments, the extracellular antigen binding region may be fully of human. In other cases, the extracellular antigen binding region can be humanized. In other cases, the extracellular antigen binding region may be of murine origin, or the chimera in the extracellular antigen binding region consists of amino acid sequences derived from at least two different animals. In some embodiments, the extracellular antigen binding region may be of non-human, or multiple antigen-binding regions may be designed. Non-limiting examples include single-chain variable fragments (scFv) derived from antibodies, fragment antigen binding regions (Fab) selected from libraries, single-domain fragments, or natural ligands conjugated to cognate receptors thereof. In some embodiments, the extracellular antigen binding region may comprise scFv, Fab or natural ligand, and any derivatives thereof. The extracellular antigen binding region may refer to a molecule other than the intact antibody, which may comprise a part of the intact antibody and may bind to the antigen to which the intact antibody binds. Examples of antibody fragments may include, but are not limited to, Fv, Fab, Fab′, Fab′-SH, F(ab′)2; bifunctional antibodies, linear antibodies; single-chain antibody molecules (e.g., scFv); and multispecific antibodies formed from antibody fragments.
The term “engineered” and other grammatical forms thereof may refer to one or more changes of nucleic acids, such as nucleic acids within the genome of an organism. The term “engineered” may refer to a change, addition and/or deletion of a gene. Engineered cells can also refer to cells that contain added, deleted, and/or changed genes.
The term “cell” or “engineered cell” and other grammatical forms thereof may refer to a cell derived from human or non-human animal. Engineering cells can also refer to cells that express CAR.
The term “transfection” refers to the introduction of a foreign nucleic acid into an eukaryotic cell. Transfection can be achieved by various means known in the art, including calcium phosphate-DNA co-precipitation, DEAE-dextran-mediated transfection, polybrene-mediated transfection, electroporation, microinjection, liposome fusion, lipofection, protoplast fusion, retrovirus infection, and biolistics.
As used herein, the terms “encoding nucleic acid molecule” and “encoding nucleic acid sequence” refer to the order of deoxyribonucleotides along a deoxyribonucleic acid chain, and the order of these deoxyribonucleotides determines the order of amino acids in a polypeptide (protein) chain. Therefore, the nucleic acid sequence encodes an amino acid sequence.
The term “peripheral blood lymphocytes” and other grammatical forms thereof may refer to lymphocytes circulating in blood (e.g., peripheral blood). Peripheral blood lymphocytes may refer to lymphocytes not limited in organs. The peripheral blood lymphocytes may comprise T cells, NK cells, B cells, or any combination thereof.
The term “immune cell” refers to a cell that can elicit an immune response, including but not limited to T cells, B cells, NK cells, NKT cells, DNT cells, etc., their respective precursor cells and progenies. Immune response cells can also refer to cells of the lymphoid or bone marrow lineage.
The term “immune cell” and other grammatical forms thereof may refer to immune cells of any origin. For example, immune cells may be derived from blood, such as autologous T cells, allogeneic T cells, autologous NK cells, xenogeneic NK cells, or may be derived from cell lines, such as NK cell line prepared by infection with EBV virus, NK cells and NK92 cell line induced from embryonic stem cells and iPSC.
The term “immune cell” may also be of human or non-human.
When used to refer to a nucleotide sequence, the term “sequence” and other grammatical forms thereof may include DNA or RNA, and may be single-stranded or double-stranded. The nucleic acid sequence can be mutated. The nucleic acid sequence can be of any length.
The term “effective amount” refers to an amount that provides therapeutic or preventive benefits.
The term “promoter” as used herein is defined as a DNA sequence that is recognized by the cell's synthetic mechanism or the introduced synthetic mechanism required to initiate specific transcription of the polynucleotide sequence.
The term “vector” as used herein is a composition that comprises an isolated nucleic acid and can be used to deliver the isolated nucleic acid inside a cell. Many vectors are known in the art, including but not limited to linear polynucleotides, polynucleotides related to ionic or amphiphilic compounds, plasmids, and viruses. Therefore, the term “vector” includes autonomously replicating plasmids or viruses. The term should also be interpreted to include non-plasmid and non-viral compounds facilitating the transfer of nucleic acids into cells, such as polylysine compounds, liposomes, and the like. Examples of viral vectors include, but are not limited to, adenovirus vectors, adeno-associated virus vectors, retrovirus vectors, and the like.
The term sequence “identity” as used herein determines the percent identity by comparing two best-matched sequences on a comparison window, where portions of the polynucleotide or polypeptide sequences in the comparison window may contain additions or deletions (i.e., gaps), for example, for two sequences that best match, a gap of 20% or less (e.g., 5 to 15%, or 10 to 12%) compared with a reference sequence (which does not include an addition or deletion). The percentage is usually calculated by determining the number of positions where the same nucleic acid base or amino acid residue is present in the two sequences to produce the number of correctly matched positions, and dividing the number of correctly matched positions by the total number of positions in the reference sequence (i.e., window size), and multiply the result by 100 to produce the percentage of sequence identity.
The terms “antiGPC3”, “anti-GPC3” and “anti GPC3” can be used interchangeably and have the same meaning.
The terms “IL12”, “Interleukin 12” and “interleukin-12” can be used interchangeably and have the same meaning. The term “IL12” is an immunomodulatory factor with multiple biological activities. For example, the term “IL12” may refer to human IL12 as defined in SEQ ID NO: 27 or active fragments thereof, or may be from other species.
In some embodiments, the elements used to construct the receptor specifically binding to GPC3 or IL12 may be naturally occurring. For example, it may be isolated or purified from a mammal; it may also be artificially prepared, such as the elements or IL12 can be recombination-produced according to conventional genetic engineering recombination technology. Preferably, recombinant elements or IL12 can be used in the present invention.
Amino acid sequences formed by substitution, deletion, or addition of one or more amino acid residues based on the aforementioned elements or IL12 polypeptide sequence are also included in the present invention. Proper replacement of amino acids is a technique well known in the art, which can be easily implemented and ensure that biological activities of the resulting molecule will not be altered. According to these techniques, a skilled person in the art will appreciate that changing a single amino acid in a non-essential region of a polypeptide will generally not substantially alter biological activities thereof.
Each of the elements or the biologically active fragments of IL12 polypeptide can be used in the present invention. The biologically active fragment herein means a polypeptide, as a part of a full-length polypeptide, that can maintain all or part of the functions of the full-length polypeptide. The biologically active fragment generally maintains at least 50% of the activity of the full-length polypeptide. In a preferred embodiment, the active fragment can maintain 60%, 70%, 80%, 90%, 95%, 99%, or 100% of the activity of the full-length polypeptide.
Modified or improved polypeptides can also be used in the present invention based on the elements or IL12 polypeptide sequence, for example, a polypeptide modified or improved for promoting half-life, effectiveness, metabolism, and/or efficacy of the polypeptide. That is, any variation forms not affecting the biological activity of the polypeptide can be used in the present invention.
The term “tumor” refers to a disease characterized by a pathological proliferation of cells or tissues, and the subsequent migration or invasion thereof to other tissues or organs. The growth of a tumor is usually uncontrolled and progressive, and does not induce or inhibit the proliferation of normal cells. Tumors can affect a variety of cells, tissues or organs, including but not limited to bladder, breast, esophagus, intestine, kidney, liver, lung, lymph nodes, nervous tissue, ovary, pancreas, prostate, skeletal muscle, skin, spinal cord, spleen, stomach, uterine organs, or tissues or corresponding cells. The tumors of the present invention may include, but are not limited to, liver cancer, stomach cancer, lung cancer, breast cancer, head and neck cancer, bladder cancer, ovarian cancer, cervical cancer, renal cancer, pancreatic cancer, cervical cancer, liposarcoma, melanoma, adrenal gland cancer, schwannoma, malignant fibrous histiocytoma, esophageal cancer. Preferably, the “tumor” includes but is not limited to: liver cancer, gastric cancer, lung cancer, breast cancer.
The extracellular antigen binding region can bind to any complementary target. The extracellular antigen binding region can be derived from antibodies with known variable region sequences. The extracellular antigen binding region can be obtained from antibody sequences obtained from available mouse hybridomas. Alternatively, the extracellular antigen-binding region can be obtained from whole external cleavage sequencing of tumor cells or primary cells, such as tumor infiltrating lymphocytes (TIL).
In some cases, the binding specificity of extracellular antigen binding regions can be determined by complementarity determining regions or CDRs, such as light chain CDRs or heavy chain CDRs. In many cases, the binding specificity can be determined by the light chain CDR and the heavy chain CDR. Compared with other reference antigens, a given binding pocket can be provided by a given combination of heavy and light chain CDRs, which can confer greater affinity and/or specificity for the antigen (e.g., GPC3). For example, CDRs specific for Glypican-3 can be expressed in the extracellular binding region of CAR, so that CAR targeting GPC3 can target immune response cells to tumor cells expressing GPC3.
In certain aspects of any embodiment disclosed herein, the extracellular antigen binding region, such as scFv, may comprise light chain CDRs specific for an antigen. The light chain CDR may be the complementarity determining region of scFv light chain of an antigen binding unit, such as CAR. The light chain CDR may comprise a continuous sequence of amino acid residues, or two or more continuous sequences of amino acid residues separated by non-complementarity determining regions (e.g., framework region). In some cases, the light chain CDR may comprises two or more light chain CDRs, which may be named as light chain CDR-1, CDR-2, etc. In some cases, the light chain CDR may comprise three light chain CDRs, which may be named as light chain CDR-1, light chain CDR-2, and light chain CDR-3, respectively. In some embodiments, a group of CDRs present on a common light chain may be collectively named as light chain CDRs.
In certain aspects of any embodiments disclosed herein, the extracellular antigen-binding region, such as scFv, may comprises heavy chain CDRs specific for an antigen. The heavy chain CDR may be a heavy chain complementarity determining region of an antigen binding unit, such as scFv. The heavy chain CDR may comprise a continuous sequence of amino acid residues, or two or more continuous sequences of amino acid residues separated by non-complementarity determining regions (e.g., framework region). In some cases, the heavy chain CDR may comprise two or more heavy chain CDRs, which may be named as heavy chain CDR-1, CDR-2, and the like. In some cases, the heavy chain CDR may comprise three heavy chain CDRs, which may be named as heavy chain CDR-1, heavy chain CDR-2, and heavy chain CDR-3, respectively. In some cases, a group of CDRs present on a common heavy chain may be collectively named as heavy chain CDRs.
The extracellular antigen-binding region can be modified in various ways through genetic engineering. In some cases, the extracellular antigen binding region can be mutated so that the extracellular antigen binding region can be selected to have a higher affinity for a target. In some cases, the affinity of the extracellular antigen-binding region to a target can be optimized for the target expressed at low levels on normal tissues. Such optimization can be performed to minimize potential toxicity. In other cases, clones of the extracellular antigen-binding region with higher affinity for the membrane-bound form of the target may be superior to the soluble form counterpart. Such modifications can be conducted since different levels of the target in soluble form can also be detected, and undesirable toxicities can be caused by such targeting.
In some cases, the extracellular antigen-binding region includes hinges or spacers. The terms hinge and spacer can be used interchangeably. The hinge may be considered as a part for providing flexibility to the extracellular antigen binding region.
The term “treatment” refers to a clinical intervention trying to change an individual or processing a disease caused by cells, which can be of preventive and performed during the clinical pathological process. Therapeutic effects include, but not limited to, preventing the occurrence or recurrence of a disease, reducing symptoms, reducing the direct or indirect pathological consequences of any disease, preventing metastasis, slowing the progress of a disease, improving or alleviating conditions, alleviating or improving prognosis, etc.
The term “constitutive expression” refers to an expression under all physiological conditions.
The term “inducible expression” refers to an expression under certain conditions, for example when T cells bind to an antigen. A skilled person will know how to perform a conventional “inducoble expression”.
The term “Notch receptor” includes 3 key components: 1) ligand binding epidermal growth factor (EGF) repeat sequence, 2) notch core that controls the cleavage of the receptor during activation, and 3) intracellular domain which is released and regulates the transcription.
The term “Notch core” is the smallest scaffold that controls ligand-dependent cleavage and activation, including Lin12-Notch repeat sequence (LNR) that controls the accessibility of the S2 cleavage site to metalloproteases, heterodimerization domain (HD), and transmembrane domain (TMD) comprising γ-secretase cleavage site required for the release of Notch intracellular domain (NICD).
Immune Cells
In some embodiments, the present invention provides an immune cell expressing a pair of plasmid vectors.
In some embodiments, the immune cell is capable of locally secreting IL12 or regulating the expression of IL12.
In some embodiments, the immune cell is capable of enhancing tumor killing effects of CAR-T cells.
Composition
The immune cells of the present invention can be used in combination with CAR-T cells. In addition to an effective amount of immune cells, the pharmaceutical composition may also comprise an effective amount of CAR-T cells.
Combination with Anti-Tumor Drugs
In some embodiments, the immune cells of the invention can be administered in combination with another therapeutic agent. In some embodiments, the another therapeutic agent is a chemotherapeutic agent. Chemotherapy drugs that can be used in combination with the immune cells of the present invention include, but not limited to, mitotic inhibitors (vinca alkaloids), including vincristine, vinblastine, vindesine, and Novibin™ (vinorelbine, 5′-dehydrohydrogen sulfide); topoisomerase I inhibitors, such as camptothecin compounds, including Camptosar™ (Irinotecan HCL), Hycamtin™ (Topotecan HCL) and other compounds derived from camptothecin and analogs thereof; podophyllotoxin derivatives, such as etoposide, teniposide, and midoxazole; alkylating agents cisplatin, cyclophosphamide, nitrogen mustard, trimethylene thiophosphoramide, Carmustine, busulfan, chlorambucil, buquinazine, uracil mustard, cloprofen, and dacarbazine; antimetabolites, including cytarabine, fluorouracil, methotrexate, mercaptopurine, azathioprine, and procarbazine; antibiotics, including but not limited to doxorubicin, bleomycin, dactinomycin, daunorubicin, mycomycin, mitomycin, sarcomycin C and daunomycin; and other chemotherapeutic drugs, including but not limited to anti-tumor antibodies, dacarbazine, azacytidine, amsacang, melphalan, ifosfamide, and mitoxantrone.
In some embodiments, chemotherapeutic drugs that can be used in combination with immune cells of the invention include, but are not limited to, anti-angiogenic agents, including anti-VEGF antibodies (including humanized and chimeric antibodies, anti-VEGF aptamers, and antisense oligonucleotides) and other angiogenesis inhibitors, such as angiostatin, endostatin, interferon, retinoic acid, and tissue inhibitors of metalloproteinases-1 and -2.
Combination Kit
The invention also provides a combination kit comprising the immune cells of the invention. The kit can be used to treat or prevent cancer, pathogen infection, immune disorders, or allotransplantation. In one embodiment, the kit may include a therapeutic or prophylactic composition comprising an effective amount of immune cells of one or more unit dosage forms.
In some embodiments, the kit includes a sterile container that may comprise a therapeutic or prophylactic composition.
In some cases, the kit may include about 1×104 cells to about 1×106 cells. In some cases, the kit may include at least about 1×105 cells, at least about 1×106 cells, at least about 1×107 cells, at least about 4×107 cells, at least about 5×107 cells, at least about 6×107 cells, at least about 6×107 cells, 8×107 cells, at least about 9×107 cells, at least about 1×108 cells, at least about 2×108 cells, at least about 3×108 cells, at least about 4×108 cells, at least about 5×108 cells, at least about 6×108 cells, at least about 6×108 cells, at least about 8×108 cells, at least about 9×108 cells, at least about 1×109 cells, at least about 2×109 cells, at least about 3×109 cells, at least about 4×109 cells, at least about 5×109 cells, at least about 6×109 cells, at least about 8×109 cells, at least about 9×109 cells, at least about 1×1010 cells, at least about 2×1010 cells, at least about 3×1010 cells, at least about 4×1010 cells, at least about 5×1010 cells, at least about 6×1010 cells, at least about 9×1010 cells, at least about 9×1010 cells, at least about 1×1011 cells, at least about 2×1011 cells, at least about 3×1011 cells, at least about 4×1011 cells, at least about 5×1011 cells, at least about 8×1011 cells, at least about 9×1011 cells, or at least about 1×1012 cells. For example, approximately 5×1010 cells can be comprised in the kit.
Table 1 below shows the connection sequence of the parts of the chimeric antigen receptor of the Examples of the present invention.
1. Amplification of nucleic acid fragment of antiGPC3-synNotch-GAL4VP64
1) Amplification of GPC3 scFv sequence
The nucleic acid sequence of antiGPC3 scFv (SEQ ID NO: 2) was obtained by conventional PCR method.
PHR-PGK-antiCD19-synNotch-GAL4VP64 (purchased by addgene) was used as a template to obtain other nucleic acid sequences by PCR. The signal sequence (SEQ ID NO: 1) was PCR-amplified with a primer pair [upstream primer: 5′-tctcacgcgtcaagtggagc-3′ (SEQ ID NO: 14), downstream primer: 5′-tctgcaccagctgcacctcgaggtcctcttcagag-3′ (SEQ ID NO: 15)]; and the synNotch-GAL4VP64 sequence was PCR-amplified with a primer pair [upstream primer: 5′-atcctggactacagcttcacaggtggcgc-3′ (SEQ ID NO: 16), downstream primer: 5′-agagccggcagcaggccgcgggaag-3′ (SEQ ID NO: 17)].
2. Slicing of nucleic acid fragment of antiGPC3-synNotch-GAL4VP64
The antiGPC3 scfv nucleic acid fragment, an equimolar signal sequence nucleic acid fragment and equimolar synNotch-GAL4VP64 nucleic acid fragment were subjected to three-segment splicing and PCR. The splicing conditions were: pre-denaturation: 94° C., 4 min; denaturation: 94° C., 40 s; annealing: 42° C., 40 s; extension: 68° C., 3 min 20 s, 7 cycles, then total extension 68° C., 10 min. And then DNA polymerase, forward primer and reverse primer were supplemented, and PCR amplification was performed for 30 cycles, wherein the amplification conditions were: pre-denaturation: 94° C., 4 min; denaturation: 94° C., 40 s; annealing: 60° C., 40 s; extension: 68° C., 3 min 20 s, for 30 cycles, then a total extension 68° C., 10 min. The amplified fragment was antiGPC3-synNotch-GAL4VP64.
3. Amplification of Nucleic Acid Fragment of GAL4UAS-IL12-PGK-Mcherry
Firstly, pHR-GAL4UAS-tBFP-PGK-mcherry (purchased from addgene) was used as a template to insert an MluI restriction site between tBFP and PGK-mcherry, and then this plasmid was used as a template for further construction.
1) Amplification of IL12 Sequence
The IL12 sequence is obtained by PCR amplification (wherein, the nucleic acid sequence of IL12 P40 is shown in SEQ ID NO: 7 and the nucleic acid sequence of IL12 P35 is shown in SEQ ID NO: 8).
2) Nucleic Acid Sequence of Other Parts
The nucleic acid sequences of other parts were obtained by PCR using pHR-GAL4UAS-tBFP-PGK-mcherry as a template. The GAL4UAS sequence was PCR-amplified with a primer pair [upstream primer: 5′-agatcgcgatgggaaaaaattc-3′ (SEQ ID NO: 28), downstream primer: 5% tgctgaacttcactctcatgatccaacgaatgtcgag-3′ (SEQ ID NO: 29)].
4. Slicing of Nucleic Acid Fragment of GAL4UAS-IL12
The above obtained IL12 nucleic acid fragment and an equimolar GAL4UAS nucleic acid fragment were subjected to two-segment splicing and PCR. The splicing conditions were: pre-denaturation: 94° C., 4 min; denaturation: 94° C., 40 s; annealing: 42° C., 40 s; extension: 68° C., 3 min 20 s, 7 cycles, then total extension 68° C., 10 min. And then DNA polymerase, forward primer and reverse primer were supplemented, and PCR amplification was performed for 30 cycles, wherein the amplification conditions were: pre-denaturation: 94° C., 4 min; denaturation: 94° C., 40 s; annealing: 60° C., 40 s; extension: 68° C., 3 min 20 s, for 30 cycles, then a total extension 68° C., 10 min. The amplified fragment was GAL4UAS-IL12.
5. Construction of Lentiviral Plasmid Vector
The vector system used in the lentiviral plasmid vector belongs to the third-generation of self-inactivating lentiviral vector system. There are three plasmids in the system, namely the encoding protein Gag/Pol, the packaging plasmid psPAX2 (purchased from addgene) encoding Rev protein; and envelope plasmid PMD2.G (purchased from addgene) encoding VSV-G protein.
The target gene antiGPC3-synNotch-GAL4VP64 obtained in the above steps 1 and 2 was digested with MluI and SacII restriction enzymes, and then connected to the pHRLSIN vector (purchased from addgene) which was subjected to the same double digestion; and the target gene GAL4UAS-IL12 was digested with NruI and MluI restriction enzymes, and then connected to the pHRLSIN vector which was subjected to the same double digestion and addition of MluI. The successfully constructed vector was sequenced as being correct, so that can be used for lentivirus packaging.
The obtained vectors containing the target fragments are shown as follows (see
pHRLSIN-antiGPC3-synNotch-GAL4VP64 (i.e., pHR-antiGPC3-synNotch-GAL4VP64, wherein the sequence of antiGPC3-synNotch-GAL4VP64 was shown in SEQ ID NO: 21);
pHRLSIN-GAL4UAS-IL12-PGK-mcherry (i.e., pHR-GAL4UAS-IL12-PGK-mcherry, the sequence of which was shown in SEQ ID NO: 22).
6. Transfection of 293T Cells with Plasmids to Package Lentivirus
1) 293T cells cultured to the 6th˜10th passages were inoculated into a 10 cm petri dish at a density of 5×106, and cultured overnight at 37° C. and 5% CO2 to prepare for transfection, and the medium was a medium containing 10% fetal bovine serum DMEM;
2) 10 μs of target gene plasmids pHRLSIN-antiGPC3-synNotch-GAL4VP64, pHRLSIN-GAL4UAS-IL12-PGK-mcherry were added with 3 μg of the envelope plasmid pMD2.G and 7.5 μg of the packaging plasmid pAX2 were added into 800 μl of blank DMEM medium, respectively and mixed well;
3) 60 μg of polyetherimide (PEI) (1 μg/μ1) was dissolved in 800 μl serum-free DMEM medium, mixed gently (or vortexed at 1000 rpm for 5 seconds) and incubated for 5 min;
4) formation of transfection complex: the plasmid mixture was added into the PEI mixture, vortexed or gently mixed immediately upon addition, and incubated for 20 min at room temperature;
5) 1.6 ml of transfection complex was dropped into a 10 cm petri dish containing 11 ml of DMEM medium (it is not necessary to change the medium);
6) After 4-5 h, the medium was change with DMEM medium containing 10% FBS for the transfected 293T cells;
7) After 72 hours of transfection, the virus supernatant was filtered and collected with a 0.45 μm filter;
8) The virus was concentrated at 5×PEG-8000 NaCl, and 7.5 ml of mother liquid was added per 30 ml of initial solution. The obtained liquid was mixed every 20-30 min for a total of 3-5 times, and placed overnight at 4° C.;
9) The next day, the obtained liquid was subjected to centrifuge at 4000 rpm for 60 min at 4° C., the supernatant was discarded, and the precipitate obtained from the centrifugation was resuspended in a dissolving solution at 1/10-1/50 of the original volume and stored in aliquots (100 μl/tube) at −80° C. to obtain lentivirus 1.
7. Determination of Lentivirus Titer
1) 293T cells were inoculated in a 12-well culture plate at 1×105 cells, 1 ml/well; a polybrene solution, the initial concentration of which was 10 μg/μl, was added at 0.6 μl/ml and the final concentration was 6 μg/ml; the cells were incubated at 37° C., 5% CO2 for 1 hour, and the culture medium was DMEM containing 10% fetal bovine serum;
2) 10 μl/well of virus concentrate was added for 5-fold dilution, 3 gradients, and incubated at 37° C. and 5% CO2;
3) After 72 hours, 293T cells were trypsinized (30 s), and 1 ml DMEM (10% FBS) was added to terminate the digestion. The cell suspension was transferred to a 2 ml centrifuge tube (half), centrifuged at 5000 rpm for 5 min, the supernatant was discarded, and the precipitate washed twice with PBS (2% N-bromosuccinimide (NBS));
4) Cells in the pHRLSIN-antiGPC3-synNotch-GAL4VP64 virus control group were washed twice with PBS (2% NBS) and resuspended as a control; the cells in the test group were described as above, the cells in the test group+50 μl 1:50 diluted Alexa(R)-647-labeled anti-myc antibody were incubated on ice for 45 min, 5000 rpm/min and centrifuged for 5 min, and the supernatant was discarded; the above procedure was repeated twice; 500 μl PBS (2% NBS) was added, transferred to the flow tube, and Alexa (R)-647 channel was detected with a flow cytometer.
5) For PHRLSIN-GAL4UAS-IL12-PGK-mcherry virus, PE-CF594 channel was directly detected with a flow cytometer;
6) The number of cells with a positive rate of 5-20% was appropriate, and the titer was calculated as: the titer (U/mL)=the number of cells×positive rate/virus volume. The virus titer measured after concentration was about 1×108 U/ml for pHRLSIN-antiGPC3-synnotch-GAL4VP64; and 3×108 U/ml for pHRLSIN-GAL4UAS-IL12-PGK-mcherry.
NK92 cells were infected with the lentivirus 1 prepared in Example 1 to obtain GPC3-SYN-IL12-NK92 cells. The specific operations are listed as follows:
1) On the day before infection, a 24-well plate was coated with recombinant human fibronectin (Retronectin), and 380 μl of 5 μg/ml recombinant human fibronectin solution (PBS) was added to each well, and incubated overnight at 4° C.;
2) At the time of infection, the recombinant human fibronectin solution (PBS) in the 24-well plate was discarded, and the plate was washed twice with 1 ml PBS. The above recombinant lentivirus was used in infection at MOI=30, polybrene at a final concentration of 10 μg/ml was added to improve the infection efficiency. The number of cells per well was 5×105, the volume of the culture medium was 500 μl, and the cells were centrifuged at 32° C., 1800 g for 90 min, and then transferred to an incubator;
3) The infected cells were passaged at a density of 5×105/ml every other day.
On the 7th day of culture, NK92 cells infected with lentivirus were tested for the expression of different receptors by flow cytometry. Since a Myc tag is present at the N-terminal of antiGPC3, the detected Myc expression means a positive cell successfully infected with pHRLSIN-antiGPC3-synNotch-GAL4VP64, the detected mcherry expression means a positive cell successfully infected with pHRLSIN-GAL4UAS-IL12-PGK-mcherry, and the simultaneous expression of Myc and mcherry means a positive cells GPC3-SYN-IL12-NK92 with successful double infection.
1) 1×106 cells were taken from different infected NK92 cells respectively, divided into 2 ml centrifuge tubes, and centrifuged at 4° C., 5000 rpm for 5 min, the supernatant was discarded, and the precipitate was washed twice with PBS;
2) The cells in the control group for detecting myc expression were directly washed twice with PBS (2% NBS) and resuspended as a control; the cells in the detection group cells are described as above, and the cells in the detection group+50 μl of 1:50 diluted Alexa(R)-647 labeled anti-myc antibody were incubated for 45 minutes on ice;
3) 2 ml of PBS (2% NBS) was added to resuspend the cells, the cells were centrifuged at 5000 rpm/min, 4° C. for 5 min and the supernatant was discarded; and the procedure was repeated twice;
4) 500 μl of PBS (2% NBS) was added and transferred to a flow tube. Alexa(R)-647 and PE-CF594 channels were detected by a Flow cytometer to determine the proportion of positive NK92 cells.
The results are shown in
GPC3-SYN-IL12-NK92 cells were subcultured and counted every other day at a cell density of 5×105/ml. On the 11th day of culture, there was about 20-40 times expansion, indicating that there were a certain number of in vitro expansion for the double-infected NK92 cells, thereby guaranteeing the subsequent in vitro toxicity test and in vivo test.
1) The materials used for regulating expression are listed as follows: liver cancer cell line (Huh7 (high expression of GPC3), PLC/PFR/5 (low expression of GPC3), SK-Hep-1 (no expression of GPC3), SK-Hep-1-GPC3 (overexpression of GPC3)) as a target cell antigen for stimulation. The expressions of GPC3 in each target cells are shown in
2) The effector to target ratio (effector: target) is 1:1, the cells were spreaded in a 12-well plate at 2×105/well; and centrifuged at 400 g for 1 min to increase mutual contact;
3) Each experimental group and each control group are listed as follows:
experimental group: each target cell +GPC3-SYN-IL12-NK92;
control group: each target cell+NK92
4) The supernatant was collected after co-culture at 37° C. and 5% CO2 for 24 hours, and the expression of IL12 was detected by Elisa kit.
From the results of Elisa in
During the co-incubation of GPC3-Syn-IL12 NK92 cells with Huh7 cells and SK-Hep-1-GPC3, the secretion of IL12 at different time points is shown in
As an example, CAR-T cells targeting GPC3 were constructed in this example, the CAR of which has the amino acid sequence as shown in SEQ ID NO: 23. It should be understood that CARs of other generations also have similar effects, for example, GPC-BBZ, GPC-28BBZ, GPC3-z as shown in SEQ ID NO: 24, SEQ ID NO: 25, SEQ ID NO: 24 and SEQ ID NO: 26.
pRRLSIN-cPPT.EF-1α was used as a vecto to construct a lentiviral plasmid expressing the second-generation of chimeric antigen receptor of the humanized antibody huGPC3, PRRLSIN-cPPT.EF-1a-huGPC3-28Z. The sequence of HuGPC3-28Z consists of CD8a signal peptide (SEQ ID NO: 9), huGPC3 scFV (SEQ ID NO: 2), CD8 hinge (SEQ ID NO: 10), CD28 transmembrane region (SEQ ID NO: 11), intracellular signaling domain (SEQ ID NO: 12) and intracellular segment of CD3, CD3ξ (SEQ ID NO: 13).
According to the operation of Example 1, 293T cells were transfect to package lentivirus, thereby obtaining lentivirus 2.
T cells were infected with Lentivirus 2 to obtain GPC3-28Z CAR-T cells.
CytoTox 96 non-radioactive cytotoxicity detection kit (Promega Company) was used according to the instructions of CytoTox 96 non-radioactive cytotoxicity detection kit.
1) Target cells: 50 μL of 2×105/mL huh? cells, PLC/PRF/5, SK-Hep-1-GPC3, SK-Hep-1 cells were inoculated into 96 well plates, respectively;
2) Effector cells: UTD, UTD+GPC3-Syn-IL12, GPC3-28Z, and GPC3-28Z+GPC3-Syn-IL12 cells were added at an effector target ratio of 3:1, 1:1 or 1:3.
The effector cells and target cells were co-incubated for 12 hours. The experiment results are shown in
a. NSG mice were inoculated with Huh7 transplanted tumor
Huh7 cells were subcutaneously inoculated, 2×106 per mouse.
b. Preparation of UTD, GPC3-28Z CAR-T cells and double-infected GPC3-SYN-IL12-NK92
1) On day d0, 3×107 PBMC cells were taken, magnetic beads were added at CD3-CD28 antibody coated magnetic beads: cells =2:1, medium was AIM-V (2% AB serum), and the total volume was 5 ml. And IL-2 was added with a final concentration of 500 IU/ml;
2) On day 1, a 24-well cell culture plate was coated with recombinant human fibronectin: the concentration of recombinant human fibronectin was 5 μg/ml at 380 μl/well, and incubated overnight at 4° C.;
3) On day d2, the activated cells were taken for virus infection. The number of PBMC infected by each virus was 3×106 and MOI=10. The cells and virus liquid were transferred to a 24-well plate coated with recombinant human fibronectin, and the infection conditions were 32° C. and centrifugation at 1800 rpm for 40 min;
4) On day 3, the infected PBMC cells were centrifuged at low speed (500 rpm, 10 min) to remove dead cells and then the medium was changed;
5) On day 5, the CD3-CD28 antibody-coated magnetic beads were removed with magnetic poles, and incubated for up to 12 days.
c. Combined adoptive immunotherapy of GPC3-28Z CAR-T cells and GPC3-SYN-IL12-NK92 cells were performed on Huh7 transplanted tumors.
On day 18, the volume of the transplanted tumor of Huh7 in NSG mice was measured, which was about 150 mm3. Mice were divided into 4 groups, including: UTD control group, GPC3-28Z CAR-T single treatment group, GPC3-SYN-IL12-NK92 single treatment group, and GPC3-28Z CAR-T+GPC3-SYN-IL12-NK92 combined treatment groups, 6 mice in each group; and adoptive immunotherapy was performed on the mice in each group. 200 μl of cells were injected through the tail vein.
(a) UTD group (T cell group without being transfected with vector): 1×106/UTD.
(b) GPC3-28Z CAR-T cell group: 1×106/positive cells.
(c) GPC3-SYN-IL12-NK92 group: 1×106/positive cells.
(d) GPC3-28Z CAR-T+GPC3-SYN-IL12-NK92 combined treatment group: 1×106/positive cells, and then every 3-4 days, GPC3-SYN-IL12-NK92 cells were administered again, for a total of four times, each time 1×106/positive cell.
d. the volume of Huh7 transplanted tumor was measured every 3-4 days, the change of tumor volume in each group of mice was recorded, and tumor volume was calculated according to: (length×width2)/2. The results are shown in
On Day 45, the mice were killed by cervical dislocation, the subcutaneous tumor in the mouse was peeled off and weighed. The results are shown in
When recording the changes in the tumor volume of mice in each group, the weight changes of the mice are shown in
The tumor tissues of mice were prepared into tissue sections by using conventional tissue section preparation methods. The tissue sections were immunohistochemically stained, and anti-human CD3 antibody (Thermo Scientific) was used to detect human CAR-T cells in the tumor tissue sections. The results are shown in
Conclusion: In in vitro experiments, compared with the control group, GPC3-28Z+GPC3-Syn-IL12 cells exhibit no significant difference in killing tumor cells. In in vivo experiments, compared with the control group, in GPC3-28Z CAR-T+GPC3-SYN-IL12-NK92 combination treatment group, the tumor growth of mice was significantly inhibited.
The description of the above embodiments is only helpful for understanding the core idea of the present invention. It should be pointed out that a skilled person in the art can make improvements and modifications to the solid powder composition of the present invention and the preparation method thereof without departing from the principle of the present invention, and these improvements and modifications also fall within the scope of the claims of the present invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201810053219.6 | Jan 2018 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2019/072497 | 1/21/2019 | WO | 00 |
