Chimeric antigen receptor cells targeting ROBO1, preparation method and use thereof

Abstract

The present invention relates to chimeric antigen receptor cells targeting ROBO1, in particular, enhanced CAR-T cells and CAR-NK cells targeting ROBO1, and preparation and application thereof. The cells can stably expressing CAR elements, while secreting extracellular domain molecules expressing PD-1 protein or mutants thereof, and thus may block PD-11PD-L1 molecular interaction. It has been found through animal experiments that the cells have very good anti-tumor effects, and the above-mentioned cells can significantly reduce tumor recurrence and improve the survival rate compared with the conventional ROBO1-targeted CAR modified cells.

Claims

1. A polynucleotide comprising a nucleotide encoding chimeric antigen receptor and a nucleotide encoding extracellular secretory protein, wherein the chimeric antigen receptor comprises an antigen-binding domain, a transmembrane domain and a costimulatory signaling region, and the antigen-binding domain is capable of specifically binding to FN3 domain of the tumor specific antigen ROBO1, and activating immune cells through the transmembrane domain and the costimulatory signaling region; the extracellular secretory protein is capable of preventing or inhibiting the binding of the wild type PD-1 protein to PD-L1 ligand; wherein, the extracellular secretory protein is the extracellular domain of PD-1 protein or the mutant of the extracellular domain, and the mutant of the extracellular domain is capable of binding PD-L1 with high affinity; wherein, the polynucleotide is a nucleotide encoding anti-ROBO1-FN3 scFv-CD8 transmembrane-4-1BB-CD3ζ-IRES-(the extracellular domain of PD-1 protein or mutant thereof), which has a sequence as shown in SEQ ID NO: 7.

2. The polynucleotide according to claim 1, wherein the antigen-binding domain is an antigen-binding fragment, and the antigen-binding fragment is scFv; the anti-ROBO1-FN3 scFv has an amino acid sequence as shown in SEQ ID NO:9; and/or, the extracellular domain or the mutant thereof has an amino acid sequence as shown in SEQ ID NO: 8.

3. The polynucleotide according to claim 2, wherein the nucleotide encoding antigen-binding domain has a sequence as shown in SEQ ID NO: 2; and/or, the nucleotide encoding the extracellular domain or the mutant thereof has a sequence as shown in SEQ ID NO: 1.

4. The polynucleotide according to claim 1, wherein the nucleotide encoding chimeric antigen receptor and the nucleotide encoding extracellular secretory protein are not in the same reading frame; and/or, wherein the nucleotide encoding IRES (internal ribosome entry site) is located between the nucleotide encoding chimeric antigen receptor and the nucleotide encoding extracellular secretory protein, and the IRES-encoding nucleotide has a sequence as shown in SEQ ID NO: 3.

5. The polynucleotide according to claim 1, wherein the CD8 transmembrane domain has a sequence as shown in SEQ ID NO:10; and/or, the 4-1BB intracellular domain has a sequence as shown in SEQ ID NO: 11; the CD3ζ intracellular domain has a sequence as shown in SEQ ID NO:12.

6. The polynucleotide according to claim 5, wherein the nucleotide encoding the CD8 transmembrane domain has a sequence as shown in SEQ ID NO: 4; and/or, the nucleotide encoding 4-1BB intracellular domain has a sequence as shown in SEQ ID NO: 5, and/or, the coding nucleotide of CD3ζ intracellular domain has a sequence as shown in SEQ ID NO: 6.

7. The polynucleotide according to claim 1, wherein the polynucleotide comprises a nucleotide encoding anti-ROBO1-FN3 scFv-CD8 transmembrane-4-1BB-CD3ζ, which has a sequence as shown in SEQ ID NO: 13.

8. A pharmaceutical composition comprising one or more of the polynucleotide according to claim 1.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 illustrates a schematic construction map of a lentiviral expression vector provided in Example 1 of the present invention.

(2) FIG. 2 illustrates a flow cytometry result of CAR-T provided in Example 3 of the present invention, wherein FIG. 2-A illustrates T cells without virus infection, and serve as a control; FIG. 2-B illustrates virus-infected T cells.

(3) FIG. 3 illustrates a flow cytometry result of CAR-NK-92 provided in Example 4 of the present invention, wherein FIG. 3-A illustrates NK-92 cells without virus infection, and serve as a control;

(4) FIG. 3-B illustrates NK-92 cells that are infected by the virus and then subjected to a flow sort and cultured for 1 month.

(5) FIG. 4 illustrates an analysis result of the specific lysis activity of CAR-cells provided in Example 5 of the present invention.

(6) FIG. 5 illustrates a result of efficacy evaluation of the drug provided in Example 6 of the present invention in mouse tumor models.

(7) FIG. 6 illustrates the survival rate for ROBO1-(PD-1 protein extracellular domain or mutants thereof) CAR-T group and the ROBO1 CAR-T group, respectively, at the end point of the experiment provided in Example 6 of the present invention.

(8) FIG. 7 illustrates the tumor recurrence rate for ROBO1-(PD-1 protein extracellular domain or mutants thereof) CAR-T group and the ROBO1 CAR-T group, respectively, at the end point of the experimental provided in Example 6 of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

(9) Unless otherwise defined, all technical and scientific terms used in the present invention have the same meaning as commonly understood by one of ordinary skill in the technical field of the invention.

(10) In the present invention, the term “antibody” refers to an immunoglobulin molecule specifically binding to an antigen. An antibody may be an intact immunoglobulin derived from natural source or recombinant source, and may be the immune response portion of intact immunoglobulin. The antibody is usually a tetramer of immunoglobulin molecules. The antibodies of the invention may be present in a variety of forms, including polyclonal antibodies, monoclonal antibodies, FV, Fab and F(ab).sub.2, and a single-chain antibody and a humanized antibody, etc (Harlow et al. 1999, in: Using Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory Press, NY; Harlow et al. 1989, In: Antibodies: A Laboratory Manual, Cold Spring Harbor, New York; Houston et al. 1989, Proc. Natl. Acad. Sci. USA 85; 5879-5883; Bird et al. 1988, Science 242: 423-426).

(11) The term “antibody fragment” refers to a part of an intact antibody, and refers to an antigen-determinant variable region of an intact antibody. Examples of antibody fragments include, but are not limited to, Fab, Fab′, F(ab′)2 and Fv fragments, a linear antibody formed from an antibody fragment, a scFv antibody and a multi-specific antibody.

(12) The term “antigen-binding fragment” is composed of an intact light chain, a heavy chain VH and a CHI domain, and can be specifically bind to an antigen.

(13) The term “encoding” refers to the intrinsic properties of specific sequences of nucleotides in polynucleotides such as a gene, cDNA or mRNA used as templates for synthesis of other polymers and macromolecules, wherein the polymers and the macromolecules have any one of a defined sequence of nucleotides (i.e., rRNA, tRNA and mRNA) or an amino acid sequence and biological properties produced by them. Thus, if the transcription and translation of mRNA corresponding to a gene produce a protein in cells or other biological systems, the gene encodes the protein. The nucleotide sequence is equivalent to the mRNA sequence and is generally provided in a coding strand, and a non-coding strand used as a template of a transcription gene or a cDNA in a sequence listing, both of which can be referred to as encoding protein or other product for gene or cDNA.

(14) Unless stated otherwise, “nucleotide sequence encoding amino acid sequence” includes all nucleotide sequences that are degenerate each other and encode the same amino acid sequence. Nucleotide sequences encoding protein and RNA can include introns.

(15) The term “costimulatory molecule” refers to an associated binding chaperone on T cells specifically binding to costimulatory ligand, thereby mediating costimulatory response of T cell, such as, but not limited to, proliferation. Costimulatory molecules include, but are not limited to, MHCI molecules, BTLA and Toll ligand receptors.

(16) The term “lentivirus” refers to a genus of retrovirus, which can effectively infect non-periodic and post-mitotic cells; and it can deliver significant amount of genetic information to the DNA of host cell, so that it is one of the most effective methods of gene delivery vectors.

(17) The term “promoter” is defined as DNA sequence that is necessary for start of specific transcription of polynucleotide sequence, and can be recognized by synthesis machinery of cell, or can direct the synthesis machinery of cell.

(18) The term “specifically binding” refers to recognizing specific antigen but not substantially recognizing or binding other molecules in samples.

(19) The term “vector” is a composition comprising isolated nucleic acids, which can be used to deliver isolated nucleic acids into cells. Many vectors are known in the art, and including but are not limited to, linear polynucleotides, polynucleotides associated with ionic or amphiphilic compounds, plasmids, and viruses. Thus, the term “vector” includes autonomously replicating plasmids or viruses. The term should also be interpreted as including non-plasmid and non-viral compound that facilitates delivering 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, reverse transcription virus vectors and the like.

(20) The term “isolated” refers to changing or removing from natural state. For example, nucleic acids or peptides naturally present in living animals are not “isolated”, but the same nucleic acid or peptide which is partially or completely separated from the coexisting substance of its natural state is “isolated”. The isolated nucleic acid or protein may be present in substantially purified form, or, for example, may be present in non-natural environment, such as a host cell.

(21) The term “cancer” is defined as disease characterized by the rapid and uncontrolled growth of aberrant cells. Cancer cells can spread locally or through the bloodstream and lymph system to other parts of the body. Examples of various cancers include, but are not limited to, breast cancer, prostate cancer, ovarian cancer, cervical cancer, skin cancer, pancreatic cancer, colorectal cancer, kidney cancer, liver cancer, brain cancer, lymphoma, leukemia, lung cancer and the like.

(22) The term “anti-tumor effect” refers to biological effect, which can be manifested by reduction in tumor volume, decrease in the number of tumor cells, decrease in the number of metastases, increase of the expected life, or the improvement of various physiological symptoms associated with the cancer condition.

(23) The terms “patient”, “subject” and “individual” and the like can be used interchangeably herein, and refers to any animal or cell that follows the methods described herein, whether in vitro or in situ. In some non-limiting embodiments, patients, subjects, or individuals are human.

(24) The “-” linkage of the amino acid sequence of the present invention is that the N-terminus of one fragment is directly linked to the C-terminus of the other fragment, and no linker peptide exists in the middle.

(25) The technical solutions of the present invention will be clearly and completely described below with reference to the Examples of the present invention, the Examples described are merely a part of the embodiments of the present invention rather than all of the embodiments. Based on the Examples of the present invention, all other embodiments obtained by ordinary skilled persons in the field without inventive efforts shall fall within the protection scope of the present invention.

Example 1: Preparation of Lentiviral Expression Vector

(26) According to the sequence information of PD-1 mutant molecule(HAC) reported by “Engineering high-affinity PD-1 variants for optimized immunotherapy and immune-PET imaging” (Maute R L, Gordon S R, Mayer A T, et al. Proceedings of the National Academy of Sciences, 2015, 112(47): E6506-E6514.), the gene sequence of PD-1 protein extracellular domain or mutant thereof was synthesized, as shown in SEQ ID NO: 1. Based on Genebank database the following sequences were searched and synthesized: the known human anti-ROBO1-FN3scFv (hereinafter referred to as scFv for short) gene sequence, IRES inner ribosome entry site, human CD8 transmembrane region gene sequence, human 4-1BB intracellular region gene sequence, and CD3ζ intracellular region gene sequences were shown in SEQ ID NO: 2-6, respectively.

(27) The above gene sequences were sequentially linked in the order of scFv gene, CD8 gene, human 4-1BB intracellular region gene and CD3ζ intracellular region, IRES ribosome internal ribosome entry site, and the extracellular domain of PD-1 protein or the mutant gene thereof, and different restriction enzyme sites were introduced at the linking positions of the sequences, so as to form an intact scFv-CD8.sup.TM-4-1BB-CD3ζ-IRES-(the PD-1 protein extracellular domain or mutant thereof) gene sequence as shown in SEQ ID NO: 7.

(28) The scFv-CD8.sup.TM-4-1BB-CD3ζ-IRES-(the extracellular domain of the PD-1 protein or mutant thereof) gene sequence was transformed into a pRRSLIN vector by double enzyme digestion, wherein the upstream of the gene was an EF-1α promoter. After the vector was transformed into Stbl3 Escherichia coli strain, the strain was transferred to solid culture medium containing ampicillin to culture, and screened to obtain positive clones. Plasmids were extracted, and identified by enzyme digestion, and the vectors were successfully constructed through sequencing to obtain a pRRSLIN-scFv-CD8.sup.TM-4-BB-CD3ζ-IRES-(PD-1 protein extracellular domain or mutant thereof) lentivirus expression vector. The construction map of the lentivirus expression vector is shown in FIG. 1.

Example 2: Preparation of Lentivirus

(29) 1. 24 Hours before transfection, 293T cells were inoculated into a 15 cm culture dish at a cell density of about 8×10.sup.6 cells per dish. It was ensured that the cells were at a confluence degree of about 80%, and evenly distributed in the culture dish at the time of the transfection.

(30) 2. Preparation of solution A and solution B

(31) Solution A: 6.25 mL 2×HEPES buffer solution (the amount of 5 large vessels for packaging was used for the best effect).

(32) Solution B: A mixture with the following plasmids respectively added: 112.5 μg scFv-CD8.sup.TM-4-1BB-CD3ζ-IRES-(the PD-1 protein extracellular domain or mutant thereof) (target plasmid), 39.5 μg pMD2.G(VSV-G envelop), 73 μg pCMVR8.74(gag, pol, tat, rev), 625 μL 2M calcium ion solution. The total volume of solution B was 6.25 ml.

(33) 3. The solution B was thoroughly mixed, and the solution B was added dropwise to Solution A while the solution A was lightly vortexed, and allowed to stand for 5-15 minutes. The mixed solution of A and B was lightly vortexed, and added dropwise to a culture dish containing 293T cells. The culture dish was slightly shaken back and forth to evenly distribute the mixture of DNA and calcium ions (without rotating the culture dish). The culture dish was placed in an incubator and cultured for 16-18 hours.

(34) The medium was replaced with new fresh culture medium and continued to culture.

(35) It was centrifuged at a rotating speed of 500 g, and temperature of 25° C. for 10 min, and filtered by a PES film (0.45 μm)). A centrifuge tube (Beckmann ultra-clear SW28 centrifuge tube) was sterilized with 70% ethanol, and then disinfected under an ultraviolet lamp for 30 min. The filtered supernatant containing the lentivirus was transferred into the centrifugal tube, and a layer of 20% sucrose (1 mL sucrose/8 mL supernatant was added) was cautiously laid at the bottom of the centrifuge tube, and the centrifuge tube was equilibrated with PBS, and centrifuged at a speed of 25,000 rpm (82, 700 g) for 2 h at 4° C. The centrifuge tube was cautiously taken out, and the supernatant was discarded, and the centrifuge tube was inverted to remove the residual liquid. The centrifugal tube was added 100 μl PBS, sealed, placed at 4° C. for 2 hours with a gentle vortex every 20 minutes, and centrifuged at 500 g for 1 min (25° C.), the lentivirus-containing supernatant was collected, cooled on ice, and then stored at −80° C.

Example 3: Preparation of CAR-T Cells

(36) CAR-T cells were prepared according to the steps of CN20161022230.9 example 3.

(37) CAR-T positive rate was detected by flow cytometry after virus infection, and the flow cytometry detection result is shown in FIG. 2. The result showed that the positive rate was 51.38%, indicating that the CAR-T cells were successfully prepared. (FIG. 2: the detection of CAR-T positive expression rate by flow cytometry, FIG. 2-A illustrates T cells without virus infection, and served as a control, and FIG. 2-B illustrates virus-infected T cells. The antibody was labeled with FITC fluorescent and was represented on the abscissa. If the T cells successfully expressed the CAR molecules, the signal value would significantly increase).

Example 4: Preparation of CAR-NK92 Stable Cell Strain

(38) The density of NK92 cells was adjusted to 2-3×10.sup.5/ml. The virus was added to the NK92 cells in the volume ratio (V/V) of virus:cell medium=1:5-10, and the 8 μg/mL polybrene was added at the same time. After 4 hours, the density of the cells was adjusted to 1×10.sup.5/mL by supplementally adding equal amount of fresh complete culture medium (The complete culture medium formulation can be found in the instructions of ATCC) for further culture. On the next day, all the cells were centrifuged, fresh culture medium was added to continue to culture. The solution was supplemented every 1-2 days, so that the cell density was maintained at 2-3×10.sup.5/ml. After 72 hours, CAR antibody staining was carried out; and CAR-NK-92 positive cells were sorted by flow cytometry for culture expansion. The color change, cell density, and cell morphology of the culture medium were observed and recorded accordingly.

(39) After flow sorting, positive CAR-NK-92 cells were continuously cultured. After expanding for 1 month, the positive rate of CAR NK-92 cells was detected by flow cytometry, and the flow cytometry detection result is shown in FIG. 3. The result showed that the positive rate of the CAR-NK92 was 96.57%, indicating that NK-92 cells stably expressing CAR element were successfully prepared (FIG. 3: the positive expression rate of CAR-NK-92 was detected by flow cytometry, wherein FIG. 3-A illustrates the NK-92 cells without virus infection, and served as a control; and FIG. 3-B illustrates the NK-92 cells that were infected with virus and then subjected to flow sort and cultured for 1 month. The antibody was labeled with APC fluorescent and was represented on the abscissa. If NK-92 cells successfully expressed the CAR molecules, the signal value would significantly increase).

Example 5. In Vitro Activity Assay of CAR Cells

(40) The killing effect of CAR-T and CAR-NK-92 cells on tumor cells were detected with LDH release method, and LDH release was measured with ELISA.

(41) 1. Target cells were adjusted to 5×10.sup.4/mL with RPMI-1640 culture solution containing 5% calf serum.

(42) 2. The target cells were added into 96-well cell culture plates with 100 μL per well. Three wells were selected as control of spontaneous release of effector cells (CART cells), which were only added 100 μL of culture medium without adding target cells.

(43) 3. 100 μL effector cells were added into each well, wherein the ratio of effector cells to target cells was 10:1; 5:1:1. The wells of spontaneous release were added only with 100 μL of culture medium without adding effector cells. The effector cells were co-incubated with target cells for 6 hours; and three replicate wells were used for each experiment.

(44) 4. 10 μL Lysis Solution (10×) was added into the largest release well (positive control), and incubated for 45-60 minutes. Meanwhile, three replicate wells were used for each experiment.

(45) 5. 50 μL of each of the test sample and the control sample in the above 3 and 4 steps were taken out and added to a fresh 96-well ELISA plate, then reaction solution and substrate were added to stand for 30 minutes in the dark.

(46) 6. Adding 50 μL stop solution.

(47) 7. The optical density (OD value) of each well was measured on an enzyme-linked detector at 490 nm or 492 nm within 1 hour.

(48) 8. Calculation of specific lysis activity
killing rate=experimental group LDH(OD)/max LDH release group (OD).
Calculation formula: Specific lysis activity=(experimental group−effect spontaneous release−target spontaneous release)/(target maximum release−target spontaneous release)×100%

(49) 9. Determination of cytokine secretion with CBA kit

(50) The analysis result of the Specific lysis activity of the CAR cells is shown in FIG. 4, and the result shows that the constructed CAR-T cells and the CAR-NK-92 cells can remarkably kill tumor cells. The specific lysis activity was 95% and 83% respectively as shown in FIG. 4.

Example 6: In-Vivo Efficacy Testing of CAR Cells in Animal

(51) 1. Cell strain: H1299 lung cancer cell strain (hereinafter referred to as H1299 for short), stored in liquid nitrogen.

(52) 2. Experimental Animal

(53) 2. 1 Animal Species, Grade, Week Age, Weight and Source

(54) NOG mouse, SPF grade, 4-6 weeks old when purchased, 15-25 g of body weight, purchased from Beijing Weitong Lihua Experimental Animal Co. ltd.

(55) 2. 2 Quarantine and domestication: quarantine inspection was performed by veterinarian after all animals being purchased. The animals were performed quarantine and domesticated for 2-7 days. Only those animals that were qualified by veterinary quarantine can be qualified for further experiment.

(56) 2. 3 Animal house: barrier animal house (SPF-grade), Suzhou GenePharma Co., Ltd.

(57) 2. 4 Animal feed, mouse feed (Standard SPF-grade). A nutrient component detection report of the feed was provided by production unit. After being purchased, the feed was subjected to ultraviolet irradiation disinfection and external packaging, and was followed by being placed into barrier environment for cryopreservation. The feed was taken one small packet (2.5 kg) each time, and weighed on demand amount, and then clamped and replaced. The feed should be used up within 2 weeks.

(58) 2. 5 Animal drinking water: SPF purified water, supplied by drinking water bottle. The animals have free access to water.

(59) 2. 6 Padding materials of animals: common poplar wood shavings, and use after high-pressure sterilization.

(60) 2. 7 Feeding Condition

(61) The Animals were fed in polycarbonate cage box filled with padding material in individual room. Unless otherwise stated, the animals have free access to food the rest of time, and have free access to water.

(62) In animal house, the room temperature ranged from 20-26° C. and humidity ranged from 40% to 70%, and experienced 12 hours of light at alternating light and darkness. The padding materials were replaced twice a week, and meanwhile, the feeding boxes were replaced. When there is serious contamination such as drinking water, urine, loose stools, etc, the feeding boxes would be replaced in time. The high-pressure disinfected drinking water bottles and bottle plugs were replaced every day. After being cleaned, all the replaced cages were sterilized by autoclaving.

(63) The animal house floor was disinfected at least once every day, and the cage frames and animal house wall were disinfected at least once a week with 0.1% of bromogeramine or 0.5% of 84 disinfection solution, and the two disinfectant solutions were used interchangeably and generally alternated once every week.

(64) 3. Experimental Method

(65) 3. 1 Tumor Cell Culture and Concentration Configuration

(66) Tumor cell culture: H1299 cells were cultured in DMEM culture solution containing 10% fetal calf serum. H1299 cells in the exponential growth phase were collected, and suspended in PBS and matrix glue (0.1 mL/animal) (the ratio of PBS to matrix glue is 1:1) for subcutaneous inoculation at a concentration of 5×10.sup.6 cells/animal.

(67) 3. 2 Animal Grouping and Administration Dosage

(68) The condition and the treatment of each group of animals were shown in the following table:

(69) TABLE-US-00001 TABLE 1 Animal grouping and administration Number of administration Group animals Drug mode A 8 PBS I.V. B 8 T cell I.V. C 8 PD-1 protein extracellular domain or I.V. mutant thereof D 8 ROBO1 CAR-T(Preparation method I.V. can see patent application CN105907719A and PCT/CN2016/092578) E 8 ROBO1-(protein extracellular domain or I.V. mutant thereof) CAR-T (prepared by Example 3 of the present invention)

(70) 4. Detection Indicator

(71) 4. 1 General Clinical Observation

(72) The observation time: one time every morning and every afternoon in one day.

(73) Observation contents: tumor growth status and systemic status of rats were observed every two days after inoculation, and the contents included recording the formation time and growth status of tumor, and observed general activities, death, manure and the like of rats.

(74) 4. 2 Body Weight

(75) Weighing time: the animal was weighed once at the time of being received, and weighed once a week after the start of the experiment, and weighed and recorded when the animals were dead or endangered.

(76) Testing Animals: all animals

(77) 4. 3 Tumor Measurement

(78) The length diameter and short diameter of the tumor were measured by vernier caliper every two days, and the volume of the tumor was calculated as follows: the volume (mm.sup.3)=length diameter (mm)×short diameter (mm.sup.2)/2. It's growth curve was depicted from the average value, as shown in FIG. 5.

(79) 5. Data Acquisition and Statistical Analysis

(80) 5. 1 Data Acquisition

(81) The measured and observed result and data required for the scheme were recorded on appropriate tables by hand or the data can be acquired directly by computer.

(82) 5. 2 Data Analysis

(83) Statistical software SPSS 20.0 was used to process data in the experiment, and the data were expressed by means of an average value±standard deviation. The specific analysis process was as follows:

(84) The homogeneity of variance was checked by levene's test, and if the variance was homogeneous (P>0.05), statistical analysis was carried out in one-way ANOVA. If the ANOVA was statistically significant (P≤0.05), comparative analysis was carried out by LSD test (parameter method).

(85) If the variance was not homogeneous (P≤0.05), kruskal-Walis test was used. If the kruskal-Wallis test has statistical significance (P≤0.05), comparison between any two means was carried out by Mann-Whitney method.

(86) The result showed that the ROBO1-(PD-1 protein extracellular domain or mutant thereof) CAR-T group and ROBO1CAR-T group had significant killing tumor activity compared to the control group. However, when the animal tumor recurrence rate and animal survival rate of ROBO1-(PD-1 protein extracellular domain or mutant thereof) CAR-T group and ROBO1CAR-T group were compared at the end point of the experiment, the results showed that the recurrence rate for ROBO1-(PD-1 protein extracellular domain or mutant thereof)CAR-T group was 12.5% (recurrence occurred only in 1 mouse among 8 mice), and the survival rate was 100%. While the survival rate of the ROBO1CAR-T group was 75% (6 mice survived in 8 mice), the recurrence rate was 66.7% (Tumor recurrence occurred in 4 mice of the 6 survival mice). The result showed that the introduction of PD-1 protein extracellular domain or mutant molecules of blocking the PD-1 and PD-La into CAR structure, can significantly reduce the tumor recurrence after the tumor was treated with CAR, and meanwhile has remarkable significance on improvement of the safety of CAR drugs.

(87) The above descriptions are only preferred embodiments of the present invention, and are not intended to limit the present invention. Any modification, equivalent replacement and the like falling within the spirit and principle of the present invention, should be all included within the protection scope of the invention.