CN110526984A

CN110526984A - It is a kind of to target the Chimeric antigen receptor of PSMA, Chimeric antigen receptor T cell and its preparation method and application

Info

Publication number: CN110526984A
Application number: CN201810513548.4A
Authority: CN
Inventors: 万晓春; 刘绿艳; 唐超; 李欣
Original assignee: Shenzhen Benta Biological Technology Co Ltd
Current assignee: Shenzhen Benta Biological Technology Co Ltd
Priority date: 2018-05-25
Filing date: 2018-05-25
Publication date: 2019-12-03

Abstract

The present invention provides a kind of Chimeric antigen receptor for targeting PSMA and the Chimeric antigen receptor T cells of targeting PSMA, the Chimeric antigen receptor of the targeting PSMA can be with the targeting PSMA of specificity, and using CD27 signaling zone as costimulatory signal area, promote T cell in the amplification of patient's body, the tumour cell of the killing PSMA positive that can be efficient and specific, the vigor and lethality of cell are preferably maintained, and does not constitute injury to normal cell.The present invention also provides a kind of preparation method and application of Chimeric antigen receptor T cell for targeting PSMA.

Description

A kind of Chimeric antigen receptor, Chimeric antigen receptor T cell and its preparation targeting PSMA Methods and applications

Technical field

The present invention relates to field of medical biotechnology, in particular to a kind of Chimeric antigen receptor for targeting PSMA and chimeric antigen by Body T cell and its preparation method and application.

Background technique

Prostate cancer is the most common malignant tumour of male reproductive system, and in the U.S., prostate-cancer incidence is all pernicious First is occupied in tumour, the death rate occupies second, is only second to lung cancer.Though the disease incidence of China's patients with prostate cancer is far below west Country, but be in recent years in significant growth trend.Prostate-specific membrane antigen (prostate specific membrane Antigen, PSMA) the newly discovered prostate cancer related antigen of one kind, there is very strong prostata tissue specificity, it has also become A kind of important target protein during the diagnosis of prostate cancer and Therapy study.PSMA on normal prostate cell is simultaneously few, But canceration, the speed of growth occur for cell when be getting faster and start to start to surrounding tissue infiltration, more and more PSMA appears in tumor cell surface.In addition, studies have shown that PSMA is likely to become new marker and the treatment of lung cancer early screening Novel targets.

Currently, for this kind of malignant tumour of prostate cancer, there is no highly effective treatment means.And develop in recent years Immune cell therapy be it is existing science and technology in be uniquely possible to the method for thoroughly removing cancer cell, compensate for the disadvantage of traditional remedies A kind of end, it is considered to be most promising treatment means in 21st century combined therapy of tumour mode.Chimeric antigen by Body T cell technology (Chimeric Antigen Receptor-Modified T Cells, CAR-T) is exempted from as currently newest One of epidemic disease cell technology, because it can activate self immune system in vivo, routinely targets neoplastic cells are killed, It is finally reached fully erased malignant cell, is widely paid close attention to and is studied.But the application also office that CART technology is current It is limited to blood tumor, does not have correlative study also for the application of a variety of PSMA positive solid tumors.

Summary of the invention

In view of this, the present invention provides a kind of Chimeric antigen receptor for targeting PSMA and the chimeric antigens of targeting PSMA Recipient T cells.It is described targeting PSMA Chimeric antigen receptor can with the targeting PSMA of specificity, and using CD27 signaling zone as be total to Stimulus signal area, promotes T cell in the amplification of patient's body, and killing tumor cell that can be efficient and specific is preferably tieed up Hold the vigor and lethality of Chimeric antigen receptor T cell.The present invention also provides a kind of Chimeric antigen receptor T for targeting PSMA is thin The preparation method and application of born of the same parents.

In a first aspect, the present invention provides a kind of Chimeric antigen receptor for targeting PSMA, the inosculating antibody of the targeting PSMA Original receptor CAR-PSMA include from aminoterminal to c-terminus the sequentially connected targeting single-chain antibody of PSMA, extracellular hinge area, across The amino acid sequence in film area and intracellular signal area, wherein the single-chain antibody of the targeting PSMA includes as shown in SEQ ID NO:1 Amino acid sequence, the intracellular signal area include from aminoterminal to c-terminus sequentially connected costimulatory signal area and first letter Number area, the costimulatory signal area includes CD27 signaling zone, and the CD27 signaling zone includes the amino as shown in SEQ ID NO:2 Acid sequence.

Wherein, described " being sequentially connected with from aminoterminal to c-terminus " specifically: the ammonia of the single-chain antibody of the targeting PSMA The c-terminus of base acid sequence is connected with the aminoterminal of the amino acid sequence of the extracellular hinge area, the amino of the extracellular hinge area The c-terminus of acid sequence is connected with the aminoterminal of the amino acid sequence of the transmembrane region, the carboxylic of the amino acid sequence of the transmembrane region Cardinal extremity is connected with the aminoterminal of the amino acid sequence of the CD27 signaling zone, the carboxyl of the amino acid sequence of the CD27 signaling zone End is connected with the aminoterminal of the amino acid sequence of first signaling zone.

In the present invention, the Chimeric antigen receptor of the targeting PSMA can be specifically bound with psma protein, right Expressing the tumour cell of PSMA, especially solid tumor cell has stronger affine activity.

Optionally, the encoding gene of the single-chain antibody of the targeting PSMA includes the nucleotide as shown in SEQ ID NO:5 Sequence.

Optionally, the single-chain antibody encoding gene of the targeting PSMA should consider degeneracy base, i.e., such as SEQ ID NO:1 Shown in the encoding gene of amino acid sequence include the nucleotide sequence as shown in SEQ ID NO:5, protection scope should also protect Shield has the nucleotide sequence of base degeneracy matter with SEQ ID NO:5, and the corresponding amino acid sequence of these nucleotide sequences is still It is so SEQ ID NO:1.

The extracellular hinge area described in the present invention is used to promote the PSMA on the single-chain antibody and tumour of the targeting PSMA In conjunction with.

Optionally, the extracellular hinge area include CD8 α hinge area, CD28 hinge area, CD4 hinge area, CD5 hinge area, One of CD134 hinge area, CD137 hinge area, ICOS hinge area or a variety of combinations.

Further alternative, the extracellular hinge area is CD8 α hinge area.

Optionally, the amino acid sequence of the CD8 α hinge area includes the amino acid sequence as shown in SEQ ID NO:6.

Optionally, the encoding gene of the CD8 α hinge area includes the nucleotide sequence as shown in SEQ ID NO:7.

Optionally, the encoding gene of the CD8 α hinge area should consider degeneracy base, i.e., as shown in SEQ ID NO:6 The encoding gene of amino acid sequence includes the nucleotide sequence as shown in SEQ ID NO:7, and protection scope should also protect and SEQ ID NO:7 has the nucleotide sequence of base degeneracy matter, and the corresponding amino acid sequence of these nucleotide sequences remains as SEQ ID NO:6。

The transmembrane region is used to fix the Chimeric antigen receptor CAR-PSMA of the targeting PSMA in the present invention.

Optionally, the transmembrane region includes one of CD3 transmembrane region, CD4 transmembrane region, CD8 transmembrane region, CD28 transmembrane region Or a variety of combination.

Further alternative, the transmembrane region is CD8 transmembrane region.

Optionally, the amino acid sequence of the CD8 transmembrane region includes the amino acid sequence as shown in SEQ ID NO:8.

Optionally, the encoding gene of the CD8 transmembrane region includes the nucleotide sequence as shown in SEQ ID NO:9.

Optionally, the encoding gene of the CD8 transmembrane region should consider degeneracy base, i.e., as shown in SEQ ID NO:8 The encoding gene of amino acid sequence includes the nucleotide sequence as shown in SEQ ID NO:9, and protection scope should also protect and SEQ ID NO:9 has the nucleotide sequence of base degeneracy matter, and the corresponding amino acid sequence of these nucleotide sequences remains as SEQ ID NO:8。

The intracellular signal area is for providing the signal of T cell activation in the present invention, maintain T cell life span and Activate T cell proliferation signal access.

The intracellular signal area includes sequentially connected costimulatory signal area and the first signaling zone from aminoterminal to c-terminus, The costimulatory signal area includes CD27 signaling zone, and the CD27 signaling zone includes the amino acid sequence as shown in SEQ ID NO:2 Column.

Optionally, the encoding gene of the CD2 signaling zone includes the nucleotide sequence as shown in SEQ ID NO:10.

Optionally, the encoding gene of the CD27 signaling zone should consider degeneracy base, i.e., as shown in SEQ ID NO:2 The encoding gene of amino acid sequence include the nucleotide sequence such as SEQ ID NO:10 shown in, protection scope should also protect and SEQ ID NO:10 has the nucleotide sequence of base degeneracy matter, and the corresponding amino acid sequence of these nucleotide sequences remains as SEQ ID NO:2。

Optionally, first signaling zone includes at least one of CD3 ζ signaling zone, Fc ε RI γ signaling zone.

Further alternative, the intracellular signal area is CD3 ζ signaling zone.

Optionally, the amino acid sequence of the CD3 ζ signaling zone includes the amino acid sequence as shown in SEQ ID NO:11.

Optionally, the encoding gene of the CD3 ζ signaling zone includes the nucleotide sequence as shown in SEQ ID NO:12.

Optionally, the encoding gene of the CD3 ζ signaling zone should consider degeneracy base, i.e., as shown in SEQ ID NO:11 Amino acid sequence encoding gene include the nucleotide sequence such as SEQ ID NO:12 shown in, protection scope should also protect and SEQ ID NO:12 has the nucleotide sequence of base degeneracy matter, and the corresponding amino acid sequence of these nucleotide sequences remains as SEQ ID NO:11。

In the present invention, CD3 ζ signaling zone is intracellular signal transduction structural domain (or being the first signaling zone), can be used for mentioning For specific signals；The CD27 signaling zone is to have stimulus structure domain altogether, can be used for providing costimulatory signal, activating T cell；It is special Not, the CD27 signaling zone can preferably promote the vigor and lethality of T cell.

Optionally, the amino acid sequence of the CAR-PSMA includes the amino acid sequence as shown in SEQ ID NO:3.

Optionally, the encoding gene of the CAR-PSMA includes the nucleotide sequence as shown in SEQ ID NO:4.

Optionally, the encoding gene of the CAR-PSMA should consider degeneracy base, the i.e. ammonia as shown in SEQ ID NO:3 The encoding gene of base acid sequence includes the nucleotide sequence as shown in SEQ ID NO:4, and protection scope should also protect and SEQ ID NO:4 has the nucleotide sequence of base degeneracy matter, and the corresponding amino acid sequence of these nucleotide sequences remains as SEQ ID NO:3。

Second aspect, the present invention provides a kind of Chimeric antigen receptor T cells for targeting PSMA, including such as first aspect institute The Chimeric antigen receptor of the targeting PSMA stated.

The targeting that the Chimeric antigen receptor and second aspect for the targeting PSMA that first aspect present invention provides provide The Chimeric antigen receptor T cell of PSMA, can targeted expression PSMA in specific manner tumour cell, using CD27 signaling zone as altogether Stimulus signal area, activating T cell promote T cell in the amplification of patient's body, and efficient and specific killing tumor cell.

The third aspect, the present invention provides a kind of recombinant viral vector, the recombinant viral vector includes such as first aspect The encoding gene of the Chimeric antigen receptor CAR-PSMA of the targeting PSMA.

Optionally, the viral vectors in the recombinant viral vector includes slow virus carrier, adenovirus vector or reverse transcription Viral vectors.

Further alternative, the viral vectors is slow virus carrier.It is further optional, the slow virus carrier packet Include at least one of pWPXLD carrier, pLEX-MCS carrier, pSico carrier and pCgpV carrier.Specifically, working as the slow disease When poisonous carrier is pWPXLD carrier, it will target the CAR-PSMA's of the Chimeric antigen receptor T cell of PSMA described in second aspect Encoding gene is inserted between I restriction enzyme site of I restriction enzyme site of BamH and EcoR in pWPXLD carrier.

The recombinant viral vector that third aspect present invention provides is a safe and reliable carrier tool, can efficiently be turned Move the encoding gene of the CAR-PSMA；The recombinant viral vector can be used for preparing the coding base for carrying the CAR-PSMA The virus of cause.The recombinant viral vector can be also used for the preparation of the Chimeric antigen receptor T cell of targeting PSMA, make the T The expression of cell realization height tissue specificity.

Fourth aspect, the present invention provides a kind of host cell, the host cell includes the weight as described in the third aspect Group viral vectors.

Optionally, the host cell may include HEK293T cell, 293 cells, 293T cell, 293FT cell, SW480 cell, u87MG cell, HOS cell, COS1 cell or COS7 cell etc., but not limited to this.

Further alternative, the host cell is HEK293T cell.

The host cell that fourth aspect present invention provides is used to provide and carries the recombinant virus as described in the third aspect The assembling of body simultaneously prepares the place for generating corresponding virus, and the heredity of the CAR-PSMA is carried by virus prepared by host cell Information has strong infectivity.

5th aspect, the present invention provides a kind of preparation methods of Chimeric antigen receptor T cell for targeting PSMA, comprising:

(1) encoding gene of the Chimeric antigen receptor CAR-PSMA of targeting PSMA is provided, including sequentially from 5 ' ends to 3 ' ends The encoding gene of the signal peptide of connection, the encoding gene of single-chain antibody, the encoding gene of extracellular hinge area, cross-film for targeting PSMA The encoding gene in area and the encoding gene in intracellular signal area, wherein the encoding gene of single-chain antibody of the targeting PSMA includes The corresponding nucleotide sequence of amino acid sequence as shown in SEQ ID NO:1, the intracellular signal area includes from aminoterminal to carboxylic The sequentially connected costimulatory signal area of cardinal extremity and the first signaling zone, the costimulatory signal area includes CD27 signaling zone, described The encoding gene of CD27 signaling zone includes the corresponding nucleotide sequence of amino acid sequence as shown in SEQ ID NO:2；

(2) encoding gene of the CAR-PSMA is inserted into pWPXLD carrier, obtains pWPXLD-CAR-PSMA recombination Plasmid；

(3) it by the pWPXLD-CAR-PSMA recombinant plasmid and envelope plasmid, packaging plasmid cotransfection host cell, obtains To recombinant slow virus；

(4) recombinant slow virus is infected into CD3 positive t lymphocytes, the chimeric antigen of targeting PSMA is obtained through separation Recipient T cells.

It is above-mentioned " from 5 ' end to 3 ' end be sequentially connected with " specifically: the coding gene sequence of the signal peptide 3 ' end with it is described 5 ' the ends for targeting the encoding gene of the single-chain antibody of PSMA are connected, 3 ' ends of the encoding gene of the single-chain antibody of the targeting PSMA It is connected with 5 ' ends of the encoding gene of the extracellular hinge area, 3 ' ends of the encoding gene of the extracellular hinge area and the cross-film 5 ' ends of the encoding gene in area are connected, 3 ' ends and the encoding gene of the CD27 signaling zone of the encoding gene of the transmembrane region 5 ' ends are connected, and the 5 ' of the encoding gene of the c-terminus and first signaling zone at 3 ' ends of the encoding gene of the CD27 signaling zone End is connected.

The signal peptide is for instructing the Chimeric antigen receptor CAR-PSMA expression to cell surface, institute in the present invention Signal peptide is stated to be cut in protein translation maturation by signal peptidase.

Optionally, the amino acid sequence of the signal peptide includes the amino acid sequence as shown in SEQ ID NO:13.

Optionally, the encoding gene of the signal peptide includes the nucleotide sequence as shown in SEQ ID NO:14.

Optionally, the encoding gene of the signal peptide should consider degeneracy base, the i.e. ammonia as shown in SEQ ID NO:13 The encoding gene of base acid sequence includes the nucleotide sequence as shown in SEQ ID NO:14, and protection scope should also protect and SEQ ID NO:14 has the nucleotide sequence of base degeneracy matter, and the corresponding amino acid sequence of these nucleotide sequences remains as SEQ ID NO:13。

The extracellular hinge area, transmembrane region, the specific choice in intracellular signal area and corresponding coding gene sequence such as this hair Described in bright first aspect part, which is not described herein again.

Optionally, the amino acid sequence of the CAR-PSMA includes the amino acid sequence as shown in SEQ ID NO:15.

Optionally, the coding gene sequence of the CAR-PSMA includes the nucleotide sequence as shown in SEQ ID NO:16.

Optionally, the encoding gene of the CAR-PSMA should consider degeneracy base, i.e., as shown in SEQ ID NO:15 The encoding gene of amino acid sequence include the nucleotide sequence such as SEQ ID NO:16 shown in, protection scope should also protect and SEQ ID NO:16 has the nucleotide sequence of base degeneracy matter, and the corresponding amino acid sequence of these nucleotide sequences remains as SEQ ID NO:15。

The encoding gene of the CAR-PSMA is inserted into pWPXLD carrier between I restriction enzyme site of BamH I and EcoR, and position After the EF1 α of pWPXLD carrier, using EF1 α as promoter.The encoding gene of the CAR-PSMA is inserted into pWPXLD carrier When, I digestion of BamH in initiation codon (such as ATG) and pWPXLD carrier can be added in 5 ' ends of the encoding gene of the CAR-PSMA Site is connected, and 3 ' ends can be added terminator codon (such as TAA) and be connected with I restriction enzyme site of EcoR in pWPXLD carrier.

Optionally, the envelope plasmid is PMD2G, and the packaging plasmid is psPAX2, and the host cell is HEK293T Cell.

The envelope plasmid PMD2G encodes vesicular stomatitis virus glycoprotein capsid, the vesicular stomatitis virus sugar egg White capsid assists recombinant slow virus to adhere to cell membrane, and keeps the infectivity of recombinant slow virus.

Recombinant slow virus of the present invention can further contain the envelope protein from other viruses.For example, as this Kind protein, is preferably the virus enveloped protein for carrying out self-infection human cell.To this protein, there is no particular limitation, can example The amphophilic virus hand epithelium albumen etc. for enumerating retrovirus, can be used for example from mouse leukemia virus (MuMLV) 4070A plants of envelope protein.Alternatively, it is also possible to use the envelope protein from MuMLV 10Al.In addition, as herpetoviridae Albumen, it can be cited for example that, gB, gD, gH, gp85 albumen of herpes simplex virus, gp350, gp220 albumen of Epstein-Barr virus Deng.As the albumen of Hepadna Virus section, the S protein etc. of hepatitis B virus can be included.The envelope protein can also be morbilli It is formed after viral glycoprotein and other single chain antibody fusions.

The packaging of recombinant slow virus is generallyd use transient transfection or is packed using cell line.It may be used as wrapping when transient transfection Human cell's strain that dress cell uses, for example including 293 cells, 293T cell, 293FT cell, 293LTV cell, 293EBNA Cell and other clones separated from 293 cells；SW480 cell, u87MG cell, HOS cell, C8166 cell, MT-4 are thin Born of the same parents, Molt-4 cell, HeLa cell, HT1080 cell, TE671 cell etc..It can also be using the cell strain from monkey, example Such as, COS1 cell, COS7 cell, CV-1 cell, BMT10 cell etc..Moreover, the calcium phosphate and PEI transfection reagent that generally use, It is also well used there are also some transfection reagents such as Lipofectamine2000, FuGENE and S93fectin.

The packaging of recombinant slow virus also uses some slow virus package cell lines, such as most common Env glycoprotein of use, Stable cell lines caused by VSVG albumen or HIV-1gag-pol albumen.

For the sake of security, the slow virus carrier system of large-scale use is all the method using split gene group, i.e., will The assignment of genes gene mapping of different miscellaneous functions is played in different plasmids.There are four pUC pUCs (encoding gag-pol gene, Rev base at present Cause, VSVG gene, SIN metastatic gene be located at four different plasmids), three pUC pUCs (eliminate coding Rev gene Plasmid, gag-pol gene uses the codon of the preferences in people's cell in gag-pol plasmid) and two pUC pUCs are (slowly Auxiliary gene necessary to viral vectors is packed is located on the same plasmid, these auxiliary genes are single gene orders；Separately One is then transgenosis plasmid).Also the slow virus packaging system for having more than four pUC pUCs is using.

Optionally, in step (4), the CD3 positive t lymphocytes are to separate to obtain from source of people peripheral blood mononuclear cells .

Optionally, the source of people peripheral blood mononuclear cells derives from autologous vein blood, autologous bone marrow, Cord blood and placenta Blood etc..

Fresh peripheral that is further alternative, being acquired after cancer patient's operation one month, after chemicotherapy one month Blood or marrow.

Specifically, the acquisition process of the CD3 positive t lymphocytes is as follows: into peripheral blood mononuclear cells by certain CD3/CD28 immunomagnetic beads are added in ratio, after being incubated for a period of time, are put into magnet and are screened, it is coated to obtain immunomagnetic beads CD3 positive t lymphocytes after removing magnetic bead, obtain CD3 positive t lymphocytes.

6th aspect, the present invention provides the Chimeric antigen receptor of targeting PSMA as described in relation to the first aspect a kind of or such as Described in second aspect or the Chimeric antigen receptor T cell of targeting PSMA made from the preparation method as described in terms of the 5th or Recombinant viral vector as described in the third aspect or the host cell as described in fourth aspect are disliked in preparation prevention, diagnosing and treating Application in the drug of property tumour.Specifically, can be used for preventing, diagnosing and treating kinds of tumors, including prostate cancer, lung cancer etc. Expression has the cancer cell of PSMA, is particularly suitable for prostate gland cancer cell or solid tumor tissue.

The application specifically: provide a kind of kit, the kit includes targeting as described in relation to the first aspect The Chimeric antigen receptor T cell of PSMA, the recombinant viral vector as described in second aspect, the host cell as described in the third aspect One of or it is a variety of.

Beneficial effects of the present invention:

The Chimeric antigen receptor of targeting PSMA provided by the invention can be with the targeting PSMA of specificity, especially generation PSMA Malignant cell, target the Chimeric antigen receptor T cell of PSMA1 using CD27 signaling zone as costimulatory signal area, promote T Cell is in the amplification of patient's body, combination tumour cell that can be efficient and specific, generates killing effect to malignant cell Fruit.

Detailed description of the invention

Fig. 1 is the plasmid map of pWPXLd-CAR-PSMA recombinant plasmid provided in an embodiment of the present invention.

Specific embodiment

The following is a preferred embodiment of the present invention, it is noted that for those skilled in the art For, various improvements and modifications may be made without departing from the principle of the present invention, these improvements and modifications are also considered as Protection scope of the present invention.

Embodiment one

A kind of preparation method for the Chimeric antigen receptor T cell targeting PSMA, comprising the following steps:

(1) gene order of the Chimeric antigen receptor CAR-PSMA of preparation targeting PSMA

Prepare respectively signal peptide, target the single-chain antibody of PSMA, CD8 α hinge area, CD8 transmembrane region, CD27 signaling zone and The encoding gene of CD3 ζ signaling zone, the encoding gene of the signal peptide is as shown in SEQ ID NO:14, the list of the targeting PSMA The encoding gene of chain antibody as shown in SEQ ID NO:5, the encoding gene of the CD8 α hinge area as shown in SEQ ID NO:7, The encoding gene of the CD8 transmembrane region is as shown in SEQ ID NO:9, the encoding gene of the CD27 signaling zone such as SEQ ID NO: Shown in 10, the encoding gene of the CD3 ζ signaling zone is as shown in SEQ ID NO:12.

By the method for PCR by above-mentioned signal peptide, the single-chain antibody for targeting PSMA, CD8 α hinge area, CD8 transmembrane region, CD27 signaling zone is successively connected together from 5 ' ends to 3 ' ends with the encoding gene of CD3 ζ signaling zone, obtains the chimeric of targeting PSMA The encoding gene of antigen receptor CAR-PSMA, the encoding gene of the CAR-PSMA is as shown in SEQ ID NO:16.

(2) pWPXLd-CAR-PSMA recombinant plasmid is constructed

The encoding gene of CAR-PSMA is inserted between I restriction enzyme site of BamH I and EcoR of pWPXLD carrier, and After pWPXLD carrier EF1 α, using EF1 α as promoter.When the encoding gene of the CAR-PSMA is inserted into pWPXLD carrier, institute I restriction enzyme site of BamH in initiation codon (such as ATG) and pWPXLD carrier can be added in the 5 ' ends for stating the encoding gene of CAR-PSMA It is connected, 3 ' ends can also be added terminator codon (such as TAA) and be connected with I restriction enzyme site of EcoR in pWPXLD carrier.Then it is transferred to Competent escherichia coli cell DH5 α carries out positive colony PCR identification and sequencing identification.By PCR product detected through gel electrophoresis Meet target fragment size and sequence with sequencing identification, successfully constructs pWPXLd-CAR-PSMA recombinant plasmid, be as shown in Figure 1 PWPXLd-CAR-PSMA recombinant plasmid.

(3) recombinant slow virus constructs

PWPXLd-CAR-PSMA recombinant plasmid, packaging plasmid psPAX2, envelope plasmid pMD2G three cotransfection are entered into training The HEK293T cell supported.48h harvest is protected in -80 DEG C of ultra low temperature freezers containing the supernatant of virus through 0.45 μm of membrane filtration It deposits；Supernatant of the 72h aftercrop containing virus, 0.45 μm of membrane filtration merge with the viral supernatants of 48h harvest and are added together It in ultracentrifugation pipe, is put into Beckman ultracentrifuge one by one, setting parameter of noncentricity is 25000rpm, and centrifugation time is 2h, centrifuging temperature are controlled at 4 DEG C；It after centrifugation, discards supernatant, removal as far as possible remains in the liquid on tube wall, and virus is added Liquid is saved, gently piping and druming is resuspended repeatedly；Through after completely dissolution, high speed centrifugation 10000rpm takes supernatant fluorescence method after being centrifuged 5min Measuring titre, virus is according to 100 μ l, and 2 × 10⁸A/mL packing, is stored in -80 DEG C of ultra low temperature freezers, obtains recombinant slow virus.

(4) preparation of the Chimeric antigen receptor T cell of PSMA is targeted

A) separation of PBMC (peripheral blood mononuclear cells)

PBMC is from autologous vein blood, autologous bone marrow, Cord blood and placental blood etc..Preferably derive from cancer patient's hand The fresh peripheral blood or marrow acquired after art one month, after chemicotherapy one month.

Extract patient blood, sample presentation to blood separating chamber；Peripheral blood mononuclear cells is acquired, is taken after Ficoll centrifuge separation Intermediate layer cell；After PBS is washed, PBMC is obtained.

B) immunomagnetic beads antigenspecific T lymphocyte

Above-mentioned PBMC is taken, the basal medium for being free of serum is added, is made into cell suspension；Ratio in magnetic bead and cell is 3:1, is added CD3/CD28 immunomagnetic beads, and room temperature incubates 1-2h；The cell for being incubated for magnetic bead is screened using magnet；PBS is washed It washs, after removing immunomagnetic beads, obtains CD3 positive t lymphocytes.

C) virus transfection method prepares antigenspecific T lymphocyte

The above-mentioned CD3 positive t lymphocytes obtained by magnetic activated cell seperation are taken, are added and CD3 positive cell number phase The recombinant slow virus for the virus titer answered is cultivated.

The 3rd day of culture carries out cell count and changes liquid, and adjustment cell concentration is 1 × 10⁶A/mL is inoculated with, culture；Training Cell state is observed in feeding the 5th day, if cell density increases, diluting cells concentration is 1 × 10⁶A/mL detects cell Activity continues to cultivate.Amplification cultivation collected cell by the 9-11 days, obtained the Chimeric antigen receptor T cell of targeting PSMA, and It is stored in and feeds back in dedicated cells frozen storing liquid.

Effect example

The tumor cell in vitro of effect example one, the Chimeric antigen receptor T cell of assessment targeting PSMA kills situation

Will by the Chimeric antigen receptor T cell (being abbreviated as CAR-T-PSMA) of targeting PSMA made from the method for the present invention with The Vitro Tumor fragmentation effect of T lymphocyte (negative control group) without preparation is compared, specific: in vitro by 10⁵ A effector cell's (CAR-T-PSMA or T lymphocyte without preparation) is with target cell (PC-3 prostate gland cancer cell) quantity ratio For 1:10,1:3,1:1,3:1 and 10:1 ratio, at 37 DEG C, 5%CO₂Under co-cultured, after incubation 15-18 hours, Cell is collected, streaming dyeing is carried out, detects cell killing situation, the results showed that the targeting PSMA of method preparation of the present invention The targeting that is significantly larger than negative control group, therefore is prepared through the method for the present invention of Chimeric antigen receptor T cell tumor-killing effect The Chimeric antigen receptor T cell of PSMA has strong tumor-killing ability.

Effect example two, the mouse interior tumor cell killing feelings of the Chimeric antigen receptor T cell of assessment targeting PSMA Condition

By the Chimeric antigen receptor T cell (CAR-T-PSMA) of the targeting PSMA by the method for the present invention preparation, without system Standby T lymphocyte (negative control group) and physiological saline (blank control group) gives every mouse in mouse tumor model Tail vein injection 1 × 10⁶A cell (n=9), obtains the survivorship curve of mouse, the results showed that the targeting prepared by this method The Chimeric antigen receptor T cell of PSMA is dead caused by capable of preferably protecting mice against because of tumour, and effect is right better than negative According to group and blank group.

The embodiments described above only express several embodiments of the present invention, and the description thereof is more specific and detailed, but simultaneously Limitations on the scope of the patent of the present invention therefore cannot be interpreted as.It should be pointed out that for those of ordinary skill in the art For, without departing from the inventive concept of the premise, various modifications and improvements can be made, these belong to guarantor of the invention Protect range.Therefore, the scope of protection of the patent of the invention shall be subject to the appended claims.

Sequence table

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Met Glu Leu Arg Ser Leu Thr Ser Glu Asp Ser Ala Val Tyr Tyr Cys

85 90 95

Ala Ala Gly Trp Asn Phe Asp Tyr Trp Gly Gln Gly Thr Thr Leu Thr

100 105 110

Val Ser Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Ser Gly Gly

115 120 125

Gly Ser Asp Ile Val Met Thr Gln Ser His Lys Phe Met Ser Thr Ser

130 135 140

Val Gly Asp Arg Val Ser Ile Ile Cys Lys Ala Ser Gln Asp Val Gly

145 150 155 160

Thr Ala Val Asp Trp Tyr Gln Gln Lys Pro Gly Gln Ser Pro Lys Leu

165 170 175

Leu Ile Tyr Trp Ala Ser Thr Arg His Thr Gly Val Pro Asp Arg Phe

180 185 190

Thr Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Ala Ile Thr Asn Val

195 200 205

Gln Ser Glu Asp Leu Ala Asp Tyr Phe Cys Gln Gln Tyr Asn Ser Tyr

210 215 220

Pro Leu Thr Phe Gly Ala Gly Thr Lys Leu Glu Ile Lys Arg Thr Thr

225 230 235 240

Thr Pro Ala Pro Arg Pro Pro Thr Pro Ala Pro Thr Ile Ala Ser Gln

245 250 255

Pro Leu Ser Leu Arg Pro Glu Ala Cys Arg Pro Ala Ala Gly Gly Ala

260 265 270

Val His Thr Arg Gly Leu Asp Phe Ala Cys Asp Ile Tyr Ile Trp Ala

275 280 285

Pro Leu Ala Gly Thr Cys Gly Val Leu Leu Leu Ser Leu Val Ile Thr

290 295 300

Leu Tyr Cys Arg Lys Tyr Arg Ser Asn Lys Gly Glu Ser Pro Val Glu

305 310 315 320

Pro Ala Glu Pro Cys Arg Tyr Ser Cys Pro Arg Glu Glu Glu Gly Ser

325 330 335

Thr Ile Pro Ile Gln Glu Asp Tyr Arg Lys Pro Glu Pro Ala Cys Ser

340 345 350

Pro Arg Val Lys Phe Ser Arg Ser Ala Asp Ala Pro Ala Tyr Lys Gln

355 360 365

Gly Gln Asn Gln Leu Tyr Asn Glu Leu Asn Leu Gly Arg Arg Glu Glu

370 375 380

Tyr Asp Val Leu Asp Lys Arg Arg Gly Arg Asp Pro Glu Met Gly Gly

385 390 395 400

Lys Pro Arg Arg Lys Asn Pro Gln Glu Gly Leu Tyr Asn Glu Leu Gln

405 410 415

Lys Asp Lys Met Ala Glu Ala Tyr Ser Glu Ile Gly Met Lys Gly Glu

420 425 430

Arg Arg Arg Gly Lys Gly His Asp Gly Leu Tyr Gln Gly Leu Ser Thr

435 440 445

Ala Thr Lys Asp Thr Tyr Asp Ala Leu His Met Gln Ala Leu Pro Pro

450 455 460

Arg

465

<210> 4

<211> 1395

<212> DNA

<213>artificial sequence (Artificial Sequence)

<400> 4

gaggtgcagc tgcagcagag cggacccgag ctggtgaaac ccggcaccag cgtgaggatc 60

agctgcaaga ccagcggcta caccttcacc gagtacacca tccactgggt gaagcagagc 120

cacggcaagt ctttagagtg gatcggcaac atcaacccca acaacggcgg caccacctac 180

aaccagaagt tcgaggacaa ggccactctg accgtggaca agagcagctc caccgcctac 240

atggagctga ggtctttaac cagcgaggac agcgccgtgt actactgtgc cgccggctgg 300

aacttcgact actggggcca aggtacaact ttaactgtga gcagcggagg cggaggatct 360

ggcggcggag gaagttctgg cggagggtct gacatcgtga tgacccagag ccacaagttc 420

atgagcacca gcgtcggcga tcgtgtgagc atcatctgca aggccagcca agatgtgggc 480

acagccgtgg actggtacca gcagaagccc ggccagagcc ccaagctgct gatctactgg 540

gccagcacaa gacacaccgg cgtgcccgat agattcaccg gcagcggctc cggcaccgat 600

ttcactttag ccatcaccaa cgtgcagagc gaggatttag ccgactactt ctgccagcag 660

tacaacagct accctctgac cttcggcgcc ggcaccaagc tggagatcaa gaggaccacg 720

acgccagcgc cgcgaccacc aacaccggcg cccaccatcg cgtcgcagcc cctgtccctg 780

cgcccagagg cgtgccggcc agcggcgggg ggcgcagtgc acacgagggg gctggacttc 840

gcctgtgata tctacatctg ggcgcccttg gccgggactt gtggggtcct tctcctgtca 900

ctggttatca ccctttactg caggaaatat agatcaaaca aaggagaaag tcctgtggag 960

cctgcagagc cttgtcgtta cagctgcccc agggaggagg agggcagcac catccccatc 1020

caggaggatt accgaaaacc ggagcctgcc tgctccccca gagtgaagtt cagcaggagc 1080

gcagacgccc ccgcgtacaa gcagggccag aaccagctct ataacgagct caatctagga 1140

cgaagagagg agtacgatgt tttggacaag agacgtggcc gggaccctga gatgggggga 1200

aagccgagaa ggaagaaccc tcaggaaggc ctgtacaatg aactgcagaa agataagatg 1260

gcggaggcct acagtgagat tgggatgaaa ggcgagcgcc ggaggggcaa ggggcacgat 1320

ggcctttacc agggtctcag tacagccacc aaggacacct acgacgccct tcacatgcag 1380

gccctgcccc ctcgc 1395

<210> 5

<211> 714

<212> DNA

<213>artificial sequence (Artificial Sequence)

<400> 5

gaggtgcagc tgcagcagag cggacccgag ctggtgaaac ccggcaccag cgtgaggatc 60

agctgcaaga ccagcggcta caccttcacc gagtacacca tccactgggt gaagcagagc 120

cacggcaagt ctttagagtg gatcggcaac atcaacccca acaacggcgg caccacctac 180

aaccagaagt tcgaggacaa ggccactctg accgtggaca agagcagctc caccgcctac 240

atggagctga ggtctttaac cagcgaggac agcgccgtgt actactgtgc cgccggctgg 300

aacttcgact actggggcca aggtacaact ttaactgtga gcagcggagg cggaggatct 360

ggcggcggag gaagttctgg cggagggtct gacatcgtga tgacccagag ccacaagttc 420

atgagcacca gcgtcggcga tcgtgtgagc atcatctgca aggccagcca agatgtgggc 480

acagccgtgg actggtacca gcagaagccc ggccagagcc ccaagctgct gatctactgg 540

gccagcacaa gacacaccgg cgtgcccgat agattcaccg gcagcggctc cggcaccgat 600

ttcactttag ccatcaccaa cgtgcagagc gaggatttag ccgactactt ctgccagcag 660

tacaacagct accctctgac cttcggcgcc ggcaccaagc tggagatcaa gagg 714

<210> 6

<211> 45

<212> PRT

<213>artificial sequence (Artificial Sequence)

<400> 6

Thr Thr Thr Pro Ala Pro Arg Pro Pro Thr Pro Ala Pro Thr Ile Ala

1 5 10 15

Ser Gln Pro Leu Ser Leu Arg Pro Glu Ala Cys Arg Pro Ala Ala Gly

20 25 30

Gly Ala Val His Thr Arg Gly Leu Asp Phe Ala Cys Asp

35 40 45

<210> 7

<211> 135

<212> DNA

<213>artificial sequence (Artificial Sequence)

<400> 7

accacgacgc cagcgccgcg accaccaaca ccggcgccca ccatcgcgtc gcagcccctg 60

tccctgcgcc cagaggcgtg ccggccagcg gcggggggcg cagtgcacac gagggggctg 120

gacttcgcct gtgat 135

<210> 8

<211> 24

<212> PRT

<213>artificial sequence (Artificial Sequence)

<400> 8

Ile Tyr Ile Trp Ala Pro Leu Ala Gly Thr Cys Gly Val Leu Leu Leu

1 5 10 15

Ser Leu Val Ile Thr Leu Tyr Cys

20

<210> 9

<211> 72

<212> DNA

<213>artificial sequence (Artificial Sequence)

<400> 9

atctacatct gggcgccctt ggccgggact tgtggggtcc ttctcctgtc actggttatc 60

accctttact gc 72

<210> 10

<211> 138

<212> DNA

<213>artificial sequence (Artificial Sequence)

<400> 10

aggaaatata gatcaaacaa aggagaaagt cctgtggagc ctgcagagcc ttgtcgttac 60

agctgcccca gggaggagga gggcagcacc atccccatcc aggaggatta ccgaaaaccg 120

gagcctgcct gctccccc 138

<210> 11

<211> 112

<212> PRT

<213>artificial sequence (Artificial Sequence)

<400> 11

Arg Val Lys Phe Ser Arg Ser Ala Asp Ala Pro Ala Tyr Lys Gln Gly

1 5 10 15

Gln Asn Gln Leu Tyr Asn Glu Leu Asn Leu Gly Arg Arg Glu Glu Tyr

20 25 30

Asp Val Leu Asp Lys Arg Arg Gly Arg Asp Pro Glu Met Gly Gly Lys

35 40 45

Pro Arg Arg Lys Asn Pro Gln Glu Gly Leu Tyr Asn Glu Leu Gln Lys

50 55 60

Asp Lys Met Ala Glu Ala Tyr Ser Glu Ile Gly Met Lys Gly Glu Arg

65 70 75 80

Arg Arg Gly Lys Gly His Asp Gly Leu Tyr Gln Gly Leu Ser Thr Ala

85 90 95

Thr Lys Asp Thr Tyr Asp Ala Leu His Met Gln Ala Leu Pro Pro Arg

100 105 110

<210> 12

<211> 336

<212> DNA

<213>artificial sequence (Artificial Sequence)

<400> 12

agagtgaagt tcagcaggag cgcagacgcc cccgcgtaca agcagggcca gaaccagctc 60

tataacgagc tcaatctagg acgaagagag gagtacgatg ttttggacaa gagacgtggc 120

cgggaccctg agatgggggg aaagccgaga aggaagaacc ctcaggaagg cctgtacaat 180

gaactgcaga aagataagat ggcggaggcc tacagtgaga ttgggatgaa aggcgagcgc 240

cggaggggca aggggcacga tggcctttac cagggtctca gtacagccac caaggacacc 300

tacgacgccc ttcacatgca ggccctgccc cctcgc 336

<210> 13

<211> 20

<212> PRT

<213>artificial sequence (Artificial Sequence)

<400> 13

Ala Leu Pro Val Thr Ala Leu Leu Leu Pro Leu Ala Leu Leu Leu His

1 5 10 15

Ala Ala Arg Pro

20

<210> 14

<211> 60

<212> DNA

<213>artificial sequence (Artificial Sequence)

<400> 14

gccctgcctg tgacagccct gctgctgcct ctggctctgc tgctgcatgc cgctagaccc 60

<210> 15

<211> 485

<212> PRT

<213>artificial sequence (Artificial Sequence)

<400> 15

Ala Leu Pro Val Thr Ala Leu Leu Leu Pro Leu Ala Leu Leu Leu His

1 5 10 15

Ala Ala Arg Pro Glu Val Gln Leu Gln Gln Ser Gly Pro Glu Leu Val

20 25 30

Lys Pro Gly Thr Ser Val Arg Ile Ser Cys Lys Thr Ser Gly Tyr Thr

35 40 45

Phe Thr Glu Tyr Thr Ile His Trp Val Lys Gln Ser His Gly Lys Ser

50 55 60

Leu Glu Trp Ile Gly Asn Ile Asn Pro Asn Asn Gly Gly Thr Thr Tyr

65 70 75 80

Asn Gln Lys Phe Glu Asp Lys Ala Thr Leu Thr Val Asp Lys Ser Ser

85 90 95

Ser Thr Ala Tyr Met Glu Leu Arg Ser Leu Thr Ser Glu Asp Ser Ala

100 105 110

Val Tyr Tyr Cys Ala Ala Gly Trp Asn Phe Asp Tyr Trp Gly Gln Gly

115 120 125

Thr Thr Leu Thr Val Ser Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly

130 135 140

Ser Ser Gly Gly Gly Ser Asp Ile Val Met Thr Gln Ser His Lys Phe

145 150 155 160

Met Ser Thr Ser Val Gly Asp Arg Val Ser Ile Ile Cys Lys Ala Ser

165 170 175

Gln Asp Val Gly Thr Ala Val Asp Trp Tyr Gln Gln Lys Pro Gly Gln

180 185 190

Ser Pro Lys Leu Leu Ile Tyr Trp Ala Ser Thr Arg His Thr Gly Val

195 200 205

Pro Asp Arg Phe Thr Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Ala

210 215 220

Ile Thr Asn Val Gln Ser Glu Asp Leu Ala Asp Tyr Phe Cys Gln Gln

225 230 235 240

Tyr Asn Ser Tyr Pro Leu Thr Phe Gly Ala Gly Thr Lys Leu Glu Ile

245 250 255

Lys Arg Thr Thr Thr Pro Ala Pro Arg Pro Pro Thr Pro Ala Pro Thr

260 265 270

Ile Ala Ser Gln Pro Leu Ser Leu Arg Pro Glu Ala Cys Arg Pro Ala

275 280 285

Ala Gly Gly Ala Val His Thr Arg Gly Leu Asp Phe Ala Cys Asp Ile

290 295 300

Tyr Ile Trp Ala Pro Leu Ala Gly Thr Cys Gly Val Leu Leu Leu Ser

305 310 315 320

Leu Val Ile Thr Leu Tyr Cys Arg Lys Tyr Arg Ser Asn Lys Gly Glu

325 330 335

Ser Pro Val Glu Pro Ala Glu Pro Cys Arg Tyr Ser Cys Pro Arg Glu

340 345 350

Glu Glu Gly Ser Thr Ile Pro Ile Gln Glu Asp Tyr Arg Lys Pro Glu

355 360 365

Pro Ala Cys Ser Pro Arg Val Lys Phe Ser Arg Ser Ala Asp Ala Pro

370 375 380

Ala Tyr Lys Gln Gly Gln Asn Gln Leu Tyr Asn Glu Leu Asn Leu Gly

385 390 395 400

Arg Arg Glu Glu Tyr Asp Val Leu Asp Lys Arg Arg Gly Arg Asp Pro

405 410 415

Glu Met Gly Gly Lys Pro Arg Arg Lys Asn Pro Gln Glu Gly Leu Tyr

420 425 430

Asn Glu Leu Gln Lys Asp Lys Met Ala Glu Ala Tyr Ser Glu Ile Gly

435 440 445

Met Lys Gly Glu Arg Arg Arg Gly Lys Gly His Asp Gly Leu Tyr Gln

450 455 460

Gly Leu Ser Thr Ala Thr Lys Asp Thr Tyr Asp Ala Leu His Met Gln

465 470 475 480

Ala Leu Pro Pro Arg

485

<210> 16

<211> 1455

<212> DNA

<213>artificial sequence (Artificial Sequence)

<400> 16

gccctgcctg tgacagccct gctgctgcct ctggctctgc tgctgcatgc cgctagaccc 60

gaggtgcagc tgcagcagag cggacccgag ctggtgaaac ccggcaccag cgtgaggatc 120

agctgcaaga ccagcggcta caccttcacc gagtacacca tccactgggt gaagcagagc 180

cacggcaagt ctttagagtg gatcggcaac atcaacccca acaacggcgg caccacctac 240

aaccagaagt tcgaggacaa ggccactctg accgtggaca agagcagctc caccgcctac 300

atggagctga ggtctttaac cagcgaggac agcgccgtgt actactgtgc cgccggctgg 360

aacttcgact actggggcca aggtacaact ttaactgtga gcagcggagg cggaggatct 420

ggcggcggag gaagttctgg cggagggtct gacatcgtga tgacccagag ccacaagttc 480

atgagcacca gcgtcggcga tcgtgtgagc atcatctgca aggccagcca agatgtgggc 540

acagccgtgg actggtacca gcagaagccc ggccagagcc ccaagctgct gatctactgg 600

gccagcacaa gacacaccgg cgtgcccgat agattcaccg gcagcggctc cggcaccgat 660

ttcactttag ccatcaccaa cgtgcagagc gaggatttag ccgactactt ctgccagcag 720

tacaacagct accctctgac cttcggcgcc ggcaccaagc tggagatcaa gaggaccacg 780

acgccagcgc cgcgaccacc aacaccggcg cccaccatcg cgtcgcagcc cctgtccctg 840

cgcccagagg cgtgccggcc agcggcgggg ggcgcagtgc acacgagggg gctggacttc 900

gcctgtgata tctacatctg ggcgcccttg gccgggactt gtggggtcct tctcctgtca 960

ctggttatca ccctttactg caggaaatat agatcaaaca aaggagaaag tcctgtggag 1020

cctgcagagc cttgtcgtta cagctgcccc agggaggagg agggcagcac catccccatc 1080

caggaggatt accgaaaacc ggagcctgcc tgctccccca gagtgaagtt cagcaggagc 1140

gcagacgccc ccgcgtacaa gcagggccag aaccagctct ataacgagct caatctagga 1200

cgaagagagg agtacgatgt tttggacaag agacgtggcc gggaccctga gatgggggga 1260

aagccgagaa ggaagaaccc tcaggaaggc ctgtacaatg aactgcagaa agataagatg 1320

gcggaggcct acagtgagat tgggatgaaa ggcgagcgcc ggaggggcaa ggggcacgat 1380

ggcctttacc agggtctcag tacagccacc aaggacacct acgacgccct tcacatgcag 1440

gccctgcccc ctcgc 1455

Claims

1. a kind of Chimeric antigen receptor for targeting PSMA, which is characterized in that the Chimeric antigen receptor CAR- of the targeting PSMA PSMA includes the sequentially connected targeting single-chain antibody of PSMA, extracellular hinge area, transmembrane region and intracellular from aminoterminal to c-terminus The amino acid sequence of signaling zone, wherein the single-chain antibody of the targeting PSMA includes the amino acid sequence as shown in SEQ ID NO:1 Column, the intracellular signal area includes sequentially connected costimulatory signal area and the first signaling zone from aminoterminal to c-terminus, described Costimulatory signal area includes CD27 signaling zone, and the CD27 signaling zone includes the amino acid sequence as shown in SEQ ID NO:2.

2. the Chimeric antigen receptor of targeting PSMA as described in claim 1, which is characterized in that the extracellular hinge area includes CD8 α hinge area, the transmembrane region include CD8 transmembrane region, and first signaling zone includes CD3 ζ signaling zone.

3. the Chimeric antigen receptor of targeting PSMA as claimed in claim 2, which is characterized in that the amino acid of the CAR-PSMA Sequence includes the amino acid sequence as shown in SEQ ID NO:3.

4. a kind of Chimeric antigen receptor T cell for targeting PSMA, which is characterized in that including as described in claim any one of 1-3 Targeting PSMA Chimeric antigen receptor.

5. a kind of recombinant viral vector, which is characterized in that the recombinant viral vector includes as described in claim any one of 1-3 Targeting PSMA Chimeric antigen receptor CAR-PSMA encoding gene.

6. recombinant viral vector as claimed in claim 5, which is characterized in that the encoding gene of the CAR-PSMA includes such as Nucleotide sequence shown in SEQ ID NO:4.

7. a kind of host cell, which is characterized in that the host cell includes such as the described in any item recombination diseases of claim 5-6 Poisonous carrier.

8. a kind of preparation method for the Chimeric antigen receptor T cell for targeting PSMA characterized by comprising

(1) encoding gene of the Chimeric antigen receptor CAR-PSMA of targeting PSMA is provided, including is sequentially connected with from 5 ' ends to 3 ' ends Signal peptide encoding gene, target the encoding gene of single-chain antibody of PSMA, the encoding gene of extracellular hinge area, transmembrane region The encoding gene of encoding gene and intracellular signal area, wherein the encoding gene of the single-chain antibody of the targeting PSMA includes such as SEQ The corresponding nucleotide sequence of amino acid sequence shown in ID NO:1, the intracellular signal area include suitable from aminoterminal to c-terminus The costimulatory signal area of secondary connection and the first signaling zone, the costimulatory signal area include CD27 signaling zone, the CD27 signal The encoding gene in area includes the corresponding nucleotide sequence of amino acid sequence as shown in SEQ ID NO:2；

(2) encoding gene of the CAR-PSMA is inserted into pWPXLD carrier, obtains pWPXLD-CAR-PSMA recombination matter Grain；

(3) by the pWPXLD-CAR-PSMA recombinant plasmid and envelope plasmid, packaging plasmid cotransfection host cell, weight is obtained Group slow virus；

(4) recombinant slow virus is infected into CD3 positive t lymphocytes, the Chimeric antigen receptor T of targeting PSMA is obtained through separation Cell.

9. the preparation method of the Chimeric antigen receptor T cell of targeting PSMA as claimed in claim 8, which is characterized in that described Envelope plasmid is PMD2G, and the packaging plasmid is psPAX2, and the host cell is HEK293T cell.

10. a kind of Chimeric antigen receptor or as claimed in claim 4 of targeting PSMA as described in any one of claims 1-3 Or as made from the described in any item preparation methods of claim 8-9 target PSMA Chimeric antigen receptor T cell or as weigh Benefit require the described in any item recombinant viral vectors of 5-6 or host cell as claimed in claim 7 preparation prevention, diagnosis and Treat the application in the drug of malignant tumour.