OCTS technology-based prostatic cancer CAR-T therapy vector and construction method and application thereof

A prostate cancer and carrier technology, applied in the field of medical biology, can solve problems that have not yet been overcome, and achieve the effects of saving economic expenses, improving quality of life, and high transduction efficiency

Active Publication Date: 2017-09-15
SHANGHAI UNICAR THERAPY BIOPHARM TECH CO LTD
View PDF8 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009] At present, there are no relevant reports on CAR-T therapy targeting PSMA and PD-L1 antigens to overcome the above shortcomings

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • OCTS technology-based prostatic cancer CAR-T therapy vector and construction method and application thereof
  • OCTS technology-based prostatic cancer CAR-T therapy vector and construction method and application thereof
  • OCTS technology-based prostatic cancer CAR-T therapy vector and construction method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0094] Example 1 Construction of OCTS-CAR-T cells

[0095] 1. Construction, purification and detection methods of recombinant lentiviral vectors lvOCTS-PDL1PSMAs and lvOCTS-PDL1PSMAt.

[0096] see image 3 , the construction method of the recombinant lentiviral vector of the present invention is as follows:

[0097] 1. Human EF1α promoter (SEQ ID NO.14), OCTS structure [OCTS-PDL1PSMAs, OCTS-PDL1PSMAt] (CD8 leader chimeric receptor signal peptide (SEQ ID NO.15), PSMA single-chain antibody light chain VL (SEQ ID NO.16), PSMA single-chain antibody heavy chain VH (SEQ ID NO.17), PDL1 single-chain antibody light chain VL (SEQ ID NO.18), PDL1 single-chain antibody heavy chain VH (SEQ ID NO.19 ), the hinge Inner-Linker (SEQ ID NO.20) in the antibody, the hinge Inter-Linker (SEQ ID NO.21) between single-chain antibodies, the CD8Hinge chimeric receptor hinge (SEQ ID NO.22), the CD8Transmembrane chimeric receptor body transmembrane region (SEQ ID NO.23), CD28 chimeric receptor costim...

Embodiment 2

[0206] OCTS-CAR-T cell pathogen detection and expression detection.

[0207] 1. Endotoxin detection;

[0208] (1), endotoxin working standard is 15EU / branch;

[0209] (2), Limulus reagent sensitivity λ=0.25EU / ml, 0.5ml / tube

[0210] (3) Dilution of endotoxin standard substance: Take one endotoxin standard substance, dilute it with BET water in proportion to dissolve into 4λ and 2λ respectively, seal with parafilm, shake and dissolve for 15min; each step of dilution should be mixed in the vortex Mix on the mixer for 30s;

[0211] (4) Adding samples: Take several LAL reagents, add 0.5 ml of BET water to each tube to dissolve, and distribute to several endotoxin-free test tubes, each tube has 0.1 ml. Two of them are negative control tubes, add 0.1ml of BET water;

[0212] Two are positive control tubes, add 0.1ml of endotoxin working standard solution with 2λ concentration;

[0213] 2 tubes are sample positive control tubes, add 0.1ml sample solution containing 2λ endotoxin ...

Embodiment 3

[0243] Example 3 Functional testing of OCTS-CAR-T cells.

[0244] 1. Evaluation of target cell killing effect.

[0245] (1) Culture target cells separately [PSMA + K562, PDL1 + K562, PDL1 + PSMA + K562, K562 cells] and effector cells [OCTS-CAR-T cells];

[0246] (2) Collect target cells 4x10 5 cells and OCTS-CAR-T cells 2.8x10 6 cells, 800g, centrifuge for 6min, discard the supernatant;

[0247] (3) Resuspend the target cells and effector cells in 1ml D-PBS(-) solution, centrifuge at 800g for 6min, discard the supernatant;

[0248] (4) Repeat step 3 once;

[0249] (5) Resuspend effector cells with 700ul medium (AIM-V medium + 1-10% FBS), and resuspend target cells with 2ml medium (AIM-V medium + 1-10% FBS);

[0250] (6) Experimental wells with effect-to-target ratios of 1:1, 5:1, and 10:1 were set, and the grouping of effector cells co-incubated with single-target cells and double-target cells was shown in Table 6, and a control group ( K562 cells), 3 replicate wells...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses an OCTS technology-based prostatic cancer CAR-T therapy vector which comprises a lentivirus framework plasmid, a human EP1alpha promoter (SEQ ID NO.14), an OCTS chimeric receptor structure domain and a PDL1 single-chain antibody, wherein the OCTS chimeric receptor structure domain comprises A CD8 leader chimeric receptor signal peptide (SEQ ID NO.15), a PSMA single-chain antibody light chain VL (SEQ ID NO.16), a PSMA single-chain antibody heavy chain VH (SEQ ID NO.17), a PDL1 single-chain antibody light chain VL (SEQ ID NO.18), a PDL1 single-chain antibody heavy chain VH (SEQ ID NO.19), an antibody Inner-Linker (SEQ ID NO.20), a single-chain antibody Inter-Linker (SEQ ID NO.21), a CD8 Hinge chimeric receptor hinge (SED ID NO.22), a CD8 Transmembrane chimeric receptor transmembrane domain (SEQ ID NO.23), a TCR chimeric receptor T cell activation domain (SEQ ID NO.26) and a chimeric receptor co-stimulus factor domain. In addition, the invention further discloses a construction method of the vector and an application of the vector in preparation of drugs for treating a prostatic cancer.

Description

technical field [0001] The invention belongs to the field of medical biology, and in particular relates to a carrier, in particular to a CAR-T treatment carrier for prostate cancer based on OCTS technology. In addition, the present invention also relates to the construction method and application of the carrier. Background technique [0002] The theoretical basis of tumor immunotherapy is that the immune system has the ability to recognize tumor-associated antigens and regulate the body's ability to attack tumor cells (highly specific cytolysis). In the 1950s, Burnet and Thomas put forward the theory of "immune surveillance", thinking that the mutated tumor cells that often appear in the body can be recognized and eliminated by the immune system, which laid the theoretical foundation for tumor immunotherapy [Burnet FM. Immunological aspects of malignant disease. Lancet, 1967; 1:1171-4]. Subsequently, various tumor immunotherapies, including cytokine therapy, monoclonal ant...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C12N15/867C12N15/62C12N5/10A61K35/17A61P35/00
Inventor 祁伟俞磊康立清林高武余宙
Owner SHANGHAI UNICAR THERAPY BIOPHARM TECH CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap