CAR-T vector capable of targeting Her2 and disturbing PD-L1 to reduce tumor immune escape and construction method and use thereof

A PD-1, immune escape technology, applied in the field of medical biology, to achieve the effect of increasing secretion, reducing immune escape, and improving curative effect

Inactive Publication Date: 2018-06-26
上海生博生物医药科技有限公司
View PDF5 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] At present, there are no reports about CAR-T vectors that can target Her2 and interfere with PD-1 to reduce tumor immune escape

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
  • CAR-T vector capable of targeting Her2 and disturbing PD-L1 to reduce tumor immune escape and construction method and use thereof
  • CAR-T vector capable of targeting Her2 and disturbing PD-L1 to reduce tumor immune escape and construction method and use thereof
  • CAR-T vector capable of targeting Her2 and disturbing PD-L1 to reduce tumor immune escape and construction method and use thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0045] The present invention is further described below in conjunction with specific embodiments. It should be understood that the specific embodiments described herein are presented by way of example and not limitation of the invention. The principal features of this invention may be employed in various embodiments without departing from the scope of the invention. Example 1 Construction of CAR recombinant lentiviral vector

[0046] 1. Materials

[0047] 1. Lentiviral backbone plasmid pLenti-3G ​​basic (see lentiviral vector structure figure 2 ), lentiviral packaging plasmids pPac-GP, pPac-R and membrane protein pEnv-G, HEK293T / 17 cells, and homologous recombinase were provided by Shiao (Shanghai) Biomedical Technology Co., Ltd.;

[0048]2. Human EF1α promoter (SEQ ID NO.1), CD8 leader chimeric receptor signal peptide (SEQ ID NO.2), Her2 single-chain antibody light chain VL (SEQ ID NO.3), single-chain antibody hinge Linker (SEQ ID NO.4), Her2 heavy chain VH (SEQ ID NO.5)...

Embodiment 2

[0087] Example 2 Packaging of recombinant lentivirus lvCAR-Her2, lvCAR-Her2-NC-shRNA, and lvCAR-Her2-PD1-shRNA.

[0088] (1) Complete medium: take out the preheated fresh medium, add 10% FBS + 5ml Pen-Srep, mix up and down;

[0089] (2) 1XPBS solution: Weigh NaCl 8g, KCl 0.2, NaCl 2 HPO 4 .12H 2 O 3.58g, KH 2 Put 0.24g of PO4 in a 1000ml beaker, add 900ml Milli-Q grade ultrapure water to dissolve, after the dissolution is completed, use a 1000ml graduated cylinder to set the volume to 1000ml, and sterilize at 121℃ for 20min;

[0090](3) 0.25% Trypsin solution: Weigh 2.5g of Trypsin, put 0.19729g of EDTA in a 1000ml beaker, add 900ml of 1XPBS to dissolve, after the dissolution is completed, use a 1000ml graduated cylinder to set the volume to 1000ml, 0.22μM filter sterilization, long-term use can be stored To -20 ℃ refrigerator;

[0091] (4) 0.5M CaCl2 solution: weigh 36.75g CaCl 2 Dissolve in 400ml Milli-Q grade ultrapure water; use Milli-Q grade ultrapure water to make ...

Embodiment 3

[0108] Example 3 Concentration and detection of recombinant lentiviral vector

[0109] 1. Purification of recombinant lentivirus by ion exchange chromatography

[0110] (1) Use a Thermo vacuum pump to filter the collected supernatant through a 0.22 μm-0.8 μm PES filter to remove impurities;

[0111] (2) Add 1.5M NaCl 250mM Tris-HCl (pH 6-8) to the supernatant at a ratio of 1:1 to 1:10;

[0112] (3) Place two ion exchange columns in series, and pass through the columns sequentially with 4ml 1M NaOH, 4ml 1M NaCl, 5ml 0.15M NaCl25mM Tris-HCl (pH 6-8);

[0113] (4) The solution obtained in step 2 is loaded on the ion exchange column with a speed of 1-10ml / min by a peristaltic pump;

[0114] (5) After passing all the supernatant through the column, wash it once with 10ml 0.15M NaCl 25mM Tris-HCl (pH 6-8) solution;

[0115] (6) Use 1-5ml 1.5M NaCl 25mM Tris-HCl (pH 6-8) for elution according to the loading amount, and collect the eluate;

[0116] (7) Divide the eluate into 25 to...

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 a CAR-T vector capable of targeting Her2 and disturbing PD-L1 to reduce tumor immune escape. The CAR-T vector comprises a human EF1 alpha promoter for eukaryotic transcriptionof a chimeric antigen receptor gene, wherein the human EF1 alpha promoter is shown in the formula of SEQ ID NO. 1, PD-1 shRNA in the 3'UTR, wherein the sequence of the PD-1 shRNA is shown in the formula of SEQ ID NO. 25, a gene delivery vector, and a second-generation CAR or third-generation CAR chimeric antigen receptor combining recognition, delivery and starting, wherein the chimeric antigen receptor comprises a Her2 single-chain antibody light chain VL and a Her2 single-chain antibody heavy chain VH. The invention also discloses a construction method of the vector and a use of the vector in preparation of drugs for disturbing PD-L1 to reduce tumor immune escape. Through a Her2 CAR-T technology and interference of PD-1 expression in T lymphocytes, the tumor immune escape is inhibited and the T lymphocyte effects of killing tumor cells are improved so that the CAR-T immunotherapy effects of resisting brain glioma are improved.

Description

technical field [0001] The invention belongs to the field of medical biology, in particular to a carrier, in particular to a CAR-T carrier that can target Her2 and interfere with PD-1 to reduce tumor immune escape. In addition, the present invention also relates to the construction method and application of the vector. Background technique [0002] With the development of tumor immunology theory and technology, the role of immune cell therapy in tumor therapy has been paid more and more attention. Studies have found that T lymphocytes are the natural enemies of tumor cells, play a major role in the tumor immune response, and have a strong killing effect on tumor cells. [0003] Chimeric antigen receptor T cell immunotherapy (Chimeric Antigen Receptor T-Cell Immunotherapy, CAR-T immunotherapy) is a new type of cellular immunotherapy technology that has developed rapidly in recent years [Eleanor J.Cheadle, et al.CAR T cells : driving the road from the laboratory to the clini...

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): C12N15/85C12N15/867A61K48/00A61K39/395A61K35/17A61P35/00
CPCA61K35/17A61K39/3955A61K48/005A61K2039/53C12N15/85C12N15/867C12N2740/15043C12N2800/107
Inventor 吴小江王聪顾莉萍
Owner 上海生博生物医药科技有限公司
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