Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Therapeutic molecules that bind to lag3 and pd1

A technology of LAG-3 and PD-1, applied in the field of protein, can solve problems such as blocking

Pending Publication Date: 2020-09-29
CRESCENDO BIOLOGICS
View PDF11 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Bispecific antibodies that bind both PD-1 and LAG-3 may also offer advantages over combination therapies, since use of the latter results in the general blockade of each target on cells expressing either target

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
  • Therapeutic molecules that bind to lag3 and pd1
  • Therapeutic molecules that bind to lag3 and pd1
  • Therapeutic molecules that bind to lag3 and pd1

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0366] The construction of embodiment 1Tg / TKO mouse

[0367] Mice carrying the human heavy chain antibody transgenic locus in germline configuration in the context of silencing endogenous heavy and light chain antibody expression (triple knockout, or TKO) were created as previously described (WO2004 / 076618, WO2003 / 000737, Ren et al., Genomics, 84, 686, 2004; Zou et al., J. Immunol., 170, 1354, 2003 and WO2016 / 062990). Briefly, transgenic mice were obtained after pronuclear microinjection of freshly fertilized oocytes with yeast artificial chromosomes (YACs) containing and lacking C H 1 domain of mouse immunoglobulin constant region genes, mouse enhancers and regulatory regions combined with excess human VH, D and J genes. Yeast artificial chromosomes (YACs) are vectors that can be used to clone very large DNA inserts in yeast. They accept large DNA insertions in addition to containing all three cis-acting structural elements (autonomously replicating sequence (ARS), centrom...

Embodiment 2

[0370] Example 2 Antigens used for immunization and characterization

[0371] LAG-3

[0372] Human and monkey LAG-3 extracellular domains were made as IgG fusion proteins for immunization of transgenic mice or for binding studies. Human LAG-3 sequence accession number NM_002286. Rhesus monkey LAG-3 accession number XM_001108923. For LAG3 domains 1-3 (NC_022282), the amino acid sequence of the rhesus monkey matched that of the cynomolgus monkey. Mouse LAG3 was from R&DBiotechne (catalogue 3328-L3). Human LAG-3 domains 1-4 and 1-2 were cloned using standard molecular biology techniques. Domains were identified according to Huard et al. 1997 PNAS 94:5744-9. Expression was performed in HEK 293 cells, and LAG3 protein was purified using size exclusion chromatography. Chinese hamster ovary (CHO) cells expressing human LAG-3 were generated using the human LAG-3 sequence in an inducible expression vector. Plasmids were transfected using lipofection and stable cell pools were se...

Embodiment 4

[0378] Example 4 Generates an anti-LAG3 library from immunized mice

[0379] Generation of libraries from the above immunized mice followed the standard protocol for library generation as described below:

[0380] a) Tissue collection and homogenization, RNA extraction and RT-PCR

[0381] Spleen, inguinal and brachial lymph nodes were collected from several immunized mice to middle. Using Qiagen Kit (cat 74104) RNA was extracted from total spleen using the Pure RNA Tissue kit (cat 98040496) following the manufacturer's protocol or via the KingRNAer automated system (Thermo). V was mined from RNA samples using the Superscript III RT-PCR High-Fidelity Kit (Invitroge cat 12574-035) and according to the manufacturer's protocol. H sequence.

[0382] b) Cloning into a phagemid vector

[0383] The phagemid vector pUCG3 was used in these studies. Conventional PCR-based methods are used to amplify V from H Sequence Construction V H Phagemid library. Purified V H RT-PC...

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 relates to LAG-3 binding agents, in particular particularly variable heavy chain (VH) sdAbs and bispecific agents that target both LAG-3 and PD-1, and the use of such binding agents in the treatment, prevention and detection of disease.

Description

Background technique [0001] Antibody-based therapeutics have become an important component of the treatment of an increasing number of human malignancies in the fields of oncology, inflammatory and infectious diseases, among others. In fact, antibodies are one of the best-selling drug classes today; five of the top ten best-selling drugs are antibodies. [0002] Lymphocyte activation gene 3 (LAG-3, LAG3, CD223) is a transmembrane protein of the immunoglobulin superfamily. It has four extracellular domains and shares homology with CD4 (Triebel 1990 J. Exp. Med. 171:1393-1405). [0003] LAG-3 is expressed on CD4+ T cells, CD8+ T cells, T regulatory cells, B cells, NK cells and plasmacytoid dendritic cells (Huard 1994 Eur.J. Immunol.24:3216-21; Grosso 2007 J.Clin.Invest.117:3383-92; Huang 2004 Immunity.21:503-13; Kieslow 2005 Eur.J.Immunol.35:2081-88; Triebel 1990 J.Exp.Med.171:1393-140; Castelli 2014 Oncoimmunology. 3:11). [0004] The role of LAG-3 on T cells is to regulate...

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): A61K39/395C07K16/28A61P35/00A61K39/00
CPCA61K39/3955C07K16/2803C07K16/2818A61K2039/505A61K2039/507C07K2317/24C07K2317/31C07K2317/526C07K2317/55C07K2317/565C07K2317/622C07K2317/76C07K2317/92C07K2317/94A61P35/00A61K39/395G01N33/563A61K47/6801C12N15/10C07K2317/569C07K16/28C07K2317/626C07K16/46C07K2319/00
Inventor 卡罗琳·爱德华兹安杰莉卡·塞特伊索贝尔·奥苏赫滕毓敏詹姆斯·莱格戴维·埃斯科斯穆鲁加伦
Owner CRESCENDO BIOLOGICS
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com