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Anti-NGF antibody and antigen binding fragment thereof, and preparation method and application thereof

A technology for binding fragments and antibodies, which is applied in the preparation of the antibodies and their antigen-binding fragments, and in the field of anti-NGF antibodies and their antigen-binding fragments, which can solve the problems of different immunogenicity, different antibody tolerance speed and toxicity, and influence on drug efficacy And other issues

Active Publication Date: 2021-04-09
XIYUAN ANJIAN MEDICINE (SHANGHAI) CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The immunogenicity of different CDRs is different, resulting in different antibody tolerance speed and toxicity, which directly affects the efficacy of the drug
On the other hand, the subject's immune response to the antibody itself will form immune complexes, which will alter the pharmacokinetics and produce allergic reactions, etc., eliminating its therapeutic use

Method used

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  • Anti-NGF antibody and antigen binding fragment thereof, and preparation method and application thereof
  • Anti-NGF antibody and antigen binding fragment thereof, and preparation method and application thereof
  • Anti-NGF antibody and antigen binding fragment thereof, and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0148] Embodiment 1: the preparation of murine source anti-NGF antibody

[0149] Recombinant human NGF protein (Beijing Yiqiao Shenzhou Technology Co., Ltd., 11050-HNAC) was mixed and emulsified with an equal amount of complete Freund's adjuvant (Sigma-Alderich, F5881) as an immunogen for initial immunization. Five 6-week-old BALB / c mice and five C57 mice (Jiangsu Huafukang) were prepared, and each animal was subcutaneously injected with 50 μg of immunogen (excluding adjuvant quality, the same below). The immunogen was mixed and emulsified with Freund's incomplete adjuvant (Sigma-Alderich, F5506) for subsequent booster immunization. Two weeks after the initial immunization, each animal was intraperitoneally injected with 25 μg of immunogen for the first booster; two weeks later, each animal was subcutaneously injected with 25 μg of immunogen for the second booster. 4-5 weeks after the last immune shock, 25 μg of immunogen was injected intraperitoneally.

[0150] After the ...

Embodiment 2

[0152] Example 2: ELISA detection of murine anti-NGF antibody binding to human NGF

[0153] The binding ability of the anti-NGF antibody was studied using human NGF (Beijing Sino Biological Science and Technology Co., Ltd., 11050-HNAC) as the antigen. Each well of the 96-well ELISA plate was coated with 50ng human NGF, after washing and blocking, the antibody was added in gradient dilution and incubated at room temperature for 1 hour. After washing three times, add HRP-conjugated goat anti-mouse antibody (Biolegend, 405306), incubate at room temperature for 1 hour, add tetramethylbenzidine (TMB, Biolegend, 421101) to develop color after washing three times, stop color development with 1M HCl, and enzyme label The instrument reads the absorbance at 450nm.

[0154] Anti-NGF antibodies secreted by the three hybridomas all bound to human NGF in a dose-dependent manner ( figure 1 ), the EC50s of the three antibodies binding to human NGF were 0.082nM, 0.112nM, and 0.1nM, respect...

Embodiment 3

[0157] Example 3: Detection of binding affinity between murine anti-NGF antibody and human NGF

[0158] Antibody affinity was determined using the biomolecular interaction detection platform ForteBio Octet Red96 (PALL). Biotin-labeled human NGF was immobilized using SA (Streptavidin) Biosensor (Fortebio, 18-5021), and then combined with gradient concentrations of anti-NGF antibodies. Buffer (1X Kinetics Buffer: PBS+0.1%BSA+0.05%Tween20) was added for dissociation, and finally the affinity kinetic constant of antigen-antibody binding was calculated by instrument algorithm (Table 2).

[0159] Table 2 Binding affinity of anti-NGF antibodies to human NGF

[0160]

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Abstract

The invention provides an anti-NGF antibody or an antigen binding fragment thereof, and a preparation method and application thereof. The invention also provides an isolated polynucleotide encoding the anti-NGF antibody or the antigen binding fragment thereof, and a vector comprising the isolated polynucleotide. The invention also provides application of the antibody or the antigen binding fragment thereof in preparation of drugs for treating NGF-mediated diseases or symptoms.

Description

technical field [0001] The invention belongs to the technical field of biological immunity, and specifically relates to an anti-NGF antibody capable of specifically binding to human nerve growth factor and an antigen-binding fragment thereof, and also relates to a preparation method and application of the antibody and an antigen-binding fragment thereof. Background technique [0002] Nerve Growth Factor (NGF) is the first identified neurotrophic factor, and its role in the development and survival of peripheral and central neurons has been characterized. NGF has been shown to be a key survival and maintenance factor in the development of peripheral sympathetic and embryonic sensory neurons and basal forebrain cholinergic neurons (Smeyne et al. (1994) Nature, 368:246-249; Crowley et al. (1994) Cell, 76:1001-1011), which can upregulate the expression of neuropeptides in sensory neurons (Lindsay et al. (1989) Nature, 337:362-364). NGF contains three subunits of α, β, and γ, an...

Claims

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Application Information

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IPC IPC(8): C07K16/22C07K16/46C07K19/00C12N15/13A61K39/395A61K47/68A61P19/02A61P29/00A61P19/08A61P35/00A61P25/00G01N33/68
CPCC07K16/22C07K14/7051A61K47/6801A61P19/02A61P29/00A61P19/08A61P35/00A61P25/00G01N33/74C07K2317/24C07K2317/31C07K2317/56C07K2317/565C07K2317/92C07K2317/76C07K2319/33A61K2039/505G01N2333/48A61K47/6835C07K14/48
Inventor 原晓辉王国永刘玉姣郑东红
Owner XIYUAN ANJIAN MEDICINE (SHANGHAI) CO LTD
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