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Anti-RSV (respiratory syncytial virus) human monoclonal antibody, and its preparation method

A technology of human monoclonal antibody and monoclonal antibody, which is applied in antiviral agents, antiviral immunoglobulin, botanical equipment and methods, etc., and can solve the requirements of high price, difficult mass production, and monoclonal antibody production process advanced questions

Active Publication Date: 2013-01-02
BRAVOVAX
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The name of the antibody is palivizumab ( Manufactured by MedImmune), it has a broad spectrum of action, but the current dosage of palivizumab required for each administration is 15 mg / kg (body weight). Due to the high requirements for the production process of monoclonal antibodies and the expensive production, the current commercially available products The price is high, it is difficult to promote production in large quantities in my country

Method used

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  • Anti-RSV (respiratory syncytial virus) human monoclonal antibody, and its preparation method
  • Anti-RSV (respiratory syncytial virus) human monoclonal antibody, and its preparation method
  • Anti-RSV (respiratory syncytial virus) human monoclonal antibody, and its preparation method

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0077] 1. Mice Immunization

[0078] The cell lines expressing anti-RSV F protein were obtained by hybridoma technology screening. Add 120ul of complete Freund's adjuvant (CFA) to 120ul of RSV antigen-containing phosphate buffer solution (PBS) commercially available from Capricon, mix and emulsify to prepare 240ul of CFARSV antigen solution. In the same way, 240 ul of IFARSV antigen solution was prepared using incomplete Freund's adjuvant (IFA).

[0079] BALB / C female mice aged 7-8 weeks were intraperitoneally injected with 240ul FCARSV antigen solution for the first immunization. After the first immunization, booster immunization with FIARSV antigen solution was carried out every 2-3 weeks. 240 ul of RSV antigen (manufactured by Capricon) was intravenously injected 10 and 3 days before splenocyte isolation. On the 42nd day after the immunization, the spleen was taken out, the splenocytes were separated, and the splenocytes and SP2-0 mouse myeloma cells were fused 1 / 1 by th...

Embodiment 2

[0086]The antigen neutralization ability of three anti-RSV monoclonal antibodies obtained by screening hybridoma cell lines was confirmed. Three RSV strains were purchased from the American Standard Biological Collection (ATCC): B1 wild-type strain (10[4.5]TCID(50) / ml), A2 (10[5.5]TCID(50) / ml) and For Long strain (10[6.7]TCID(50) / ml), the obtained RSV was diluted 10 times with phosphate buffered saline (abbreviated as diluent) containing bovine serum albumin (BSA).

[0087] Antigen extraction reagents were prepared: 0.4M NaCl, 0.1M citric acid, 10mM dithiothreitol and 0.1% polyoxyethylene novel phenyl ether. The diluted RSV virus and the antigen extraction reagent are mixed in equal volumes, and the antigen extraction solution is obtained after reacting for 5-10 minutes.

[0088] Agarose gel (GE) coated with anti-mouse IgG polyclonal antibody (SANTA CRUZ) was prepared, and the colloidal concentration was 15% (v / v) of the agarose gel solution. The gel solution is mixed with t...

Embodiment 37B05

[0102] Follow the instructions of the RNesay kit (Qiagen) from 2×10 7 Total mRNA was extracted from BW01-7B05 hybridoma cells. Single-stranded cDNA was prepared using oligo-dT primers and reverse transcriptase, and an aliquot of the cDNA was used as a starting material for polymerase chain reaction (PCR) to amplify the gene of the variable region.

[0103] The preparation of single-stranded cDNA uses 1ug of total mRNA as a template, in the buffer system of 50mM Tris-cl, 8mM Mg2Cl, 30mM KCl pH8.5, add 1mM dithiothreitol (DTT), 1mM dNTP, 25 units of human Placental ribonucleic acid inhibitor, 33uM random hexamer and 10 units of AMV reverse transcriptase, the reaction system is placed at 42°C for 1-2 hours. The heavy chain variable region (VH) of the 7B05 monoclonal antibody was amplified by polymerase chain reaction (PCR) with primers P1 (SEQ ID NO: 1) and P2 (SEQ ID NO: 2), and the light chain variable region (VL) was obtained by PCR amplification using primers P3 (SEQ ID NO:...

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Abstract

The invention relates to the biotechnical field, concretely relates to a monoclonal antibody of a virus, and more concretely relates to an anti-RSV human monoclonal antibody and its preparation method. The antibody can be used for enhancing the anti-RSV infection tolerance of human subjects, and reducing the infection level in infected individual bodies or mitigating symptoms caused by the RSV infection, and the administration dosage of the anti-RSV human monoclonal antibody is lower than that of current market products.

Description

technical field [0001] The invention relates to the field of biotechnology, in particular to a virus monoclonal antibody and a preparation method thereof, more specifically to a human monoclonal antibody against respiratory syncytial virus RSV and a preparation method thereof. The antibodies can be used to increase the tolerance of human subjects against RSV infection and to reduce the level of infection in infected individuals or to alleviate the symptoms caused by RSV infection. Background technique [0002] 1. Overview and pathogenic mechanism [0003] Respiratory syncytial virus pneumonia (respiratory syncytial virus pneumonia), referred to as syncytial virus pneumonia, is a negative-strand RNA virus with a capsule, belonging to the genus Pneumovirus of the family Paramyxo-viridae (Fenner, Virology 71 : 371-378, 1975; Huang et al., J. Virol. 43, 1982). RSV is a common interstitial pneumonia in children, which mostly occurs in infants and young children. Since maternal...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07K16/10C12N15/13C12N5/20A61K39/42A61P31/14C12R1/91
Inventor 张爱晖吴克徐亚南
Owner BRAVOVAX
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