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Heavy chain and light chain variable regions of anti-human BAFF monoclonal antibody

A monoclonal antibody and variable region technology, applied in the field of biomedicine, can solve problems such as low affinity, inability to recognize cell membrane BAFF, hindering application, etc., and achieve high affinity.

Inactive Publication Date: 2010-10-06
FOURTH MILITARY MEDICAL UNIVERSITY
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] At present, the preparations that block the biological activity of BAFF mainly include anti-BAFF antibodies and BAFF soluble receptors, among which anti-BAFF antibodies include lymphostat-B, EGFP / scFv F8, anti-BAFFscFv, anti-BAFF scFv-Fc etc., but the first three types of antibodies can only recognize free BAFF, not BAFF on the cell membrane; although the latter type of antibodies can recognize both free BAFF and BAFF on the cell membrane, their affinity is low, which hinders its further application

Method used

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  • Heavy chain and light chain variable regions of anti-human BAFF monoclonal antibody
  • Heavy chain and light chain variable regions of anti-human BAFF monoclonal antibody
  • Heavy chain and light chain variable regions of anti-human BAFF monoclonal antibody

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Embodiment Construction

[0030] The complete nucleotide sequence of the variable region gene, especially the nucleotide sequence of its functional fragments (such as CDR, etc.) and the amino acid sequence of the antibody variable region, are chimeric antibodies, single-chain antibodies or humanized antibody construction The basics. For this reason, the applicant immunized BALB / c mice with recombinant human BAFF, prepared mouse anti-human BAFF monoclonal antibody, cloned and screened out the hybridization of FMMU-BAFF-NO.4 that can secrete specific human BAFF monoclonal antibody The monoclonal antibody was purified from a tumor cell line and its high affinity and specificity were verified.

[0031] And clone the monoclonal antibody light chain and heavy chain variable region gene, obtain the monoclonal antibody light chain and heavy chain variable region gene sequence and amino acid sequence, and the CDR sequence of the variable region; and confirm the amino acid sequence and gene sequence uniqueness....

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Abstract

The invention discloses heavy chain and light chain variable regions of an anti-human BAFF monoclonal antibody. The anti-human BAFF monoclonal antibody is FMMU-BAFF-4, wherein the gene sequences of the monoclonal antibody variable regions are shown as SEQ ID NO.3 and SEQ ID NO.4; and the amino acid sequences of the monoclonal antibody variable regions are shown as SEQ ID NO.1 and SEQ ID NO.2. In the variable regions, a mouse anti-human BAFF monoclonal antibody is prepared by using a recombined human BAFF immunological BALB / c mouse; the mouse anti-human BAFF monoclonal antibody is cloned and screened to obtain a hybridoma cell line which can secrete specific human BAFF monoclonal antibody FMMU-BAFF-NO.4; the genes of the monoclonal antibody light chain and heavy chain variable regions are cloned to obtain the gene sequences and the amino acid sequences of the monoclonal antibody light and heavy chain variable regions, and CDR sequences of the variable regions; and the uniqueness of the amino acid sequences and the gene sequences is determined.

Description

technical field [0001] The invention belongs to the technical field of biomedicine and relates to a monoclonal antibody, in particular to a heavy chain and light chain variable region of an anti-human BAFF monoclonal antibody, including its amino acid sequence and its nucleotide sequence. Background technique [0002] Autoimmune diseases refer to the diseases caused by the body's immune response to self-antigens, resulting in damage to its own tissues, and are diseases that seriously endanger human health. Common autoimmune diseases include systemic lupus erythematosus (SLE), Sjogren's syndrome (SS), and rheumatoid arthritis (RA). The treatment methods for autoimmune diseases are still in the research and exploration stage, mainly relying on drugs such as immunosuppressants, physical therapy and surgical treatment, but the side effects are relatively large and cannot be cured. Therefore, targeted antibody drug therapy combined with genetic engineering and protein engineerin...

Claims

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Application Information

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IPC IPC(8): C07K16/24C12N15/13A61K39/395A61P19/04A61P29/00A61P37/02
Inventor 金伯泉陈丽华肖黎明宋朝君龚玖瑜
Owner FOURTH MILITARY MEDICAL UNIVERSITY
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