Human anti-h7n9 avian influenza virus neutralizing antibody m5, its preparation method and application
An avian influenza virus and antibody technology, applied in antiviral agents, antiviral immunoglobulins, botanical equipment and methods, etc., can solve the problems of limitation, time-consuming, blood-borne disease infection, etc.
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Embodiment 1
[0032] 1 Materials and methods
[0033]1.1 Source of virus, cell and vector: H7N9 virus A / Anhui / 1 / 2013 strain has been published in the literature (Gao R, Cao B, Hu Y, Feng Z, Wang D, Hu W, Chen J, Jie Z, Qiu H, Xu K, Xu X, Lu H, Zhu W, Gao Z, Xiang N, Shen Y, He Z, Gu Y, Zhang Z, Yang Y, Zhao X, Zhou L, Li X, Zou S, Zhang Y, Li X, Yang L ,Guo J,Dong J,Li Q,Dong L,Zhu Y,Bai T,Wang S,Hao P,Yang W,Zhang Y,Han J,YuH,Li D,Gao GF,Wu G,Wang Y,Yuan Z , Shu Y.2013.Human infection with a novelavian-origin influenza A(H7N9)virus.N Engl J.Med.368:1888–1897), provided by the Institute of Pathogenic Biology, Chinese Academy of Medical Sciences. The cells used for the in vitro neutralization experiment of H7N9 avian influenza virus were MDCK cells, which were purchased from ATCC. The bacterial strain used to construct the phage antibody library was XL1-Blue (Stratagene, USA), and the vector pComb3H (provided by Scripps Research Institute, USA).
[0034] 1.2 Antigen preparation
[0035] ...
Embodiment 2
[0104] Example 2 Application of Human Anti-H7N9 Avian Influenza Virus Neutralizing Antibody M5
[0105] At present, there are no specific vaccines and drugs for the prevention and treatment of acute respiratory infectious diseases caused by the H7N9 virus. The immunoglobulins used clinically are often derived from the convalescent serum of patients infected with the virus, which limits their mass production. At the same time, because it comes from serum, it is prone to infection of blood-borne diseases. Using the human source anti-H7N9 avian influenza virus genetically engineered antibody M5 obtained by the invention to replace the blood-derived immunoglobulin provides a new approach for the treatment of acute respiratory infectious diseases caused by the H7N9 virus.
Embodiment 3
[0106] Example 3 Method for preparing full antibody immunoglobulin IgG by using neutralizing antibody M5
[0107] 1. Expression and purification of whole antibody IgG
[0108] ① Construction of whole antibody recombinant expression plasmid: first use primers (upstream primer 5'-CCCAAGCTTGTTGCTCTGGATCTCTGGTGCCTACGGGGAAATTGTGTTGACCCAGTCTCC-3', downstream primer 5'-CTAGTCTAGAATTAACACTCTCCCCTG-3') to amplify the light chain segment of FAB antibody, digest with XBAI / HINDIII, Cloned into the PIGG vector (provided by the SCRIPPS Institute of the United States) (CHRISTOPH RADER, MIKHAIL POPKOV, JOHN A.NEVES, AND CARLOS F.BARBASIII.INTEGRIN ΑVΒ3-TARGETED THERAPY FOR KAPOSI.S SARCOMA WITH AN IN VITRO-EVOLVED ANTIBODY.THE FASEB JOURNAL .(OCTOBER18, 2002) 10.1096 / FJ.02-0281FJE.), the vector PIGG-L was obtained. Then use primers (upstream primer 5'-GAGGAGCTCACTCCGAGGTGCAGCTGTTGGAGTCTGGGGGAGGCTTGGTAC-3', downstream primer 5'-GAGGGGCCCTTGGTGGAGGCTGAGGAGACGGT-3') to amplify the heavy chain s...
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