REASSORTANT INFLUENZA VIRUS PRODUCTION METHOD

    公开(公告)号:US20210338798A1

    公开(公告)日:2021-11-04

    申请号:US16316186

    申请日:2017-07-11

    Abstract: Provided is a method of producing reassortant influenza virus containing an antigenic protein of the first influenza virus strain, the method including the following steps: 1) a step of irradiating the first influenza virus strain with ultraviolet light in such an irradiation dose that the first influenza virus strain has initial infection ability and loses or is reduced in virus growth potential; 2) a step of infecting a host with the first influenza virus strain and the second influenza virus strain; 3) a step of culturing the host infected with the first influenza virus strain and the second influenza virus strain, to obtain culture product; 4) a step of inactivating influenza virus strain having an antigenic protein of the second influenza virus strain in the culture product obtained in the step 3); and 5) a step of collecting reassortant influenza virus after the step 4).

    ANTI-INFLUENZA VIRUS NEUTRALIZING ANTIBODY
    19.
    发明申请
    ANTI-INFLUENZA VIRUS NEUTRALIZING ANTIBODY 审中-公开
    抗流感病毒中和抗体

    公开(公告)号:US20160200799A1

    公开(公告)日:2016-07-14

    申请号:US14913613

    申请日:2014-08-20

    CPC classification number: C07K16/1018 C07K2317/76

    Abstract: It is an object of the present invention to provide a novel antibody having a high binding activity and a high neutralizing activity on influenza viruses. The present invention provides an antibody, which neutralizes H1 influenza virus and/or H5 influenza virus, wherein the antibody has a heavy chain variable region having CDRs consisting of a defined heavy chain first complementarity-determining region (VH CDR1), a defined heavy chain second complementarity-determining region (VH CDR2) and a defined heavy chain third complementarity-determining region (VH CDR3), and a light chain variable region having CDRs consisting of a defined light chain second complementarity-determining region (VL CDR2) and a defined light chain third complementarity-determining region (VL CDR3).

    Abstract translation: 本发明的目的是提供一种对流感病毒具有高结合活性和高中和活性的新型抗体。 本发明提供中和H1流感病毒和/或H5流感病毒的抗体,其中该抗体具有由定义的重链第一互补决定区(VH CDR1)构成的CDR的重链可变区,定义的重链 第二互补决定区(VH CDR2)和定义的重链第三互补决定区(VH CDR3)和轻链可变区,其具有由定义的轻链第二互补决定区(VL CDR2)和定义的 轻链第三互补决定区(VL CDR3)。

Patent Agency Ranking