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    Home > Active Ingredient News > Study of Nervous System > Nat Commun: "Fighting with poison", oncolytic virus enhances the anti-tumor innate immune response to glioblastoma

    Nat Commun: "Fighting with poison", oncolytic virus enhances the anti-tumor innate immune response to glioblastoma

    • Last Update: 2021-10-20
    • Source: Internet
    • Author: User
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    Glioblastoma (GBM) is the most common and aggressive primary malignant brain tumor
    .


    GBM patients receiving standard treatment, including surgical resection, chemotherapy and radiotherapy, have a median survival time of approximately 15 months


    Oncolytic virus (OV) provides a potentially unique treatment for GBM because its mechanism of action is completely different from the standard treatment of GBM
    .


    Tumor lytic herpes simplex virus-1 (oHSV) is one of the most widely studied oncolytic viruses.


    Selectively lyse cancer cells while leaving normal cells basically unchanged Selectively lyse cancer cells while leaving normal cells basically unchanged

    Talimogene laherparepvec (Imlygic) is the first oncolytic virus therapy approved by the FDA and is based on the oHSV vector
    .


    In existing studies, researchers have found that oHSV treatment greatly increases the intratumoral infiltration of immune cells


    αCD47-G1, but not αCD47-G4, can induce the cytotoxicity of human NK cells to GBM cells
    .

    αCD47-G1, but not αCD47-G4, can induce the cytotoxicity of human NK cells to GBM cells
    .


    αCD47-G1, but not αCD47-G4, can induce the cytotoxicity of human NK cells to GBM cells


    Oncolytic herpes virus expressing full- length anti-(α)-human CD47 IgG1 or IgG4 antibody Oncolytic herpes virus expressing full-length anti-(α)-human CD47 IgG1 or IgG4 antibody

    ΑCD47-IgG1 intracranial injection of virus produced in the tumor microenvironment sustained release of the corresponding antibodies, but does not enter the systemic circulation ; In addition, generating αCD47-IgG1 virus to provide better survival rate of tumor-bearing mice high
    .


    The results from a mouse tumor model with strong immunity further confirmed that macrophages, and to a lesser extent NK cells, mediate the anti-tumor cytotoxicity of the oncolytic herpes virus that produces antibodies


    The virus produced by intracranial injection of αCD47-IgG1 continuously releases the corresponding antibody in the tumor microenvironment, but does not enter the systemic circulation .


     

    Original source:

    Original source:

    Bo Xu al.


    Bo Xu al.


     

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