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    Home > Active Ingredient News > Study of Nervous System > Personalized T cell immunotherapy for pediatric brain tumors is one step closer to becoming a reality

    Personalized T cell immunotherapy for pediatric brain tumors is one step closer to becoming a reality

    • Last Update: 2021-12-05
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com
    Recent popular reports from Yimaike ★ Invitation Letter2021 CSGCT Gene and Cell Therapy Medical Summit is about to be held in Shanghai ★ Mustang Biology develops RAG1 immunodeficiency disease and obtains the first exclusive authorization of in vitro lentiviral gene therapy November 23, 2021 / Yimai Ke News eMedClub News/--Medulloblastoma is a common brain tumor in children, once it spreads, it becomes particularly difficult to treat
    .

    In order to find immunotherapies that may bring hope to these young patients, scientists at the National Children's Hospital in Washington, DC used a specific type of DNA analysis to design a new therapy that has shown promising efficacy in preclinical studies
    .

    The team identified peptides specific to medulloblastoma, and then modified the T cells so that they could recognize and target these proteins
    .

    They reported in Nature Communications that these modified T cells eliminated medulloblastoma cells in the test tube
    .

    From an immunotherapy perspective, tumor specificity is important because when clinicians treat patients with T cell therapy, they want to ensure that T cells directly target and kill the tumor without causing destructive damage to healthy cells
    .

    This paper proves that using this new method may produce better efficacy and safety
    .

    The researchers first patient samples for DNA sequencing analysis of all the proteins that affect tumor biology of cancer - they explained in a statement from the Children's Society said, this process is called "low input protein genomics"
    .

    Then, the researchers developed T cells that target specific proteins or neoantigens in each sample.
    These samples are unique to cancer and do not exist in healthy cells.

    .

    Tumor cells usually have mutations when they copy DNA.
    These mutated genes produce abnormal proteins.
    These proteins are unique for every cancer patient
    .

    In order for this process to work properly, researchers must develop a technique to filter normal peptides
    .

    The first author, Dr.
    Samuel Rivero-Hinojosa, a scientist at the National Children’s Fund, said in a statement: “Targeting antigens that are completely specific to tumors and not expressed in other parts of the body may enhance the strength of antigen-specific T cell products.
    At the same time reduce toxicity
    .

    "Personalized CAR-T Therapy Personalized CAR-T Therapy has been proven to be effective for blood cancer, but it has not been successfully transformed into the treatment of solid tumors
    .

    Several techniques for adapting this technique to brain tumors are currently being studied
    .

    Canadian scientists reported last year that they had developed a CAR-T that targets CD133, also known as prominin-1, a protein on neural stem cells found in some brain tumors
    .

    The therapy was developed by the start-up company Empirica Therapeutics
    .

    In April of this year, scientists at the University of California, San Francisco described a method they developed: They developed armed T cells to target solid tumors (including glioblastoma) through molecular circuits.
    ), these molecular circuits can cause cancer cells to be killed by T cells
    .

    The National Children's Hospital team hopes to design a clinical trial during which they will extract T cells from medulloblastoma patients, train them to recognize unique tumor neoantigens, and then reinject them into patients
    .

    Reference materials: 1.
    https:// discovery of neoantigens facilitates personalized multi-antigen targeted T cell immunotherapy for brain tumors DOI: 10.
    1038 / s41467-021-26936-y 
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