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    Home > Biochemistry News > Biotechnology News > Cell discusses what else can CAR-T cell therapy do beyond cancer?

    Cell discusses what else can CAR-T cell therapy do beyond cancer?

    • Last Update: 2023-01-05
    • Source: Internet
    • Author: User
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    Engineered immune cells, known as CAR-T cells, have shown the world how personalized immunotherapy can play
    in fighting blood cancers.
    Now, researchers have reported very promising early results
    for CAR-T therapy in a small group of patients with the autoimmune disease lupus.
    Carl June, MD, a pioneer in CAR-T at the Pennsylvania Medical School, and Daniel Baker, a doctoral student in cell and molecular biology at the University of Pennsylvania's Perelman School of Medicine, discuss the advance
    in a commentary published today in the journal Cell.

    "We've always known that CAR-T therapies can have broad applications in principle, and it's very encouraging to see early evidence that this promise is materializing," said June, the Richard W.
    Vague Professor of Immunotherapy in the Department of Pathology and Laboratory Medicine at the University of Pennsylvania School of Medicine and director of the Center for Cellular Immunotherapy at the University of
    Pennsylvania Abramson Cancer Center.

    T cells are one of the
    immune system's most powerful weapons.
    They can bind and kill other cells they deem effective targets, including virus-infected cells
    .
    CAR-T cells are T cells that are redirected through genetic engineering and can effectively kill specific cell types
    .

    CAR-T therapy is created from each patient's own cells — cells are collected from the patient's blood, then engineered and multiplied in the lab, and then reinfused into the patient as a "living drug
    .
    " The first CAR-T therapy, Kymriah, was developed by June and his team at Pennsylvania Medical School and was approved
    by the Food and Drug Administration in 2017.

    In the United States, there are currently six FDA-approved CAR-T cell therapies used to treat six different cancers
    .
    These therapies have revolutionized the treatment of certain B-cell leukemias, lymphomas and other blood cancers, allowing many patients who would otherwise have no hope of long-term remission to recover
    .

    Since the beginning of CAR-T research, experts have believed that T cells can be engineered to fight many diseases
    beyond B-cell cancer.
    Dozens of research teams around the world are working on these potential new applications, including teams at the University of Pennsylvania School of Medicine and the Biotechnology Branch, which are working to develop effective treatments
    from personalized cell therapy structures developed at the University of Pennsylvania.

    June and Baker's comments are in response to the success of these efforts in the first major clinical report: a paper
    published in Nature Medicine by German researchers on the use of CAR-T therapy to treat the autoimmune disease lupus (systemic lupus erythematosus).
    The German researchers say lupus is an obvious option for CAR-T therapy because it is also driven by B cells, so experimental CAR-T treatments against it can use existing anti-B cell designs
    .
    B cells are cells that the immune system produces antibodies, and in lupus, B cells attack the patient's own organs and tissues
    .

    In the German study, five young adults did not benefit
    from standard lupus treatment.
    However, all went into remission and were able to stop taking their lupus medication within three months of a relatively small dose of CAR-T treatment, which essentially removed their existing B cells
    .
    (Cancer patients then need to be infused with purified human antibodies from healthy volunteers to maintain some immunity
    .
    ) )

    More notably, all patients remained in remission during a follow-up period of up to one year
    .
    Unlike cancer patients, lupus patients recover B cells, which are naturally replenished
    by blood stem cells in the bone marrow.

    In their comments, Baker and June note that although the results of the German study require larger studies and longer-term follow-up to confirm, they are very promising – in fact, they suggest that lupus may be a more likely target for CAR-T than
    B-cell carcinoma.

    "The number of disease-driven B cells in lupus erythematosus is much smaller," Baker said
    .
    "Therefore, effective CAR-T therapy for this autoimmune disease may require lower doses, which will greatly reduce the problem of
    immune side effects.
    "


                           

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