Targeting Cancer Pathways: Understanding Immune Checkpoints

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  • เผยแพร่เมื่อ 28 พ.ค. 2024
  • Participating Experts: James Allison, PhD, (MD Anderson), Gordon J. Freeman, PhD, (Dana-Farber), and Philip J. Gotwals, PhD) (Novartis)
    ⬇️ Expand “Show More” to view abstract and table of contents
    Explore/download the signaling pathway diagram for Immune Checkpoint Signaling in the Tumor Microenvironment
    cst-science.com/2q5jtr
    Tumors manipulate their microenvironment in order to evade surveillance and elimination by the immune system. To do this, cancer cells can co-opt inhibitory ligands and their receptors that regulate T cell effector function. Intervention targeting these pathways, known as immune checkpoint therapies, have been the subject of intense translational research and clinical development. This webinar explores how tumors exploit immune modulatory mechanisms to generate and thrive in their own immunosuppressive microenvironment, and how these mechanisms can be targeted to develop better therapeutic options. Topics covered include:
    • A historical overview of immune checkpoint research and examination of the effect of mutational load on clinical response.
    • How PD-1 immunotherapy stops certain cancers from turning off the anticancer immune response.
    • Discuss general therapeutic approaches to activating the immune system to treat cancer.
    Table of Contents
    0:00 Welcome and overview
    2:46 James Allison speaker profile
    3:35 Immune checkpoint blockade in cancer therapy: New inishgts, opportunities, and prospects for cures
    4:18 FDA approval of antibodies targeting immune chckpoints
    6:10 Dynamic integration of TCR and costimulatory signals
    7:49 CTLA-4 blockade enhances tumor-specific immune responses
    9:04 Anti-CTLA-4 induces regression of transplantable colon carcinoma
    10:29 Anti-CTLA-4/GVAX therapy activates the tumor vasculature and increases infiltration of tumors by CD4 and CD8 effector cells
    12:10 The longest survivor on ipilimumab?
    13:12 Ipilimumab in metastatic melanoma: pooled OS analysis including EAP data
    14:16 Anti-CTLA-4, Anti-PD-1 comparison
    15:13 Clinical activity: Ipilimumba and Nivolumab combination therapy
    16:05 Mutational load varies in human cancers
    17:12 Potential characteristics of immunogenic and nonimmunogenic tumors
    17:21 Infiltrates in prostate cancer pre and post anti-CTLA4 therapy
    18:09 Improving survival with immunotherapy
    18:55 Gordon Freeman speaker profile
    19:34 Immunology has offered hope for 100 years
    20:43 T cells need antigen recognition + co-stimulatory signals; PD-1 pathway inhibits T cell activation
    23:34 PD-1 or PD-L1 blockade allows reactivation of anti-tumor T cell responses
    24:29 Phase I clinical trial of nivolumab - kidney cancer cohort
    25:45 PD-1 cancer immunotherapy tolerance, safety, adverse events
    27:25 PD-1 is better than chemotherapy for melanoma; overall response rates
    28:39 The immune system recognizes protein coding changes in the tumor cell called neoantigens
    30:04 Durable responses to immunotherapy compared to Braf tyrosine kinase inhibition
    32:32 Understanding immunology and genetics has identified groups that respond well to PD-1 and PD-L1 therapy
    33:40 Exhausted tumor infiltrating lymphocytes express multiple immunoinhibitory receptors
    35:47 Future directions
    38:08 Philip Gotwals speaker profile
    38:53 Therapeutic targeting of the immune system to treat cancer
    40:45 Targeted and immune-modulatory therapeutics are being combined in melanoma
    43:55 A wealth of important targets for T cell modulation
    44:37 LAG-3 as a target for therapeutic approaches
    46:06 Chimeric Antigen Receptor (CAR-T) engineering
    47:22 CTL019 therapy: overview of recent clinical data in hematologic malignancies
    48:47 Targeting the immunosuppressive tumor microenvironment: IDO
    50:50 Talimogene (T-VEC) study
    51:29 Local delivery may lead to systemic therapy: The abscopal effect
    52:28 STING agonist for enhancing immune reponse to tumors
    53:44 Towards complete, durable remission for cancer patients
    54:32 Question and Answer
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    #Antibody #CSTWebinar #immunotherap
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ความคิดเห็น • 11

  • @bruceleroybell8139
    @bruceleroybell8139 4 ปีที่แล้ว +5

    Thank you for sharing this valuable and exciting information as a cancer patient I feel blessed to be living in these promising cancer treatment times.

  • @smca7271
    @smca7271 4 ปีที่แล้ว +6

    its working for me...stage 4 melanoma head and lung...good info , thanks

  • @NikhilMandrekar
    @NikhilMandrekar 4 ปีที่แล้ว +1

    At 48:00 "have not seen the impressive efficacy results (in GBM) that we've seen in hematological tumors" - why?

  • @tbbionkoloji2755
    @tbbionkoloji2755 4 ปีที่แล้ว +1

    thanks for this webinar

  • @swisschaesar2701
    @swisschaesar2701 2 ปีที่แล้ว +3

    Gordon Freeman

    • @zalxder
      @zalxder ปีที่แล้ว

      better grab that HEV suit again

  • @mikedaniels3009
    @mikedaniels3009 3 ปีที่แล้ว +1

    Looks so bloody simple on paper. But HOW is it done in real, when you can't see those molecules?

    • @aidan4943
      @aidan4943 ปีที่แล้ว

      Science 🥸🥽🧪

  • @oscarcordero2351
    @oscarcordero2351 4 ปีที่แล้ว

    My dad diagnosed liver cancer and he has spread other places in his body . He’s on stage 4 . Will this work on it ? How promising this treatment and this will cure cancer ?

    • @cellsignaldotcom
      @cellsignaldotcom  4 ปีที่แล้ว +2

      Hi Oscar, I'm sorry to hear about your dad's diagnosis. As you may have read elsewhere, different types of cancer are quite different from each other, and immune checkpoint therapies are very narrow in the types of cancers they target. Our company makes research tools for the scientists who are trying to better understand the molecular mechanisms of cancer, but we don't make therapeutic antibodies. So I would encourage you to discuss with your physicians and oncologist.

    • @mikedaniels3009
      @mikedaniels3009 3 ปีที่แล้ว

      My heart goes out to your father, Oscar.