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Oncolytic Viruses Trigger Hyperacute Cancer Rejection

  • Oncolytic viruses are being explored as a novel approach to induce hyperacute rejection against tumors, revolutionizing cancer therapy.
  • This strategy aims to utilize viruses to trigger rapid and potent immune responses, leading to the destruction of cancer cells with exceptional speed and specificity.
  • The approach involves manipulating the immune system through oncolytic viruses, which selectively infect and destroy cancer cells while sparing normal tissue.
  • By inducing hyperacute rejection, researchers aim to mimic swift rejection mechanisms observed in organ transplantation immunology to achieve rapid tumor clearance.
  • Engineering oncolytic viruses involves balancing viral replication, tumor specificity, and immunostimulatory capacity to provoke acute immune responses.
  • The viral vectors serve as cytotoxic agents and immune stimulants, triggering complement activation, antibody-dependent cellular cytotoxicity, and recruitment of cytotoxic lymphocytes.
  • Safety measures include tumor-selective promoters, localized viral administration, and safety switches to mitigate risks of normal tissue damage or off-target effects.
  • Combining oncolytic viruses with immune checkpoint inhibitors or other therapies could enhance therapeutic outcomes by synergizing rapid tumor debulking with immune-based interventions.
  • The induction of hyperacute rejection involves complex immune crosstalk, including the upregulation of pro-inflammatory signals and enhanced antigen presentation.
  • Long-lasting anti-tumor immunity is essential for preventing cancer recurrence, with oncolytic viruses promoting the development of durable tumor-specific memory T cells and B cells.

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