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Related Concept Videos

Cytotoxic T Cells-mediated Immune Response01:27

Cytotoxic T Cells-mediated Immune Response

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Cytotoxic T cells are a vital component of the immune system. They have the remarkable ability to identify and target antigens on infected or abnormal cells. These antigens often originate from intracellular pathogens such as viruses or abnormal proteins cancer cells produce.
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
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Overview of Cell Death01:30

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Cell death is an essential process where the body gets rid of old or damaged cells. Cell proliferation and death need to be balanced, as an imbalance between the two may lead to cancer or autoimmune diseases.
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the...
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The Extrinsic Apoptotic Pathway01:17

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The extrinsic apoptotic pathway is initiated when extracellular death-inducing signals, such as specific cytokines, activate the death receptors expressed on the cell surface. The immune cells involved in this pathway are natural killer cells (NK cells) and cytotoxic T-lymphocytes. NK cells are critical in innate immune response, while cytotoxic T-lymphocytes are associated with adaptive immune response. These cells recognize specific receptors expressed on the altered cells and activate...
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Biological Effects of Radiation02:59

Biological Effects of Radiation

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All radioactive nuclides emit high-energy particles or electromagnetic waves. When this radiation encounters living cells, it can cause heating, break chemical bonds, or ionize molecules. The most serious biological damage results when these radioactive emissions fragment or ionize molecules. For example, α and β particles emitted from nuclear decay reactions possess much higher energies than ordinary chemical bond energies. When these particles strike and penetrate matter, they...
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Mutations01:35

Mutations

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Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations can be characterized in a number of different ways: whether and how they alter the amino acid sequence of the protein, whether they occur over a small or large area of DNA, and whether they occur in somatic cells or germline cells.
Chromosomal Alterations Are Large-Scale Mutations
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Cells of the Innate Immune Response01:28

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The innate immune response is an immediate and non-specific response against pathogens, acting swiftly to prevent the spread of infections. The primary cells involved in this response are phagocytes and natural killer (NK) cells.
Phagocytes
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Updated: Oct 21, 2025

One-step Protocol for Evaluation of the Mode of Radiation-induced Clonogenic Cell Death by Fluorescence Microscopy
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Immunogenic Cell Death Induction by Ionizing Radiation.

Mengqin Zhu1,2, Mengdie Yang1,2, Jiajia Zhang1,2

  • 1Department of Nuclear Medicine, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.

Frontiers in Immunology
|September 7, 2021
PubMed
Summary
This summary is machine-generated.

Immunogenic cell death (ICD) is a regulated cell death process that enhances antitumor immunity. Ionizing radiation (IR) can induce ICD, and strategies exist to boost this response for cancer therapy.

Keywords:
chemotherapydamage-associated molecular patternsferroptosishyperthermiaimmunogenic cell deathionizing radiationnanoparticlesnecroptosis

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Area of Science:

  • Oncology
  • Immunology
  • Radiation Biology

Background:

  • Immunogenic cell death (ICD) is a regulated cell death (RCD) process that elicits antitumor immune responses through the release of damage-associated molecular patterns (DAMPs).
  • Ionizing radiation (IR) is known to induce cell death, with emerging evidence suggesting it can trigger ICD, influenced by radiation parameters like dose and fractionation.
  • Current evidence for IR-induced ICD is primarily from in vitro and murine models, with limited clinical validation.

Purpose of the Study:

  • To review the molecular mechanisms underlying ICD.
  • To explore factors associated with IR that promote ICD.
  • To summarize clinical evidence and strategies for enhancing IR-induced ICD to improve antitumor immunity.

Main Methods:

  • Literature review focusing on molecular mechanisms of ICD.
  • Analysis of studies investigating IR-induced ICD in vitro and in vivo.
  • Examination of synergistic strategies combining IR with other therapies (e.g., hyperthermia, nanoparticles, chemotherapy).

Main Results:

  • IR can induce ICD, with its efficacy dependent on irradiation parameters.
  • Various DAMPs (HMGB1, CRT, ATP, HSPs) are key mediators of IR-induced ICD.
  • Combinatorial approaches show promise in enhancing IR-induced ICD and antitumor immune responses.

Conclusions:

  • IR is a potential inducer of ICD, contributing to antitumor immunity.
  • Further clinical research is needed to validate IR-induced ICD.
  • Strategies combining IR with other modalities can significantly boost ICD and enhance cancer immunotherapy.