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Related Concept Videos

Forced Transdifferentiation01:28

Forced Transdifferentiation

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Transdifferentiation, also known as lineage reprogramming, was first discovered by Selman and Kafatos in 1974 in silkmoths. They observed that the moths’ cuticle-producing cells transformed into salt-producing cells. Many such cases of natural transdifferentiation occur in organisms. In humans, pancreatic alpha cells can become beta cells. In newts, the loss of the eye’s lens causes the pigmented epithelial cells to transdifferentiate into the lens cells.
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Tumor Immunotherapy01:27

Tumor Immunotherapy

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Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
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Tissue Transplantation01:24

Tissue Transplantation

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Tissue transplantation is a significant medical procedure involving the transfer of cells, tissues, or organs from a donor to a recipient, with the primary aim of restoring lost functions. This procedure is crucial in treating a broad spectrum of diseases, including kidney diseases, liver failure, heart disease, and certain types of cancers.
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Bone Marrow Sampling and Transplants01:22

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Bone marrow transplant is a potential cure for several diseases, including cancer and specific genetic disorders. Notably, this procedure is applicable for patients suffering from aplastic anemia, certain types of leukemia, severe combined immunodeficiency disease (SCID), Hodgkin's disease, non-Hodgkin's lymphoma, multiple myeloma, thalassemia, sickle-cell disease, and certain cancers.
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iPS Cell Differentiation01:22

iPS Cell Differentiation

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The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.
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Cell-mediated Immune Responses01:40

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Updated: Jul 18, 2025

Generation of CAR T Cells for Adoptive Therapy in the Context of Glioblastoma Standard of Care
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Challenges and new technologies in adoptive cell therapy.

Pengchao Zhang1,2, Guizhong Zhang3, Xiaochun Wan4

  • 1Center for Protein and Cell-based Drugs, Institute of Biomedicine and Biotechnology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, 1068 Xueyuan Avenue, Nanshan District, Shenzhen, 518055, People's Republic of China.

Journal of Hematology & Oncology
|August 18, 2023
PubMed
Summary

Chimeric antigen receptor (CAR)-T cell therapy shows promise for blood cancers but has limitations. New CAR-engineered immune cells like CAR-NK and CAR-macrophages offer potential solutions for improved cancer immunotherapy.

Keywords:
Adoptive cell therapyCancer therapyChimeric antigen receptorGene transductionT cell receptor

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Area of Science:

  • Immunology
  • Oncology
  • Biotechnology

Background:

  • Adoptive cell therapies (ACTs) have evolved significantly, with chimeric antigen receptor (CAR)-T cell therapy revolutionizing hematologic malignancy treatment.
  • Despite successes, CAR-T cell therapy faces challenges in practicality and toxicity in both autologous and allogeneic applications.

Purpose of the Study:

  • To review the development, advantages, and challenges of novel CAR-engineered immune cell therapies beyond CAR-T cells.
  • To discuss gene transduction strategies in immunotherapy and explore future directions for cancer treatment.

Main Methods:

  • Review of existing literature on adoptive cell therapies, focusing on CAR engineering.
  • Analysis of emerging CAR-based cell therapies including CAR-NK, CAR-macrophage, CAR-γδT, and CAR-NKT cells.
  • Discussion of gene transduction techniques and strategies for creating positive feedback immune circuits.

Main Results:

  • CAR engineering has been extended to various immune cells, leading to CAR-NK, CAR-macrophage, CAR-γδT, and CAR-NKT therapies.
  • Gene transduction strategies are crucial for effective immune cell engineering in immunotherapy.
  • Positive feedback immune circuits may overcome limitations of single-cell type ACTs.

Conclusions:

  • Novel CAR-engineered immune cells offer potential to overcome CAR-T cell therapy limitations.
  • Advanced gene transduction and the development of immune circuits are key for future cancer immunotherapy.
  • Expanding CAR technology to diverse immune cells holds significant therapeutic promise.