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Related Concept Videos

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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Targeted Cancer Therapies02:57

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The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
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Related Experiment Video

Updated: Mar 5, 2026

Manufacturing Chimeric Antigen Receptor CAR T Cells for Adoptive Immunotherapy
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CAR T-Cell Therapy: Progress and Prospects.

Olivia Wilkins1, Allison M Keeler1,2, Terence R Flotte2

  • 11 Department of Biology, Wheaton College , Norton, Massachusetts.

Human Gene Therapy Methods
|March 24, 2017
PubMed
Summary

Chimeric antigen receptor (CAR) T-cell therapy, a gene therapy for cancer, uses engineered T cells for targeted immunotherapy. Advances in CAR vector design have significantly improved its efficacy and expanded its potential in treating various malignancies.

Keywords:
CAR T-cellcancer immuno therapygene therapyimmunologylentivirus

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Area of Science:

  • Immunology
  • Gene Therapy
  • Oncology

Background:

  • Chimeric antigen receptor (CAR) T-cell therapy represents a significant advancement in targeted cancer immunotherapy.
  • Early gene therapy approaches for enhancing antitumor immunity lacked specificity and efficacy compared to CAR T-cell technology.

Purpose of the Study:

  • To review the historical development and iterative improvements in CAR vector design since the 1990s.
  • To highlight emerging strategies in CAR vector engineering for future gene therapy applications.

Main Methods:

  • Review of lentivirus-mediated transduction of T cells with CARs.
  • Analysis of CAR T-cell engineering combining antibody gene sequences with T-cell receptor and activation domains.
  • Examination of CD19-directed CAR T cells for B-cell malignancies.

Main Results:

  • CAR T-cell therapy demonstrates widespread therapeutic efficacy in treating specific cancers, such as CD19-expressing B-cell malignancies.
  • The engineering of CAR T cells provides a highly specific antitumor response through a single vector approach.

Conclusions:

  • CAR T-cell therapy is a leading human gene therapy technique for cancer treatment.
  • Ongoing advancements in CAR vector design promise to broaden the scope and impact of CAR T-cell therapy in the future.