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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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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.
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Related Experiment Video

Updated: Jun 18, 2025

A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy
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Toward a comprehensive solution for treating solid tumors using T-cell receptor therapy: A review.

Peiwen Ma1, Yale Jiang1, Guo Zhao1

  • 1Clinical Trial Center, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.

European Journal of Cancer (Oxford, England : 1990)
|July 27, 2024
PubMed
Summary

T-cell receptor therapy (TCR-T) shows promise for solid tumors like melanoma. This review details TCR-T development considerations, focusing on avidity, antigen selection, and future directions for improved efficacy.

Keywords:
AffinityImmunotherapyT cell receptorTCR-T therapy

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Area of Science:

  • Immunotherapy
  • Oncology
  • Cellular Therapy

Background:

  • T-cell receptor therapy (TCR-T) has shown significant efficacy, durability, and safety in specific solid tumors.
  • Existing research highlights successes in human papillomavirus-related tumors, synovial sarcoma, and melanoma.

Purpose of the Study:

  • To provide comprehensive considerations for developing TCR-T therapies specifically for solid tumors.
  • To review current clinical applications, advantages, and key parameters influencing TCR-T efficacy and safety in solid tumors.

Main Methods:

  • Review of current literature on TCR-T clinical applications and modalities.
  • Exploration of efficacy/safety parameters: avidity, pharmacokinetics/pharmacodynamics, and indications.
  • Investigation of factors influencing T-cell receptor avidity: antigen selection, acquisition, optimization, and co-receptor engagement.
  • Analysis of tumor antigen expression using RNA-seq datasets for broader solid tumor coverage.

Main Results:

  • TCR-T therapy demonstrates potential benefits in specific solid tumor types.
  • Avidity, pharmacokinetics/pharmacodynamics, and antigen selection are critical for TCR-T success in solid tumors.
  • RNA-seq data analysis suggests opportunities for expanding TCR-T coverage across various solid tumors.

Conclusions:

  • Careful consideration of antigen selection, T-cell receptor avidity, and pharmacokinetic/pharmacodynamic profiles is essential for successful TCR-T development in solid tumors.
  • Further research into optimizing TCR-T strategies and exploring novel tumor antigens is crucial for advancing this therapy.
  • TCR-T holds significant promise for treating a wider range of solid tumors with improved outcomes.