Related Experiment Video
Updated: Sep 21, 2025

Experimental Melanoma Immunotherapy Model Using Tumor Vaccination with a Hematopoietic Cytokine
Published on: February 24, 2023
The role of neoantigens in tumor immunotherapy
Shengwen Shang1, Yongjie Zhao1, Kaiqiang Qian1
1School of Life Science, Anhui Province Key Laboratory of Translational Cancer Research, Anhui Province Key Laboratory of Immunology in Chronic Diseases, Bengbu Medical College, Bengbu, Anhui Province 233030, China.
Abstract:
Tumor neoantigens are aberrant polypeptides produced by tumor cells as a result of genomic mutations. They are also tumor-specific antigens (TSA). Neoantigens are more immunogenic than tumor-related antigens and do not induce autoimmunity. Based on the rapid development of bioinformatics and the continuous update of sequencing technology, cancer immunotherapy with tumor neoantigens has made promising breakthroughs and progress. In this review, the generation, prediction, and identification of novel antigens, as well as the individualized treatments of neoantigens, were first introduced. Secondly, the mechanism of Chimeric Antigen Receptor T-Cell Immunotherapy (CAR-T) therapy and immune checkpoint blockade therapy in the treatment of tumors were outlined, and the three treatment methods were compared. Thirdly, the application of neoantigens in CAR-T therapy and PD-1/PD-L1 blockade therapy was briefly described. The benefits of the neoantigen vaccines over common vaccines were summarized as well. Finally, the prospect of neoantigen therapy was presented.
Insights
Tumor neoantigens, unique cancer targets, are revolutionizing immunotherapy. This review explores their generation, prediction, and application in personalized cancer treatments like CAR-T cell therapy and immune checkpoint blockade.
Area of Science:
- Oncology
- Immunology
- Bioinformatics
Background:
- Tumor neoantigens are aberrant polypeptides arising from genomic mutations in cancer cells.
- Neoantigens are highly immunogenic and specific to tumors, distinguishing them from tumor-related antigens and avoiding autoimmunity.
- Advances in bioinformatics and sequencing technologies are driving progress in neoantigen-based cancer immunotherapy.
Purpose of the Study:
- To review the generation, prediction, and identification of novel tumor neoantigens.
- To outline and compare mechanisms of Chimeric Antigen Receptor T-Cell (CAR-T) Immunotherapy and immune checkpoint blockade therapy.
- To discuss the application of neoantigens in CAR-T and PD-1/PD-L1 blockade therapies and summarize the benefits of neoantigen vaccines.
Main Methods:
- Review of current literature on neoantigen generation, prediction, and identification.
- Comparative analysis of CAR-T therapy and immune checkpoint blockade mechanisms.
- Exploration of neoantigen applications in advanced cancer immunotherapies.
Main Results:
- Neoantigens offer a promising avenue for personalized cancer treatment due to their high immunogenicity and tumor specificity.
- CAR-T therapy and immune checkpoint blockade (e.g., PD-1/PD-L1) are key modalities leveraging neoantigens.
- Neoantigen vaccines demonstrate potential advantages over conventional vaccines in eliciting anti-tumor immune responses.
Conclusions:
- Neoantigen-based therapies, including personalized vaccines, CAR-T, and immune checkpoint inhibitors, represent a significant advancement in cancer immunotherapy.
- The integration of bioinformatics and sequencing is crucial for effective neoantigen discovery and application.
- Future prospects for neoantigen therapy are bright, offering hope for more effective and targeted cancer treatments.
Related Concept Videos
Tumor Immunotherapy
The Tumor Microenvironment
Cancer Vaccines
Cancer vaccines come in two categories: preventive (prophylactic) and treatment (active). Preventive vaccines, such as the Human Papillomavirus (HPV) vaccine, protect against viruses that cause certain...
Mitogens and the Cell Cycle
Targeted Cancer Therapies
There are several types of targeted therapies against...
Antigens Involved in Adaptive Immunity
Complete Antigens
Complete antigens possess both immunogenicity and...

