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NY-ESO-1 antigen: A promising frontier in cancer immunotherapy
Alaa Alsalloum1,2, Julia A Shevchenko1, Sergey Sennikov1,3
1Laboratory of Molecular Immunology, Federal State Budgetary Scientific Institution Research Institute of Fundamental and Clinical Immunology, Novosibirsk, Russia.
Abstract:
Significant strides have been made in identifying tumour-associated antigens over the past decade, revealing unique epitopes crucial for targeted cancer therapy. Among these, the New York esophageal squamous cell carcinoma (NY-ESO-1) protein, a cancer/testis antigen, stands out. This protein is presented on the cell surface by major histocompatibility complex class I molecules and exhibits restricted expression in germline cells and various cancers, marking it as an immune-privileged site. Remarkably, NY-ESO-1 serves a dual role as both a tumour-associated antigen and its own adjuvant, implying a potential function as a damage-associated molecular pattern. It elicits strong humoural immune responses, with specific antibody frequencies significantly correlating with disease progression. These characteristics make NY-ESO-1 an appealing candidate for developing effective and specific immunotherapy, particularly for advanced stages of disease. In this review, we provide a comprehensive overview of NY-ESO-1 as an immunogenic tumour antigen. We then explore the diverse strategies for targeting NY-ESO-1, including cancer vaccination with peptides, proteins, DNA, mRNA, bacterial vectors, viral vectors, dendritic cells and artificial adjuvant vector cells, while considering the benefits and drawbacks of each strategy. Additionally, we offer an in-depth analysis of adoptive T-cell therapies, highlighting innovative techniques such as next-generation NY-ESO-1 T-cell products and the integration with lymph node-targeted vaccines to address challenges and enhance therapeutic efficacy. Overall, this comprehensive review sheds light on the evolving landscape of NY-ESO-1 targeting and its potential implications for cancer treatment, opening avenues for future tailored directions in NY-ESO-1-specific immunotherapy. HIGHLIGHTS: Endogenous immune response: NY-ESO-1 exhibited high immunogenicity, activating endogenous dendritic cells, T cells and B cells. NY-ESO-1-based cancer vaccines: NY-ESO-1 vaccines using protein/peptide, RNA/DNA, microbial vectors and artificial adjuvant vector cells have shown promise in enhancing immune responses against tumours. NY-ESO-1-specific T-cell receptor-engineered cells: NY-ESO-1-targeted T cells, along with ongoing innovations in engineered natural killer cells and other cell therapies, have improved the efficacy of immunotherapy.
Insights
The New York esophageal squamous cell carcinoma-1 (NY-ESO-1) protein is a promising target for cancer immunotherapy due to its immunogenicity. Various NY-ESO-1 targeting strategies, including vaccines and T-cell therapies, are being developed to enhance cancer treatment efficacy.
Area of Science:
- Immunology
- Oncology
- Biochemistry
Background:
- Tumour-associated antigens (TAAs) are critical for targeted cancer therapy.
- New York esophageal squamous cell carcinoma-1 (NY-ESO-1) is a cancer/testis antigen with restricted expression in cancer cells and germline cells.
- NY-ESO-1 acts as both a TAA and an endogenous adjuvant, eliciting strong immune responses.
Purpose of the Study:
- To provide a comprehensive review of NY-ESO-1 as an immunogenic tumour antigen.
- To explore diverse strategies for targeting NY-ESO-1 in cancer immunotherapy.
- To analyze adoptive T-cell therapies and innovative techniques for enhanced efficacy.
Main Methods:
- Review of existing literature on NY-ESO-1 immunogenicity and targeting strategies.
- Analysis of various cancer vaccination approaches (peptide, protein, DNA, mRNA, vectors, dendritic cells, artificial adjuvant vector cells).
- In-depth examination of adoptive T-cell therapies, including next-generation products and lymph node-targeted vaccines.
Main Results:
- NY-ESO-1 demonstrates high immunogenicity, activating endogenous dendritic cells, T cells, and B cells.
- NY-ESO-1-based vaccines (protein/peptide, RNA/DNA, microbial vectors, artificial adjuvant vector cells) show promise in boosting anti-tumour immune responses.
- NY-ESO-1-targeted T-cell therapies, including engineered T cells and NK cells, have improved immunotherapy efficacy.
Conclusions:
- NY-ESO-1 is a highly immunogenic target with significant potential for cancer immunotherapy.
- Diverse vaccination and adoptive T-cell strategies are effective in harnessing the immune system against NY-ESO-1-expressing tumours.
- Ongoing innovations in NY-ESO-1-specific immunotherapy offer promising avenues for future cancer treatment.
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