Neoantigen vaccine: an emerging tumor immunotherapy
By M. Peng, Yongzhen Mo, Yian Wang, Pan Wu, Yijie Zhang, F. Xiong, Can Guo, Xu Wu, Yong Li, Xiaoling Li and 3 more. Molecular Cancer, 2019
610 citations recorded by the source corpus.
Genetic instability of tumor cells often leads to the occurrence of a large number of mutations, and expression of non-synonymous mutations can produce tumor-specific antigens called neoantigens. Neoantigens are highly immunogenic as they are not expressed in normal tissues. They can activate CD4+ and CD8+ T cells to generate immune response and have the potential to become new targets of tumor immunotherapy. The development of bioinformatics technology has accelerated the identification of neoantigens. The combination of different algorithms to identify and predict the affinity of neoantigens to major histocompatibility complexes (MHCs) or the immunogenicity of neoantigens is mainly based on the whole-exome sequencing technology. Tumor vaccines targeting neoantigens mainly include nucleic acid, dendritic cell (DC)-based, tumor cell, and synthetic long peptide (SLP) vaccines. The combination with immune checkpoint inhibition therapy or radiotherapy and chemotherapy might achieve better therapeutic effects. Currently, several clinical trials have demonstrated the safety and efficacy of these vaccines. Further development of sequencing technologies and bioinformatics algorithms, as well as an improvement in our understanding of the mechanisms underlying tumor development, will expand the application of neoantigen vaccines in the future.
Subfields: Immunology, Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/9445421ac6f7def563c16edd140555f3c0d547fb
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Citations in the corpus
- Extracellular Matrix in the Tumor Microenvironment and Its Impact on Cancer Therapy (2020, background): “In addition, the application of antitumor vaccination approaches have made considerable progress in recent years (reviewed in Rammensee and Singh-Jasuja, 2013; Accolla et al., 2019; Peng et al., 2019).”