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Targeting public neoantigens for cancer immunotherapy.

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TLDR
The opportunities and challenges involved in the identification of suitable public neoantigen targets and the development of therapeutic agents targeting them are reviewed.
Abstract
Several current immunotherapy approaches target private neoantigens derived from mutations that are unique to individual patients’ tumors. However, immunotherapeutic agents can also be developed against public neoantigens derived from recurrent mutations in cancer driver genes. The latter approaches target proteins that are indispensable for tumor growth, and each therapeutic agent can be applied to numerous patients. Here we review the opportunities and challenges involved in the identification of suitable public neoantigen targets and the development of therapeutic agents targeting them. Zhou and colleagues discuss the opportunities and challenges in targeting public neoantigens for cancer immunotherapy.

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Cancer Therapy With TCR-Engineered T Cells: Current Strategies, Challenges, and Prospects

TL;DR: The differing mechanisms of T cell antigen recognition and signal transduction mediated through CARs and TCRs are described and both classical and emerging pre-clinical strategies for antigen-specific TCR discovery, enhancement, and validation are discussed.
Journal ArticleDOI

Neoantigens: promising targets for cancer therapy

TL;DR: Neoantigens are newly formed antigens generated by tumor cells as a result of various tumor-specific alterations, such as genomic mutation, dysregulated RNA splicing, disordered post-translational modification, and integrated viral open reading frames as mentioned in this paper .
Journal ArticleDOI

Translating recent advances in the pathogenesis of acute myeloid leukemia to the clinic

TL;DR: In this review, Bewersdorf and Abdel-Wahab discuss the development of promising new molecular targeted approaches for AML, including menin inhibition, novel IDH1/2 inhibitors, and preclinical means to target TET2, ASXL1, and RNA splicing factor mutations.
References
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Journal ArticleDOI

Evolutionary pressure against MHC class II binding cancer mutations

TL;DR: It is demonstrated that the M HC-II genotype constrains the mutational landscape during tumorigenesis in a manner complementary to MHC-I, emphasizing the central role of MHC -II presentation in tumor evolution.
Journal ArticleDOI

Developing neoantigen-targeted T cell-based treatments for solid tumors.

TL;DR: The prospect of targeting somatic tumor mutations to promote T cell destruction of cancer must contend with the biology that not all tumor-expressed ‘neoepitopes’ actually generate neoantigens that can be functionally recognized and provoke an effective immune response.
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