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- W2607114575 abstract "Dendritic cells (DCs) are equipped for sensing danger signals and capturing, processing, and presenting antigens to naive or effector cells and are critical in inducing humoral and adaptive immunity. Successful vaccinations are those that activate DCs to elicit both cellular and humoral responses, as well as long-lasting memory response against the target of interest. Recently, it has become apparent that tumor cells can provide new sources of antigens through nonsynonymous mutations or frame-shift mutations, leading to potentially hundreds of mutation-derived tumor antigens (MTAs) or neoantigens. T cells recognizing MTA have been detected in cancer patients and can even lead to tumor regression. Designing MTA-specific vaccination strategies will have to take into account the adjuvant activity of DC subsets and the best formulation to elicit an effective immune response. We discuss the potential of human DCs to prime MTA-specific responses." @default.
- W2607114575 created "2017-04-28" @default.
- W2607114575 creator A5031838474 @default.
- W2607114575 creator A5054194432 @default.
- W2607114575 creator A5055358847 @default.
- W2607114575 date "2017-03-01" @default.
- W2607114575 modified "2023-09-24" @default.
- W2607114575 title "Dendritic Cell Strategies for Eliciting Mutation-Derived Tumor Antigen Responses in Patients" @default.
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- W2607114575 doi "https://doi.org/10.1097/ppo.0000000000000251" @default.
- W2607114575 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5520811" @default.
- W2607114575 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28410301" @default.
- W2607114575 hasPublicationYear "2017" @default.
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