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Cynthia M. Fehres

Researcher at VU University Medical Center

Publications -  19
Citations -  692

Cynthia M. Fehres is an academic researcher from VU University Medical Center. The author has contributed to research in topics: Antigen & Cytotoxic T cell. The author has an hindex of 11, co-authored 14 publications receiving 587 citations. Previous affiliations of Cynthia M. Fehres include Vanderbilt University Medical Center.

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Glycan-modified liposomes boost CD4+ and CD8+ T-cell responses by targeting DC-SIGN on dendritic cells

TL;DR: The potency of a glycoliposome-based vaccine targeting DC-SIGN for CD4(+) and CD8(+) effector T-cell activation is demonstrated and this approach may offer improved options for treatment of cancer patients and opens the way to in situ DC-targeted vaccination.
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Understanding the biology of antigen cross-presentation for the design of vaccines against cancer

TL;DR: In this article, the authors summarize new insights in factors that affect antigen cross-presentation of human dendritic cells and discuss the possibilities to exploit antigen crosspresentation for immunotherapy against cancer.
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Glycan-based DC-SIGN targeting vaccines to enhance antigen cross-presentation.

TL;DR: The capacity of glycan-based vaccines to enhance antigen-specific CD4(+) and CD8(+) T cell responses in human skin and mouse model systems is discussed.
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Cross-presentation through langerin and DC-SIGN targeting requires different formulations of glycan-modified antigens

TL;DR: It is demonstrated that langerin and DC-SIGN have different size requirements for antigen uptake, although using glycans remains an interesting option in the design of anti-cancer vaccines targeting multiple CLRs, aspects such as molecule size and conformation need be taken in consideration.
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Topical rather than intradermal application of the TLR7 ligand imiquimod leads to human dermal dendritic cell maturation and CD8+ T‐cell cross‐priming

TL;DR: Topical application of Aldara skin cream significantly enhanced DC migration as compared with that resulting from intradermal injection of the TLR7/8 ligand R848 or the soluble form of imiquimod, and Aldara‐treated DCs showed highest levels of the costimulatory molecules CD86, CD83, CD40, and CD70.