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Amy Hobeika

Researcher at Duke University

Publications -  99
Citations -  4612

Amy Hobeika is an academic researcher from Duke University. The author has contributed to research in topics: Immunotherapy & Antigen. The author has an hindex of 33, co-authored 95 publications receiving 4087 citations. Previous affiliations of Amy Hobeika include Durham University & University of Florida.

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A phase I study of dexosome immunotherapy in patients with advanced non-small cell lung cancer

TL;DR: Production of the DEX vaccine was feasible and DEX therapy was well tolerated in patients with advanced NSCLC, and some patients experienced long term stability of disease and activation of immune effectors.
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Depletion of human regulatory T cells specifically enhances antigen-specific immune responses to cancer vaccines

TL;DR: The results indicate the potential for combining Treg-cell depletion with anticancer vaccines to enhance tumor antigen-specific immune responses and the need to explore dose and schedule of Treg depletion strategies in optimizing vaccine efforts.
Journal Article

Assays for monitoring cellular immune responses to active immunotherapy of cancer.

TL;DR: This review evaluates the currently used in vivo and in vitro methods of assessing T-cell number and function, including delayed-type hypersensitivity, tetramer analysis, ELISPOT, flow cytometry-based analysis of cytokine expression, and PCR-based detection of T- cell receptor gene usage or cytokine production.
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Increasing vaccine potency through exosome antigen targeting

TL;DR: It is demonstrated that the mode of secretion and trafficking can influence the immunogenicity of different human TAAs, and may explain the lack of immunogenicicity of non-mutated TAAs found in cancer patients, and suggested that exosomal targeting could enhance future anti-tumor vaccination protocols.
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Immunotherapy with Autologous, Human Dendritic Cells Transfected with Carcinoembryonic Antigen mRNA

TL;DR: It is feasible and safe to administer mRNA-loaded DC loaded with CEA mRNA to patients with advanced malignancies, and evidence of an immunologic response was demonstrated in biopsies of DC injection sites and peripheral blood of selected patients.