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Walter J. Storkus

Researcher at University of Pittsburgh

Publications -  285
Citations -  19025

Walter J. Storkus is an academic researcher from University of Pittsburgh. The author has contributed to research in topics: Immune system & Cytotoxic T cell. The author has an hindex of 67, co-authored 270 publications receiving 18010 citations. Previous affiliations of Walter J. Storkus include Duke University & University of Regensburg.

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Bone marrow-derived dendritic cells pulsed with synthetic tumour peptides elicit protective and therapeutic antitumour immunity

TL;DR: Treatment of animals bearing established macroscopic tumours with tumour peptide-pulsed dendritic cells resulted in sustained tumour regression and tumour-free status in more than 80% of cases, and support the clinical use of tumour Peptide-Pulsed Dendritic Cells as components in developing effective cancer vaccines and therapies.
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Therapy of murine tumors with tumor peptide-pulsed dendritic cells: dependence on T cells, B7 costimulation, and T helper cell 1-associated cytokines.

TL;DR: Using the immunogenic C3 (H-2b) tumor model in B6 mice, tumor peptide-pulsed DC therapy resulted in the erradication of established d14 tumors and long-term survival in 100% of treated animals.
Journal Article

Recombinant IL-12 administration induces tumor regression in association with IFN-gamma production.

TL;DR: IL-12 is an effective and minimally toxic antitumor agent in murine tumor models and leads to an immune-mediated rejection involving, at least in part, IFN-gamma, CD4+, and CD8+ cells.
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Peptide-pulsed dendritic cells induce antigen-specific CTL-mediated protective tumor immunity.

TL;DR: It is shown that major histocompatibility complex class I- presented peptide antigen pulsed onto dendritic APCs induces protective immunity to lethal challenge by a tumor transfected with the antigen gene.
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α-Type-1 Polarized Dendritic Cells A Novel Immunization Tool with Optimized CTL-inducing Activity

TL;DR: Serum-free generation of alphaDC1 allows, for the first time, the clinical application of DCs that combine the key three features important for their efficacy as anticancer vaccines.