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Albert B. DeLeo

Researcher at University of Pittsburgh

Publications -  94
Citations -  8248

Albert B. DeLeo is an academic researcher from University of Pittsburgh. The author has contributed to research in topics: Antigen & Cytotoxic T cell. The author has an hindex of 40, co-authored 92 publications receiving 7965 citations.

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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.
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Detection of a transformation-related antigen in chemically induced sarcomas and other transformed cells of the mouse.

TL;DR: In this article, a protein with an apparent molecular weight of 53,000 in extracts of transformed BALB/c cells was detected in normal adult mouse fibroblasts, lymphoid cells, or hematopoietic cells or in mouse embryo cells.
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Tumor rejection antigens of chemically induced sarcomas of inbred mice.

TL;DR: In this paper, isolated membrane and cytosol fractions from two antigenically distinct BALB/c sarcomas, Meth A and CMS5, have TRA activity, and biochemical characterization of the active components from the cytosolic and plasma membranes of these two tumors identified a glycoprotein of Mr 96,000.
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Monoclonal antibody to a triggering structure expressed on rat natural killer cells and adherent lymphokine-activated killer cells.

TL;DR: An mAb is described that recognizes a triggering structure that is expressed on rat LGL/NK cells and A-LAK cells and is a useful tool for the study of NK cell ontogeny and function, and the development of cells with LAK activity from the NK cell compartment.