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Douglas J. Loftus

Researcher at National Institutes of Health

Publications -  21
Citations -  1607

Douglas J. Loftus is an academic researcher from National Institutes of Health. The author has contributed to research in topics: T cell & Antigen. The author has an hindex of 14, co-authored 21 publications receiving 1567 citations.

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A mutated beta-catenin gene encodes a melanoma-specific antigen recognized by tumor infiltrating lymphocytes.

TL;DR: The isolation of a cDNA clone encoding beta- catenin was reported, which was shown to be recognized by the tumor-infiltrating lymphocyte (TIL) 1290, a HLA-A24 restricted melanoma-specific CTL line from patient 888, indicating that this represented a unique mutation in this patient's melanoma.
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Identification of epitope mimics recognized by CTL reactive to the melanoma/melanocyte-derived peptide MART-1((27-35))

TL;DR: In this paper, a protein database search for potential MART-1 epitope mimics was done using criteria developed from analyses of effector recognition of singly substituted peptide analogues of MART27-35.
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Report of immune monitoring of prostate cancer patients undergoing T-cell therapy using dendritic cells pulsed with HLA-A2-specific peptides from prostate-specific membrane antigen (PSMA)

TL;DR: The program for the immune monitoring of phase II participants given dendritic cell (DC)/prostate‐specific membrane antigen (PSMA)‐based immunotherapy, and some initial findings are presented.
Journal Article

A Superagonist Variant of Peptide MART1/Melan A27–35 Elicits Anti-Melanoma CD8+ T Cells with Enhanced Functional Characteristics: Implication for More Effective Immunotherapy

TL;DR: In this article, a singly substituted peptide derived from the epitope MART127-35 and containing a Leu in position 1 (LAGIGILTV; 1L) behaves as a superagonist by in vitro inducing specific T cells with enhanced immunological functions.
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The ability of variant peptides to reverse the nonresponsiveness of T lymphocytes to the wild-type sequence p53(264-272) epitope.

TL;DR: The use of variant peptides of the wt p53264–272 epitope represents a promising approach to overcoming the nonresponsiveness of certain cancer patients to this self epitope, thereby enhancing its potential use in tumor vaccines for appropriately selected cancer patients.