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Cleavage and polyadenylation specificity factor (CPSF)-derived peptides can induce HLA-A2-restricted and tumor-specific CTLs in the majority of gastrointestinal cancer patients.

Abstract
To identify CTL-directed antigens in gastrointestinal cancer, we have investigated antigens recognized by the HLA-A2-restricted CTL line established from T cells infiltrating into colon cancer and report herein cleavage and polyadenylation specificity factor (CPSF) as a potent antigen holding peptides capable of inducing CTLs. Five peptides at amino acid positions 250-258, 392-400, 534-542, 1296-1304 and 1359-1368 of CPSF, which were recognized by the CTL line, were found to have the ability to induce HLA-A2-restricted and tumor-specific CTLs in peripheral blood mononuclear cells of the majority (69%, 11/16) of gastrointestinal cancer patients with different HLA-A2 subtypes. Thus, these peptides might be appropriate molecules for use in the peptide-based specific immunotherapy of HLA-A2(+) patients with gastrointestinal cancers.
AuthorsYoshiaki Maeda, Masaaki Ito, Nanae Harashima, Tetsuya Nakatsura, Naoya Hida, Nobue Imai, Yuuji Sato, Shigeki Shichijo, Satoru Todo, Kyogo Itoh
JournalInternational journal of cancer (Int J Cancer) Vol. 99 Issue 3 Pg. 409-17 (May 20 2002) ISSN: 0020-7136 [Print] United States
PMID11992410 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2002 Wiley-Liss, Inc.
Chemical References
  • Cancer Vaccines
  • DNA, Complementary
  • HLA-A2 Antigen
  • Interleukin-2
  • Peptides
  • RNA-Binding Proteins
  • mRNA Cleavage and Polyadenylation Factors
  • Interferon-gamma
  • Sepharose
Topics
  • Amino Acid Sequence
  • Blotting, Northern
  • Cancer Vaccines
  • DNA, Complementary (metabolism)
  • Dose-Response Relationship, Drug
  • Gastrointestinal Neoplasms (metabolism)
  • HLA-A2 Antigen (metabolism)
  • Humans
  • Immunotherapy (methods)
  • Interferon-gamma (metabolism)
  • Interleukin-2 (metabolism)
  • Molecular Sequence Data
  • Peptides (chemistry)
  • RNA-Binding Proteins (biosynthesis)
  • Sepharose (metabolism)
  • T-Lymphocytes, Cytotoxic (metabolism)
  • Tumor Cells, Cultured
  • mRNA Cleavage and Polyadenylation Factors

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