Nucleophosmin is recognized by a cytotoxic T cell line derived from a rectal carcinoma patient

Rolf K. Swoboda, Rajasekharan Somasundaram, Laura Caputo, Klara Berencsi, Paul Von Franzke, Douglas D. Taylor, Francesco M. Marincola, Neal J. Meropol, Elin Sigurdson, Eric Miller, Dorothee Herlyn

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Immunotherapy of colorectal carcinoma (CRC) has great promise as the presence of T lymphocytes in CRC tissues in situ is correlated with reduced recurrence and increased survival. Thus, identification of the antigens recognized by T cells of CRC patients may permit development of vaccines with potential benefit for these patients. Using expression cloning, we identified the antigen, nucleophosmin (Npm), recognized by an HLA-A1 restricted cytotoxic T lymphocyte (CTL) line derived from the peripheral blood mononuclear cells (PBMC) of a rectal cancer patient. A decamer peptide derived from the Npm sequence sensitized peptide-pulsed HLA-A1 positive cells to lysis by the CTL line. The peptide also induced proliferative and cytotoxic T lymphocytes in the PBMC of 4 of 6 CRC patients, which lysed HLA-A1 positive peptide-pulsed target cells and CRC cells endogenously expressing Npm. Overexpression of Npm by tumors of various histological types, recognition of the antigen by T cells derived from different CRC patients and association of the antigen with poor prognostic outcome make it a promising target for immunotherapeutic intervention in cancer patients.

Original languageEnglish
Pages (from-to)1124-1130
Number of pages7
JournalInternational Journal of Cancer
Volume127
Issue number5
DOIs
StatePublished - Sep 1 2010

Keywords

  • Antigen Presentation
  • Antigens, Neoplasm/immunology
  • Breast Neoplasms/immunology
  • Cells, Cultured
  • Colorectal Neoplasms/immunology
  • Female
  • HLA-A1 Antigen/immunology
  • Humans
  • Immunotherapy
  • Lymphocyte Activation
  • Melanoma/immunology
  • Nuclear Proteins/immunology
  • Nucleophosmin
  • Peptide Fragments/immunology
  • Rectal Neoplasms/immunology
  • T-Lymphocytes, Cytotoxic/immunology

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