TY - JOUR
T1 - Nucleophosmin is recognized by a cytotoxic T cell line derived from a rectal carcinoma patient
AU - Swoboda, Rolf K.
AU - Somasundaram, Rajasekharan
AU - Caputo, Laura
AU - Berencsi, Klara
AU - Von Franzke, Paul
AU - Taylor, Douglas D.
AU - Marincola, Francesco M.
AU - Meropol, Neal J.
AU - Sigurdson, Elin
AU - Miller, Eric
AU - Herlyn, Dorothee
PY - 2010/9/1
Y1 - 2010/9/1
N2 - 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.
AB - 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.
KW - Antigen Presentation
KW - Antigens, Neoplasm/immunology
KW - Breast Neoplasms/immunology
KW - Cells, Cultured
KW - Colorectal Neoplasms/immunology
KW - Female
KW - HLA-A1 Antigen/immunology
KW - Humans
KW - Immunotherapy
KW - Lymphocyte Activation
KW - Melanoma/immunology
KW - Nuclear Proteins/immunology
KW - Nucleophosmin
KW - Peptide Fragments/immunology
KW - Rectal Neoplasms/immunology
KW - T-Lymphocytes, Cytotoxic/immunology
UR - http://www.scopus.com/inward/record.url?scp=77955482633&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:000280653800013&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.1002/ijc.25133
DO - 10.1002/ijc.25133
M3 - Article
C2 - 20027629
SN - 0020-7136
VL - 127
SP - 1124
EP - 1130
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 5
ER -