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Nucleophosmin is recognized by a cytotoxic T cell line derived from a rectal carcinoma patient
- Source :
- International Journal of Cancer. 127:1124-1130
- Publication Year :
- 2009
- Publisher :
- Wiley, 2009.
-
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.
- Subjects :
- Cancer Research
medicine.medical_treatment
Antigen presentation
Breast Neoplasms
Lymphocyte Activation
Peripheral blood mononuclear cell
Article
Immune system
Antigen
Antigens, Neoplasm
medicine
Humans
Cytotoxic T cell
Melanoma
Cells, Cultured
HLA-A1 Antigen
Antigen Presentation
integumentary system
Rectal Neoplasms
business.industry
Nuclear Proteins
Cancer
Immunotherapy
medicine.disease
Peptide Fragments
CTL
Oncology
Immunology
Female
Colorectal Neoplasms
business
Nucleophosmin
T-Lymphocytes, Cytotoxic
Subjects
Details
- ISSN :
- 10970215 and 00207136
- Volume :
- 127
- Database :
- OpenAIRE
- Journal :
- International Journal of Cancer
- Accession number :
- edsair.doi.dedup.....398d01631f4877e5eada23347e22e119
- Full Text :
- https://doi.org/10.1002/ijc.25133