Abstract
Chronic myelogenous leukemia (CML) 28 is a broadly immunogenic antigen that can have an antileukemia effect. We adopted the SYFPEITHI database to predict human leukocyte antigen-A2 restricted CML28 peptide. We designed artificial antigen-presenting cells (aAPCs) by coating micro beads with human leukocyte antigen-A2-immunoglobulin dimer and CD28-specific antibody. We used the selected peptides-pulsed aAPCs to induce cytotoxic T lymphocytes (CTLs), to choose the CML28 peptide, which was best for inducing CTLs. The result showed that the peptides-pulsed aAPCs could induce CTLs and that the peptide VLTFALDSV was the best choice for significantly inducing specific CTLs.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Antigen-Presenting Cells / immunology*
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Antigens, Neoplasm / immunology*
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Antigens, Surface / immunology*
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CD8-Positive T-Lymphocytes / cytology
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CD8-Positive T-Lymphocytes / immunology
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Cell Proliferation
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Cells, Cultured
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Coculture Techniques
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Epitopes / immunology
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Exoribonucleases / immunology*
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Exosome Multienzyme Ribonuclease Complex
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HLA-A2 Antigen / chemistry
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HLA-A2 Antigen / immunology*
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Humans
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RNA-Binding Proteins
Substances
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Antigens, Neoplasm
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Antigens, Surface
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EXOSC5 protein, human
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Epitopes
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HLA-A2 Antigen
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RNA-Binding Proteins
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Exoribonucleases
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Exosome Multienzyme Ribonuclease Complex