Identification of an HLA-A*0201 restricted Bcl2-derived epitope expressed on tumors.
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Identification of an HLA-A*0201 restricted Bcl2-derived epitope expressed on tumors. / Wang, Mingjun; Johansen, Britta; Nissen, Mogens H; Thorn, Mette; Kløverpris, Henrik; Fomsgaard, Anders; Buus, Søren; Claësson, Mogens H.
In: Cancer Letters, Vol. 251, No. 1, 2006, p. 86-95.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Identification of an HLA-A*0201 restricted Bcl2-derived epitope expressed on tumors.
AU - Wang, Mingjun
AU - Johansen, Britta
AU - Nissen, Mogens H
AU - Thorn, Mette
AU - Kløverpris, Henrik
AU - Fomsgaard, Anders
AU - Buus, Søren
AU - Claësson, Mogens H
N1 - Keywords: Amino Acid Sequence; Animals; Apoptosis Regulatory Proteins; Blotting, Western; Cell Line, Tumor; Cytotoxicity Tests, Immunologic; Cytotoxicity, Immunologic; Enzyme-Linked Immunosorbent Assay; Epitopes; Female; HLA-A Antigens; Humans; K562 Cells; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Neoplasms; Oligopeptides; Proto-Oncogene Proteins c-bcl-2; T-Lymphocytes, Cytotoxic; Transfection
PY - 2006
Y1 - 2006
N2 - A large number of human tumor-associated antigen-derived peptides have been identified that are recognized by CTLs in a MHC-I restricted fashion. The apoptosis inhibitory protein Bcl2 is overexpressed in many human cancers as part of their neoplastic phenotype. Since inhibition or loss of Bcl2 expression might impair tumor growth and survival, this protein may serve as a rational target for vaccine-induced CTL responses. By Western blot technique, we screened a panel of established human tumor cell lines for proteins involved in the apoptotic process. Two of eight tumor cell lines, a B lymphoma (Loukes) and a colon carcinoma (CCL220) cell line showed increased Bcl2 protein expression whereas the majority of tumor cell lines expressed proapoptotic proteins. Neither fibroblasts nor peripheral blood mononuclear cells showed Bcl2 expression. An HLA-A*0201 restricted CTL epitope was deduced in silica from the amino acid sequence of the Bcl2 protein and its binding affinity for HLA-A*0201 was confirmed using a biochemical binding assay. We here demonstrate that the 9-mer peptide Bcl2(85-93) induces specific CTL reactivity in immunized C57-A2K(b) or -A2D(b) tg mice. These Bcl2(85-93) specific CTLs react with and lyse Bcl2-expressing human colon carcinoma CCL220 cells which have been transfected with a chimeric HLA-A*0201/H2-K(b) DNA construct similar to that expressed in the transgenic mice. Based on these observations, we suggest that Bcl2(85-93) may be a target for immune therapy.
AB - A large number of human tumor-associated antigen-derived peptides have been identified that are recognized by CTLs in a MHC-I restricted fashion. The apoptosis inhibitory protein Bcl2 is overexpressed in many human cancers as part of their neoplastic phenotype. Since inhibition or loss of Bcl2 expression might impair tumor growth and survival, this protein may serve as a rational target for vaccine-induced CTL responses. By Western blot technique, we screened a panel of established human tumor cell lines for proteins involved in the apoptotic process. Two of eight tumor cell lines, a B lymphoma (Loukes) and a colon carcinoma (CCL220) cell line showed increased Bcl2 protein expression whereas the majority of tumor cell lines expressed proapoptotic proteins. Neither fibroblasts nor peripheral blood mononuclear cells showed Bcl2 expression. An HLA-A*0201 restricted CTL epitope was deduced in silica from the amino acid sequence of the Bcl2 protein and its binding affinity for HLA-A*0201 was confirmed using a biochemical binding assay. We here demonstrate that the 9-mer peptide Bcl2(85-93) induces specific CTL reactivity in immunized C57-A2K(b) or -A2D(b) tg mice. These Bcl2(85-93) specific CTLs react with and lyse Bcl2-expressing human colon carcinoma CCL220 cells which have been transfected with a chimeric HLA-A*0201/H2-K(b) DNA construct similar to that expressed in the transgenic mice. Based on these observations, we suggest that Bcl2(85-93) may be a target for immune therapy.
U2 - 10.1016/j.canlet.2006.11.004
DO - 10.1016/j.canlet.2006.11.004
M3 - Journal article
C2 - 17182178
VL - 251
SP - 86
EP - 95
JO - Cancer Letters
JF - Cancer Letters
SN - 0304-3835
IS - 1
ER -
ID: 8724809