Expression of synovial sarcoma X (SSX) antigens in epithelial ovarian cancer and identification of SSX-4 epitopes recognized by CD4+ T cells Journal Article


Authors: Valmori, D.; Qian, F.; Ayyoub, M.; Renner, C.; Merlo, A.; Gnjatic, S.; Stockert, E.; Driscoll, D.; Lele, S.; Old, L. J.; Odunsi, K.
Article Title: Expression of synovial sarcoma X (SSX) antigens in epithelial ovarian cancer and identification of SSX-4 epitopes recognized by CD4+ T cells
Abstract: Purpose: Synovial sarcoma X (SSX) breakpoint genes are expressed in a variety of cancers but not in normal tissues, except for testis, and are potential targets for immunotherapy. The aims of this study were to determine the expression and immunogenicity of these antigens in patients with epithelial ovarian cancer (EOC). Experimental Design: SSX-1-, SSX-2-, and SSX-4-specific reverse transcription-PCR were done on a panel of EOC specimens. Sera from a subgroup of the patients were tested for SSX-2 and SSX-4 antibody by ELISA and recombinant antigen expression on yeast surface (RAYS), in vitro stimulation of peripheral blood mononuclear cells from a patient bearing SSX-4-expressing tumor with a pool of long peptides spanning the protein sequence was used for assessment of SSX-4-specific CD4+ T cells recognizing distinct antigenic sequences restricted by HLA class II alleles. Results: Our results indicate expression of SSX-1, SSX-2, and SSX-4 in 2.5%, 10%, and 16% of 120 EOC specimens, respectively. When all three SSX antigens are considered, aberrant expression was found in 26% of ovarian tumors. Antibodies to SSX-2 and SSX-4 were detectable by ELISA and RAYS in two patients. SSX-4-specific CD4 + T cells recognizing two previously undescribed SSX-4-derived T-cell epitopes in association with HLA-DR (SSX-4: 51-70 and SSX-4: 61-180) were identified. Conclusions: Our study shows aberrant expression of SSX antigens in a proportion of patients with EOC. The evidence of humoral immunity to SSX-2 and SSX-4, and SSX-4-specific CD4+ T cells among circulating lymphocytes in patients with antigen expressing EOC suggest that these antigens are attractive targets for specific immunotherapy in EOC. © 2006 American Association for Cancer Research.
Keywords: adult; controlled study; human tissue; aged; aged, 80 and over; middle aged; survival rate; unclassified drug; human cell; major clinical study; overall survival; cancer staging; cancer grading; antigen expression; ovarian neoplasms; gene; cancer immunotherapy; reverse transcription polymerase chain reaction; ovary cancer; gene expression; neoplasm proteins; cancer cell culture; tumor antigen; enzyme linked immunosorbent assay; statistical analysis; amino acid sequence; antigens, neoplasm; immunogenicity; hla antigen class 2; hla dr antigen; antigen recognition; cd4+ t lymphocyte; cd4-positive t-lymphocytes; hla-dr antigens; epitope; kaplan meier method; cell stimulation; hla typing; epitopes, t-lymphocyte; humoral immunity; repressor proteins; antibodies, neoplasm; peripheral blood mononuclear cell; neoplasms, glandular and epithelial; hla dq antigen; synovial sarcoma x 1 antigen; synovial sarcoma x 2 antigen; synovial sarcoma x 4 antigen; synovial sarcoma x antigen; synovial sarcoma x gene
Journal Title: Clinical Cancer Research
Volume: 12
Issue: 2
ISSN: 1078-0432
Publisher: American Association for Cancer Research  
Date Published: 2006-01-15
Start Page: 398
End Page: 404
Language: English
DOI: 10.1158/1078-0432.ccr-05-1902
PUBMED: 16428478
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 16" - "Export Date: 4 June 2012" - "CODEN: CCREF" - "Source: Scopus"
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  1. Sacha Gnjatic
    113 Gnjatic
  2. Lloyd J Old
    593 Old