CD4+ T Cell Responses to SSX-4 in Melanoma Patients
Author(s) -
Maha Ayyoub,
Andrea Merlo,
Charles S. Hesdorffer,
Donata Rimoldi,
Daniel E. Speiser,
Jean-Charles Cerottini,
Yao-Tseng Chen,
Lloyd J. Old,
Stefan Stevanović,
Danila Valmori
Publication year - 2005
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.174.8.5092
Subject(s) - immunogenicity , melanoma , breakpoint , peripheral blood mononuclear cell , biology , cancer research , antigen , t cell , gene , cancer , immunology , in vitro , microbiology and biotechnology , immune system , genetics , chromosomal translocation
Genes of the synovial sarcoma X breakpoint (SSX) family are expressed in different human tumors, including melanomas, but not in adult somatic tissues. Because of their specific expression at the tumor site, SSX-encoded Ags are potential targets for anticancer immunotherapy. In this study, we have analyzed CD4+ T cell responses directed against the Ag encoded by SSX-4. Upon in vitro stimulation of PBMC from four melanoma patients bearing Ag-expressing tumors with a pool of long peptides spanning the protein sequence, we detected and isolated SSX-4-specific CD4+ T cells recognizing several distinct antigenic sequences, mostly restricted by frequently expressed HLA class II alleles. The majority of the identified sequences were located within the Krüppel-associated box domain in the N-terminal region of the protein, indicating a high potential immunogenicity of this region. Together our data document the existence of CD4+ T cells specific for multiple SSX-4 derived sequences in circulating lymphocytes from melanoma patients and encourage further studies to assess the impact of SSX-4-specific T cell responses on disease evolution in cancer patients.
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