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SSX-2 epitope presented by dendritic cells to CD4+ T cells identified.

Vaccine Weekly

| August 04, 2004 | COPYRIGHT 2004 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2004 AUG 4 - (NewsRx.com & NewsRx.net) -- Scientists have identified an SSX-2 epitope presented by dendritic cells to circulating autologous CD4+ T cells.

According to recent research from the United States, "Accumulating evidence supports the requirement for both tumor-specific CD8+ and CD4+ T cell responses for efficient tumor rejection to occur. Because of its expression in different tumor types, the cancer/testis antigen encoded by the synovial sarcoma X breakpoint 2 (SSX-2) gene is among the most relevant candidates for the development of generic cancer vaccines. The immunogenicity of SSX-2 has been previously corroborated by detection of specific humoral and CD8+ T cell responses in cancer patients."

"In this study, we report identification of the first CD4+ T cell epitope encoded by SSX-2," stated Maha Ayyoub at Columbia University and collaborators in the United States and Switzerland. "The identified epitope mapped to the 19-34 region of the protein and was recognized by CD4+ T cells from an antigen-expressing melanoma patient in association with HLADPBI*0101. The absence of detectable response in healthy donors and other patients suggests that SSX-2-specific CD4+ T cells in the responder patient had been previously expanded in vivo in response to the autologous tumor."

"The epitope did not appear to be presented on ...

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