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Expression of Tumor‐associated Glycoantigen, Sialyl Lewis(a), in Human Head and Neck Squamous Cell Carcinoma and Its Application to Tumor Immunotherapy

The glycoantigen sialyl Lewis(a) (sLe(a)) is widely expressed on a variety of gastrointestinal tumor cells. Here, we immunohistochemically demonstrated the expression of sLe(a) antigen in 54% (7 out of 13) of human head and neck squamous cell carcinoma (H‐NSCG) samples. Frequent expression of sLe(a)...

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Detalles Bibliográficos
Autores principales: Makino, Koji, Ogata, Tetsuro, Miyake, Hirosato, Habu, Sonoko, Nishimura, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919591/
https://www.ncbi.nlm.nih.gov/pubmed/7961115
http://dx.doi.org/10.1111/j.1349-7006.1994.tb02964.x
Descripción
Sumario:The glycoantigen sialyl Lewis(a) (sLe(a)) is widely expressed on a variety of gastrointestinal tumor cells. Here, we immunohistochemically demonstrated the expression of sLe(a) antigen in 54% (7 out of 13) of human head and neck squamous cell carcinoma (H‐NSCG) samples. Frequent expression of sLe(a) antigen was also demonstrated on a variety of H‐NSCC cell lines using flow cytometry. Both CD4(+) and CD8(+) T cells, which were activated with immobilized OKT3 monoclonal antibody plus inter‐leukin‐2, showed augmented cytotoxicity against sLe(a)‐positive H‐NSCC, including autologous tumor cells, on targeting with anti‐CD3 x anti‐sLe(a) bispccific antibody, suggesting that sLe(a) antigen is a good target molecule for bispecific antibody‐dependent adoptive tumor immunotherapy of human head and neck cancer.