作者: Ian Spendlove , Lindy G. Durrant , Li Li , James Carmichael
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摘要: The 791Tgp72 antigen has been used successfully as a target for tumor imaging and T-cell immunotherapy. We have characterized this using the monoclonal antibody 791T/36 72/66 kDa doublet. NH 2 -terminal protein sequencing of two bands revealed identity with complement regulatory CD55. Antibodies recognizing different domains CD55 were also shown to bind purified 791Tgp72, although sequence analysis cDNA cloned from 791T cells showed 100% homology transfection into antigen-negative CHO resulted in binding 791T/36. This identifies protects attack; however, it can transduce signals lymphocytes is ligand CD97, expressed by activated T cells. These results suggest that plays roll signaling between innate adaptive immune responses. It therefore very intriguing target, because absence molecule makes susceptible complement, whereas protective overexpression being