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In vitro co-stimulation of anti-tumor activity by soluble B7 molecules.
Author(s) -
Wei He,
Zhongbo Hu,
Fang Liu,
Xianqi Feng,
Ping Zou
Publication year - 2006
Publication title -
acta biochimica polonica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.452
H-Index - 78
eISSN - 1734-154X
pISSN - 0001-527X
DOI - 10.18388/abp.2006_3310
Subject(s) - fusion protein , chinese hamster ovary cell , in vitro , immune system , recombinant dna , microbiology and biotechnology , antibody , stimulation , biology , t cell , interleukin 2 , cell fusion , chemistry , biochemistry , cell , immunology , receptor , gene , endocrinology
In order to investigate the anti-tumor activity of a soluble B7-1/immunoglobulin G fusion protein and explore an effective method to eliminate immune escape of tumor cells, a recombinant vector encoding this fusion protein was constructed and constitutively expressed in Chinese hamster ovary cells. After purification with protein G affinity chromatography, the soluble fusion protein was tested for bioactivity. Results showed that the fusion protein could significantly increase the density of B7-1 molecules on WEHI-3 cells, a mouse leukemia cell line. Through allogeneic mixed lymphocyte tumor cultures, it was demonstrated that, with the presence of the first signal, it could also significantly enhance T cell activation and killing activity against WEHI-3 cells and interleukin-2 secretion by activated mouse T lymphocytes. The conclusion can be drawn that the soluble B7-IgG fusion protein has a potent capacity to generate or enhance anti-tumor immune response in vitro, and its clinical value deserves further investigation.

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