Abstract
Transforming growth factor-β (TGF-β) is a potent inhibitor of immune cells including T-lymphocytes, natural killer (NK) cells, and antigen presenting cells (APCs). Because large amounts of TGF-β are often produced by tumors, it has been hypothesized that blockade of TGF-β would prevent the loss of antitumor immune activity and exert effective antitumor efficacy. Thus, a number of experimental studies have been performed in tumor models blocking TGF-β production, TGF-β receptor binding, or TGF-β signaling to augment host antitumor immune responses. In this chapter, we review studies employing blockade of TGF-β using a soluble type II transforming growth factor-β receptor (sTGF-βR) and discuss future ways in which TGF-β inhibition might enhance cancer immuno-therapy.
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Suzuki, E., Albelda, S.M. (2008). Soluble Type II Transforming Growth Factor-β Receptor Inhibits Tumorigenesis by Augmenting Host Antitumor Immunity. In: Jakowlew, S.B. (eds) Transforming Growth Factor-β in Cancer Therapy, Volume II. Cancer Drug Discovery and Development. Humana Press. https://doi.org/10.1007/978-1-59745-293-9_42
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DOI: https://doi.org/10.1007/978-1-59745-293-9_42
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