Abstract
Genetically modified T cells expressing chimeric antigen receptors (CARs) demonstrate potent clinical antitumor effects in a variety of blood cancers. However, clinical activity in solid tumors has been disappointing and toxicity has been a serious concern (Lamers et al., 2013; Morgan et al., 2010). We recently found that a CAR composed of a scFv antibody fragment specific for the Tn-glycoform of MUC1 had potent activity in preclinical models of blood cancer and adenocarcinoma (Posey et al., 2016).
Originalsprog | Engelsk |
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Tidsskrift | Immunity |
Vol/bind | 45 |
Udgave nummer | 5 |
Sider (fra-til) | 947-948 |
Antal sider | 2 |
ISSN | 1074-7613 |
DOI | |
Status | Udgivet - 15 nov. 2016 |