| Literature DB >> 26934353 |
Beatrix Kotlan1, Orsolya Csuka2, László Tóth3, Emil Farkas3, Vanda Plótár4, Szabolcs Horváth4, Klára Éles4, Judit Olasz2, József Tóth4, Miklós Kásler5, Gabriella Liszkay6.
Abstract
The rapidly growing field of gene therapy techniques to modify T cells with chimeric antigen receptors (CARs) for cancer care solutions, reached considerable achievements. However, there is an urgent need of reliable, well tolerable tumor-associated antigen specific antibodies. Tumor-infiltrating B (TIL-B) cell originated single chain Fv (scFv) gene regions could be selected with tumor specificity. DNA sequences of these antibody variable regions were subjects to get engineered into new CAR constructs. Our novel strategy harnesses tumor-infiltrating B cells' unique capacity to reveal highly tumor-associated disialylated glycosphingolipids (GD3 gangliosides). We used these human antibody fragments for generating GD3 ganglioside specific CAR gene constructs for potential usage in solid tumors.Entities:
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Year: 2016 PMID: 26934353
Source DB: PubMed Journal: Magy Onkol ISSN: 0025-0244