Abken, Hinrich (2015). Adoptive therapy with CAR redirected T cells: the challenges in targeting solid tumors. Immunotherapy, 7 (5). S. 535 - 545. LONDON: FUTURE MEDICINE LTD. ISSN 1750-7448

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Abstract

Recent spectacular success in the adoptive cell therapy of leukemia and lymphoma with chimeric antigen receptor (CAR)-modified T cells raised the expectations that this therapy may be efficacious in a wide range of cancer entities. The expectations are based on the predefined specificity of CAR T cells by an antibody-derived binding domain that acts independently of the natural T-cell receptor, recognizes targets independently of presentation by the major histocompatibility complex and allows targeting toward virtually any cell surface antigen. We here discuss that targeting CAR T cells toward solid tumors faces certain circumstances critical for the therapeutic success. Targeting tumor stroma and taking advantage of TRUCK cells, in other words, CAR T cells with inducible release of a transgenic payload, are some strategies envisaged to overcome current limitations in the near future.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Abken, HinrichUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-419020
DOI: 10.2217/IMT.15.15
Journal or Publication Title: Immunotherapy
Volume: 7
Number: 5
Page Range: S. 535 - 545
Date: 2015
Publisher: FUTURE MEDICINE LTD
Place of Publication: LONDON
ISSN: 1750-7448
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
CHIMERIC ANTIGEN RECEPTORS; PHASE-I; GENETIC-MODIFICATION; ESTABLISHED TUMORS; ANTITUMOR-ACTIVITY; ADVERSE EVENT; IMMUNOTHERAPY; PERSISTENCE; LYMPHOCYTES; EXPRESSIONMultiple languages
ImmunologyMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/41902

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