Literature DB >> 20408760

Development of adoptive cell therapy for cancer: a clinical perspective.

Robert E Hawkins1, David E Gilham, Reno Debets, Zelig Eshhar, Naomi Taylor, Hinrich Abken, Ton N Schumacher.   

Abstract

Adoptive cellular therapy provides the promise of a potentially powerful general treatment for cancer. Although this is a complex and challenging field, there have been major advances in basic and translational research resulting in clinical trial activity that is now beginning to confirm this promise. However, these trials are also identifying new challenges and this review focuses on these clinical issues. For tumors such as melanoma, in which tumor-specific T cells can be readily identified and isolated, the adoptive transfer of "tumor-infiltrating lymphocytes" (TILs) already appears to offer significant patient benefit and this approach now warrants further development. Genetically engineered T cells offer a means to endow peripheral blood T cells with antitumor activity and in principle these techniques could allow the treatment of a wide range of cancers. Genetic engineering also offers the means to endow T cells with new properties and enhanced functions. There have been clear proof-of-principle trials showing responses with T cell receptor (TCR)-engineered T cells and this can be built on with further development. By contrast, other trials have produced significant toxicity related to expression of target antigen on normal tissue, particularly with enhanced receptors. The challenge ahead lies in understanding how to achieve the balance between targeted antitumor immune responses while avoiding toxicity associated with on-target destruction of antigen-expressing normal tissues. Cellular therapy of cancer will need continued preclinical evaluation as well as carefully designed clinical trials addressing the various issues. For these challenges to be fully assessed, and for progression to a widely used, effective and safe therapy, development as cooperative groups is an appropriate way forward.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20408760     DOI: 10.1089/hum.2010.086

Source DB:  PubMed          Journal:  Hum Gene Ther        ISSN: 1043-0342            Impact factor:   5.695


  20 in total

1.  Generation of CD8(+) T cells expressing two additional T-cell receptors (TETARs) for personalised melanoma therapy.

Authors:  Sandra Höfflin; Sabrina Prommersberger; Ugur Uslu; Gerold Schuler; Christopher W Schmidt; Volker Lennerz; Jan Dörrie; Niels Schaft
Journal:  Cancer Biol Ther       Date:  2015-07-15       Impact factor: 4.742

Review 2.  Living in the liver: hepatic infections.

Authors:  Ulrike Protzer; Mala K Maini; Percy A Knolle
Journal:  Nat Rev Immunol       Date:  2012-02-24       Impact factor: 53.106

Review 3.  Cancer immunotherapy: Progress and challenges in the clinical setting.

Authors:  Hassane M Zarour; Soldano Ferrone
Journal:  Eur J Immunol       Date:  2011-06       Impact factor: 5.532

4.  Activating systemic T-cell immunity against self tumor antigens to support oncolytic virotherapy with vesicular stomatitis virus.

Authors:  Phonphimon Wongthida; Rosa Maria Diaz; Christine Pulido; Diana Rommelfanger; Feorillo Galivo; Karen Kaluza; Timothy Kottke; Jill Thompson; Alan Melcher; Richard Vile
Journal:  Hum Gene Ther       Date:  2011-04-11       Impact factor: 5.695

Review 5.  Research progress of therapeutic vaccines for treating chronic hepatitis B.

Authors:  Jianqiang Li; Mengru Bao; Jun Ge; Sulin Ren; Tong Zhou; Fengchun Qi; Xiuying Pu; Jia Dou
Journal:  Hum Vaccin Immunother       Date:  2017-01-24       Impact factor: 3.452

6.  Inducible T-cell receptor expression in precursor T cells for leukemia control.

Authors:  S S Hoseini; M Hapke; J Herbst; D Wedekind; R Baumann; N Heinz; B Schiedlmeier; D A A Vignali; M R M van den Brink; A Schambach; B R Blazar; M G Sauer
Journal:  Leukemia       Date:  2015-02-05       Impact factor: 11.528

7.  Treatment of metastatic renal cell carcinoma with CAIX CAR-engineered T cells: clinical evaluation and management of on-target toxicity.

Authors:  Cor Hj Lamers; Stefan Sleijfer; Sabine van Steenbergen; Pascal van Elzakker; Brigitte van Krimpen; Corrien Groot; Arnold Vulto; Michael den Bakker; Egbert Oosterwijk; Reno Debets; Jan W Gratama
Journal:  Mol Ther       Date:  2013-02-19       Impact factor: 11.454

8.  Elimination of progressive mammary cancer by repeated administrations of chimeric antigen receptor-modified T cells.

Authors:  Anat Globerson-Levin; Tova Waks; Zelig Eshhar
Journal:  Mol Ther       Date:  2014-02-27       Impact factor: 11.454

9.  PD-1 blockade enhances T-cell migration to tumors by elevating IFN-γ inducible chemokines.

Authors:  Weiyi Peng; Chengwen Liu; Chunyu Xu; Yanyan Lou; Jieqing Chen; Yan Yang; Hideo Yagita; Willem W Overwijk; Gregory Lizée; Laszlo Radvanyi; Patrick Hwu
Journal:  Cancer Res       Date:  2012-08-20       Impact factor: 12.701

10.  Selective immunotargeting of diabetogenic CD4 T cells by genetically redirected T cells.

Authors:  Shira Perez; Sigal Fishman; Amos Bordowitz; Alon Margalit; F Susan Wong; Gideon Gross
Journal:  Immunology       Date:  2014-12       Impact factor: 7.397

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.