Literature DB >> 20373147

Adoptive T-cell immunotherapy of cancer using chimeric antigen receptor-grafted T cells.

David Marc Davies1, John Maher.   

Abstract

Harnessing the power of the immune system to target cancer has long been a goal of tumor immunologists. One avenue under investigation is the modification of T cells to express a chimeric antigen receptor (CAR). Expression of such a receptor enables T-cell specificity to be redirected against a chosen tumor antigen. Substantial research in this field has been carried out, incorporating a wide variety of malignancies and tumor-associated antigens. Ongoing investigations will ensure this area continues to expand at a rapid pace. This review will explain the evolution of CAR technology over the last two decades in addition to detailing the associated benefits and disadvantages. The outcome of recent phase I clinical trials and the impact that these have had upon the direction of future research in this field will also be addressed.

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Year:  2010        PMID: 20373147     DOI: 10.1007/s00005-010-0074-1

Source DB:  PubMed          Journal:  Arch Immunol Ther Exp (Warsz)        ISSN: 0004-069X            Impact factor:   4.291


  7 in total

Review 1.  Potential targets for pancreatic cancer immunotherapeutics.

Authors:  Lindzy F Dodson; William G Hawkins; Peter Goedegebuure
Journal:  Immunotherapy       Date:  2011-04       Impact factor: 4.196

2.  Chimeric antigen receptor T cells targeting HERV-K inhibit breast cancer and its metastasis through downregulation of Ras.

Authors:  Fuling Zhou; Janani Krishnamurthy; Yongchang Wei; Ming Li; Kelly Hunt; Gary L Johanning; Laurence Jn Cooper; Feng Wang-Johanning
Journal:  Oncoimmunology       Date:  2015-05-26       Impact factor: 8.110

3.  Genetically modified T cells targeting neovasculature efficiently destroy tumor blood vessels, shrink established solid tumors and increase nanoparticle delivery.

Authors:  Xinping Fu; Armando Rivera; Lihua Tao; Xiaoliu Zhang
Journal:  Int J Cancer       Date:  2013-07-11       Impact factor: 7.396

4.  Flexible targeting of ErbB dimers that drive tumorigenesis by using genetically engineered T cells.

Authors:  David M Davies; Julie Foster; Sjoukje J C Van Der Stegen; Ana C Parente-Pereira; Laura Chiapero-Stanke; George J Delinassios; Sophie E Burbridge; Vincent Kao; Zhe Liu; Leticia Bosshard-Carter; May C I Van Schalkwyk; Carol Box; Suzanne A Eccles; Stephen J Mather; Scott Wilkie; John Maher
Journal:  Mol Med       Date:  2012-05-09       Impact factor: 6.354

5.  An HSV-2 based oncolytic virus can function as an attractant to guide migration of adoptively transferred T cells to tumor sites.

Authors:  Xinping Fu; Armando Rivera; Lihua Tao; Xiaoliu Zhang
Journal:  Oncotarget       Date:  2015-01-20

Review 6.  Targeting the Microenvironment for Treating Multiple Myeloma.

Authors:  Peter Neumeister; Eduard Schulz; Katrin Pansy; Marta Szmyra; Alexander Ja Deutsch
Journal:  Int J Mol Sci       Date:  2022-07-10       Impact factor: 6.208

7.  Trafficking of CAR-engineered human T cells following regional or systemic adoptive transfer in SCID beige mice.

Authors:  Ana Caterina Parente-Pereira; Jerome Burnet; David Ellison; Julie Foster; David Marc Davies; Sjoukje van der Stegen; Sophie Burbridge; Laura Chiapero-Stanke; Scott Wilkie; Stephen Mather; John Maher
Journal:  J Clin Immunol       Date:  2011-04-20       Impact factor: 8.317

  7 in total

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