Producer T cells: Using genetically engineered T cells as vehicles to generate and deliver therapeutics to tumors

被引:15
|
作者
Tsai, Alexander K. [1 ]
Davila, Eduardo [1 ,2 ]
机构
[1] Univ Maryland, Marlene & Stewart Greenebaum Canc Ctr, Baltimore, MD 21201 USA
[2] Univ Maryland, Dept Microbiol & Immunol, Baltimore, MD 21201 USA
来源
ONCOIMMUNOLOGY | 2016年 / 5卷 / 05期
关键词
Adoptive transfer; cell vehicle; cancer therapy; drug delivery; genetic engineering; T cell; STEM-CELLS; IN-VIVO; ANTITUMOR-ACTIVITY; EXOGENOUS IL-2; CLINICAL-TRIAL; LONG-TERM; CANCER; LYMPHOCYTES; INTERLEUKIN-12; EXPRESSION;
D O I
10.1080/2162402X.2015.1122158
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adoptive cell transfer (ACT) is an emerging anticancer therapy that has shown promise in various malignancies. Redirecting antigen specificity by genetically engineering T cells to stably express receptors has become an effective variant of ACT. A novel extension of this approach is to utilize engineered T cells to produce and deliver anticancer therapeutics that enhance cytotoxic T cell function and simultaneously inhibit immunosuppressive processes. Here, we review the potential of using T cells as therapeutic-secreting vehicles for immunotherapies and present theoretical and established arguments in support of further development of this unique cell-based immunotherapy.
引用
收藏
页数:9
相关论文
共 50 条
  • [41] Validation of cGMP-Generation of Genetically Engineered T Cells on the CliniMACS Prodigy™
    Daley, Heather
    Rodriguez, Diego Hernandez
    Khelladi, Radia
    Cunningham, Amy
    Mason, Andrew
    Kelley, Mary Ann
    Silva, Michelle C.
    Sturtevant, Olive J.
    Shaw, Kit L.
    Nikiforow, Sarah
    Ritz, Jerome
    MOLECULAR THERAPY, 2020, 28 (04) : 67 - 68
  • [42] In vivo cervical cancer growth inhibition by genetically engineered cytotoxic T cells
    Dall, P
    Herrmann, I
    Durst, B
    Stoff-Khalili, M
    Bauerschmitz, G
    Hanstein, B
    Niederacher, D
    CANCER IMMUNOLOGY IMMUNOTHERAPY, 2005, 54 (01) : 51 - 60
  • [43] Engineered T cells for all
    Gemma K. Alderton
    Nature Reviews Cancer, 2017, 17 : 206 - 207
  • [44] TUMORS AND T CELLS
    不详
    NATURE, 1973, 245 (5423) : 235 - 236
  • [45] Boosting engineered T cells
    Singh, Nathan
    June, Carl H.
    SCIENCE, 2019, 365 (6449) : 119 - 120
  • [46] Engineered T cells for all
    Alderton, Gemma K.
    NATURE REVIEWS CANCER, 2017, 17 (04) : 206 - 206
  • [47] Delivery of nucleic acid therapeutics by genetically engineered hematopoietic stem cells
    Doering, Christopher B.
    Archer, David
    Spencer, H. Trent
    ADVANCED DRUG DELIVERY REVIEWS, 2010, 62 (12) : 1204 - 1212
  • [48] Beyond CAR T cells: Engineered Vγ9Vδ2 T cells to fight solid tumors
    Rafia, Chirine
    Harly, Christelle
    Scotet, Emmanuel
    IMMUNOLOGICAL REVIEWS, 2020, 298 (01) : 117 - 133
  • [49] Adoptive cancer immunotherapy using genetically engineered designer T-cells: First steps into the clinic
    Eshhar, Zelig
    CURRENT OPINION IN MOLECULAR THERAPEUTICS, 2010, 12 (01) : 55 - 63
  • [50] Imaging of genetically engineered T cells by PET using gold nanoparticles complexed to Copper-64
    Bhatnagar, Parijat
    Li, Zheng
    Choi, Yoonsu
    Guo, Jianfeng
    Li, Feng
    Lee, Daniel Y.
    Figliola, Matthew
    Huls, Helen
    Lee, Dean A.
    Zal, Tomasz
    Li, King C.
    Cooper, Laurence J. N.
    INTEGRATIVE BIOLOGY, 2013, 5 (01) : 231 - 238