Next generation natural killer cells for cancer immunotherapy: the promise of genetic engineering

被引:162
作者
Daher, May [1 ]
Rezvani, Katayoun [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Stem Cell Transplantat & Cellular Therapy, Houston, TX 77030 USA
关键词
CHIMERIC ANTIGEN RECEPTOR; BETA SIGNALING PATHWAY; OFF-THE-SHELF; TUMOR-CELLS; NK CELLS; T-CELL; IMMUNE EVASION; STEM-CELLS; LINE NK-92; IN-VITRO;
D O I
10.1016/j.coi.2018.03.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent advances in the field of cellular therapy have focused on autologous T cells engineered to express a chimeric antigen receptor (CAR) against tumor antigens. Remarkable responses have been observed in patients receiving autologous CD19-redirected T cells for the treatment of B-lymphoid malignancies. However, the generation of autologous products for each patient is logistically challenging and expensive. Extensive research efforts are ongoing to generate an off-theshelf cellular product for the treatment of cancer patients. Natural killer (NK) cells are attractive contenders since they have potent anti-tumor activity, and their safety in the allogeneic setting expands the cell sources for NK cell therapy beyond an autologous one. In this review, we discuss advantages and limitations of NK cellular therapy, and novel genetic engineering strategies that may be applied to overcome some of the limitations. Next-generation engineered NK cells are showing great promise in the preclinical setting and it is likely that in the next few years CAR-engineered NK cells will be incorporated into the current armamentarium of cell-based cancer therapeutics.
引用
收藏
页码:146 / 153
页数:8
相关论文
共 64 条
  • [1] [Anonymous], 2017, Cancer Discov, V7, pOF1, DOI 10.1158/2159-8290.CD-NB2017-126
  • [2] [Anonymous], CANC DISCOV
  • [3] Infusion of the allogeneic cell line NK-92 in patients with advanced renal cell cancer or melanoma: a phase I trial
    Arai, S.
    Meagher, R.
    Swearingen, M.
    Myint, H.
    Rich, E.
    Martinson, J.
    Klingemann, H.
    [J]. CYTOTHERAPY, 2008, 10 (06) : 625 - 632
  • [4] Control of NK Cell Activation by Immune Checkpoint Molecules
    Beldi-Ferchiou, Asma
    Caillat-Zucman, Sophie
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (10)
  • [5] The cell biology of the human natural killer cell CD94/NKG2A inhibitory receptor
    Borrego, F
    Masilamani, M
    Kabat, J
    Sanni, TB
    Coligan, JE
    [J]. MOLECULAR IMMUNOLOGY, 2005, 42 (04) : 485 - 488
  • [6] Improving efficacy of cancer immunotherapy by genetic modification of natural killer cells
    Burga, Rachel A.
    Tuongvan Nguyen
    Zulovich, Jane
    Madonna, Sarah
    Ylisastigui, Loyda
    Fernandes, Rohan
    Yvon, Eric
    [J]. CYTOTHERAPY, 2016, 18 (11) : 1410 - 1421
  • [7] Natural killer cell biology: An update and future directions
    Campbell, Kerry S.
    Hasegawa, Jun
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2013, 132 (03) : 536 - 544
  • [8] Efficient mRNA-Based Genetic Engineering of Human NK Cells with High-Affinity CD16 and CCR7 Augments Rituximab-Induced ADCC against Lymphoma and Targets NK Cell Migration toward the Lymph Node-Associated Chemokine CCL19
    Carlsten, Mattias
    Levy, Emily
    Karambelkar, Amrita
    Li, Linhong
    Reger, Robert
    Berg, Maria
    Peshwa, Madhusudan V.
    Childs, Richard W.
    [J]. FRONTIERS IN IMMUNOLOGY, 2016, 7
  • [9] Genetic manipulation of NK cells for cancer immunotherapy: techniques and clinical implications
    Carlsten, Mattias
    Childs, Richard W.
    [J]. FRONTIERS IN IMMUNOLOGY, 2015, 6
  • [10] Antibody-dependent cell cytotoxicity: immunotherapy strategies enhancing effector NK cells
    Carmen Ochoa, Maria
    Minute, Luna
    Rodriguez, Inmaculada
    Garasa, Saray
    Perez-Ruiz, Elisabeth
    Inoges, Susana
    Melero, Ignacio
    Berraondo, Pedro
    [J]. IMMUNOLOGY AND CELL BIOLOGY, 2017, 95 (04) : 347 - 355