Molecular Imaging: A Useful Tool for the Development of Natural Killer Cell-Based Immunotherapies

被引:38
作者
Gangadaran, Prakash [1 ]
Ahn, Byeong-Cheol [1 ]
机构
[1] Kyungpook Natl Univ, Dept Nucl Med, Sch Med & Hosp, Daegu, South Korea
基金
新加坡国家研究基金会;
关键词
bioluminescence; cell trafficking; molecular imaging; natural killer cell; positron-emission tomography; single photon-emission computed tomography; therapy; GREEN FLUORESCENT PROTEIN; NK CELLS; CANCER-IMMUNOTHERAPY; ADOPTIVE IMMUNOTHERAPY; GENE-THERAPY; T-CELLS; ACTIVATION; TRACKING; EXPANSION; MICE;
D O I
10.3389/fimmu.2017.01090
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Molecular imaging is a relatively new discipline that allows visualization, characterization, and measurement of the biological processes in living subjects, including humans, at a cellular and molecular level. The interaction between cancer cells and natural killer (NK) cells is complex and incompletely understood. Despite our limited knowledge, progress in the search for immune cell therapies against cancer could be significantly improved by dynamic and non-invasive visualization and tracking of immune cells and by visualization of the response of cancer cells to therapies in preclinical and clinical studies. Molecular imaging is an essential tool for these studies, and a multimodal molecular imaging approach can be applied to monitor immune cells in vivo, for instance, to visualize therapeutic effects. In this review, we discuss the usefulness of NK cells in cancer therapies and the preclinical and clinical usefulness of molecular imaging in NK cell-based therapies. Furthermore, we discuss different molecular imaging modalities for use with NK cell-based therapies, and their preclinical and clinical applications in animal and human subjects. Molecular imaging has contributed to the development of NK cell-based therapies against cancers in animal models and to the refinement of current cell-based cancer immunotherapies. Developing sensitive and reproducible non-invasive molecular imaging technologies for in vivo NK cell monitoring and for real-time assessment of therapeutic effects will accelerate the development of NK cell therapies.
引用
收藏
页数:12
相关论文
共 104 条
[1]
Abdel-Magid AF, 2017, FUNDAMENTALS EARLY C
[4]
CD107a as a functional marker for the identification of natural killer cell activity [J].
Alter, G ;
Malenfant, JM ;
Altfeld, M .
JOURNAL OF IMMUNOLOGICAL METHODS, 2004, 294 (1-2) :15-22
[5]
Natural killer cell behavior in lymph nodes revealed by static and real-time imaging [J].
Bajénoff, M ;
Breart, B ;
Huang, AYC ;
Qi, H ;
Cazareth, J ;
Braud, VM ;
Germain, RN ;
Glaichenhaus, N .
JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 203 (03) :619-631
[6]
Live Cell Linear Dichroism Imaging Reveals Extensive Membrane Ruffling within the Docking Structure of Natural Killer Cell Immune Synapses [J].
Benninger, Richard K. P. ;
Vanherberghen, Bruno ;
Young, Stephen ;
Taner, Sabrina B. ;
Culley, Fiona I. ;
Schnyder, Tim ;
Neil, Mark A. A. ;
Wuestner, Daniel ;
French, Paul M. W. ;
Davis, Daniel M. ;
Onfelt, Bjorn .
BIOPHYSICAL JOURNAL, 2009, 96 (02) :L13-L15
[7]
Dynamic behavior of NK cells during activation in lymph nodes [J].
Beuneu, Helene ;
Deguine, Jacques ;
Breart, Beatrice ;
Mandelboim, Ofer ;
Di Santo, James P. ;
Bousso, Philippe .
BLOOD, 2009, 114 (15) :3227-3234
[8]
Retargeting NK-92 cells by means of CD19-and CD20-specific chimeric antigen receptors compares favorably with antibody-dependent cellular cytotoxicity [J].
Boissel, Laurent ;
Betancur-Boissel, Monica ;
Lu, Weiquan ;
Krause, Daniela S. ;
Van Etten, Richard A. ;
Wels, Winfried S. ;
Klingemann, Hans .
ONCOIMMUNOLOGY, 2013, 2 (10)
[9]
The role of interleukin-2 during homeostasis and activation of the immune system [J].
Boyman, Onur ;
Sprent, Jonathan .
NATURE REVIEWS IMMUNOLOGY, 2012, 12 (03) :180-190
[10]
Super-resolution imaging of remodeled synaptic actin reveals different synergies between NK cell receptors and integrins [J].
Brown, Alice C. N. ;
Dobbie, Ian M. ;
Alakoskela, Juha-Matti ;
Davis, Ilan ;
Davis, Daniel M. .
BLOOD, 2012, 120 (18) :3729-3740