Natural Killer Cell-targeted Immunotherapy for Cancer

被引:4
作者
Tang, Jingyi [1 ]
Zhu, Qi [2 ]
Li, Zhaoyang [1 ,3 ]
Yang, Jiahui [1 ]
Lai, Yu [1 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Sch Basic Med, Chengdu, Sichuan, Peoples R China
[2] Sichuan Fine Arts Inst, Chongqing, Peoples R China
[3] Xinjiang Med Univ, Urumqi, Xinjiang Uygur, Peoples R China
关键词
NK cells; immunotherapy; genetic engineering; chimeric antigen receptor; inhibitory checkpoints; cancerous cells; HUMAN NK CELLS; CORD BLOOD; GENE-EXPRESSION; IN-VIVO; MEDIATED CYTOTOXICITY; TIM-3; EXPRESSION; ANTIBODY; CHECKPOINT; BLOCKADE; INTERLEUKIN-2;
D O I
10.2174/1574888X17666220107101722
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Natural Killer (NK) cells were initially described in the early 1970s as major histocompatibility complex unrestricted killers due to their ability to spontaneously kill certain tumor cells. In the past decade, the field of NK cell-based treatment has been accelerating exponentially, holding a dominant position in cancer immunotherapy innovation. Generally, research on NK cell-mediated antitumor therapies can be categorized into three areas: choosing the optimal source of allogeneic NK cells to yield massively amplified "off-the-shelf' products, improving NK cell cytotoxicity and longevity, and engineering NK cells with the ability of tumor-specific recognition. In this review, we focused on NK cell manufacturing techniques, some auxiliary methods to enhance the therapeutic efficacy of NK cells, chimeric antigen receptor NK cells, and monoclonal antibodies targeting inhibitory receptors, which can significantly augment the antitumor activity of NK cells. Notably, emerging evidence suggests that NK cells are a promising constituent of multi-pronged therapeutic strategies, strengthening immune responses to cancer.
引用
收藏
页码:513 / 526
页数:14
相关论文
共 105 条
[1]   CAR Natural Killer Cell Therapy Safe and Effective in First Trial [J].
Abbasi, Jennifer .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2020, 323 (10) :916-916
[2]   Differential activation of cord blood and peripheral blood natural killer cells by cytokines [J].
Alnabhan, Rehab ;
Madrigal, Alejandro ;
Saudemont, Aurore .
CYTOTHERAPY, 2015, 17 (01) :73-85
[3]   New nomenclature for MHC receptors [J].
André, P ;
Biassoni, R ;
Colonna, M ;
Cosman, D ;
Lanier, LL ;
Long, EO ;
Lopez-Botet, M ;
Moretta, A ;
Moretta, L ;
Parham, P ;
Trowsdale, J ;
Vivier, E ;
Wagtmann, N ;
Wilson, MJ .
NATURE IMMUNOLOGY, 2001, 2 (08) :661-661
[4]   Improved cancer immunotherapy by a CD25-mimobody conferring selectivity to human interleukin-2 [J].
Arenas-Ramirez, Natalia ;
Zou, Chao ;
Popp, Simone ;
Zingg, Daniel ;
Brannetti, Barbara ;
Wirth, Emmanuelle ;
Calzascia, Thomas ;
Kovarik, Jiri ;
Sommer, Lukas ;
Zenke, Gerhard ;
Woytschak, Janine ;
Regnier, Catherine H. ;
Katopodis, Andreas ;
Boyman, Onur .
Science Translational Medicine, 2016, 8 (367)
[5]   Echinococcus multilocularis vesicular fluid induces the expression of immune checkpoint proteins in vitro [J].
Bellanger, Anne-Pauline ;
Courquet, Sandra ;
Pallandre, Jean-Rene ;
Godet, Yann ;
Millon, Laurence .
PARASITE IMMUNOLOGY, 2020, 42 (06)
[6]   A First-in-Human Study and Biomarker Analysis of NKTR-214, a Novel 1L2Rβγ-Biased Cytokine, in Patients with Advanced or Metastatic Solid Tumors [J].
Bentebibel, Salah-Eddine ;
Hurwitz, Michael E. ;
Bernatchez, Chantale ;
Haymaker, Cara ;
Hudgens, Courtney W. ;
Kluger, Harriet M. ;
Tetzlaff, Michael T. ;
Tagliaferri, Mary A. ;
Zalevsky, Jonathan ;
Hoch, Ute ;
Fanton, Christie ;
Aung, Sandra ;
Hwu, Patrick ;
Curti, Brendan D. ;
Tannir, Nizar M. ;
Sznol, Mario ;
Diab, Adi .
CANCER DISCOVERY, 2019, 9 (06) :711-721
[7]   Human natural killer cells produce abundant macrophage inflammatory protein-1 in response to monocyte-derived cytokines [J].
Bluman, EM ;
Bartynski, KJ ;
Avalos, BR ;
Caligiuri, MA .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (12) :2722-2727
[8]   Antibody-Dependent Cellular Cytotoxicity Activity of a Novel Anti-PD-L1 Antibody Avelumab (MSB0010718C) on Human Tumor Cells [J].
Boyerinas, Benjamin ;
Jochems, Caroline ;
Fantini, Massimo ;
Heery, Christopher R. ;
Gulley, James L. ;
Tsang, Kwong Yok ;
Schlom, Jeffrey .
CANCER IMMUNOLOGY RESEARCH, 2015, 3 (10) :1148-1157
[9]   HUMAN UMBILICAL-CORD BLOOD AS A POTENTIAL SOURCE OF TRANSPLANTABLE HEMATOPOIETIC STEM PROGENITOR CELLS [J].
BROXMEYER, HE ;
DOUGLAS, GW ;
HANGOC, G ;
COOPER, S ;
BARD, J ;
ENGLISH, D ;
ARNY, M ;
THOMAS, L ;
BOYSE, EA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (10) :3828-3832
[10]   Human anti-CAIX antibodies mediate immune cell inhibition of renal cell carcinoma in vitro and in a humanized mouse model in vivo [J].
Chang, De-Kuan ;
Moniz, Raymond J. ;
Xu, Zhongyao ;
Sun, Jiusong ;
Signoretti, Sabina ;
Zhu, Quan ;
Marasco, Wayne A. .
MOLECULAR CANCER, 2015, 14