| Literature DB >> 34050690 |
Faroogh Marofi1, Omar F Abdul-Rasheed2, Heshu Sulaiman Rahman3, Hendrik Setia Budi4, Abduladheem Turki Jalil5, Alexei Valerievich Yumashev6, Ali Hassanzadeh7, Mahboubeh Yazdanifar8, Roza Motavalli9, Max Stanley Chartrand10, Majid Ahmadi9, Angel Cid-Arreguid11, Mostafa Jarahian12.
Abstract
Chimeric antigen receptors (CARs) have a unique facet of synthetic biology and offer a paradigm shift in personalized medicine as they can use and redirect the patient's immune cells to attack cancer cells. CAR-natural killer (NK) cells combine the targeted specificity of antigens with the subsequent intracellular signaling ability of the receptors to increase their anti-cancer functions. Importantly, CAR-NK cells can be utilized as universal cell-based therapy without requiring human leukocyte antigen (HLA) matching or earlier contact with tumor-associated antigens (TAAs). Indeed, CAR-NK cells can be adapted to recognize various antigens, hold higher proliferation capacity, and in vivo persistence, show improved infiltration into the tumors, and the ability to overcome the resistant tumor microenvironment leading to sustained cytotoxicity against tumors. Accumulating evidence from recent in vivo studies rendering CAR-NK cell anti-cancer competencies renewed the attention in the context of cancer immunotherapy, as these redirected effector cells can be used in the development of the "off-the-shelf" anti-cancer immunotherapeutic products. In the current review, we focus on the therapeutic efficacy of CAR-NK cell therapies for treating various human malignancies, including hematological malignancies and solid tumors, and will discuss the recent findings in this regard, with a special focus on animal studies.Entities:
Keywords: CAR-NK; cancer; chimeric antigen receptors; immunotherapy; natural killer cells
Year: 2021 PMID: 34050690 DOI: 10.1111/cas.14993
Source DB: PubMed Journal: Cancer Sci ISSN: 1347-9032 Impact factor: 6.716