| Literature DB >> 31026116 |
Shuanghui Yang1,2, Jianguo Wen2, Huan Li2,3, Ling Xu2,4, Yanting Liu2, Nianxi Zhao2, Zihua Zeng2, Jianjun Qi2, Wenqi Jiang2, Wei Han2,5, Youli Zu2.
Abstract
Natural killer (NK) cells are a key component of the innate immune system as they can attack cancer cells without prior sensitization. However, due to lack of cell-specific receptors, NK cells are not innately able to perform targeted cancer immunotherapy. Aptamers are short single-stranded oligonucleotides that specifically recognize their targets with high affinity in a similar manner to antibodies. To render NK cells with target-specificity, synthetic CD30-specific aptamers are anchored on cell surfaces to produce aptamer-engineered NK cells (ApEn-NK) without genetic alteration or cell damage. Under surface-anchored aptamer guidance, ApEn-NK specifically bind to CD30-expressing lymphoma cells but do not react to off-target cells. The resulting specific cell binding of ApEn-NK triggers higher apoptosis/death rates of lymphoma cells compared to parental NK cells. Additionally, experiments with primary human NK cells demonstrate the potential of ApEn-NK to specifically target and kill lymphoma cells, thus presenting a potential new approach for targeted immunotherapy by NK cells.Entities:
Keywords: adaptive immunotherapy; aptamer-engineering; lymphoma; natural killer (NK) cells; oligonucleotide aptamers
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Year: 2019 PMID: 31026116 PMCID: PMC6541510 DOI: 10.1002/smll.201900903
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281