← 返回

CTLs、NK 细胞和 NK 来源的 EVs 抗乳腺癌

英文原题:CTLs, NK cells and NK-derived EVs against breast cancer.

查看英文原题

CTLs, NK cells and NK-derived EVs against breast cancer.

PubMed 2023/03/14(内容时间) Hum Immunol Q4 · IF 2.1(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

晚期乳腺癌患者需要新的治疗方法。新的潜在治疗方法已经被开发出来,例如过继性细胞疗法和替代性无细胞免疫疗法。本研究的目的是评估三种患者来源的免疫成分,CTLs、NK细胞和NK来源的EVs的细胞毒性,并评估开发针对乳腺癌的新疗法的潜力。CTLs被激活以针对MUC-1抗原。用流式细胞术评估了三种成分的体外细胞毒性活性,体内研究揭示了过继性细胞疗法的疗效。总体而言,CTLs对MCF7乳腺腺癌球体表现出最高的细胞毒性,在所有情况下均达到NK细胞细胞毒性百分比的两倍以上。与这两种细胞群体相比,NK来源的EVs对MCF7球体表现出最低的作用。通过过继性细胞疗法小鼠研究评估了MUC-1特异性CTLs,似乎耐受性良好且中等有效。需要对CTLs进行更多研究以评估安全性和有效性,从而评估其临床潜力,而NK细胞和NK来源的EVs是有前景的候选者,需要更多实验来增强其细胞毒性。

展开英文摘要原文

Patients with advanced stage breast cancer need novel therapies. New potential treatments have been developed, such as adoptive cellular therapies and alternative cell-free immunotherapies. The goal of this study was to assess the cytotoxicity of three of the patient-derived immune components, CTLs, NK cells and NK-derived EVs, and evaluate the potential for the development of novel therapy against breast cancer.

CTLs were activated against MUC-1 antigen. The in vitro cytotoxic activity of three components was assessed with flow cytometry and in vivo study revealed the efficacy of adoptive cell therapy.

Overall, CTLs exhibited the highest cytotoxicity against spheroids of MCF7 breast adenocarcinoma, reaching in all cases higher than double the percentage of NK cells' cytotoxicity. NK-derived EVs exhibited the lowest effect against MCF7 spheroids comparing to the two cell populations.

MUC-1 specific CTLs were evaluated with adoptive cell therapy mice study and appeared to be well tolerable and moderately efficacious. More studies need to be performed with CTLs to evaluate safety and efficacy in order to assess their clinical potential, while NK cells and NK-derived EVs are promising candidates that require more experiments to enhance their cytotoxicity.

论文信息

作者
Parsonidis P、Mamagkaki A、Papasotiriou I
第一作者单位
Research Genetic Cancer Centre S.A., Florina, Greece.Greece
通讯作者单位
Research Genetic Cancer Centre International GmbH, Zug, Switzerland. Electronic address: papasotiriou.ioannis@rgcc-international.com.Switzerland
期刊
Human immunology2023 May-Jul
原文标识
PubMed 36925436 · DOI 10.1016/j.humimm.2023.03.001