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抗原呈递树突状细胞-TIL(肿瘤浸润淋巴细胞)对卵巢癌细胞细胞毒性作用的体外研究

英文原题:An in vitro investigation into the cytotoxic impact of antigen-presenting dendritic cell-tumor infiltrating lymphocytes on ovarian cancer cells.

查看英文原题

An in vitro investigation into the cytotoxic impact of antigen-presenting dendritic cell-tumor infiltrating lymphocytes on ovarian cancer cells.

PubMed 2024/11/07(内容时间) BMC Cancer Q2 · IF 4.1(JCR 2025)

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研究概要

TIL 在 DC 刺激后具有增强针对肿瘤细胞的细胞毒作用的能力。

中文摘要

本研究旨在开发一种治疗卵巢癌的新方法,并探讨TIL(肿瘤浸润淋巴细胞)在卵巢癌治疗中的作用。首要目标是建立技术流程,从卵巢癌组织或腹水中分离肿瘤细胞、淋巴细胞和树突状细胞(DC)。随后,重点制备具有特异性细胞毒作用的DC-TIL,以用于靶向治疗。我们通过体外实验研究DC-TIL相互作用对肿瘤细胞的细胞毒作用,旨在为未来卵巢癌TIL疗法的临床发展提供基础实验依据。

实验样本包括3例患者(年龄32至75岁)的新鲜手术标本和腹水标本,来源于吉林大学第三医院妇科。通过体外分离从实体瘤组织中获取TIL,并从腹水标本中获取原代肿瘤细胞和DC。采用患者肿瘤细胞来源的肿瘤特异性抗原刺激DC成熟,随后将TIL与抗原刺激后的DC共培养,获得具有特异杀伤作用的TIL,并在体外检测DC-TIL对肿瘤细胞的细胞毒作用。

(1)成功从一例卵巢癌患者的肿瘤组织中扩增获得TIL。(2)成功从卵巢癌患者腹水细胞诱导获得DC。(3)经DC刺激后,TIL显著增强了对肿瘤细胞的细胞毒作用。

DC刺激后,TIL能够增强针对肿瘤细胞的细胞毒作用。

展开英文摘要原文

The objective of this study is to develop a novel therapeutic approach for the treatment of ovarian cancer while investigating the role of tumor-infiltrating lymphocytes (TILs) in the context of ovarian cancer therapy. The primary aim is to establish a technical procedure for the isolation of tumor cells, lymphocytes, and dendritic cells (DCs) derived from ovarian cancer tissues or ascites. Subsequently, the focus lies on the generation of dendritic cell-tumor infiltrating lymphocytes (DC-TILs) exhibiting specific cytotoxic capabilities aimed at targeted therapeutic interventions. The cytotoxic impact of DC-TIL interactions on tumor cells was investigated through in vitro experimentation. This research aims to provide fundamental experimental insights for the future clinical advancement of TIL therapy in ovarian cancer.

The experimental samples included fresh surgical specimens and ascites specimens procured from three patients (ranging in age from 32 to 75), sourced from the Department of Gynecology at the Third Bethune Hospital of Jilin University. TILs were extracted through in vitro isolation from solid tumor tissues, while primary tumor cells and DCs were obtained from ascites specimens. Tumor-specific antigens derived from patient tumor cells were utilized to stimulate the maturation of DCs. TILs were subsequently co-cultured with antigen-stimulated DC cells. Subsequently, TILs with specific killing effects were obtained, and the cytotoxic impact of DC-TILs on tumor cells was detected in vitro.

(1) TILs were successfully obtained through expansion from the tumor tissue of a patient diagnosed with ovarian cancer. (2) DCs were successfully induced from ascites cells harvested from patients diagnosed with ovarian cancer. (3) TILs significantly enhanced the cytotoxicity of tumor cells following DC stimulation.

TILs have the capacity to augment the cytotoxicity directed towards tumor cells following DC stimulation.

论文信息

作者
Yang S、Wang J、Du Z、Sheng C、Liu Q、Lao X、Xu D、Pan Y
第一作者单位
Department of Gynecologic, The Third Bethune Hospital of Jilin University, 130033, Changchun, China.China
通讯作者单位
Department of Gynecologic, The Third Bethune Hospital of Jilin University, 130033, Changchun, China. panying@jlu.edu.cn.China
期刊
BMC cancer2024 Nov 7
原文标识
PubMed 39511530 · DOI 10.1186/s12885-024-13131-7