[Tumor infiltrating T lymphocyte components in malignant pleural effusion of lung adenocarcinoma and their killing activities to autologous tumor cells].

医学 肿瘤浸润淋巴细胞 白细胞介素12 癌症研究 淋巴因子激活杀伤细胞 腺癌 病理 白细胞介素21 细胞毒性T细胞 胸腔积液 免疫学 生物 T细胞 免疫疗法 免疫系统 癌症 体外 内科学 生物化学
作者
Zhenkun Xia,Jiamiao Liu,Bei Qing,Wei Wang,Mingjiu Chen,Yunchang Yuan
出处
期刊:PubMed 卷期号:44 (10): 1107-1112
标识
DOI:10.11817/j.issn.1672-7347.2019.180747
摘要

To analyze the components of tumor infiltrating T lymphocyte (TIL) cells in malignant pleural effusion of lung adenocarcinoma, and evaluate their killing activities to autologous tumor cells. Methods: Malignant pleural effusions were collected from 17 patients with lung adenocarcinoma. Mononuclear cells were isolated by Ficoll density gradient centrifugation and flow cytometer was used to analyze TIL cell components. TIL and tumor cells were separated through adherent culture. The tumor cells were identified via intramuscular injection of adherent cells into nude mice and the killing effect of cultured lymphocytes on autologous tumor cells was studied. Results: Of the TIL in malignant pleural effusions, T cells accounted for 60.6%-79.3%, while T helper cells were significantly higher than T killer cells (36.63%±1.90% vs 24.64%±2.32%, P<0.001). There were also natural killer (NK) cells and NK T cells in the effusions. Tumor cells were successfully isolated and cultured. The killing activity of cultured TIL to autologous tumor cells was 39.14%±12.04%, and the killing activity of TIL with high proliferation rate to autologous tumor cells was higher than that of low proliferation group (50.51%±3.80% vs 29.04%±5.77%, P<0.001). Conclusion: T lymphocytes are the major components of TIL in malignant pleural effusions derived from lung adenocarcinoma, and T helper cells are more than T killer cells. The killing activity of TIL with strong proliferation ability to autologous tumor cells is higher than that of TIL with weak proliferation ability. Therefore, cells from malignant pleural effusions could be used for cellular immunotherapy against tumor.目的:分析恶性胸水中的肿瘤浸润T淋巴细胞(tumor infiltrating T lymphocyte,TIL)的细胞成分,探究其对自体肿瘤细胞的杀伤活性。方法:收集17例肺腺癌患者的胸水,采用Ficoll密度梯度离心法分离恶性胸水中的单个核细胞,流式细胞检测仪分析TIL细胞成分,贴壁培养法分离肿瘤细胞和TIL,裸鼠成瘤实验明确贴壁细胞为肿瘤细胞,MTT法检测培养的TIL对自体肿瘤细胞的杀伤活性。结果:恶性胸水TIL中T细胞占60.6%~79.3%,辅助性T细胞占比显著高于细胞毒性T细胞(36.63%±1.90% vs 24.64%±2.32%,P<0.001),同时还含有少量自然杀伤(natural killer,NK)细胞和NK T细胞;采用贴壁培养法成功分离培养肿瘤细胞,体外培养增殖的TIL对自体肿瘤细胞杀伤活性为39.14%±12.04%,且体外高增殖组的TIL对自体肿瘤细胞的杀伤活性高于低增殖组(50.51%±3.80% vs 29.04%±5.77%,P<0.001)。结论:肺腺癌恶性胸水中TIL主要以T细胞为主,辅助性T细胞多于细胞毒性T细胞,体外增殖能力强的TIL对自体肿瘤细胞的杀伤活性高于增殖能力弱者,恶性胸水可能为肿瘤细胞免疫治疗提供细胞来源。.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI

祝大家在新的一年里科研腾飞
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
斯文败类应助科研通管家采纳,获得10
刚刚
Akim应助科研通管家采纳,获得10
刚刚
ding应助科研通管家采纳,获得10
刚刚
刚刚
specialling发布了新的文献求助10
2秒前
爆米花应助奋斗的雅柔采纳,获得10
2秒前
cyfmlt发布了新的文献求助10
2秒前
4秒前
5秒前
排骨通通完成签到,获得积分10
5秒前
syl完成签到 ,获得积分10
5秒前
zhenya发布了新的文献求助10
8秒前
lijingwen发布了新的文献求助10
9秒前
雪白的听寒完成签到 ,获得积分10
10秒前
丹dan完成签到 ,获得积分10
10秒前
bkagyin应助小奶瓶_采纳,获得10
11秒前
ovo233发布了新的文献求助10
12秒前
12秒前
大模型应助莫华龙采纳,获得10
13秒前
15秒前
失眠的诗蕊应助肥羊七号采纳,获得20
16秒前
16秒前
17秒前
18秒前
文献缺缺应助llkk采纳,获得30
19秒前
liang发布了新的文献求助10
20秒前
judy发布了新的文献求助10
21秒前
失眠的诗蕊应助肥羊七号采纳,获得20
24秒前
li完成签到,获得积分10
24秒前
徐开心发布了新的文献求助10
26秒前
大喜子给大喜子的求助进行了留言
27秒前
28秒前
我是老大应助花花采纳,获得10
28秒前
打打应助liang采纳,获得10
29秒前
852应助ovo233采纳,获得10
31秒前
莫华龙发布了新的文献求助10
31秒前
JJDS完成签到,获得积分10
32秒前
精神小伙完成签到,获得积分10
33秒前
南瓜完成签到,获得积分10
35秒前
CodeCraft应助zbb采纳,获得10
35秒前
高分求助中
Востребованный временем 2500
The Three Stars Each: The Astrolabes and Related Texts 1500
Very-high-order BVD Schemes Using β-variable THINC Method 990
Les Mantodea de Guyane 800
Mantids of the euro-mediterranean area 700
Field Guide to Insects of South Africa 660
Mantodea of the World: Species Catalog 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 细胞生物学 免疫学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3396635
求助须知:如何正确求助?哪些是违规求助? 3006253
关于积分的说明 8820217
捐赠科研通 2693343
什么是DOI,文献DOI怎么找? 1475279
科研通“疑难数据库(出版商)”最低求助积分说明 682394
邀请新用户注册赠送积分活动 675645