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从保存的人肿瘤组织标本中分离 TIL(肿瘤浸润淋巴细胞)用于下游表征

英文原题:Isolation of tumor-infiltrating lymphocytes from preserved human tumor tissue specimens for downstream characterization.

查看英文原题

Isolation of tumor-infiltrating lymphocytes from preserved human tumor tissue specimens for downstream characterization.

PubMed 2022/07/18(内容时间) STAR Protoc Q4 · IF 1.4(JCR 2025)

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中文摘要

流式细胞术对TIL(肿瘤浸润淋巴细胞)进行免疫表型分析可预测免疫治疗疗效,但从实体瘤标本建立流式检测方法仍面临若干障碍。本文提供一种详细酶法流程,用于从人肿瘤组织中分离TIL。该流程经过优化,可从活检组织获得足量存活TIL,以供流式免疫表型分析;组织样本还可保存最长72小时再进行后续表征。该流程的完整细节及操作说明请参阅Kumagai等(2020、2022年)。

展开英文摘要原文

Immunophenotyping of tumor-infiltrating lymphocytes (TILs) by flow cytometry can predict clinical efficacy of immunotherapy.

However, several obstacles need to be overcome for developing a flow cytometry assay starting from solid tumor specimens.

Here, we show a detailed enzyme-based protocol to isolate TILs from human tumor tissues. The protocol was optimized to obtain enough viable TILs from a biopsy tissue specimen for flow cytometry-based TIL immunophenotyping.

Additionally, tissue samples could be preserved for up to 72 h for subsequent characterization. For complete details on the use and execution of this protocol, please refer to Kumagai et al. (2020, 2022).

论文信息

作者
Kobayashi T、Kumagai S、Doi R、Afonina E、Koyama S、Nishikawa H
第一作者单位
Division of Cancer Immunology, Research Institute/Exploratory Oncology Research & Clinical Trial Center (EPOC), National Cancer Center, Tokyo/Chiba 104-0045/277-8577, Japan; Becton, Dickinson and Company, Biosciences, Tokyo 107-0052, Japan. Electronic address: tamiyo.kobayashi@bd.com.Japan
通讯作者单位
Division of Cancer Immunology, Research Institute/Exploratory Oncology Research & Clinical Trial Center (EPOC), National Cancer Center, Tokyo/Chiba 104-0045/277-8577, Japan; Department of Immunology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan. Electronic address: hnishika@ncc.go.jp.Japan
文献类型
非美国政府资助研究
期刊
STAR protocols2022 Sep 16
原文标识
PubMed 35852944 · DOI 10.1016/j.xpro.2022.101557