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Best Practices for Preparing a Single Cell Suspension from Solid Tissues for Flow Cytometry.单细胞悬液制备的最佳实践:从固体组织用于流式细胞术。
Cytometry A. 2019 Feb;95(2):219-226. doi: 10.1002/cyto.a.23690. Epub 2018 Dec 6.
2
Normative data for flow cytometry immunophenotyping of benign lymph nodes sampled by surgical biopsy.通过手术活检获取的良性淋巴结流式细胞术免疫表型分析的标准数据。
J Clin Pathol. 2018 Feb;71(2):174-179. doi: 10.1136/jclinpath-2017-204687. Epub 2017 Sep 15.
3
Preparing Viable Single Cells from Human Tissue and Tumors for Cytomic Analysis.从人体组织和肿瘤中制备用于细胞组学分析的活单细胞。
Curr Protoc Mol Biol. 2017 Apr 3;118:25C.1.1-25C.1.23. doi: 10.1002/cpmb.37.
4
A Basic Approach to Lymph Node and Flow Cytometry Fine-Needle Cytology.淋巴结及流式细胞术细针穿刺细胞学的基本方法
Acta Cytol. 2016;60(4):284-301. doi: 10.1159/000448679. Epub 2016 Sep 17.
5
Fine-needle aspiration is superior to needle core biopsy as a sample acquisition method for flow cytometric analysis in suspected hematologic neoplasms.对于疑似血液系统肿瘤的流式细胞术分析,细针穿刺作为一种样本采集方法优于粗针活检。
Cytometry B Clin Cytom. 2015 Jan;88(1):64-8. doi: 10.1002/cyto.b.21183. Epub 2014 Sep 4.

一项关于确定自动组织解离器在基于流式细胞术评估血液淋巴肿瘤组织活检中的效用的初步研究。

A Pilot Study to Determine the Utility of Automated Tissue Dissociator for Flowcytometry Based Evaluation of Hematolymphoid Tumor Tissue Biopsies.

作者信息

Karmakar Tanusri, Banerjee Sambhunath, Brahma Subhajit, Dey Debdeep, Radhakrishnan Vivek, Chandy Mammen, Ghara Niharendu, Krishnan Shekhar, Mukherjee Geetashree, Mishra Deepak Kumar, Arora Neeraj

机构信息

Department of Laboratory Hematology and Molecular Genetics, Tata Medical Center, Kolkata, 700160 India.

Department of Histopathology, Tata Medical Center, Kolkata, India.

出版信息

Indian J Hematol Blood Transfus. 2022 Apr;38(2):403-410. doi: 10.1007/s12288-021-01481-2. Epub 2021 Aug 15.

DOI:10.1007/s12288-021-01481-2
PMID:35496962
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9001761/
Abstract

Routine diagnostic biopsy tissue processing, conventional histology/immunohistochemistry (IHC) method is a multi-step and time consuming practice. With the advanced tissue dissociation protocols and panel designing, flow cytometric immunophenotyping (FCI) can be performed on diagnostic hematolymphoid tissue samples using single cell suspensions that economize steps and the time taken. Diagnostic tissue samples from lymph node, mediastinal mass, testicular biopsies and similar sites were dissociated using gentle MACS Octo-dissociator and FCI was performed thereafter. Oral tissue biopsy samples were also processed as a validation set for the protocol. 21 prospective tissue biopsy samples with suspected involvement by a known hematolymphoid neoplasm were processed and evaluated. These included B lymphoblastic lymphoma (n = 12), T lymphoblastic lymphomas (n = 3), Burkitts lymphoma (n = 3) and one case each of granulocytic sarcoma, Hodgkin lymphoma and granulomatous disease. Tissue FCI and IHC were found concordant with identified profile FCI obtained from blood/bone marrow analyses. FCI can produce a highly sensitive and reliable report, within hours, by processing fresh tumor tissue samples from suspected hematolymphoid malignancies. This method can be considered as an effective adjunct to IHC and can be applicable in routine clinical diagnostics, especially in cases that needs quick diagnosis and immediate clinical treatment.

摘要

常规诊断活检组织处理,传统组织学/免疫组织化学(IHC)方法是一个多步骤且耗时的操作。通过先进的组织解离方案和面板设计,流式细胞免疫表型分析(FCI)可以使用单细胞悬液对诊断性血液淋巴组织样本进行检测,从而节省步骤和时间。使用温和MACS Octo解离器对来自淋巴结、纵隔肿块、睾丸活检及类似部位的诊断组织样本进行解离,随后进行FCI检测。口腔组织活检样本也作为该方案的验证集进行处理。对21例疑似患有已知血液淋巴肿瘤的前瞻性组织活检样本进行了处理和评估。这些样本包括B淋巴母细胞淋巴瘤(n = 12)、T淋巴母细胞淋巴瘤(n = 3)、伯基特淋巴瘤(n = 3)以及各1例粒细胞肉瘤、霍奇金淋巴瘤和肉芽肿性疾病。发现组织FCI和IHC与从血液/骨髓分析中获得的已识别的FCI谱一致。通过处理疑似血液淋巴恶性肿瘤的新鲜肿瘤组织样本,FCI可以在数小时内生成一份高度敏感且可靠的报告。该方法可被视为IHC的有效辅助手段,可应用于常规临床诊断,尤其是在需要快速诊断和立即临床治疗的病例中。