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本文引用的文献

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Evaluation of Immunophenotypic and Molecular Biomarkers for Sézary Syndrome Using Standard Operating Procedures: A Multicenter Study of 59 Patients.使用标准操作程序评估蕈样肉芽肿综合征的免疫表型和分子生物标志物:一项对59例患者的多中心研究。
J Invest Dermatol. 2016 Jul;136(7):1364-1372. doi: 10.1016/j.jid.2016.01.038. Epub 2016 Feb 28.
2
Flow cytometric identification of immunophenotypically aberrant T-cell clusters on skin shave biopsy specimens from patients with mycosis fungoides.蕈样肉芽肿患者皮肤剃刮活检标本中免疫表型异常T细胞簇的流式细胞术鉴定
Am J Clin Pathol. 2015 Jun;143(6):785-96. doi: 10.1309/AJCPWE2HBFCGDIDS.
3
Blood flow cytometry in Sézary syndrome: new insights on prognostic relevance and immunophenotypic changes during follow-up.Sézary综合征中的血流式细胞术:随访期间预后相关性及免疫表型变化的新见解
Am J Clin Pathol. 2015 Jan;143(1):57-69. doi: 10.1309/AJCP1NA3YCHCDEIG.
4
Expression of helper T cell master regulators in inflammatory dermatoses and primary cutaneous T-cell lymphomas: diagnostic implications.辅助性 T 细胞主调控因子在炎症性皮肤病和原发性皮肤 T 细胞淋巴瘤中的表达:诊断意义。
J Am Acad Dermatol. 2015 Jan;72(1):159-67. doi: 10.1016/j.jaad.2014.09.022. Epub 2014 Oct 18.
5
Primary cutaneous lymphomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.原发性皮肤淋巴瘤:ESMO 诊断、治疗及随访临床实践指南
Ann Oncol. 2013 Oct;24 Suppl 6:vi149-54. doi: 10.1093/annonc/mdt242. Epub 2013 Jul 17.
6
The role of extracorporeal photopheresis in the treatment of cutaneous T-cell lymphomas.体外光化学疗法在皮肤T细胞淋巴瘤治疗中的作用。
Transfus Apher Sci. 2012 Apr;46(2):195-202. doi: 10.1016/j.transci.2011.10.016. Epub 2011 Nov 8.
7
Regulatory T cells and immunodeficiency in mycosis fungoides and Sézary syndrome.调节性 T 细胞与蕈样肉芽肿和赛泽里综合征中的免疫缺陷。
Leukemia. 2012 Mar;26(3):424-32. doi: 10.1038/leu.2011.237. Epub 2011 Sep 9.
8
Clinical end points and response criteria in mycosis fungoides and Sézary syndrome: a consensus statement of the International Society for Cutaneous Lymphomas, the United States Cutaneous Lymphoma Consortium, and the Cutaneous Lymphoma Task Force of the European Organisation for Research and Treatment of Cancer.蕈样肉芽肿和塞扎里综合征的临床终点和反应标准:国际皮肤淋巴瘤学会、美国皮肤淋巴瘤联盟以及欧洲癌症研究与治疗组织皮肤淋巴瘤工作组的共识声明。
J Clin Oncol. 2011 Jun 20;29(18):2598-607. doi: 10.1200/JCO.2010.32.0630. Epub 2011 May 16.
9
The usefulness of CD26 in flow cytometric analysis of peripheral blood in Sézary syndrome.CD26在蕈样肉芽肿外周血流式细胞术分析中的应用价值。
Am J Clin Pathol. 2008 Jan;129(1):146-56. doi: 10.1309/05GFG3LY3VYCDMEY.

通过免疫表型分析监测一名 Sézary 综合征患者的体外光化学疗法。

Monitoring the extracorporeal photopheresis by immunophenotyping in a Sézary syndrome patient.

作者信息

Rodrigues Tânia, Lopes Sérgio, Pinho Catarina, Roncon Susana

机构信息

Liga Portuguesa Contra o Cancro, Núcleo Regional do Norte, Porto, Portugal.

Serviço de Terapia Celular, Instituto Português de Oncologia do Porto Francisco Gentil, EPE, Porto, Portugal.

出版信息

Porto Biomed J. 2017 Nov-Dec;2(6):340-343. doi: 10.1016/j.pbj.2017.04.008. Epub 2017 May 30.

DOI:10.1016/j.pbj.2017.04.008
PMID:32258791
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6806760/
Abstract

The extracorporeal photopheresis is indicated as immunomodulatory treatment in primary cutaneous T-cell lymphoma. There are no guidelines about the most suitable immunophenotypic panel to monitor and correlate clinical evolution and laboratory parameters. In this study we characterize a patient with Sézary syndrome stage III, who performed 98 sessions of photopheresis; in the last 30, the expression of T-cells in peripheral blood was evaluated. The patient had exfoliative dermatitis (mainly in the lower limbs) and several analytical disorders: anemia, neutropenia and lymphocytosis; abnormal number of effector T-cells and a CD4/CD8 ratio higher than 10; atypical cells (CD7, CD26) with aberrant phenotype (characteristic of malignant T-cell clones); and regulatory T-cells indicating an immunotolerance state. The clinical evolution verified can be related with the therapeutic scheme adopted. We propose a multiparameter flow cytometry approach to monitor patients with Sézary syndrome that realize photopheresis, including the aberrant cases.

摘要

体外光化学疗法被用作原发性皮肤T细胞淋巴瘤的免疫调节治疗。目前尚无关于最适合监测临床进展和实验室参数并将其关联起来的免疫表型检测组合的指南。在本研究中,我们对一名III期塞扎里综合征患者进行了特征描述,该患者接受了98次光化学疗法治疗;在最后30次治疗中,对外周血中的T细胞表达进行了评估。该患者患有剥脱性皮炎(主要在下肢)以及多种分析指标异常:贫血、中性粒细胞减少和淋巴细胞增多;效应T细胞数量异常且CD4/CD8比值高于10;具有异常表型的非典型细胞(CD7、CD26)(恶性T细胞克隆的特征);以及表明免疫耐受状态的调节性T细胞。观察到的临床进展可能与所采用的治疗方案有关。我们提出一种多参数流式细胞术方法,用于监测接受光化学疗法的塞扎里综合征患者,包括异常病例。