调节性T淋巴细胞浸润影响卵巢癌患者的临床预后

C. Valverde, Karen López Miguel, J. A. Sánchez-Villanueva, Alej, R. Lambert, Tania Carmenate Portilla, María del Carmen Arango Prado
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引用次数: 0

摘要

背景:卵巢癌(OC)是女性最严重和最致命的癌症之一。调节性T (Treg)细胞可能参与介导肿瘤组织中的抑制微环境,并有助于肿瘤逃避免疫应答。具体而言,一些研究表明,恶性腹水和外周血中Treg细胞浸润与临床预后不良有关。方法:采用流式细胞术检测24例上皮性卵巢癌(EOC)患者的腹水和外周血中CD4+、CD25+、叉头盒p3+ (Foxp3+)淋巴细胞的数量。总生存率与Treg水平有关。结果:研究表明,与健康对照组相比,EOC患者外周血Treg细胞亚群增加。EOC患者腹水Treg浸润高于血液Treg浸润。与Treg水平正常的患者相比,Treg在血液中高浸润的患者总体生存率较低。关于腹水中Treg水平升高的患者与总体生存期之间的关系,与Treg水平正常的患者腹水相比,没有发现不利因素。结论:研究提示EOC患者腹水和外周血中Treg淋巴细胞增加,并可能通过损害抗肿瘤免疫应答而降低总生存期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Infiltration of Regulatory T Lymphocytes Impair Clinical Outcome in Ovarian Cancer Patients
Background: Ovarian carcinoma (OC) is one of the most severe and lethal cancers in women. Regulatory T (Treg) cells may participate in mediating a suppressive microenvironment in tumor tissue and contribute to tumor evasion from immune response. Specifically, some studies have indicated that Treg cell infiltration in malignant ascites and peripheral blood has been associated with poor clinical outcome. Methods: The number of CD4+, CD25+, forkhead box p3+ (Foxp3+) lymphocytes was assessed via flow cytometry in ascites and peripheral blood from 24 women with epithelial ovarian cancer (EOC). Overall survival was associated with Treg levels. Results: The study indicated an increase in the Treg cell subset from peripheral blood of EOC patients compared with those in healthy controls. Treg infiltration in ascites was higher than in blood into EOC patients. The patients with high infiltration of Treg in blood revealed less overall survival compared to a counterpart with normal levels of Treg. Regarding the association between patients with increased levels of Treg in ascites with overall survival there was no disadvantage found, compared to ascites from patients with normal levels of Treg. Conclusion: Study suggests that Treg lymphocytes were increased in ascites and peripheral blood in EOC patients and could be associated with diminished overall survival, via impairment antitumor immune response.
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