去核葡萄膜黑色素瘤中的浸润性T调节细胞。

Evan Lagouros, Diva Salomao, Erik Thorland, David O Hodge, Richard Vile, Jose S Pulido
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引用次数: 0

摘要

目的:T调节细胞(Treg)在减弱癌症免疫反应中的作用似乎是显著的,但Treg细胞在葡萄膜黑色素瘤中的存在尚未得到广泛的研究。因此,我们评估了葡萄膜黑色素瘤中肿瘤浸润性Treg细胞的存在。方法:回顾性检索梅奥诊所2000年至2005年的记录,以确定因葡萄膜黑色素瘤导致的眼睛去核病例。组织学检查包括肿瘤的位置、是否存在传质管侵犯、巩膜直接延伸、眼外延伸、细胞类型和优势细胞类型、每40倍视场有丝分裂图、淋巴细胞肿瘤侵犯、坏死、微血管模式、CD3、CD4、CD25和foxp3细胞的存在。我们还评估了通过图表复习获得的因素,包括去核前肿瘤的临床大小和超声厚度,患者去核时的年龄,去核前后对转移性疾病的全身评估,单体3,以及患者最后一次就诊时的全身状态。结果:42例去核眼中,淋巴细胞浸润17例(40.5%),Treg细胞(CD3+CD4+CD25+Foxp3+或CD3+CD4+CD25-Foxp3+)阳性5例(11.9%)。17例淋巴细胞浸润者中有5例(29.4%)存在Treg细胞,5例Treg细胞浸润者中有4例存在较大的淋巴细胞浸润(CD3细胞>1400个)。当使用“因病死亡”作为风险比终点时,CD3存在的风险比为5.5 (P = .03),临床大小的风险比为1.2 (P = .03)。此外,当以“是否存在转移”作为终点时,CD3存在的HR为3.6 (P = 0.05),临床大小的HR为1.3 (P = 0.003)。结论:虽然T淋巴细胞浸润是一个不良的预后指标,但Treg细胞在去核脉络膜黑色素瘤中很少见到,因此与其他肿瘤相比,Treg细胞的局部作用可能有限。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Infiltrative T regulatory cells in enucleated uveal melanomas.

Purpose: The role of T regulatory (Treg) cells in blunting immune response to cancer appears to be significant, but the presence of Treg cells in uveal melanoma has not been extensively examined. We therefore evaluated the presence of tumor-infiltrating Treg cells in uveal melanomas.

Methods: A retrospective search of Mayo Clinic records from 2000 to 2005 was performed to identify cases of eyes enucleated as a consequence of uveal melanoma. Histologic examination included location of the tumor, presence of emissary canal invasion, direct sclera extension, extraocular extension, cell type and predominant cell type, mitotic figures per 40 high-power fields, lymphocytic tumor invasion, necrosis, microvascular pattern, and presence of CD3, CD4, CD25, and Foxp3cells. Factors obtained by chart review were also evaluated, including clinical size and ultrasound thickness of tumor before enucleation, patient age at time of enucleation, systemic evaluation for metastatic disease both before and after enucleation, monosomy 3, and systemic status at last patient visit.

Results: Of 42 enucleated eyes, 17 (40.5 %) were found to have lymphocytic infiltrate and 5 (11.9%) were considered positive for the presence of Treg cells (CD3+CD4+CD25+Foxp3+ or CD3+CD4+CD25-Foxp3+). Thus 29.4% (5 of 17) of those with lymphocytic infiltates had Treg cells, and 4 of the 5 with Treg cells had a large lymphocytic infiltrate (>1400 CD3 cells). When using "death due to disease" as the hazard ratio (HR) end point, the HR for presence of CD3 was 5.5 (P = .03) and for clinical size, 1.2 (P = .03). Furthermore, when using "presence of metastasis" as the end point, the HR for presence of CD3 was 3.6 (P = .05) and for clinical size, 1.3 (P = .003).

Conclusion: Though T lymphocyte infiltration is a bad prognostic indicator, Treg cells are rarely seen in enucleated choroidal melanoma, so their local effect may be limited in contradistinction to other cancers.

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