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通过联合评估CD127和FOXP3来定义不同癌症亚型中调节性T细胞增加的比较方法。

Comparative approach to define increased regulatory T cells in different cancer subtypes by combined assessment of CD127 and FOXP3.

作者信息

Beyer Marc, Classen Sabine, Endl Elmar, Kochanek Matthias, Weihrauch Martin R, Debey-Pascher Svenja, Knolle Percy A, Schultze Joachim L

机构信息

Laboratory for Genomics and Immunoregulation, LIMES-Institute, University of Bonn, Carl-Troll-Street 31, 53115 Bonn, Germany.

出版信息

Clin Dev Immunol. 2011;2011:734036. doi: 10.1155/2011/734036. Epub 2011 Aug 28.

DOI:10.1155/2011/734036
PMID:21904560
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3166761/
Abstract

In recent years an increase of functional CD4(+)CD25(+) regulatory T cells (T(reg) cells) has been established for patients with solid tumors, acute leukemias, and lymphomas. We have reported an expanded pool of CD4(+)CD25(high) T(reg) cells in patients with chronic lymphatic leukemia (CLL), multiple myeloma (MM) as well as its premalignant precursor monoclonal gammopathy of undetermined significance (MGUS). In healthy individuals, low-level expression of CD127 on T cells in addition to the expression of FOXP3 has been associated with T(reg) cells. Here, we demonstrate that the expanded FOXP3(+) T-cell population in patients with colorectal cancer, CLL, MGUS, MM, follicular lymphoma, and Hodgkin's disease are exclusively CD127(low) T(reg) cells and were strongly suppressive. A significant portion of CD127(low)FOXP3(+) T(reg) cells expressed only low levels of CD25 suggesting that the previously reported expansion of CD25(+) T(reg) cells underestimates the true expansion. The assessment of CCR7 and CD45RA expression on the expanded CD4(+)CD127(low)FOXP3(+) T(reg) cells revealed an increase of both naïve as well as central and effector memory T(reg) cells in peripheral blood. Our data strongly support superiority of combined CD127 and FOXP3 analysis in comparison to CD25 and FOXP3 assessment for further quantification of T(reg) cells in malignant diseases.

摘要

近年来,已证实实体瘤、急性白血病和淋巴瘤患者体内功能性CD4(+)CD25(+)调节性T细胞(T(reg)细胞)数量增加。我们报道过,慢性淋巴细胞白血病(CLL)、多发性骨髓瘤(MM)及其癌前病变意义未明的单克隆丙种球蛋白病(MGUS)患者体内CD4(+)CD25(高)T(reg)细胞池有所扩大。在健康个体中,T细胞上除了表达FOXP3外,CD127低水平表达也与T(reg)细胞有关。在此,我们证明,结直肠癌、CLL、MGUS、MM、滤泡性淋巴瘤和霍奇金病患者体内扩增的FOXP3(+) T细胞群体均为CD127(低)T(reg)细胞,且具有强抑制性。相当一部分CD127(低)FOXP3(+) T(reg)细胞仅低水平表达CD25,这表明先前报道的CD25(+) T(reg)细胞扩增低估了实际的扩增情况。对扩增的CD4(+)CD127(低)FOXP3(+) T(reg)细胞上CCR7和CD45RA表达的评估显示,外周血中幼稚型以及中枢和效应记忆T(reg)细胞均有所增加。我们的数据有力地支持了与CD25和FOXP3评估相比,联合CD127和FOXP3分析在进一步定量恶性疾病中T(reg)细胞方面具有优越性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/388b/3166761/36441afcf4ef/CDI2011-734036.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/388b/3166761/401b86fb66ec/CDI2011-734036.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/388b/3166761/90591cc1ea55/CDI2011-734036.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/388b/3166761/72a3846aabd1/CDI2011-734036.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/388b/3166761/88655135ce84/CDI2011-734036.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/388b/3166761/36441afcf4ef/CDI2011-734036.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/388b/3166761/401b86fb66ec/CDI2011-734036.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/388b/3166761/90591cc1ea55/CDI2011-734036.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/388b/3166761/72a3846aabd1/CDI2011-734036.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/388b/3166761/88655135ce84/CDI2011-734036.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/388b/3166761/36441afcf4ef/CDI2011-734036.005.jpg

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