免疫系统
细胞毒性T细胞
CTL公司*
淋巴瘤
免疫学
FOXP3型
里德-斯特恩伯格细胞
免疫
生物
癌症研究
Treg细胞
医学
白细胞介素2受体
T细胞
霍奇金淋巴瘤
CD8型
体外
遗传学
作者
Sabine Schreck,D Friebel,Maike Buettner,Luitpold Distel,Gerhard G. Grabenbauer,Lawrence S. Young,Gerald Niedobitek
摘要
Abstract Classical Hodgkin Lymphoma (cHL) is morphologically characterized by a small number of tumour cells, Hodgkin and Reed–Sternberg (HRS) cells, surrounded by numerous tumour‐infiltrating lymphocytes (TIL). The functional role of these TIL is still controversial. While generally considered to represent an anti‐tumour immune response, TIL in cHL might result from the profoundly deregulated immunity of cHL patients. Eighty‐seven cases of cHL were available to evaluate the prognostical significance of tumour‐infiltrating cytotoxic T lymphocytes (CTL), T helper 1 (Th1) cells, T helper 2 (Th2) cells and regulatory T cells (Treg). We confirm that in cHL the microenvironment is dominated by Th2 cells and Treg and show that large numbers of Th2 cells are associated with significantly improved disease‐free survival ( p = 0.021) and event‐free survival ( p = 0.012). Furthermore, a high ratio of Treg over Th2 cells resulted in a significantly shortened disease‐free survival ( p = 0.025). These observations suggest that Treg may exert inhibitory effects on anti‐tumour immune responses mediated through Th2 cells and that Th2 cells may be more important for effective anti‐tumour immunity than anticipated. Copyright © 2008 John Wiley & Sons, Ltd.
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