FOXP3+ regulatory T cells in cutaneous T-cell lymphomas: association with stage and survival

被引:122
作者
Gjerdrum, L. M.
Woetmann, A.
Odum, N.
Burton, C. M.
Rossen, K.
Skovgaard, G. L.
Ryder, L. P.
Ralfkiaer, E.
机构
[1] Univ Copenhagen Hosp, Rigshosp, Dept Pathol, DK-2100 Copenhagen, Denmark
[2] Univ Copenhagen, Inst Mol Biol, Dept Med Microbiol & Immunol, DK-2100 Copenhagen, Denmark
[3] Bispebjerg Hosp, Dept Pathol, DK-2100 Copenhagen, Denmark
[4] Bispebjerg Hosp, Dept Dermatol, DK-2100 Copenhagen, Denmark
[5] Univ Copenhagen, Dept Immunol, Tissue Typing Lab, DK-2100 Copenhagen, Denmark
关键词
cutaneous T-cell lymphoma; FOXP3; immunohistochemistry; regulatory T cells; survival;
D O I
10.1038/sj.leu.2404913
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
FOXP3 is a unique marker for CD4+CD25+ regulatory T cells (Tregs). In solid tumours, high numbers of Tregs are associated with a poor prognosis. Knowledge about the implications of Tregs for the behaviour of haematological malignancies is limited. In this study, skin biopsies from 86 patients with mycosis fungoides (MF) and cutaneous T-cell lymphoma (CTCL) unspecified were analysed for the expression of FOXP3 on tumour cells and tumour-infiltrating Tregs. Labelling of above 10% of the neoplastic cells was seen in one case classified as an aggressive epidermotropic CD8+ cytotoxic CTCL. In the remaining 85 cases, the atypical neoplastic infiltrate was either FOXP3 negative (n=80) or contained only very occasional weakly positive cells (n=5). By contrast, all biopsies showed varying numbers of strongly FOXP3+ tumour-infiltrating Tregs. MF with early or infiltrated plaques had significantly higher numbers of FOXP3+ Tregs than CTCL unspecified or advanced MF with tumours or transformation to large cell lymphoma. An analysis of all patients demonstrated that increasing numbers of FOXP3+ Tregs were associated with improved survival in both MF and CTCL unspecified. In conclusion, our data indicate that the presence of FOXP3+ Tregs in CTCL is associated with disease stage and patient survival.
引用
收藏
页码:2512 / 2518
页数:7
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