Regulatory T cells and immunodeficiency in mycosis fungoides and Sezary syndrome

被引:88
作者
Krejsgaard, T. [1 ,2 ]
Odum, N. [2 ]
Geisler, C.
Wasik, M. A. [3 ]
Woetmann, A. [2 ]
机构
[1] Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, Panum Inst, DK-2200 Copenhagen N, Denmark
[2] Univ Copenhagen, Dept Biol, DK-2200 Copenhagen N, Denmark
[3] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
关键词
cutaneous T-cell lymphoma; Sezary syndrome; immunodeficiency; regulatory T cells; FOXP3; mycosis fungoides; TUMOR-INFILTRATING LYMPHOCYTES; GROWTH-FACTOR-BETA; NF-KAPPA-B; FOXP3; EXPRESSION; FAS-LIGAND; CONSTITUTIVE ACTIVATION; MALIGNANT PROLIFERATION; CD127; LYMPHOMA-CELLS; RECEPTOR;
D O I
10.1038/leu.2011.237
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cutaneous T-cell lymphoma (CTCL) is the term for diseases characterized by primary accumulation of malignant T cells in the skin. Patients with the two predominant clinical forms of CTCL called mycosis fungoides (MF) and Sezary syndrome (SS) characteristically develop severe immunodeficiency during disease progression and consequently patients with advanced disease frequently die of infections and not from the tumor burden. For decades, it has been suspected that the malignant T cells actively drive the evolving immunodeficiency to avoid antitumor immunity, yet, the underlying mechanisms remain unclear. The identification of a subset of highly immunosuppressive regulatory T cells (Tregs) triggered a variety of studies investigating if MF and SS are malignant proliferations of Tregs but seemingly discordant findings have been reported. Here, we review the literature to clarify the role of Tregs in MF and SS and discuss the potential mechanisms driving the immunodeficiency. Leukemia (2012) 26, 424-432; doi:10.1038/leu.2011.237; published online 9 September 2011
引用
收藏
页码:424 / 432
页数:9
相关论文
共 105 条
  • [21] Cutting edge:: Self-peptides drive the peripheral expansion of CD4+CD25+ regulatory T cells
    Cozzo, C
    Larkin, J
    Caton, AJ
    [J]. JOURNAL OF IMMUNOLOGY, 2003, 171 (11) : 5678 - 5682
  • [22] INTERLEUKIN-7 IS A GROWTH-FACTOR FOR SEZARY LYMPHOMA-CELLS
    DALLOUL, A
    LAROCHE, L
    BAGOT, M
    MOSSALAYI, MD
    FOURCADE, C
    THACKER, DJ
    HOGGE, DE
    MERLEBERAL, H
    DEBRE, P
    SCHMITT, C
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (03) : 1054 - 1060
  • [23] Natural and Adaptive Foxp3+ Regulatory T Cells: More of the Same or a Division of Labor?
    de Lafaille, Maria A. Curotto
    Lafaille, Juan J.
    [J]. IMMUNITY, 2009, 30 (05) : 626 - 635
  • [24] Interleukin-15 is an autocrine/paracrine viability factor for cutaneous T-cell lymphoma cells
    Döbbeling, U
    Dummer, R
    Laine, E
    Potoczna, N
    Gin, JZ
    Burg, G
    [J]. BLOOD, 1998, 92 (01) : 252 - 258
  • [25] Isoform-specific inhibition of RORα-mediated transcriptional activation by human FOXP3
    Du, Jianguang
    Huang, Chunjian
    Zhou, Baohua
    Ziegler, Steven F.
    [J]. JOURNAL OF IMMUNOLOGY, 2008, 180 (07) : 4785 - 4792
  • [26] A phase II open-label study of recombinant human interleukin-12 in patients with stage IA, IB, or IIA mycosis fungoides
    Duvic, Madeleine
    Sherman, Matthew L.
    Wood, Gary S.
    Kuzel, Timothy M.
    Olsen, Elise
    Foss, Francine
    Laliberte, Robert J.
    Ryan, John L.
    Zonno, Kristilyn
    Rook, Alain H.
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2006, 55 (05) : 807 - 813
  • [27] Regulatory T cell lineage specification by the forkhead transcription factor FoxP3
    Fontenot, JD
    Rasmussen, JP
    Williams, LM
    Dooley, JL
    Farr, AG
    Rudensky, AY
    [J]. IMMUNITY, 2005, 22 (03) : 329 - 341
  • [28] Profiles of Foxp3+ regulatory T cells in eczematous dermatitis, psoriasis vulgaris and mycosis fungoides
    Fujimura, T.
    Okuyama, R.
    Ito, Y.
    Aiba, S.
    [J]. BRITISH JOURNAL OF DERMATOLOGY, 2008, 158 (06) : 1256 - 1263
  • [29] Gavin MA, 2006, P NATL ACAD SCI USA, V103, P6659, DOI 10.1073/pnas.0509484103
  • [30] Medical progress - The pathogenesis of mycosis fungoides
    Girardi, M
    Heald, PW
    Wilson, LD
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (19) : 1978 - 1988