FoxP3: A genetic link between immunodeficiency and autoimmune diseases

被引:29
作者
Chang, Xing
Zheng, Pan
Liu, Yang
机构
[1] Ohio State Univ, Med Ctr, Dept Pathol, Div Canc Immunol, Columbus, OH 43210 USA
[2] Ctr Comprehens Canc, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
homeostatic proliferation; thymopoiesis; IPEX; Scurfy;
D O I
10.1016/j.autrev.2005.10.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It has long been observed that patients with autoimmune diseases also have immune deficiency. How these two opposite extremes of immunity can be found in the same individual is largely unclear. Here we review the evidence that a FoxP3 defect may provide a critical link between autoimmunity and immune deficiency. Disruption of FoxP3 results in severe autoimmune syndromes in both human and mice. Bone marrow chimera experiments indicate that FoxP3 defects in both hematopoietic and non-hematopoietic cells are required for the development of severe autoimmune disease. FoxP3 mutation in the hematopoietic cells impairs the development of regulatory T cells (Treg). Our data demonstrate that the mutation in non-hematopoietic cells results in deficient thymopoiesis. Defective T cell production may be an underlying cause of T cell hyperproliferation, which together with Treg defects, may lead to fatal autoimmune disease in mouse and man. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:399 / 402
页数:4
相关论文
共 36 条
  • [1] The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
    Bennett, CL
    Christie, J
    Ramsdell, F
    Brunkow, ME
    Ferguson, PJ
    Whitesell, L
    Kelly, TE
    Saulsbury, FT
    Chance, PF
    Ochs, HD
    [J]. NATURE GENETICS, 2001, 27 (01) : 20 - 21
  • [2] BLAIR PJ, 1994, J IMMUNOL, V153, P3764
  • [3] THYMIC HYPOPLASIA, AUTOIMMUNE HEMOLYTIC-ANEMIA AND JUVENILE PEMPHIGOID IN AN INFANT
    BLOOMFIELD, S
    STOCKDILL, G
    BARNETSON, RS
    [J]. BRITISH JOURNAL OF DERMATOLOGY, 1982, 106 (03) : 353 - 355
  • [4] Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse
    Brunkow, ME
    Jeffery, EW
    Hjerrild, KA
    Paeper, B
    Clark, LB
    Yasayko, SA
    Wilkinson, JE
    Galas, D
    Ziegler, SF
    Ramsdell, F
    [J]. NATURE GENETICS, 2001, 27 (01) : 68 - 73
  • [5] The Scurfy mutation of FoxP3 in the thymus stroma leads to defective thymopoiesis
    Chang, X
    Gao, JX
    Jiang, Q
    Wen, J
    Seifers, N
    Su, LS
    Godfrey, VL
    Zuo, T
    Zheng, P
    Liu, Y
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (08) : 1141 - 1151
  • [6] JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome
    Chatila, TA
    Blaeser, F
    Ho, N
    Lederman, HM
    Voulgaropoulos, C
    Helms, C
    Bowcock, AM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (12) : R75 - R81
  • [7] Homeostasis-stimulated proliferation drives naive T cells to differentiate directly into memory T cells
    Cho, BK
    Rao, VP
    Ge, Q
    Eisen, HN
    Chen, JZ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (04) : 549 - 556
  • [8] Davies K, 2001, J RHEUMATOL, V28, P2326
  • [9] MYASTHENIA-GRAVIS AND LYMPHOMA - CLINICAL AND IMMUNOLOGICAL ASSOCIATION
    DAVIS, S
    SCHUMACHER, MJ
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1979, 242 (19): : 2096 - 2097
  • [10] Dudley ME, 2002, SCIENCE, V298, P850, DOI 10.1126/science.1076514