Immunological and genetic bases of new primary immunodeficiencies

被引:63
作者
Marodi, Laszlo [1 ]
Notarangelo, Luigi D. [1 ]
机构
[1] Harvard Univ, Sch Med, Div Immunol, Childrens Hosp, Boston, MA 02115 USA
基金
匈牙利科学研究基金会;
关键词
D O I
10.1038/nri2195
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Since 1952, when congenital agammaglobulinaemia was described by Bruton, the characterization of genetically defined immunodeficiencies in humans has been crucial for a better understanding of the biology of the innate and adaptive immune responses. This Review focuses on the characterization of new primary immunodeficiencies and diseaserelated genes. A series of primary defects of innate immunity have recently been discovered and are discussed here. Moreover, new defects in pre- B- cell and B- cell differentiation and antibody maturation are summarized and recently discovered monogenic immunodeficiencies that disturb the homeostasis of both the innate and the adaptive immune systems are discussed.
引用
收藏
页码:851 / 861
页数:11
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共 103 条
  • [1] A novel genetic leukocyte adhesion deficiency in subsecond triggering of integrin avidity by endothelial chemokines results in impaired leukocyte arrest on vascular endothelium under shear flow
    Alon, R
    Aker, M
    Feigelson, S
    Sokolovsky-Eisenberg, M
    Staunton, DE
    Cinamon, G
    Grabovsky, V
    Shamri, R
    Etzioni, A
    [J]. BLOOD, 2003, 101 (11) : 4437 - 4445
  • [2] Germline mutations in HRAS proto-oncogene cause Costello syndrome
    Aoki, Y
    Niihori, T
    Kawame, H
    Kurosawa, K
    Filocamo, M
    Kato, K
    Suzuki, Y
    Kure, S
    Matsubara, Y
    [J]. NATURE GENETICS, 2005, 37 (10) : 1038 - 1040
  • [3] 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
  • [4] The Toll-like receptors: analysis by forward genetic methods
    Beutler, B
    [J]. IMMUNOGENETICS, 2005, 57 (06) : 385 - 392
  • [5] Genetic disorders of programmed cell death in the immune system
    Bidere, Nicolas
    Su, Helen C.
    Lenardo, Michael J.
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 2006, 24 : 321 - 352
  • [6] Development of human lymphoid cells
    Blom, Blanca
    Spits, Hergen
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 2006, 24 : 287 - 320
  • [7] A novel human primary immunodeficiency syndrome caused by deficiency of the endosomal adaptor protein p14
    Bohn, Georg
    Allroth, Anna
    Brandes, Gudrun
    Thiel, Jens
    Glocker, Erik
    Schaffer, Alejandro A.
    Rathinam, Chozhavendan
    Taub, Nicole
    Teis, David
    Zeidler, Cornelia
    Dewey, Ricardo A.
    Geffers, Robert
    Buer, Jan
    Huber, Lukas A.
    Welte, Karl
    Grimbacher, Bodo
    Klein, Christoph
    [J]. NATURE MEDICINE, 2007, 13 (01) : 38 - 45
  • [8] Defective interleukin-12/interferon-γ pathway in patients with hyperimmunoglobulinemia E syndrome
    Borges, WG
    Augustine, NH
    Hill, HR
    [J]. JOURNAL OF PEDIATRICS, 2000, 136 (02) : 176 - 180
  • [9] The induction of Bim expression in human T-cell blasts is dependent on nonapoptotic Fas/CD95 signaling
    Bosque, Alberto
    Ignacio Aguilo, Juan
    Angeles Alava, M.
    Paz-Artal, Estela
    Naval, Javier
    Allende, Luis M.
    Anel, Alberto
    [J]. BLOOD, 2007, 109 (04) : 1627 - 1635
  • [10] Primary immunodeficiency diseases due to defects in lymphocytes.
    Buckley, RH
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (18) : 1313 - 1324