CD56bright natural killer (NK) cells: an important NK cell subset

被引:694
作者
Poli, Aurelie [1 ]
Michel, Tatiana [1 ]
Theresine, Maud [1 ]
Andres, Emmanuel [2 ]
Hentges, Francois [1 ]
Zimmer, Jacques [1 ]
机构
[1] CRP Sante, Lab Immunogenet Allergol, L-1526 Luxembourg, Luxembourg
[2] Hop Univ Strasbourg, Serv Med Interne, Clin Med B, Strasbourg, France
关键词
CD56(bright); immunoregulation; natural killer cells; HUMAN CYTOMEGALOVIRUS-INFECTION; PERIPHERAL-BLOOD; RHEUMATOID-ARTHRITIS; RECEPTOR EXPRESSION; GENE-EXPRESSION; ACTIVATION; CD56(DIM); SUBPOPULATIONS; DYSFUNCTION; CD94/NKG2C;
D O I
10.1111/j.1365-2567.2008.03027.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human natural killer (NK) cells can be subdivided into different populations based on the relative expression of the surface markers CD16 and CD56. The two major subsets are CD56(bright) CD16(dim/-) and CD56(dim) CD16(+), respectively. In this review, we will focus on the CD56(bright) NK cell subset. These cells are numerically in the minority in peripheral blood but constitute the majority of NK cells in secondary lymphoid tissues. They are abundant cytokine producers but are only weakly cytotoxic before activation. Recent data suggest that under certain conditions, they have immunoregulatory properties, and that they are probably immediate precursors of CD56(dim) NK cells. CD56(bright) NK cell percentages are expanded or reduced in a certain number of diseases, but the significance of these variations is not yet clear.
引用
收藏
页码:458 / 465
页数:8
相关论文
共 54 条
[1]   Modification of P-selectin glycoprotein ligand-1 with a natural killer cell-restricted sulfated lactosamine creates an alternate ligand for L-selectin [J].
André, P ;
Spertini, O ;
Guia, S ;
Rihet, P ;
Dignat-George, F ;
Brailly, H ;
Sampol, J ;
Anderson, PJ ;
Vivier, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3400-3405
[2]  
Anumanthan A, 1998, J IMMUNOL, V161, P2780
[3]   Natural killer cell subpopulations in putative resistant individuals and patients with active Mycobacterium tuberculosis infection [J].
Barcelos, W. ;
Sathler-Avelar, R. ;
Martins-Filho, O. A. ;
Carvalho, B. N. ;
Guimaraes, T. M. P. D. ;
Miranda, S. S. ;
Andrade, H. M. ;
Oliveira, M. H. P. ;
Toledo, V. P. C. P. .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2008, 68 (01) :92-102
[4]   Regulatory CD56bright natural killer cells mediate immunomodulatory effects of IL-2Rα-targeted therapy (daclizumab) in multiple sclerosis [J].
Bielekova, B ;
Catalfamo, M ;
Reichert-Scrivner, S ;
Packer, A ;
Cerna, M ;
Waldmann, TA ;
McFarland, H ;
Henkart, PA ;
Martin, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (15) :5941-5946
[5]   Recalcitrant warts, associated with natural killer cell dysfunction, treated with systemic IFN-α [J].
Cac, Natalie N. ;
Ballas, Zuhair K. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 118 (02) :526-528
[6]   Human natural killer cells [J].
Caligiuri, Michael A. .
BLOOD, 2008, 112 (03) :461-469
[7]   Unique subpopulations of CD56+ NK and NK-T peripheral blood lymphocytes identified by chemokine receptor expression repertoire [J].
Campbell, JJ ;
Qin, SX ;
Unutmaz, D ;
Soler, D ;
Murphy, KE ;
Hodge, MR ;
Wu, LJ ;
Butcher, EC .
JOURNAL OF IMMUNOLOGY, 2001, 166 (11) :6477-6482
[8]  
Carson William, 1996, Methods (Orlando), V9, P327, DOI 10.1006/meth.1996.0038
[9]   CD56bright human NK cells differentiate into CD56dim cells:: Role of contact with peripheral fibroblasts [J].
Chan, Antoni ;
Hong, Deng-Li ;
Atzberger, Ann ;
Kollnberger, Simon ;
Filer, Andrew D. ;
Buckley, Christopher D. ;
McMichael, Andrew ;
Enver, Tariq ;
Bowness, Paul .
JOURNAL OF IMMUNOLOGY, 2007, 179 (01) :89-94
[10]   The biology of human natural killer-cell subsets [J].
Cooper, MA ;
Fehniger, TA ;
Caligiuri, MA .
TRENDS IN IMMUNOLOGY, 2001, 22 (11) :633-640