Natural killer and dendritic cell liaison: Recent insights and open questions

被引:32
作者
Ferlazzo, G [1 ]
机构
[1] Ist Nazl Ric Canc, Immunol Lab, I-16132 Genoa, Italy
关键词
dendritic cells; natural killer cells; secondary lymphoid organs; innate immunity; cell activation;
D O I
10.1016/j.imlet.2005.04.015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The functional links between natural killer (NK) and dendritic cells (DCs) have been widely investigated in the last years and different studies have demonstrated that reciprocal activations ensue upon NK/DC interactions. More recently, the anatomical sites were these interactions take place have been identified together with the related cell subsets involved. Remarkably, as predicted by pioneering studies, there is now "in vivo" evidence that this cellular cross-talk occurring during the innate phase of the immune response can deeply affects the magnitude and the quality of the subsequent adaptive response. Thus, NK cells are not merely cytotoxic lymphocytes competent in containing viral and tumor spreading but can now rather be considered as crucial fine-tuning effector cells. Despite the large mass of information rapidly obtained in this field, several fundamental questions still remain to be addressed. Among them, two central issues require additional consideration: (a) what mediates the activation of NK cell cytotoxicity induced by DCs and (b) what factors are responsible for NK-dependent maturation of DCs. Unexpectedly, for both of these questions insufficient or inconsistent results are so far available; factors either dependent or independent from cell contacts between DCs and NK cells have been convincingly described, and it is likely that several mechanisms, rather than a single one, are responsible for each of these novel innate functions. Understanding the molecular bases of this complex liaison will pave the way to new and more effective immune adjuvants. The most recent advances about NK/DC interplay are here reviewed and possible answers to still open questions in this field are considered. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:12 / 17
页数:6
相关论文
共 52 条
[1]  
ADAM C, 2005, BLOOD MAR
[2]   Functional interactions between dendritic cells and NK cells during viral infection [J].
Andrews, DM ;
Scalzo, AA ;
Yokoyama, WM ;
Smyth, MJ ;
Degli-Esposti, MA .
NATURE IMMUNOLOGY, 2003, 4 (02) :175-181
[3]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[4]   A survival game of hide and seek: Cytomegaloviruses and MHC class I antigen presentation pathways [J].
Basta, S ;
Bennink, JR .
VIRAL IMMUNOLOGY, 2003, 16 (03) :231-242
[5]   A new class of membrane-bound chemokine with a CX(3)C motif [J].
Bazan, JF ;
Bacon, KB ;
Hardiman, G ;
Wang, W ;
Soo, K ;
Rossi, D ;
Greaves, DR ;
Zlotnik, A ;
Schall, TJ .
NATURE, 1997, 385 (6617) :640-644
[6]   Natural killer and dendritic cell contact in lesional atopic dermatitis skin -: Malassezia-influenced cell interaction [J].
Buentke, E ;
Heffler, LC ;
Wilson, JL ;
Wallin, RPA ;
Löfman, C ;
Chambers, BJ ;
Ljunggren, HG ;
Scheynius, A .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2002, 119 (04) :850-857
[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]   The natural killer cell-mediated killing of autologous dendritic cells is confined to a cell subset expressing CD94/NKG2A, but lacking inhibitory killer Ig-like receptors [J].
Chiesa, MD ;
Vitale, M ;
Carlomagno, S ;
Ferlazzo, G ;
Moretta, L ;
Moretta, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2003, 33 (06) :1657-1666
[9]   Human natural killer cells:: a unique innate immunoregulatory role for the CD56bright subset [J].
Cooper, MA ;
Fehniger, TA ;
Turner, SC ;
Chen, KS ;
Ghaheri, BA ;
Ghayur, T ;
Carson, WE ;
Caligiuri, MA .
BLOOD, 2001, 97 (10) :3146-3151
[10]   Preventing NK cell activation by donor dendritic cells enhances allospecific CD4 T cell priming and promotes Th type 2 responses to transplantation antigens [J].
Coudert, RD ;
Coureau, C ;
Guéry, JC .
JOURNAL OF IMMUNOLOGY, 2002, 169 (06) :2979-2987