Human NK cells and their receptors

被引:59
作者
Moretta, L [1 ]
Biassoni, R
Bottino, C
Cantoni, C
Pende, D
Mingari, MC
Moretta, A
机构
[1] Univ Genoa, Dipartimento Med Sperimentale, Genoa, Italy
[2] Ist Giannina Gaslini, I-16148 Genoa, Italy
[3] Univ Genoa, Ctr Eccellenza Ric Biomed, Genoa, Italy
[4] Ist Nazl Ric Canc, I-16132 Genoa, Italy
[5] Univ Genoa, Dipartimento Oncol Biol & Genet, Genoa, Italy
关键词
NK cells; HLA-Cl I-specific inhibitory receptors; triggering NK receptors; killer Ig-like receptors; NK-like activity; cytolytic T lymphocytes; HLA-E; acute myeloid leukemias; haploidentical bone marrow transplantation; NK cell alloreactivity;
D O I
10.1016/S1286-4579(02)00037-0
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 past decade has witnessed important progress in our understanding of how natural killer (NK) cells function. This is primarily consequent to the identification and functional characterization of MHC-specific inhibitory receptors that allow NK cells to discriminate between normal cells and potentially harmful cells that have lost or express insufficient amounts of MHC class I molecules. More recently, a number of activating receptors or coreceptors have been identified that are involved in the process of natural cytotoxicity but may also play a role in the direct recognition of pathogen-associated structures. Surprisingly, none of the triggering receptors identified in NK cells appears to be involved in the "NK-like activity" of a subset of CD8(+) cytolytic T lymphocytes. In this case, lysis of NK-susceptible tumor target cells is the result of the TCR alpha/beta-mediated recognition of HLA-E. The potent cytolytic activity of NK cells as well as their unique mode of functioning may be exploited in therapy. An important breakthrough is the recent report that "alloreactive" NK cells, generated in haploidentical bone marrow transplantation in patients with acute myeloid leukemias, may efficiently prevent leukemic relapses as well as graft rejection and graft-vs.-host disease. This may lead to a true revolution in bone marrow transplantation, based on the exploitation of appropriate HLA-Cl I mismatches that can put NK cells in action. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:1539 / 1544
页数:6
相关论文
共 60 条
[41]   Contact-dependent stimulation and inhibition of dendritic cells by natural killer cells [J].
Piccioli, D ;
Sbrana, S ;
Melandri, E ;
Valiante, NM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (03) :335-341
[42]  
Pietra G, 2001, EUR J IMMUNOL, V31, P3687, DOI 10.1002/1521-4141(200112)31:12<3687::AID-IMMU3687>3.0.CO
[43]  
2-C
[44]   A POPULATION OF EARLY FETAL THYMOCYTES EXPRESSING FC-GAMMA-RII/III CONTAINS PRECURSORS OF LYMPHOCYTES-T AND NATURAL-KILLER-CELLS [J].
RODEWALD, HR ;
MOINGEON, P ;
LUCICH, JL ;
DOSIOU, C ;
LOPEZ, P ;
REINHERZ, EL .
CELL, 1992, 69 (01) :139-150
[45]   Effectiveness of donor natural killer cell alloreactivity in mismatched hematopoietic transplants [J].
Ruggeri, L ;
Capanni, M ;
Urbani, E ;
Perruccio, K ;
Shlomchik, WD ;
Tosti, A ;
Posati, S ;
Rogaia, D ;
Frassoni, F ;
Aversa, F ;
Martelli, MF ;
Velardi, A .
SCIENCE, 2002, 295 (5562) :2097-2100
[46]   Cellular therapy: exploiting NK cell alloreactivity in transplantation [J].
Ruggeri, L ;
Capanni, M ;
Martelli, MF ;
Velardi, A .
CURRENT OPINION IN HEMATOLOGY, 2001, 8 (06) :355-359
[47]   X-LINKED LYMPHOPROLIFERATIVE DISEASE - 25 YEARS AFTER THE DISCOVERY [J].
SEEMAYER, TA ;
GROSS, TG ;
EGELER, RM ;
PIRRUCCELLO, SJ ;
DAVIS, JR ;
KELLY, CM ;
OKANO, M ;
LANYI, A ;
SUMEGI, J .
PEDIATRIC RESEARCH, 1995, 38 (04) :471-478
[48]  
Sivori S, 2000, EUR J IMMUNOL, V30, P787, DOI 10.1002/1521-4141(200003)30:3<787::AID-IMMU787>3.0.CO
[49]  
2-I
[50]   Early expression of triggering receptors and regulatory role of 2134 in human natural killer cell precursors undergoing in vitro differentiation [J].
Sivori, S ;
Falco, M ;
Marcenaro, E ;
Parolini, S ;
Biassoni, R ;
Bottino, C ;
Moretta, L ;
Moretta, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (07) :4526-4531