The role of natural killer cells in immunity against multiple myeloma

被引:64
作者
Godfrey, James [1 ]
Benson, Don M., Jr. [1 ,2 ]
机构
[1] Ohio State Univ, Coll Med, Columbus, OH 43210 USA
[2] Ohio State Univ, Ctr Comprehens Canc, Div Hematol, Columbus, OH 43210 USA
关键词
Natural killer cells; immunotherapy; multiple myeloma; INTERFERON-GAMMA-PRODUCTION; REGULATORY T-CELLS; LENALIDOMIDE PLUS DEXAMETHASONE; CLONAL PLASMA-CELLS; HLA CLASS-I; PERIPHERAL-BLOOD; BONE-MARROW; LYMPHOCYTE RECOVERY; TUMOR-CELLS; NK CELLS;
D O I
10.3109/10428194.2012.676175
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multiple myeloma (MM) is an essentially incurable malignancy associated with profound immune dysregulation. Despite the advent of novel therapies and improvements in survival over the last 10 years, death from progressive disease and infection remains a common outcome. Natural killer (NK) cells are CD56(+)CD3(-) large granular lymphocytes that constitute a key cellular subset of the innate immune system. For over 30 years, the relationship between NK cells and MM has been described in the clinical setting and characterized in the laboratory. Data suggest that NK cells may play a role in the immune response to MM; however, this effect is lost due to immunoevasive strategies utilized by MM. Nevertheless, progress in the understanding of the mechanisms perpetuating this effect have led to new opportunities to recover or augment NK cell function therapeutically in MM. In fact, the novel agents thalidomide, lenalidomide and bortezomib all confer anti-MM effects, in part, through enhancement of NK cell function. Currently, the development of therapies designed specifically to increase NK cell cytotoxicity against MM is under way. The present review summarizes the current understanding of the NK cell versus MM effect and characterizes therapeutic interventions that exert anti-MM efficacy via NK cell function against the disease.
引用
收藏
页码:1666 / 1676
页数:11
相关论文
共 143 条
[51]   CD4+ CD25+ regulatory T cells inhibit natural killer cell functions in a transforming growth factor-β-dependent manner [J].
Ghiringhelli, F ;
Ménard, C ;
Terme, M ;
Flament, C ;
Taieb, J ;
Chaput, N ;
Puig, PE ;
Novault, S ;
Escudier, B ;
Vivier, E ;
Lecesne, A ;
Robert, C ;
Blay, JY ;
Bernard, J ;
Caillat-Zucman, S ;
Freitas, A ;
Tursz, T ;
Wagner-Ballon, O ;
Capron, C ;
Vainchencker, W ;
Martin, F ;
Zitvogel, L .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (08) :1075-1085
[52]  
Gisslinger H, 1997, LEUKEMIA, V11, pS52
[53]   Immunomodulatory effects of lenalidomide and pomalidomide on interaction of tumor and bone marrow accessory cells in multiple myeloma [J].
Goerguen, Guellue ;
Calabrese, Elisabetta ;
Soydan, Ender ;
Hideshima, Teru ;
Perrone, Giulia ;
Bandi, Madhavi ;
Cirstea, Diana ;
Santo, Loredana ;
Hu, Yiguo ;
Tai, Yu-Tzu ;
Nahar, Sabikun ;
Mimura, Naoya ;
Fabre, Claire ;
Raje, Noopur ;
Munshi, Nikhil ;
Richardson, Paul ;
Anderson, Kenneth C. .
BLOOD, 2010, 116 (17) :3227-3237
[54]   INCREASED EXPRESSION OF NATURAL-KILLER-ASSOCIATED AND ACTIVATION ANTIGENS IN MULTIPLE-MYELOMA [J].
GONZALEZ, M ;
MIGUEL, JFS ;
GASCON, A ;
MORO, J ;
HERNANDEZ, JM ;
ORTEGA, F ;
JIMENEZ, R ;
GUERRAS, L ;
ROMERO, M ;
CASANOVA, F ;
SANZ, MA ;
PORTERO, JA ;
ORFAO, A .
AMERICAN JOURNAL OF HEMATOLOGY, 1992, 39 (02) :84-89
[55]   MALIGNANT PLASMA-CELLS ARE SENSITIVE TO LAK CELL-LYSIS - PRECLINICAL AND CLINICAL-STUDIES OF INTERLEUKIN-2 IN THE TREATMENT OF MULTIPLE-MYELOMA [J].
GOTTLIEB, DJ ;
PRENTICE, HG ;
MEHTA, AB ;
GALAZKA, AR ;
HESLOP, HE ;
HOFFBRAND, AV ;
BRENNER, MK .
BRITISH JOURNAL OF HAEMATOLOGY, 1990, 75 (04) :499-505
[56]  
GOTTLIEB DJ, 1989, BLOOD, V74, P2335
[57]  
Hall PD, 1997, PHARMACOTHERAPY, V17, P248
[58]   Sensitization of tumor cells to NK cell-mediated killing by proteasome inhibition [J].
Hallett, William H. D. ;
Ames, Erik ;
Motarjemi, Milad ;
Barao, Isabel ;
Shanker, Anil ;
Tamang, David L. ;
Sayers, Thomas J. ;
Hudig, Dorothy ;
Murphy, William J. .
JOURNAL OF IMMUNOLOGY, 2008, 180 (01) :163-170
[59]   Molecular mechanisms whereby immunomodulatory drugs activate natural killer cells: clinical application [J].
Hayashi, T ;
Hideshima, T ;
Akiyama, M ;
Podar, K ;
Yasui, H ;
Raje, N ;
Kumar, S ;
Chauhan, D ;
Treon, SP ;
Richardson, P ;
Anderson, KC .
BRITISH JOURNAL OF HAEMATOLOGY, 2005, 128 (02) :192-203
[60]  
Herberman RB, 1985, INT J CANCER, V16, P216