At the Bedside: Innate immunity as an immunotherapy tool for hematological malignancies

被引:40
作者
Locatelli, Franco [1 ,2 ]
Merli, Pietro [1 ]
Rutella, Sergio [1 ]
机构
[1] Bambino Gesu Pediat Hosp, IRCCS, Dept Paediat Haematol & Oncol, I-00165 Rome, Italy
[2] Univ Pavia, I-27100 Pavia, Italy
关键词
NK cells; Haploidentical hematopoietic stem cell transplantation; - T cells; graft-versus-host disease; graft-versus-leukemia effect; DELTA-T-CELLS; KIR-LIGAND INCOMPATIBILITY; NATURAL-KILLER-CELLS; CLASS-I MOLECULES; LYMPHOID STRESS-SURVEILLANCE; NON-HODGKINS-LYMPHOMA; RISK ACUTE-LEUKEMIA; GAMMA-DELTA; NK CELLS; ANTIGEN RECEPTOR;
D O I
10.1189/jlb.0613343
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Clinical Review for Basic Researchers: The available clinical evidence supporting the role of NK cells, and T lymphocytes, in killing tumor cells in haematological malignancies, focusing on strategies optimizing these cells in clinical practice. The identification of an anti-tumor effect displayed by cells of innate immunity has opened new scenarios, not only in the field of allo-HSCT but also for nontransplanted patients with hematological malignancies or solid tumors. Donor-derived NK cells have been shown to contribute to the eradication of malignant cells after allo-HSCT, when recipients lack ligands for their inhibitory receptors. These alloreactive donor NK cells can also kill recipient APCs and CTLs, thus preventing the occurrence of GvHD and graft rejection. The role of activating receptors on the capacity of NK cells to kill leukemia targets has become evident in the last years. The adoptive infusion of ex vivo-activated NK cells has been investigated recently in Phase I/II trials on patients with hematological malignancies and solid tumors, with promising results. T lymphocytes are also able to display anti-tumor activitythis providing the biological rationale for Phase I/II trials in lymphoproliferative disorders and solid tumors. Aminobisphosphonates are clinically available compounds able to boost T cell function. As T cells do not cause GvHD, they could also be transduced with tumor-associated chimeric antigen receptors and safely infused in allo-HSCT recipients. Basic aspects of innate immunity relevant to the field will be covered by a companion review article.
引用
收藏
页码:1141 / 1157
页数:17
相关论文
共 145 条
[1]   Clinical and immunological evaluation of zoledronate-activated Vγ9γδ T-cell-based immunotherapy for patients with multiple myeloma [J].
Abe, Yu ;
Muto, Masato ;
Nieda, Mie ;
Nakagawa, Yasunori ;
Nicol, Andrew ;
Kaneko, Touru ;
Goto, Shigenori ;
Yokokawa, Kiyoshi ;
Suzuki, Kenshi .
EXPERIMENTAL HEMATOLOGY, 2009, 37 (08) :956-968
[2]   Association of γδ T Cells with Disease Severity and Mortality in Septic Patients [J].
Andreu-Ballester, Juan C. ;
Tormo-Calandin, Constantino ;
Garcia-Ballesteros, Carlos ;
Perez-Griera, J. ;
Amigo, Victoria ;
Almela-Quilis, Amadeo ;
del Castillo, Juan Ruiz ;
Penarroja-Otero, Carlos ;
Ballester, Ferran .
CLINICAL AND VACCINE IMMUNOLOGY, 2013, 20 (05) :738-746
[3]   Haematopoietic cell transplantation as immunotherapy [J].
Appelbaum, FR .
NATURE, 2001, 411 (6835) :385-389
[4]   Reduced number and impaired function of circulating γδ T cells in patients with cutaneous primary melanoma [J].
Argentati, K ;
Re, F ;
Serresi, S ;
Tucci, MG ;
Bartozzi, B ;
Bernardini, G ;
Provinciali, M .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 120 (05) :829-834
[5]   SUCCESSFUL ENGRAFTMENT OF T-CELL-DEPLETED HAPLOIDENTICAL 3-LOCI INCOMPATIBLE TRANSPLANTS IN LEUKEMIA PATIENTS BY ADDITION OF RECOMBINANT HUMAN GRANULOCYTE-COLONY-STIMULATING FACTOR-MOBILIZED PERIPHERAL-BLOOD PROGENITOR CELLS TO BONE-MARROW INOCULUM [J].
AVERSA, F ;
TABILIO, A ;
TERENZI, A ;
VELARDI, A ;
FALZETTI, F ;
GIANNONI, C ;
IACUCCI, R ;
ZEI, T ;
MARTELLI, MP ;
GAMBELUNGHE, C ;
ROSSETTI, M ;
CAPUTO, P ;
LATINI, P ;
ARISTEI, C ;
RAYMONDI, C ;
REISNER, Y ;
MARTELLI, MF .
BLOOD, 1994, 84 (11) :3948-3955
[6]   Treatment of high-risk acute leukemia with T-cell-depleted stem cells from related donors with one fully mismatched HLA haplotype [J].
Aversa, F ;
Tabilio, A ;
Velardi, A ;
Cunningham, I ;
Terenzi, A ;
Falzetti, F ;
Ruggeri, L ;
Barbabietola, G ;
Aristei, C ;
Latini, P ;
Reisner, Y ;
Martelli, MF .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (17) :1186-1193
[7]   Full haplotype-mismatched hematopoietic stem-cell transplantation: A phase II study in patients with acute leukemia at high risk of relapse [J].
Aversa, F ;
Terenzi, A ;
Tabilio, A ;
Falzetti, F ;
Carotti, A ;
Ballanti, S ;
Felicini, R ;
Falcinelli, F ;
Velardi, A ;
Ruggeri, L ;
Aloisi, T ;
Saab, JP ;
Santucci, A ;
Perruccio, K ;
Martelli, MP ;
Mecucci, C ;
Reisner, Y ;
Martelli, MF .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (15) :3447-3454
[8]   MEGADOSE OF T-CELL-DEPLETED BONE-MARROW OVERCOMES MHC BARRIERS IN SUBLETHALLY IRRADIATED MICE [J].
BACHARLUSTIG, E ;
RACHAMIM, N ;
LI, HW ;
LAN, FS ;
REISNER, Y .
NATURE MEDICINE, 1995, 1 (12) :1268-1273
[9]   Understanding and harnessing the graft-versus-leukaemia effect [J].
Barrett, A. John .
BRITISH JOURNAL OF HAEMATOLOGY, 2008, 142 (06) :877-888
[10]   3-formyl-1-butyl pyrophosphate A novel mycobacterial metabolite-activating human γδ T cells [J].
Belman, C ;
Espinosa, E ;
Poupot, R ;
Peyrat, MA ;
Guiraud, M ;
Poquet, Y ;
Bonneville, M ;
Fournié, JJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (45) :32079-32084