Immunotherapy in allogeneic hematopoietic stem cell transplantation - not just a case for effector cells

被引:12
作者
Troeger, A
Meisel, R
Moritz, T
Dilloo, D
机构
[1] Univ Dusseldorf, Klin Kinderhamatol Onkol & Immunol, D-40225 Dusseldorf, Germany
[2] Univ Duisburg Essen, Dept Internal Med Canc Res, W German Canc Ctr, Duisburg, Germany
关键词
allogeneic hematopoietic stem cell transplantation; leukemia; vaccination; dendritic cells; mesenchymal stem cells;
D O I
10.1038/sj.bmt.1704849
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The concept that in allogeneic hematopoietic stem cell transplantation (alloHSCT) the immune system plays a prominent role in the control of leukemic disease is supported by the clinical observation that immunological effector mechanisms contribute to the elimination of leukemic blasts. The failure to induce prolonged remission after alloHSCT has led to resurgent interest in complementing concepts of immune modulation to improve the antileukemic reponse. Whil e the general focus has been placed on manipulation of cytotoxic effector cell populations, we will explore the dual role of leukemia cells as both antigen-presenting and target cells and describe various vaccination strategies to facilitate a protective antileukemic immune response in this setting. In addition, we will introduce mesenchymal stem cells ( MSC) as another cell population recently recognized for their immunomodulatory properties. The potential benefits and hazards of MSC-cotransplantation in alloHSCT with regard to the graft versus leukemia (GvL) and the graft versus host (GvH) response will be discussed.
引用
收藏
页码:S59 / S64
页数:6
相关论文
共 72 条
[51]   Multilineage potential of adult human mesenchymal stem cells [J].
Pittenger, MF ;
Mackay, AM ;
Beck, SC ;
Jaiswal, RK ;
Douglas, R ;
Mosca, JD ;
Moorman, MA ;
Simonetti, DW ;
Craig, S ;
Marshak, DR .
SCIENCE, 1999, 284 (5411) :143-147
[52]   Veto-like activity of mesenchymal stem cells: Functional discrimination between cellular responses to alloantigens and recall antigens [J].
Potian, JA ;
Aviv, H ;
Ponzio, NM ;
Harrison, JS ;
Rameshwar, P .
JOURNAL OF IMMUNOLOGY, 2003, 171 (07) :3426-3434
[53]   Mesenchymal stem cells inhibit the formation of cytotoxic T lymphocytes, but not activated cytotoxic T lymphocytes or natural killer cells [J].
Rasmusson, I ;
Ringdén, O ;
Sundberg, B ;
Le Blanc, K .
TRANSPLANTATION, 2003, 76 (08) :1208-1213
[54]   Idiotype vaccination using dendritic cells after autologous peripheral blood stem cell transplantation for multiple myeloma - A feasibility study [J].
Reichardt, VL ;
Okada, CY ;
Liso, A ;
Benike, CJ ;
Stockerl-Goldstein, KE ;
Engleman, EG ;
Blume, KG ;
Levy, R .
BLOOD, 1999, 93 (07) :2411-2419
[55]   Identification of novel survivin-derived CTL epitopes [J].
Reker, S ;
Meier, A ;
Holten-Andersen, L ;
Svane, IM ;
Becker, JC ;
Straten, PT ;
Andersen, MH .
CANCER BIOLOGY & THERAPY, 2004, 3 (02) :173-179
[56]   Stimulation by soluble CD70 promotes strong primary and secondary CD8+ cytotoxic T cell responses in vivo [J].
Rowley, TF ;
Al-Shamkhani, A .
JOURNAL OF IMMUNOLOGY, 2004, 172 (10) :6039-6046
[57]   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
[58]   A pilot study of combined immunotherapy with autologous adoptive tumour-specific T-cell transfer, vaccination with CD40-activated malignant B cells and interleukin 2 [J].
Schultze, JL ;
Anderson, KC ;
Gilleece, MH ;
Gribben, JG ;
Nadler, LM .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 113 (02) :455-460
[59]  
SIEGEL S, 2004, LEUKEMIA
[60]   Combination of CD80 and granulocyte-macrophage colony-stimulating factor coexpression by a leukemia cell vaccine: Preclinical studies in a murine model recapitulating Philadelphia chromosome-positive acute lymphoblastic leukemia [J].
Stripecke, R ;
Skelton, DC ;
Pattengale, PK ;
Shimada, H ;
Kohn, DB .
HUMAN GENE THERAPY, 1999, 10 (13) :2109-2122