Allogeneic transplantation using non-myeloablative transplant regimens

被引:10
作者
Battiwalla, M [1 ]
Barrett, J [1 ]
机构
[1] NHLBI, Stem Cell Allotransplantat Sect, Haematol Branch, Bethesda, MD 20892 USA
关键词
non-myeloablative stem cell transplants; graft-versus-tumour effect; mixed chimerism; adoptive immunotherapy; lymphocytes; stem cell transplantation conditioning;
D O I
10.1053/beha.2001.0168
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Reduced intensity (non-myeloablative) stem cell transplant (NST) preparative regimens are being increasingly used to exploit the curative potential of allogeneic stem cell transplantation without the morbidity and mortality associated with conventional transplantation. Growing confidence in the power of the allogeneic graft-versus-malignancy (GVM) effect makes such an approach attractive. Lower intensity transplants increase the degree of mixed chimerism, both in T cell and myeloid cell lineages. Currently a variety of NST treatment approaches are being developed and in this chapter their safety profile and the immunological characteristics of the mixed chimeric state are described. Results of NST in specific disease categories are still limited but the NST approach appears to have promise in the treatment of both haematological and non-haematological malignancies because of the benefit of low toxicity coupled with a strong graft-versus-malignancy effect. NST regimens are also being explored in high-risk patients with non-malignant disorders. However, at present, there is insufficient data to determine whether NST should replace standard myeloablative transplants in specific disease groups. With their low toxicity, NST are well placed as platforms for future developments in transplant immunology to avoid GVHD and enhance the allograft effect against malignant diseases.
引用
收藏
页码:701 / 722
页数:22
相关论文
共 79 条
[1]   Nonmyeloablative stem cell transplantation for congenital immunodeficiencies [J].
Amrolia, P ;
Gaspar, HB ;
Hassan, A ;
Webb, D ;
Jones, A ;
Sturt, N ;
Mieli-Vergani, G ;
Pagliuca, A ;
Mufti, G ;
Hadzic, N ;
Davies, G ;
Veys, P .
BLOOD, 2000, 96 (04) :1239-1246
[2]   Long-term survive of ex-thalassemic patients with persistent mixed chimerism after bone marrow transplantation [J].
Andreani, M ;
Nesci, S ;
Lucarelli, G ;
Tonucci, P ;
Rapa, S ;
Angelucci, E ;
Persini, B ;
Agostinelli, F ;
Donati, M ;
Manna, M .
BONE MARROW TRANSPLANTATION, 2000, 25 (04) :401-404
[3]  
Bacigalupo A, 2000, BRIT J HAEMATOL, V108, P99
[4]   High response rate in refractory and poor-risk multiple myeloma after allotransplantation using a nonmyeloablative conditioning regimen and donor lymphocyte infusions [J].
Badros, A ;
Barlogie, B ;
Morris, C ;
Desikan, R ;
Martin, SR ;
Munshi, N ;
Zangari, M ;
Toor, A ;
Cottler-Fox, M ;
Fassas, A ;
Aniassie, E ;
Schichman, S ;
Tricot, G .
BLOOD, 2001, 97 (09) :2574-2579
[5]  
Bahçeci E, 2000, BRIT J HAEMATOL, V108, P408
[6]   TREATMENT OF MURINE LEUKAEMIA WITH X-RAYS AND HOMOLOGOUS BONE MARROW - PRELIMINARY COMMUNICATION [J].
BARNES, DWH ;
CORP, MJ ;
LOUTIT, JF ;
NEAL, FE .
BRITISH MEDICAL JOURNAL, 1956, 2 (SEP15) :626-627
[7]   Graft-versus-leukaemia: Understanding and using the alloimmune response to treat haematological malignancies [J].
Barrett, AJ ;
Malkovska, V .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 93 (04) :754-761
[8]   Non-myeloablative stem cell transplants [J].
Barrett, J ;
Childs, R .
BRITISH JOURNAL OF HAEMATOLOGY, 2000, 111 (01) :6-17
[9]  
BENSINGER W, 1999, HEMATOPOIETIC CELL T, P1260
[10]   Massive immune haemolysis after allogeneic peripheral blood stem cell transplantation with minor ABO incompatibility [J].
Bolan, CD ;
Childs, RW ;
Procter, JL ;
Barrett, AJ ;
Leitman, SF .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 112 (03) :787-795