Immune reconstitution after allogeneic stem cell transplantation with reduced-intensity conditioning regimens

被引:35
作者
Jimenez, M.
Ercilla, G.
Martinez, C.
机构
[1] Univ Barcelona, Hosp Clin, IDIBAPS, Dept Hematol,Inst Hematol & Oncol, Barcelona 08036, Spain
[2] Univ Barcelona, Hosp Clin, IDIBAPS, Dept Immunol, Barcelona 08036, Spain
关键词
immune reconstitution; reduced; intensity conditioning regimen; allogeneic stem cell transplantation; TREC;
D O I
10.1038/sj.leu.2404681
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Reduced-intensity conditioning (RIC) regimens have been increasingly used as an alternative to conventional myeloablative conditioning (MAC) regimens for elderly patients, for patients medically infirm to qualify for conventional allogeneic stem cell transplantation (SCT), and for disorders in which traditional MAC-SCT are associated with high rates of non-relapse mortality. One of the theoretical advantages of RIC-SCT is that it might lend to better immune reconstitution after transplantation due to less damage of the thymus, allowing regeneration of naive T cells derived from prethymic donor stem cells, and due to the proliferation of immunologically competent host T cells that survive the conditioning regimen. Although limited, studies comparing immune recovery following RIC and MAC-SCT have been insightful. One of the main difficulties of these studies is the current spectrum of RIC protocols, which vary considerably in myeloablative and immunosuppressive potential, resulting in apparently contradictory findings. In spite of this, most reports have shown significant quantitative and/or qualitative differences in T-and B-cell reconstitution after RIC-SCT in comparison with conventional SCT. This paper will review current knowledge of immune reconstitution following RIC-SCT.
引用
收藏
页码:1628 / 1637
页数:10
相关论文
共 98 条
[1]   Rapid establishment of dendritic cell chimerism in allogeneic hematopoietic cell transplant recipients [J].
Auffermann-Gretzinger, S ;
Lossos, IS ;
Vayntrub, TA ;
Leong, W ;
Grumet, FC ;
Blume, KG ;
Stockerl-Goldstein, KE ;
Levy, R ;
Shizuru, JA .
BLOOD, 2002, 99 (04) :1442-1448
[2]  
Bacigalupo A, 2004, BONE MARROW TRANSPL, V33, pS29, DOI 10.1038/sj.bmt.1704416
[3]   Early reconstitution of the T-cell repertoire after non-myeloablative peripheral blood stem cell transplantation is from post-thymic T-cell expansion and is unaffected by graft-versus-host disease or mixed chimaerism [J].
Bahceci, E ;
Epperson, D ;
Douek, DC ;
Melenhorst, JJ ;
Childs, RC ;
Barrett, AJ .
BRITISH JOURNAL OF HAEMATOLOGY, 2003, 122 (06) :934-943
[4]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[5]   Graft-versus-tumor effects after allogeneic hematopoietic cell transplantation with nonmyeloablative conditioning [J].
Baron, F ;
Maris, MB ;
Sandmaier, BM ;
Storer, BE ;
Sorror, M ;
Diaconescu, R ;
Woolfrey, AE ;
Chauncey, TR ;
Flowers, MED ;
Mielcarck, M ;
Maloney, DG ;
Storb, R .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (09) :1993-2003
[6]   Kinetics of dendritic cell chimerism and T cell chimerism in allogeneic hematopoietic stem cell recipients [J].
Boeck, S ;
Hamann, M ;
Pihusch, V ;
Heller, T ;
Diem, H ;
Rolf, B ;
Pihusch, R ;
Kolb, HJ ;
Pihusch, M .
BONE MARROW TRANSPLANTATION, 2006, 37 (01) :57-64
[7]  
Breit TM, 1997, J IMMUNOL, V159, P4341
[8]  
BRETAGNE S, 1990, BLOOD, V75, P296
[9]  
Busca Alessandro, 2003, Hematology, V8, P303, DOI 10.1080/10245330310001612125
[10]   Respiratory virus infections in transplant recipients after reduced-intensity conditioning with Campath-1H: high incidence but low mortality [J].
Chakrabarti, S ;
Avivi, I ;
Mackinnon, S ;
Ward, K ;
Kottaridis, PD ;
Osman, H ;
Waldmann, H ;
Hale, G ;
Fegan, CD ;
Yong, K ;
Goldstone, AH ;
Linch, DC ;
Milligan, DW .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 119 (04) :1125-1132