Immune reconstitution following hematopoietic progenitor cell transplantation: challenges for the future

被引:48
作者
Fry, TJ [1 ]
Mackall, CL [1 ]
机构
[1] NCI, Pediat Oncol Branch, Bethesda, MD 20892 USA
关键词
thymopoiesis; GVHD; IL-7; keratinocyte growth factor; homeostatic peripheral expansion;
D O I
10.1038/sj.bmt.1704848
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Successful hematopoietic progenitor cell transplantation requires rapid and complete transfer of the donor hematopoietic and immune systems to the host. Whereas the uncontrolled transfer of a nontolerant donor immune system results in GVHD in many cases, strategies which diminish GVHD also diminish immune reconstitution. Thus, the reliable, rapid and safe transfer of immunity from donor to host remains a major challenge for the field. Advances in the understanding of the biology of immune reconstitution have elucidated that thymic-dependent immune reconstitution can restore global immunity, but is especially vulnerable to toxicities associated with transplant. Alternatively, homeostatic peripheral expansion can be exploited for targeted immunity toward pathogens and tumors, but is difficult to manipulate without exacerbating GVHD risk. New translatable strategies are needed to safely augment one or both of these pathways in the setting of allogeneic hematopoietic progenitor cell transplantation.
引用
收藏
页码:S53 / S57
页数:5
相关论文
共 34 条
[1]   Massive activation-induced cell death of alloreactive T cells with apoptosis of bystander postthymic T cells prevents immune reconstitution in mice with graft-versus-host disease [J].
Brochu, S ;
Rioux-Massé, B ;
Roy, J ;
Roy, DC ;
Perreault, C .
BLOOD, 1999, 94 (02) :390-400
[2]   Incidence, risk factors, and mortality from pneumonia developing late after hematopoietic stem cell transplantation [J].
Chen, CS ;
Boeckh, M ;
Seidel, K ;
Clark, JG ;
Kansu, E ;
Madtes, DK ;
Wagner, JL ;
Witherspoon, RP ;
Anasetti, C ;
Appelbaum, FR ;
Bensinger, WI ;
Deeg, HJ ;
Martin, PJ ;
Sanders, JE ;
Storb, R ;
Storek, J ;
Wade, J ;
Siadak, M ;
Flowers, MED ;
Sullivan, KM .
BONE MARROW TRANSPLANTATION, 2003, 32 (05) :515-522
[3]   Donor lymphocyte infusions for relapse of chronic myeloid leukemia after allogeneic stem cell transplant: Where we now stand [J].
Dazzi, F ;
Szydlo, RM ;
Goldman, JM .
EXPERIMENTAL HEMATOLOGY, 1999, 27 (10) :1477-1486
[4]   Assessment of thymic output in adults after haematopoietic stem-cell transplantation and prediction of T-cell reconstitution [J].
Douek, DC ;
Vescio, RA ;
Betts, MR ;
Brenchley, JM ;
Hill, BJ ;
Zhang, L ;
Berenson, JR ;
Collins, RH ;
Koup, RA .
LANCET, 2000, 355 (9218) :1875-1881
[5]  
Dudley ME, 2002, SCIENCE, V298, P850, DOI 10.1126/science.1076514
[6]   Flt3 ligand enhances thymic-dependent and thymic-independent immune reconstitution [J].
Fry, TJ ;
Sinha, M ;
Milliron, M ;
Chu, YW ;
Kapoor, V ;
Gress, RE ;
Thomas, E ;
Mackall, CL .
BLOOD, 2004, 104 (09) :2794-2800
[7]   Interleukin-7 restores immunity in athymic T-cell-depleted hosts [J].
Fry, TJ ;
Christensen, BL ;
Komschlies, KL ;
Gress, RE ;
Mackall, CL .
BLOOD, 2001, 97 (06) :1525-1533
[8]   IL-7 therapy dramatically alters peripheral T-cell homeostasis in normal and SIV-infected nonhuman primates [J].
Fry, TJ ;
Moniuszko, M ;
Creekmore, S ;
Donohue, SJ ;
Douek, DC ;
Giardina, S ;
Hecht, TT ;
Hill, BJ ;
Komschlies, K ;
Tomaszewski, J ;
Franchini, G ;
Mackall, CL .
BLOOD, 2003, 101 (06) :2294-2299
[9]   THYMUS - A DIRECT TARGET TISSUE IN GRAFT-VERSUS-HOST REACTION AFTER ALLOGENEIC BONE-MARROW TRANSPLANTATION THAT RESULTS IN ABROGATION OF INDUCTION OF SELF-TOLERANCE [J].
FUKUSHI, N ;
ARASE, H ;
WANG, BY ;
OGASAWARA, K ;
GOTOHDA, T ;
GOOD, RA ;
ONOE, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (16) :6301-6305
[10]  
GHAYUR T, 1988, AM J PATHOL, V133, P39