CD34 positive blood cells for allogeneic progenitor and stem cell transplantation

被引:6
作者
Link, H
Arseniev, L
机构
[1] Department of Hematology, Medical School Hannover
关键词
CD34+ stem cells; allogeneic transplantation; blood progenitor cell transplantation;
D O I
10.3109/10428199709050882
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The transplantation of allogeneic peripheral blood progenitor cells (PBPC) provides complete and sustained hematopoietic and lymphopoietic engraftment,In healthy donors, large amounts of PBPC can be mobilized with hematopoietic growth factors. However, the high content of immunocompetent T-cells in apheresis products may expose recipients of allogeneic PBPC to an elevated risk of acute and chronic graft-versus-host disease. Thus, the use of appropriate T-cell reduction, but not depletion might reduce this risk. The hazards of graft rejection and a higher relapse rate can be avoided by maintaining a portion of the T-cells in the graft. The positive selection of CD34+ cells from peripheral blood preparations simultaneously provides an approximately 1000-fold reduction of T-cells. These purified CD34+ cells containing committed and pluripotent stem cells are suitable for allogeneic transplantation and can be used in the following instances: 1. As hematopoietic stem and progenitor cell transplantation instead of bone marrow cells, from HLA-identical family donors; 2. for increasing the stem cell numbers from HLA-mismatched or three HLA-loci different family donors in order to reduce the incidence of rejection but without increasing the T-cell number; 3. boosting of poor marrow graft function with stem cells from the same family donors; 4. transplantation from volunteer matched unrelated donors ; 5. split transplantation of CD34+ and T-cells; 6. addition of ex vivo expanded CD34+ cells to blood cell or bone marrow transplantation; 7. generation of antigen specific immune effector cells and antigen presenting cells for cell therapy.
引用
收藏
页码:451 / 465
页数:15
相关论文
共 94 条
[71]   USE OF GENE-MODIFIED VIRUS-SPECIFIC T-LYMPHOCYTES TO CONTROL EPSTEIN-BARR-VIRUS-RELATED LYMPHOPROLIFERATION [J].
ROONEY, CM ;
SMITH, CA ;
NG, CYC ;
LOFTIN, S ;
LI, CF ;
KRANCE, RA ;
BRENNER, MK ;
HESLOP, HE .
LANCET, 1995, 345 (8941) :9-13
[72]   Randomised trial of filgrastim-mobilised peripheral blood progenitor cell transplantation versus autologous bone-marrow transplantation in lymphoma patients [J].
Schmitz, N ;
Linch, DC ;
Dreger, P ;
Goldstone, AH ;
Boogaerts, MA ;
Ferrant, A ;
Demuynck, HMS ;
Link, H ;
Zander, A ;
Barge, A ;
Borkett, K .
LANCET, 1996, 347 (8998) :353-357
[73]   PRIMARY TRANSPLANTATION OF ALLOGENEIC PERIPHERAL-BLOOD PROGENITOR CELLS MOBILIZED BY FILGRASTIM (GRANULOCYTE-COLONY-STIMULATING FACTOR) [J].
SCHMITZ, N ;
DREGER, P ;
SUTTORP, M ;
ROHWEDDER, EB ;
HAFERLACH, T ;
LOFFLER, H ;
HUNTER, A ;
RUSSELL, NH .
BLOOD, 1995, 85 (06) :1666-1672
[74]  
Schmitz N, 1996, BONE MARROW TRANSPL, V17, pS40
[75]   FREQUENCY OF ANTI-RECIPIENT ALLOREACTIVE HELPER T-CELL PRECURSORS IN DONOR BLOOD AND GRAFT-VERSUS-HOST DISEASE AFTER HLA-IDENTICAL SIBLING BONE-MARROW TRANSPLANTATION [J].
SCHWARER, AP ;
JIANG, YZ ;
BROOKES, PA ;
BARRETT, AJ ;
BATCHELOR, JR ;
GOLDMAN, JM ;
LECHLER, RI .
LANCET, 1993, 341 (8839) :203-205
[76]   TRANSPLANTATION OF ENRICHED CD34-POSITIVE AUTOLOGOUS MARROW INTO BREAST-CANCER PATIENTS FOLLOWING HIGH-DOSE CHEMOTHERAPY - INFLUENCE OF CD34-POSITIVE PERIPHERAL-BLOOD PROGENITORS AND GROWTH-FACTORS ON ENGRAFTMENT [J].
SHPALL, EJ ;
JONES, RB ;
BEARMAN, SI ;
FRANKLIN, WA ;
ARCHER, PG ;
CURIEL, T ;
BITTER, M ;
CLAMAN, HN ;
STEMMER, SM ;
PURDY, M ;
MYERS, SE ;
HAMI, L ;
TAFFS, S ;
HEIMFELD, S ;
HALLAGAN, J ;
BERENSON, RJ .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (01) :28-36
[77]  
SIENA S, 1989, BLOOD, V74, P1905
[78]  
STOCKSCHLADER M, 1995, BONE MARROW TRANSPL, V16, P719
[79]  
STOCKSCHLADER M, IN PRESS LEUK LYMPH
[80]   PREDICTIVE FACTORS IN CHRONIC GRAFT-VERSUS-HOST DISEASE IN PATIENTS WITH APLASTIC-ANEMIA TREATED BY MARROW TRANSPLANTATION FROM HLA-IDENTICAL SIBLINGS [J].
STORB, R ;
PRENTICE, RL ;
SULLIVAN, KM ;
SHULMAN, HM ;
DEEG, HJ ;
DONEY, KC ;
BUCKNER, CD ;
CLIFT, RA ;
WITHERSPOON, RP ;
APPELBAUM, FA ;
SANDERS, JE ;
STEWART, PS ;
THOMAS, ED .
ANNALS OF INTERNAL MEDICINE, 1983, 98 (04) :461-466