Erythroid-lineage-specific engraftment in patients with severe hemoglobinopathy following allogeneic hematopoietic stem cell transplantation

被引:5
作者
Armistead, Paul M. [2 ,3 ]
Mohseni, Mehrdad [1 ]
Gerwin, Roslyn [1 ]
Walsh, Emily C. [4 ,5 ]
Iravani, Masoud [6 ]
Chahardouli, Bahram [6 ]
Rostami, Shahrbano [6 ]
Zhang, Wandi [1 ]
Neuberg, Donna [7 ]
Rioux, John [4 ,5 ]
Ghavamzadeh, Ardeshir [6 ]
Ritz, Jerome [1 ,2 ,8 ]
Antin, Joseph H. [1 ,2 ,8 ]
Wu, Catherine J. [1 ,2 ,8 ]
机构
[1] Harvard Univ, Inst Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[3] Univ Texas Houston, MD Anderson Canc Ctr, Dept Med Oncol, Houston, TX 77030 USA
[4] Broad Inst Harvard, Program Med & Populat Genet, Boston, MA USA
[5] MIT, Boston, MA USA
[6] Univ Tehran, Sch Med Sci, Hematol Oncol & Bone Marrow Transplant Res Ctr, Tehran, Iran
[7] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02115 USA
[8] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
关键词
D O I
10.1016/j.exphem.2008.04.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. We aimed to create a molecular assay to monitor erythroid (red blood cell [RBC]) engraftment in any patient following allogeneic hematopoietic stem cell transplantation, independent of disease-specific mutations. Materials and Methods. We identified 10 common single nucleotide polymorphisms (SNPs), expressed by genes encoding RBC antigens and structural proteins. These SNPs were polymerase chain reaction-amplified from total RNA extracted from peripheral blood, which contains nucleated erythroid progenitors. Mixing studies validated that each SNP can quantitatively measure donor/recipient DNA and RNA. Results. We directly genotyped 23 patients who underwent hematopoietic stem cell transplantation and their human leukocyte antigen-matched donors and found a median of three informative SNPs (i.e., discordant between donor and recipient) per pair. By using the informative RBC SNPs to quantify donor-derived RBC transcripts, we compared rates of RBC engraftment in 13 patients with hemoglobinopathies vs donor mononuclear cell (white blood cell [WBC]) engraftment. Consistent with known ineffective erythropoiesis associated with hemoglobinopathies, we detected up to threefold greater RBC-specific compared to overall WBC engraftment in five of eight patients who were mixed chimeras by transplant day 30. The remaining three of eight who received ABH-incompatible grafts, demonstrated at least 0.5-fold lower RBC compared to WBC engraftment that was related to persistence of host-derived anti-isohemagglutinin antibodies. Conclusion. This RNA-based assay can be used to monitor RBC-specific engraftment regardless of a patient's specific hemoglobin mutation or even diagnosis. We propose that panels of expressed SNPs informative for other cell lineages can be created to comprehensively assess the impact of novel stem cell-based therapies on lineage-specific engraftment. (C) 2008 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc.
引用
收藏
页码:1205 / 1215
页数:11
相关论文
共 40 条
[1]   Distinct roles for donor- and host-derived antigen-presenting cells and costimulatory molecules in murine chronic graft-versus-host disease: requirements depend on target organ [J].
Anderson, BE ;
McNiff, JM ;
Jain, D ;
Blazar, BR ;
Shlomchik, WD ;
Shlomchik, MJ .
BLOOD, 2005, 105 (05) :2227-2234
[2]   Persistence of mixed chimerism in patients transplanted for the treatment of thalassemia [J].
Andreani, M ;
Manna, M ;
Lucarelli, G ;
Tonucci, P ;
Agostinelli, F ;
Ripalti, M ;
Rapa, S ;
Talevi, N ;
Galimberti, M ;
Nesci, S .
BLOOD, 1996, 87 (08) :3494-3499
[3]   Establishment of complete and mixed donor chimerism after allogeneic lymphohematopoietic transplantation: Recommendations from a Workshop at the 2001 Tandem Meetings [J].
Antin, JH ;
Childs, R ;
Filipovich, AH ;
Giralt, S ;
Mackinnon, S ;
Spitzer, T ;
Weisdorf, D .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2001, 7 (09) :473-485
[4]   Evaluation of KIR ligand incompatibility in mismatched unrelated donor hematopoietic transplants [J].
Davies, SM ;
Ruggieri, L ;
DeFor, T ;
Wagner, JE ;
Weisdorf, DJ ;
Miller, JS ;
Velardi, A ;
Blazar, BR .
BLOOD, 2002, 100 (10) :3825-3827
[5]  
Frankel W, 1996, AM J HEMATOL, V52, P281, DOI 10.1002/(SICI)1096-8652(199608)52:4<281::AID-AJH7>3.0.CO
[6]  
2-O
[7]   The structure of haplotype blocks in the human genome [J].
Gabriel, SB ;
Schaffner, SF ;
Nguyen, H ;
Moore, JM ;
Roy, J ;
Blumenstiel, B ;
Higgins, J ;
DeFelice, M ;
Lochner, A ;
Faggart, M ;
Liu-Cordero, SN ;
Rotimi, C ;
Adeyemo, A ;
Cooper, R ;
Ward, R ;
Lander, ES ;
Daly, MJ ;
Altshuler, D .
SCIENCE, 2002, 296 (5576) :2225-2229
[8]   Bone marrow transplantation from alternative donors for thalassemia: HLA-phenotypically identical relative and HLA-nonidentical sibling or parent transplants [J].
Gaziev, D ;
Galimberti, M ;
Lucarelli, G ;
Polchi, P ;
Giardini, C ;
Angelucci, E ;
Baronciani, D ;
Sodani, P ;
Erer, B ;
De Biagi, M ;
Andreani, M ;
Agostinelli, F ;
Donati, M ;
Nesci, S ;
Talevi, N .
BONE MARROW TRANSPLANTATION, 2000, 25 (08) :815-821
[9]   Adoptive immunotherapy in canine mixed chimeras after nonmyeloablative hematopoietic cell transplantation [J].
Georges, GE ;
Storb, R ;
Thompson, JD ;
Yu, C ;
Gooley, T ;
Bruno, B ;
Nash, RA .
BLOOD, 2000, 95 (10) :3262-3269
[10]   A novel rapid single nucleotide polymorphism (SNP)-based method for assessment of hematopoietic chimerism after allogeneic stem cell transplantation [J].
Hochberg, EP ;
Miklos, DB ;
Neuberg, D ;
Eichner, DA ;
McLaughlin, SF ;
Mattes-Ritz, A ;
Alyea, EP ;
Antin, JH ;
Soiffer, RJ ;
Ritz, J .
BLOOD, 2003, 101 (01) :363-369