Prognostic value of pretransplantation host thymic function in HLA-identical sibling hematopoietic stem cell transplantation

被引:60
作者
Clave, E
Rocha, V
Talvensaari, K
Busson, M
Douay, C
Appert, ML
Rabian, C
Carmagnat, M
Garnier, F
Filion, A
Socié, G
Gluckman, E
Charron, D
Toubert, A
机构
[1] Hop St Louis, Lab Immunol & Histocompatibilite, Ctr G Hayem,Serv Hematol Greffe Moelle, INSERM U396,AP HP,Inst Univ Hematol, F-75475 Paris, France
[2] Inst Univ Hematol, INSERM ERM0220, Paris, France
[3] Finnish Red Cross & Blood Transfus Serv, Dept Tissue Typing, Finnish Bone Marrow Donor Registry, Helsinki, Finland
关键词
D O I
10.1182/blood-2004-04-1667
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Thymic function is critical for immune reconstitution after hematopoietic stem cell transplantation (HSCT). We evaluated recipient thymic function before HSCT by quantifying T-cell receptor excision circles (TRECs) in pretransplantation peripheral blood lymphocytes from 102 patients who received HSCs from an HLA-identical sibling for malignant (n = 87) or nonmalignant diseases (n = 15). Median TREC value before transplantation was 257 TRECs per 150 000 CD3(+) cells (range,. 0-42 746). We assessed 1 2 TRECs per 150 000 CD3(+) cells as the most discriminating TREC value for survival in a first cohort of patients (n = 62). This cut-off was validated in a second independent prospective group of 40 patients. In the 102 patients, a TREC value greater than or equal to 172 was associated with a better survival (P < .000 01), a decreased incidence of grade II-IV acute graft-versus-host disease (GVHD; P = .017), chronic GVHD (P = .03), and bacterial (P = .003) and cytomegalovirus (CMV) infection (P = .024). In a multivariate analysis, low pretransplantation TREC values were associated with a higher incidence of CMV infection (hazard ratio [HR] = 2.0, P = .06) and severe bacterial infections (HR = 2.8, P = .036). Finally, high TREC values (HR = 6.6, P = .002) and ABO compatibility (HR = 2.7, P = .02) were associated with a better survival. Therefore, recipient host thymic function assessment could be helpful in predicting HSCT outcome and identifying patients who require a close immunologic monitoring. (c) 2005 by The American Society of Hematology
引用
收藏
页码:2608 / 2613
页数:6
相关论文
共 26 条
[1]   Prediction of T-cell reconstitution by assessment of T-cell receptor excision circle before allogeneic hematopoietic stem cell transplantation in pediatric patients [J].
Chen, XH ;
Barfield, R ;
Benaim, E ;
Leung, W ;
Knowles, J ;
Lawrence, D ;
Otto, M ;
Shurtleff, SA ;
Neale, GAM ;
Behm, FG ;
Turner, V ;
Handgretinger, R .
BLOOD, 2005, 105 (02) :886-893
[2]   Acute and chronic graft-versus-host disease after allogeneic peripheral-blood stem-cell and bone marrow transplantation: A meta-analysis [J].
Cutler, C ;
Giri, S ;
Jeyapalan, S ;
Paniagua, D ;
Viswanathan, A ;
Antin, JH .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (16) :3685-3691
[3]   Changes in thymic function with age and during the treatment of HIV infection [J].
Douek, DC ;
McFarland, RD ;
Keiser, PH ;
Gage, EA ;
Massey, JM ;
Haynes, BF ;
Polis, MA ;
Haase, AT ;
Feinberg, MB ;
Sullivan, JL ;
Jamieson, BD ;
Zack, JA ;
Picker, LJ ;
Koup, RA .
NATURE, 1998, 396 (6712) :690-695
[4]   Factors affecting reconstitution of the T cell compartment in allogeneic haematopoietic cell transplant recipients [J].
Fallen, PR ;
McGreavey, L ;
Madrigal, JA ;
Potter, M ;
Ethell, M ;
Prentice, HG ;
Guimaraes, A ;
Travers, PJ .
BONE MARROW TRANSPLANTATION, 2003, 32 (10) :1001-1014
[5]  
FERRARA JLM, 1991, NEW ENGL J MED, V324, P667
[6]   A proportional hazards model for the subdistribution of a competing risk [J].
Fine, JP ;
Gray, RJ .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1999, 94 (446) :496-509
[7]   CLINICAL MANIFESTATIONS OF GRAFT VERSUS HOST DISEASE IN HUMAN RECIPIENTS OF MARROW FROM HL-A-MATCHED SIBLING DONORS [J].
GLUCKSBERG, H ;
STORB, R ;
FEFER, A ;
BUCKNER, CD ;
NEIMAN, PE ;
CLIFT, RA ;
LERNER, KG ;
THOMAS, ED .
TRANSPLANTATION, 1974, 18 (04) :295-304
[8]   ABO incompatibility between donor and recipient and clinical outcomes in allogeneic stem cell transplantation [J].
Goldman, J ;
Liesveld, J ;
Nichols, D ;
Heal, J ;
Blumberg, N .
LEUKEMIA RESEARCH, 2003, 27 (06) :489-491
[9]   The role of the thymus in immune reconstitution in aging, bone marrow transplantation, and HIV-1 infection [J].
Haynes, BF ;
Markert, ML ;
Sempowski, GD ;
Patel, DD ;
Hale, LP .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :529-560
[10]   Direct evidence for new T-cell generation by patients after either T-cell-depleted or unmodified allogeneic hematopoietic stem cell transplantations [J].
Lewin, SR ;
Heller, G ;
Zhang, LQ ;
Rodrigues, E ;
Skulsky, E ;
van den Brink, MRM ;
Small, TN ;
Kernan, NA ;
O'Reilly, RJ ;
Ho, DD ;
Young, JW .
BLOOD, 2002, 100 (06) :2235-2242