In vitro methotrexate as a practical approach to selective allodepletion

被引:7
作者
Sathe, Atul
Ortega, Sterling B.
Mundy, Dorothy I.
Collins, Robert H.
Karandikar, Nitin J.
机构
[1] Univ Texas, SW Med Ctr, Dept Pathol, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
allodepletion; GVBD;
D O I
10.1016/j.bbmt.2007.01.081
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Graft-versus-host disease (GVHD) is a major cause of transplant-related morbidity and mortality in recipients of allogeneic hematopoietic stem cell transplantation. As GVHD is mediated predominantly by alloreactive donor T cells, selective allodepletion from the graft may alleviate GVHD, whereas potentially maintaining other advantages conferred by donor T cells, such as graft survival, antiviral immunity, and graft-versus-leukemia effect. In this study, we evaluated the ability of methotrexate, a clinically approved antimetabolite drug, to deplete alloreactive T cells in HLA-mismatched mixed lymphocyte reactions (MLR). We observed that methotrexate could inhibit the proliferation of alloreactive T cells in primary in vitro MLR. On reexposure of methotrexate-treated cells to the same allostimulus, a significant reduction in the alloreactive immune response was observed, whereas responses to third-party allostimuli and viral antigens were preserved. Thus, our results provide preclinical evidence that in vitro methotrexate treatment results in specific allodepletion and may be used as an effective agent for preventing GVHD. (C) 2007 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:644 / 654
页数:11
相关论文
共 43 条
[1]   Selective depletion of donor alloreactive T cells without loss of antiviral or antileukernic responses [J].
Amrolia, PJ ;
Muccioli-Casadei, G ;
Yvon, E ;
Huls, H ;
Sili, U ;
Wieder, ED ;
Bollard, C ;
Heslop, HE ;
Molldrem, JJ ;
Rooney, CM ;
Brenner, MK .
BLOOD, 2003, 102 (06) :2292-2299
[2]   The current status of hematopoietic cell transplantation [J].
Appelbaum, FR .
ANNUAL REVIEW OF MEDICINE-SELECTED TOPICS IN THE CLINICAL SCIENCES, 2003, 54 :491-512
[3]   Medical progress: Hematopoietic stem-cell transplantation [J].
Copelan, EA .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (17) :1813-1826
[4]   Acute graft-versus-host disease: Pathophysiology, clinical manifestations, and management [J].
Couriel, D ;
Caldera, H ;
Champlin, R ;
Komanduri, K .
CANCER, 2004, 101 (09) :1936-1946
[5]   High prevalence of autoreactive, neuroantigen-specific CD8+ T cells in multiple sclerosis revealed by novel flow cytometric assay [J].
Crawford, MP ;
Yan, SX ;
Ortega, SB ;
Mehta, RS ;
Hewitt, RE ;
Price, DA ;
Stastny, P ;
Douek, DC ;
Koup, RA ;
Racke, MK ;
Karandikar, NJ .
BLOOD, 2004, 103 (11) :4222-4231
[6]   Low-dose methotrexate: A mainstay in the treatment of rheumatoid arthritis [J].
Cronstein, BN .
PHARMACOLOGICAL REVIEWS, 2005, 57 (02) :163-172
[7]  
DATTA AR, 1994, BONE MARROW TRANSPL, V14, P517
[8]   Antiviral immunity and T-regulatory cell function are retained after selective alloreactive T-cell depletion in both the HLA-identical and HLA-mismatched settings [J].
Davies, JK ;
Koh, MBC ;
Lowdell, MW .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2004, 10 (04) :259-268
[9]   GRAFT FAILURE AFTER T-CELL DEPLETED HLA IDENTICAL ALLOGENEIC BONE-MARROW TRANSPLANTATION - RISK-FACTORS IN LEUKEMIC PATIENTS [J].
DELAIN, M ;
CAHN, JY ;
RACADOT, E ;
FLESCH, M ;
PLOUVIER, E ;
MERCIER, M ;
TIBERGHIEN, P ;
PAVY, JJ ;
DESCHASEAUX, M ;
DECONINCK, E ;
COUTERET, Y ;
BRION, A ;
HERVE, P .
LEUKEMIA & LYMPHOMA, 1993, 11 (5-6) :359-368
[10]   Efficient depletion of alloreactive donor T lymphocytes based on expression of two activation-induced antigens (CD25 and CD69) [J].
Fehse, B ;
Frerk, O ;
Goldmann, M ;
Bulduk, M ;
Zander, AR .
BRITISH JOURNAL OF HAEMATOLOGY, 2000, 109 (03) :644-651