Effectiveness and risks of total body irradiation for conditioning in the treatment of autoimmune disease with autologous bone marrow transplantation

被引:25
作者
van Bekkum, DW [1 ]
机构
[1] IntroGene BV, NL-2301 CA Leiden, Netherlands
关键词
D O I
10.1093/rheumatology/38.8.757
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The results of experiments with the induced autoimmune diseases adjuvant arthritis and allergic encephalomyelitis in rats, which led to the discovery of the curative effect of autologous bone marrow transplantation following high-dose myeloablative treatment, are reviewed. The rationale is eradication of the autoreactive lymphocytes and memory cells, and the prevention of relapse due to transfer of lymphocytes with the autograft. Comparison of various conditioning regimens in the animal models indicates that a combination conditioning with low-dose total body irradiation (TBI) and high-dose cyclophosphamide is optimal. These findings were the basis for the conditioning currently employed in the treatment of polyarticular juvenile chronic arthritis (JCA) by the teams in Utrecht and Leiden, which consists of cyclophosphamide 50 mg/kg for 4 days, 4 Gy TBI and anti-thymocyte globulin (ATG). The use of TBI for the treatment of non-malignant disease is regarded as undesirable by many physicians in view of the risks, in particular, of growth inhibition in children and the induction of tumours. Experimental and clinical data show that a dose of 4 Gy does not cause significant inhibition of skeletal growth in infants. The risk of excess cancer due to TBI has been well established in quantitative terms and is compared with the expected risk of high-dose cyclophosphamide and the risk associated with the highly immunosuppressive regimens currently used for the treatment of JCA.
引用
收藏
页码:757 / 761
页数:5
相关论文
共 26 条
[1]  
[Anonymous], 1977, ANN ICRP, V1, DOI DOI 10.1016/J.ICRP.2004.12.002
[2]   Complete remission in severe aplastic anemia after high-dose cyclophosphamide without bone marrow transplantation [J].
Brodsky, RA ;
Sensenbrenner, LL ;
Jones, RJ .
BLOOD, 1996, 87 (02) :491-494
[3]  
CROOK PR, 1986, BRIT J RHEUMATOL, V25, P384
[4]   Effect of long-term immunosuppression in kidney-graft recipients on cancer incidence: randomised comparison of two cyclosporin regimens [J].
Dantal, J ;
Hourmant, M ;
Cantarovich, D ;
Giral, M ;
Blancho, G ;
Dreno, B ;
Soulillou, JP .
LANCET, 1998, 351 (9103) :623-628
[5]   TREATMENT-FREE REMISSION IN SEVERE SYSTEMIC LUPUS-ERYTHEMATOSUS FOLLOWING SYNCHRONIZATION OF PLASMAPHERESIS WITH SUBSEQUENT PULSE CYCLOPHOSPHAMIDE [J].
EULER, HH ;
SCHROEDER, JO ;
HARTEN, P ;
ZEUNER, RA ;
GUTSCHMIDT, HJ .
ARTHRITIS AND RHEUMATISM, 1994, 37 (12) :1784-1794
[6]   LONG-TERM OBSERVATIONS OF AUTOIMMUNE-PRONE MICE TREATED FOR AUTOIMMUNE-DISEASE BY ALLOGENEIC BONE-MARROW TRANSPLANTATION [J].
IKEHARA, S ;
YASUMIZU, R ;
INABA, M ;
IZUI, S ;
HAYAKAWA, K ;
SEKITA, KI ;
TOKI, J ;
SUGIURA, K ;
IWAI, H ;
NAKAMURA, T ;
MUSO, E ;
HAMASHIMA, Y ;
GOOD, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (09) :3306-3310
[7]  
KNAANSHANZER S, 1991, BONE MARROW TRANSPL, V8, P333
[8]   RADIATION-THERAPY OF SPONTANEOUS AUTOIMMUNITY - A REVIEW OF MOUSE MODELS [J].
LOOR, F ;
JACHEZ, B ;
MONTECINORODRIGUEZ, E ;
KLEIN, AS ;
KUNTZ, L ;
PFLUMIO, F ;
FONTENEAU, P ;
ILLINGER, D .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1988, 53 (01) :119-136
[9]  
MARMONT AM, 1995, BONE MARROW TRANSPL, V16, P497
[10]  
ORME IM, 1989, IMMUNOLOGY, V68, P93