Stem cell transplantation in experimental models of autoimmune disease

被引:88
作者
van Bekkum, DW
机构
[1] Introgene BV, PO Box 2048
关键词
autoimmune disease; hematopoietic stem cells; autologous transplant;
D O I
10.1023/A:1006682225181
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
A review of the experiments with animal models of autoimmune disease (AID) that have provided the rationale for the present clinical investigations on the use of autologous stem cells for treating patients with severe refractory AID. The various types of AID in laboratory animals and the recognition of the key-role of hematopoitic stem cells (HSC) in AID are discussed. Two animal models were employed for translational research on autologous bone marrow transplantation (BMT): adjuvant arthritis (AA) as model for rheumatoid arthritis (RA) and experimental allergic encephalomyelitis (EAE) as model for multiple sclerosis (MS). The principal aspects of the treatment, i.e., conditioning agents and doses and T cell depletion of the autograft, were investigated in relation to remission induction and the incidence of relapses.
引用
收藏
页码:10 / 16
页数:7
相关论文
共 34 条
[1]
BIGGS J, 1999, PERIPHERAL BLOOD STE
[2]
TRANSFER OF THE INFLAMMATORY DISEASE OF HLA-B27 TRANSGENIC RATS BY BONE-MARROW ENGRAFTMENT [J].
BREBAN, M ;
HAMMER, RE ;
RICHARDSON, JA ;
TAUROG, JD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (05) :1607-1616
[3]
BREBAN MA, 1993, CLIN EXP RHEUMATOL, V11, P61
[4]
BRODSKY RA, 1999, HIGH DOSE CYCLOPHOSP
[5]
Treatment of autoimmune disease by intense immunosuppressive conditioning and autologous hematopoietic stem cell transplantation [J].
Burt, RK ;
Traynor, AE ;
Pope, R ;
Schroeder, J ;
Cohen, B ;
Karlin, KH ;
Lobeck, L ;
Goolsby, C ;
Rowlings, P ;
Davis, FA ;
Stefoski, D ;
Terry, C ;
Keever-Taylor, C ;
Rosen, S ;
Vesole, D ;
Fishman, M ;
Brush, M ;
Mujias, S ;
Villa, M ;
Burns, WH .
BLOOD, 1998, 92 (10) :3505-3514
[6]
Charron D, 1990, Adv Immunol, V48, P107, DOI 10.1016/S0065-2776(08)60753-1
[7]
Early recurrence or persistence of autoimmune diseases after unmanipulated autologous stem cell transplantation [J].
Euler, HH ;
Marmont, AM ;
Bacigalupo, A ;
Fastenrath, S ;
Dreger, P ;
Hoffknecht, M ;
Zander, AR ;
Schalke, B ;
Hahn, U ;
Haas, R ;
Schmitz, N .
BLOOD, 1996, 88 (09) :3621-3625
[8]
Peripheral blood stem cell transplantation in the treatment of progressive multiple sclerosis: first results of a pilot study [J].
Fassas, A ;
Anagnostopoulos, A ;
Kazis, A ;
Kapinas, K ;
Sakellari, I ;
Kimiskidis, V ;
Tsompanakou, A .
BONE MARROW TRANSPLANTATION, 1997, 20 (08) :631-638
[9]
ORGAN-SPECIFIC AND SYSTEMIC AUTOIMMUNE-DISEASES ORIGINATE FROM DEFECTS IN HEMATOPOIETIC STEM-CELLS [J].
IKEHARA, S ;
KAWAMURA, M ;
TAKAO, F ;
INABA, M ;
YASUMIZU, R ;
THAN, S ;
HISHA, H ;
SUGIURA, K ;
KOIDE, Y ;
YOSHIDA, TO ;
IDA, T ;
IMURA, H ;
GOOD, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (21) :8341-8344
[10]
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