Optimal protocol for total body irradiation for allogeneic bone marrow transplantation in mice

被引:62
作者
Cui, YZ
Hisha, H
Yang, GX
Fan, TX
Jin, T
Li, Q
Lian, Z
Ikehara, S
机构
[1] Kansai Med Univ, Dept Pathol 1, Osaka 5708506, Japan
[2] Kansai Med Univ, Transplantat Ctr, Osaka 5708506, Japan
[3] Kansai Med Univ, Regenerat Res Ctr Intractable Dis, Osaka 5708506, Japan
关键词
bone marrow transplantation; fractionated irradiation; reconstitution;
D O I
10.1038/sj.bmt.1703766
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
We have previously demonstrated, using chimeric resistant MRL/lpr mice, that a fractionated total body irradiation (FTBI) (5 Gy x 2 with a 4 h interval on the day before allogeneic bone marrow transplantation (BMT)) is the best conditioning regimen for the treatment of autoimmune diseases in radiosensitive MRL/lpr mice. In the present study, using various standard strains of mice (not radiosensitive mice), we explore the best protocol for irradiation (doses and intervals) as the conditioning regimen for allogeneic BMT. Recipient mice were exposed to various irradiation regimens: a single total body irradiation (TBI) of 9.5 or 12 Gy and FTBI of (5+5) Gy to (7+7) Gy with a 1 to 24 h interval. The method generally utilized for humans ((2+2) Gy with a 4 h interval for 3 days (total 12 Gy)) was also used. One day, after the last irradiation, donor BMCs from BALB/c, C3H, or C57BL/6 (B6) mice were transplanted into C3H or B6 mice. The irradiation protocol of (2+2) Gy for 3 days was found to be insufficient to enable the complete removal of recipient immunocompetent cells, since donor-reactive T cells were observed in the recipient spleens and many recipient-type NK and CD4(+) cells were also detected in the recipient hematolymphoid tissues. In all the combinations, the highest survival rate was achieved in the recipients irradiated with (6+6) or (6.5+6.5) Gy with a 4 h interval. In the surviving mice, the hematolymphoid tissues had been fully reconstituted with donor cells.
引用
收藏
页码:843 / 849
页数:7
相关论文
共 20 条
[1]
Immediate toxicity during fractionated total body irradiation as conditioning for bone marrow transplantation [J].
Buchali, A ;
Feyer, P ;
Groll, J ;
Massenkeil, G ;
Arnold, R ;
Budach, V .
RADIOTHERAPY AND ONCOLOGY, 2000, 54 (02) :157-162
[2]
Mouse strain-dependent changes in frequency and proliferation of hematopoietic stem cells during aging: Correlation between lifespan and cycling activity [J].
deHaan, G ;
Nijhof, W ;
VanZant, G .
BLOOD, 1997, 89 (05) :1543-1550
[3]
Intrinsic and extrinsic control of hemopoietic stem cell numbers: Mapping of a stem cell gene [J].
deHaan, G ;
VanZant, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (04) :529-536
[4]
DOWN JD, 1991, BLOOD, V77, P661
[5]
HISHA H, 1995, EXP HEMATOL, V23, P347
[6]
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
[7]
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
[8]
IKEHARA S, 1991, UCLA SYM BI, V137, P251
[9]
ISHIDA T, 1994, J IMMUNOL, V152, P3119
[10]
Multi-organ, multi-lineage engraftment by a single bone marrow-derived stem cell [J].
Krause, DS ;
Theise, ND ;
Collector, MI ;
Henegariu, O ;
Hwang, S ;
Gardner, R ;
Neutzel, S ;
Sharkis, SJ .
CELL, 2001, 105 (03) :369-377