Mixed allogeneic chimerism induced by a sublethal approach prevents autoimmune diabetes and reverses insulitis in nonobese diabetic (NOD) mice

被引:0
作者
Li, H [1 ]
Kaufman, CL [1 ]
Boggs, SS [1 ]
Johnson, PC [1 ]
Patrene, KD [1 ]
Ildstad, ST [1 ]
机构
[1] UNIV PITTSBURGH,DEPT SURG,DIV CELLULAR THERAPEUT,PITTSBURGH,PA 15261
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中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Evidence in experimental models suggests that many autoimmune diseases can be prevented by transplantation of bone marrow from disease-resistant donors, For potential clinical application, it would be important to avoid the morbidity and mortality associated with lethal conditioning and achieve mixed chimerism using less than complete recipient ablation, We report here for the first time that stable chimerism achieved in NOD mice using a sublethal radiation-based conditioning approach is sufficient to prevent beta-cell destruction and abrogate insulitis in prediabetic NOD mice, The percentage of NOD mouse recipients (8 wk of age) that engrafted with donor bone marrow correlated with the dose of irradiation and number of bone marrow cells transplanted, Engraftment of B10.BR bone marrow occurred in greater than or equal to 94% of animals receiving greater than or equal to 750 cGy of total body irradiation before bone marrow transplantation and greater than or equal to 30 x 10(6) bone marrow cells, while reproducible engraftment did not occur at radiation doses of less than 700 cGy and cellular doses of less than 30 x 10(6) bone marrow cells, All chimeric animals remained free of diabetes (n = 38) for 10 mo following bone marrow transplantation. Moreover, in all animals examined, no insulitis was present from 12 to 36 wk following reconstitution, In striking contrast, 61% (22 of 36) of NOD recipients that were conditioned but did not receive bone marrow developed acute diabetes by 12 mo, Insulitis was present in all remaining animals, These results suggest that allogeneic chimerism achieved using a sublethal conditioning approach can prevent the onset of diabetes and even reverse preexisting insulitis in NOD mice.
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页码:380 / 388
页数:9
相关论文
共 47 条
[1]   PREVENTIVE EFFECTS OF AZATHIOPRINE (AZA) ON THE ONSET OF DIABETES-MELLITUS IN NOD MICE [J].
CALAFIORE, R ;
BASTA, G ;
FALORNI, A ;
IETROPAOLO, M ;
PICCHIO, ML ;
CALCINARO, F ;
BRUNETTI, P .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1993, 16 (11) :869-873
[2]  
CASTANO L, 1990, ANNU REV IMMUNOL, V8, P647, DOI 10.1146/annurev.iy.08.040190.003243
[3]   MONOCLONAL-ANTIBODIES TO PROMOTE MARROW ENGRAFTMENT AND TISSUE GRAFT TOLERANCE [J].
COBBOLD, SP ;
MARTIN, G ;
QIN, S ;
WALDMANN, H .
NATURE, 1986, 323 (6084) :164-166
[4]   COMPETITION FOR FOLLICULAR NICHES EXCLUDES SELF-REACTIVE CELLS FROM THE RECIRCULATING B-CELL REPERTOIRE [J].
CYSTER, JG ;
HARTLEY, SB ;
GOODNOW, CC .
NATURE, 1994, 371 (6496) :389-395
[5]  
EPSTEIN SL, 1980, J IMMUNOL, V125, P129
[6]  
HARADA M, 1986, INSULITIS TYPE 1 DIA, P143
[7]   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
[8]   PREVENTION OF TYPE-I DIABETES IN NONOBESE DIABETIC MICE BY ALLOGENEIC BONE-MARROW TRANSPLANTATION [J].
IKEHARA, S ;
OHTSUKI, H ;
GOOD, RA ;
ASAMOTO, H ;
NAKAMURA, T ;
SEKITA, K ;
MUSO, E ;
TOCHINO, Y ;
IDA, T ;
KUZUYA, H ;
IMURA, H ;
HAMASHIMA, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (22) :7743-7747
[9]   CROSS-SPECIES BONE-MARROW TRANSPLANTATION - EVIDENCE FOR TOLERANCE INDUCTION, STEM-CELL ENGRAFTMENT, AND MATURATION OF LYMPHOCYTES-T IN A XENOGENEIC STROMAL ENVIRONMENT (RAT-]MOUSE) [J].
ILDSTAD, ST ;
WREN, SM ;
BOGGS, SS ;
HRONAKES, ML ;
VECCHINI, F ;
VANDENBRINK, MRM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 174 (02) :467-478
[10]   CHARACTERIZATION OF MIXED ALLOGENEIC CHIMERAS - IMMUNOCOMPETENCE, INVITRO REACTIVITY, AND GENETIC SPECIFICITY OF TOLERANCE [J].
ILDSTAD, ST ;
WREN, SM ;
BLUESTONE, JA ;
BARBIERI, SA ;
SACHS, DH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 162 (01) :231-244