EVIDENCE THAT ANTI-ASIALO GM1 INVIVO IMPROVES ENGRAFTMENT OF T-CELL-DEPLETED BONE-MARROW IN HYBRID RECIPIENTS

被引:16
作者
FERRARA, JLM
MAUCH, P
VANDIJKEN, PJ
CROSIER, KE
MICHAELSON, J
BURAKOFF, SJ
机构
[1] HARVARD UNIV, SCH MED, DANA FARBER CANC INST, ROOM 1632, BINNEY ST, BOSTON, MA 02115 USA
[2] CHILDRENS HOSP MED CTR, DIV PEDIAT HEMATOL ONCOL, BOSTON, MA 02115 USA
[3] MASSACHUSETTS GEN HOSP, BOSTON, MA 02114 USA
[4] HARVARD UNIV, SCH MED, DEPT PEDIAT, BOSTON, MA 02115 USA
[5] HARVARD UNIV, SCH MED, DEPT RADIOTHERAPY, BOSTON, MA 02115 USA
关键词
D O I
10.1097/00007890-199001000-00030
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Engraftment of T cell-depleted bone marrow was studied in a P-F1 murine bone marrow transplant model which features long-term stability of mixed chimerism of donor (B6) and host (B6AF1) cells after BMT. We report that a polyclonal antibody to asialo GM1 (anti-ASGM1) given in vivo after transplant was able to increase long-term donor bone marrow engraftment. In vivo anti-ASGM1 eliminated NK activity but did not affect the generation of cytotoxic T cells nor did it stimulate hematopoiesis in vitro. Anti-Thy 1.2, a pan- T cell monoclonal antibody, had no effect on donor en- graftment. We conclude that ASGM1+ cells with NK activity inhibit the long-term engraftment of bone marrowstem cells in this model and that antibodies to NK cells can be used in vivo as an effective component of the transplant conditioning regimen. © 1990 by Williams and Wilkins.
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页码:134 / 138
页数:5
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