TY - JOUR
T1 - Mixed chimerism and tolerance without whole body irradiation in a large animal model
AU - Fuchimoto, Yasushi
AU - Huang, Christene A.
AU - Yamada, Kazuhiko
AU - Shimizu, Akira
AU - Kitamura, Hiroshi
AU - Colvin, R. B.
AU - Ferrara, Vincent
AU - Murphy, Michael C.
AU - Sykes, Megan
AU - White-Scharf, Mary
AU - Neville, David M.
AU - Sachs, David H.
PY - 2000
Y1 - 2000
N2 - Mixed hematopoietic chimerism may provide a treatment for patients with nonmalignant hematologic diseases, and may tolerize patients to organ allografts without requiring chronic immunosuppression. However, the toxicity of the usual conditioning regimens has limited the clinical applicability of this approach. These regimens generally include some level of whole body irradiation (WBI), which is thought to facilitate engraftment either by making room for donor hematopoietic stem cells or by providing sufficient host immunosuppression to enable donor cells to engraft. Here, we have established mixed chimerism across both minor and major histocompatibility barriers in swine, by using high doses of peripheral blood stem cells in the absence of WBI. After mixed chimerism was established, swine leukocyte antigen-matched (SLA-matched) donor skin grafts were tolerated and maintained for a prolonged period, whereas third-party SLA-matched skin was rejected promptly. Donor-matched kidney allografts were also accepted without additional immunosuppression. Because of its low toxicity, this approach has potential for a wide range of clinical applications. Our data may indicate that niches for engrafting stem cells are filled by mass action and that WBI, which serves to empty some of these niches, can be omitted if the donor inoculum is sufficiently large and if adequate host T-cell depletion is achieved before transplant.
AB - Mixed hematopoietic chimerism may provide a treatment for patients with nonmalignant hematologic diseases, and may tolerize patients to organ allografts without requiring chronic immunosuppression. However, the toxicity of the usual conditioning regimens has limited the clinical applicability of this approach. These regimens generally include some level of whole body irradiation (WBI), which is thought to facilitate engraftment either by making room for donor hematopoietic stem cells or by providing sufficient host immunosuppression to enable donor cells to engraft. Here, we have established mixed chimerism across both minor and major histocompatibility barriers in swine, by using high doses of peripheral blood stem cells in the absence of WBI. After mixed chimerism was established, swine leukocyte antigen-matched (SLA-matched) donor skin grafts were tolerated and maintained for a prolonged period, whereas third-party SLA-matched skin was rejected promptly. Donor-matched kidney allografts were also accepted without additional immunosuppression. Because of its low toxicity, this approach has potential for a wide range of clinical applications. Our data may indicate that niches for engrafting stem cells are filled by mass action and that WBI, which serves to empty some of these niches, can be omitted if the donor inoculum is sufficiently large and if adequate host T-cell depletion is achieved before transplant.
UR - http://www.scopus.com/inward/record.url?scp=0033917492&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033917492&partnerID=8YFLogxK
U2 - 10.1172/JCI8721
DO - 10.1172/JCI8721
M3 - Article
C2 - 10862793
AN - SCOPUS:0033917492
SN - 0021-9738
VL - 105
SP - 1779
EP - 1789
JO - Journal of Clinical Investigation
JF - Journal of Clinical Investigation
IS - 12
ER -