PERMANENT AND SPECIFIC TRANSPLANTATION TOLERANCE INDUCED BY A NONMYELOABLATIVE TREATMENT TO A WIDE VARIETY OF ALLOGENEIC TISSUES .1. INDUCTION OF TOLERANCE BY A SHORT-COURSE OF TOTAL LYMPHOID IRRADIATION AND SELECTIVE ELIMINATION OF THE DONOR-SPECIFIC HOST LYMPHOCYTES
Tb. Prigozhina et al., PERMANENT AND SPECIFIC TRANSPLANTATION TOLERANCE INDUCED BY A NONMYELOABLATIVE TREATMENT TO A WIDE VARIETY OF ALLOGENEIC TISSUES .1. INDUCTION OF TOLERANCE BY A SHORT-COURSE OF TOTAL LYMPHOID IRRADIATION AND SELECTIVE ELIMINATION OF THE DONOR-SPECIFIC HOST LYMPHOCYTES, Transplantation, 63(10), 1997, pp. 1394-1399
The long-term success of organ transplantation is limited by complicat
ions resulting from consistent nonspecific immunosuppression. Inductio
n of stable, donor-specific tolerance remains the main goal of transpl
antation immunology. In this article, a new, nonmyeloablative method i
s described for induction of transplantation tolerance to fully mismat
ched bone marrow cells (BMC), bone marrow stromal precursors, heart mu
scle, and skin allografts. The method is based on pretransplant condit
ioning with no postgraft immunosuppression, and consists of a short co
urse (six daily fractions of 200 cGy) of total lymphoid irradiation (s
TLI), followed by selective elimination of donor-specific alloreactive
cells of the host escaping low-dose sTLI. Donor-specific alloreactive
cells were activated by intravenous inoculation with a high dose of d
onor BMC (3x10(7) cells) 1 day after sTLI, and eliminated by a single
intraperitoneal dose (200 mg/kg) of cyclophosphamide given 1 day after
cell transfer. Infusion of a low number of T cell-depleted BMC (3x10(
6) cells) after tolerogenic preconditioning converted recipients to st
able mixed chimeras free of graft-versus-host disease. The same treatm
ent provided long-lasting acceptance of heterotopically transplanted a
llografts of the heart muscle and of the stromal precursors to the hem
atopoietic microenvironment. This treatment also led to acceptance and
life-long survival of full-thickness donor skin allografts. However,
skin allografts survived only in mice that received donor T cell-deple
ted BMC after cyclophosphamide and had 20-50% donor cells in the blood
. Our results suggest that after sTLI, additional selective clonal del
etion of residual host cells induces a state of long-lasting specific
tolerance to a wide variety of donor-derived tissues.