TY - JOUR
T1 - A short course of FK506 can induce limited donor-specific graft acceptance
AU - Hirai, Takashi
AU - Waddell, Thomas K.
AU - DeCampos, Kleber N.
AU - Compeau, Christopher G.
AU - Wada, Hiromi
AU - Hitomi, Shigeki
AU - Patterson, G. Alexander
AU - Slutsky, Arthur S.
N1 - Funding Information:
Supported by the J. P. Bickell Foundation grant 8237.
PY - 1994/8
Y1 - 1994/8
N2 - To examine the hypothesis that a short course of FK506 would induce permanent graft acceptance after lung transplantation, left lung allotransplantation was performed in 14 mongrel dogs. In group 1 (control; n = 3), no immunosuppressive agent was given. In group 2 (n = 7), FK506 (1.2 mg/kg intramuscularly) was given on posttransplantation days 0, 1, and 2. In group 3 (n = 4), FK506 was given at the same dose on posttransplantation days 0, 1, and 2 as well as on days 29 and 30. Allograft function was evaluated by temporarily occluding the right pulmonary artery. A mixed lymphocyte reaction study was performed preoperatively and monthly thereafter. Control lungs were all rejected within 8 days. Group 2 dogs showed improved survival, with a median survival of 49.5 days. One dog in group 2 lived more than 400 days after transplantation. The mixed lymphocyte reaction data suggests that some donor-specific unresponsiveness occurs, which lasts for only a limited time. Supplemental doses of FK506 did not significantly improve survival (median, 74 days). The whole blood level of FK506 was 17.7 ± 3.98 ng/mL on day 15; however, on day 29 the FK506 level was almost undetectable. We conclude that a 3-day course of 1.2 mg/kg of FK506 can induce donorspecific graft acceptance, but this acceptance is not permanent.
AB - To examine the hypothesis that a short course of FK506 would induce permanent graft acceptance after lung transplantation, left lung allotransplantation was performed in 14 mongrel dogs. In group 1 (control; n = 3), no immunosuppressive agent was given. In group 2 (n = 7), FK506 (1.2 mg/kg intramuscularly) was given on posttransplantation days 0, 1, and 2. In group 3 (n = 4), FK506 was given at the same dose on posttransplantation days 0, 1, and 2 as well as on days 29 and 30. Allograft function was evaluated by temporarily occluding the right pulmonary artery. A mixed lymphocyte reaction study was performed preoperatively and monthly thereafter. Control lungs were all rejected within 8 days. Group 2 dogs showed improved survival, with a median survival of 49.5 days. One dog in group 2 lived more than 400 days after transplantation. The mixed lymphocyte reaction data suggests that some donor-specific unresponsiveness occurs, which lasts for only a limited time. Supplemental doses of FK506 did not significantly improve survival (median, 74 days). The whole blood level of FK506 was 17.7 ± 3.98 ng/mL on day 15; however, on day 29 the FK506 level was almost undetectable. We conclude that a 3-day course of 1.2 mg/kg of FK506 can induce donorspecific graft acceptance, but this acceptance is not permanent.
UR - http://www.scopus.com/inward/record.url?scp=0028069073&partnerID=8YFLogxK
U2 - 10.1016/0003-4975(94)92238-1
DO - 10.1016/0003-4975(94)92238-1
M3 - Article
C2 - 7520685
AN - SCOPUS:0028069073
SN - 0003-4975
VL - 58
SP - 496
EP - 501
JO - The Annals of thoracic surgery
JF - The Annals of thoracic surgery
IS - 2
ER -