TY - JOUR
T1 - Spontaneous tolerance involving natural killer T cells after hepatic grafting in mice
AU - Morita, Miwa
AU - Fujino, Masayuki
AU - Li, Xiao Kang
AU - Kimura, Hiromitsu
AU - Nakayama, Toshinori
AU - Taniguchi, Masaru
AU - Sugioka, Atsushi
N1 - Funding Information:
The authors thank Naoko Funeshima-Fuji and Yusuke Kitazawa for their technical assistance. This study was supported by research grants from the Ministry of Education, Culture, Sports, Science and Technology of Japan (a Grant-in-Aid 14370367, 13671250, 17390355).
PY - 2007/11
Y1 - 2007/11
N2 - The liver contains significant numbers of invariant natural killer T (iNKT) cells, which have an invariant T cell receptor-α chain and are activated in a CD1d-restricted manner. We examined the role of iNKT cells in the spontaneous tolerance of the major histocompatibility antigen complex-mismatched liver allograft model using Jα18 knockout mice that lack iNKT cells. Liver allografts lacking iNKT cells manifested not only infiltration but also hemorrhage and necrosis with significant reduction of graft survival and much less induction of tolerance compared with wild type (WT) liver allograft. In addition, allografts lacking iNKT cells grafted into iNKT-deficient recipients result in more severe inflammation than when grafted into WT recipients, while there was no significant difference with respect to induction of tolerance and graft survival. These results demonstrated that iNKT cells, especially donor-residual iNKT cells, constitute immune regulatory cells that play an important role in induction of allograft tolerance.
AB - The liver contains significant numbers of invariant natural killer T (iNKT) cells, which have an invariant T cell receptor-α chain and are activated in a CD1d-restricted manner. We examined the role of iNKT cells in the spontaneous tolerance of the major histocompatibility antigen complex-mismatched liver allograft model using Jα18 knockout mice that lack iNKT cells. Liver allografts lacking iNKT cells manifested not only infiltration but also hemorrhage and necrosis with significant reduction of graft survival and much less induction of tolerance compared with wild type (WT) liver allograft. In addition, allografts lacking iNKT cells grafted into iNKT-deficient recipients result in more severe inflammation than when grafted into WT recipients, while there was no significant difference with respect to induction of tolerance and graft survival. These results demonstrated that iNKT cells, especially donor-residual iNKT cells, constitute immune regulatory cells that play an important role in induction of allograft tolerance.
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U2 - 10.1016/j.trim.2007.05.015
DO - 10.1016/j.trim.2007.05.015
M3 - Article
C2 - 18005859
AN - SCOPUS:36049000898
SN - 0966-3274
VL - 18
SP - 142
EP - 145
JO - Transplant Immunology
JF - Transplant Immunology
IS - 2
ER -