Cutting edge: Recipient MHC class II expression is required to achieve long-term survival of murine cardiac allografts after costimulatory blockade

被引:93
作者
Yamada, A
Chandraker, A
Laufer, TM
Gerth, AJ
Sayegh, MH
Auchincloss, H
机构
[1] Massachusetts Gen Hosp, Transplantat Unit, Surg Serv, Boston, MA 02114 USA
[2] Brigham & Womens Hosp, Dept Med, Lab Immunogenet & Transplantat, Div Renal, Boston, MA 02115 USA
[3] Univ Penn, Dept Med, Div Rheumatol, Philadelphia, PA 19104 USA
[4] Harvard Univ, Sch Publ Hlth, Dept Canc Biol, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
关键词
D O I
10.4049/jimmunol.167.10.5522
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To study the role of the direct and indirect pathways in achieving tolerance, we used genetically altered mouse strains in two ways: 1) MHC class II-deficient mice were used as donors of skin and cardiac grafts to eliminate the direct CD4(+) T cell response, and 2) B6 II(-)4(+) mice, which are MHC class II-deficient mice expressing an MHC class II transgene only on thymic epithelium, were used as recipients of normal grafts. These mice cannot mount an indirect response. Eliminating the indirect pathway actually made it more difficult to achieve prolonged allograft survival when we used costimulatory blockade than when both pathways were available. Costimulatory blockade was ineffective even when CD4(+) T cells from normal animals were transferred into recipients that lacked MHC class II molecules. These results suggest that an active CD4(+) response through the indirect pathway is necessary for costimulatory blockade to be effective in prolonging allograft survival.
引用
收藏
页码:5522 / 5526
页数:5
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