共 4 条
Artemisiae capillaris herba Induces Prolonged Survival of Fully Cardiac Allografts and Generates Regulatory Cells in Mice
被引:8
作者:
Jin, X.
[2
]
Uchiyama, M.
[3
]
Zhang, Q.
[4
]
Watanabe, T.
Niimi, M.
[1
]
机构:
[1] Teikyo Univ, Dept Surg, Itabashi Ku, Tokyo 1738605, Japan
[2] Harbin Med Univ, Affiliated Hosp 4, Dept Cardiovasc & Thorac Surg, Harbin, Peoples R China
[3] Juntendo Univ Hosp, Dept Cardiovasc Surg, Tokyo, Japan
[4] Fudan Univ, Huashan Hosp, Dept Dermatol, Shanghai 200433, Peoples R China
关键词:
D O I:
10.1016/j.transproceed.2012.03.002
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
071005 [微生物学];
100108 [医学免疫学];
摘要:
Inchingorei-san (TJ-117), a 6-component herbal medicine, is used in Japan for the treatment of vomiting, urticaria, and liver and kidney disorders with few side effects. In this study we investigated the effect of TJ-117 on alloimmune responses in murine cardiac allograft transplantation. CBA (H2(k)) mice underwent transplantation of a C57BL/6 (B6, H2(b)) heart with oral administration of TJ-117 (or 1 component of TJ-117) from the day of transplantation for 7 days. CBA recipients given 1 g/kg/d of TJ-117 showed prolonged B6 allograft survival (median survival time [MST], 23 days). Naive CBA mice rejected B6 cardiac grafts acutely (MST, 7 days). Moreover, Artemisiae capillaris herba (ACH; 1g/kg/d) 1 component of TJ-117, significantly prolonged B6 allograft survival (MST, > 100 days). However, the other 5 components of TJ-117 were individually less effective than TJ-117 or ACH. ACH also suppressed splenocyte proliferation and interferon-gamma production. Secondary CBA recipient showed prolonged survival of B6 hearts after treatments with whole splenocytes from primary ACH-treated CBA recipients carrying B6 cardiac allografts for 30 days (MST, >50 days). Flow cytometry studies showed increased CD4(+)CD25(+)Foxp3(+) regulatory cells in transplant recipients given ACH. In conclusion, ACH, 1 component of TJ-117, as well as TJ-117 induced hyporesponsiveness to fully allogeneic cardiac allografts with generation of CD4(+)CD25(+)Foxp3(+) regulatory cells.
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页码:1073 / 1075
页数:3
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