Article

Artemisiae capillaris herba induces prolonged survival of fully cardiac allografts and generates regulatory cells in mice.

Department of Surgery, Teikyo University, Tokyo, Japan.
Transplantation Proceedings (impact factor: 1). 05/2012; 44(4):1073-5. DOI:10.1016/j.transproceed.2012.03.002 pp.1073-5
Source: PubMed

ABSTRACT 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-γ 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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Keywords

1 component
 
5 components
 
6-component herbal medicine
 
7 days
 
allogeneic cardiac allografts
 
alloimmune responses
 
B6 allograft survival
 
B6 cardiac allografts
 
B6 cardiac grafts acutely
 
CBA recipients
 
Flow cytometry studies
 
interferon-γ production
 
median survival time [MST]
 
murine cardiac allograft transplantation
 
Naive CBA mice
 
oral administration
 
primary ACH-treated CBA recipients
 
Secondary CBA recipient
 
TJ-117 induced hyporesponsiveness
 
transplant recipients
 

X Jin