Assessment of adult living related liver transplantation utilizing serum anti-liver arginase autoantibody assay : a possible novel strategy prospecting its prognosis.
Assessment of adult living related liver transplantation utilizing serum anti-liver arginase autoantibody assay : a possible novel strategy prospecting its prognosis.
批准号:
11671141
负责人:
MAFUNE Naoki
金额:
$2.05万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1999
资助国家:
日本
项目状态:
已结题
起止时间:
1999 至 2000
中文摘要
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英文摘要
Background/Aims : Clinical immuno-biochemical blood test for postoperative recipients of living related liver transplantation (LRLT) is still done by combination of assaying serum liver markers as in the past. Our recent study, determining serum anti-liver arginase autoantibody in patients with liver disease, revealed that the autoantibody titre stayed high in continuous liver distraction but easily decreased after the termination of liver damage. This phenomenon prompted us to seek whether this autoantibody can be utilized as a prognostic marker for a postoperative recipient of LRLT.Based on these findings, we tried to clarify whether the serum AAA shows reasonable change even under the state of immunosupression due to postoperative regimen.Methods : Western blot and ELISA were undertaken for the detection and quantification of the anti-liver arginase autoantibody. In the ELISA system, rat liver arginase was used as a target antigen, taking advantage of its high immunological cross reactivity with human liver arginase and the ease of handling it provides.Results : In the cases with short postopcrative hospitalization (<2 months), AAA levels eventually stayed in "critical zone" settled between 5 and 26 U, including normal range (19.7 ± 6.0U), while in those with poor prognosis with prolonged hospitalization (>6months) or with recurrent short term discharge, AAA was never stayed in that level.Conclusions : AAA can be utilized as a prognostic maker that reflect both liver distraction and immunosupression, which are key factors in LRLT.With this in mind, utilization of AAA might ease clinical testing on recipients.
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T.Miyatake, S.Kubota, K.Miyazaki, S.Watanabe, N.Mafune, T.Murashita, K.Yasuda: "Analysis of cardiac function during hyperacute rejection : effects of PAF antagonist, TXA2 inhibitor/antagonists, and nitroglycerin"Transplantation Proceedings. 32 (5) :. 999-
T.Miyatake、S.Kubota、K.Miyazaki、S.Watanabe、N.Mafune、T.Murashita、K.Yasuda:“超急性排斥反应期间心脏功能的分析:PAF 拮抗剂、TXA2 抑制剂/拮抗剂和硝酸甘油的作用”
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T.Miyatake,S.Kubota,K.Miyazaki,S.Watanabe,N.Mafune,T.Murashita,K.Yasuda: "Analysis of cardiac function during hyperacute rejection : effects of PAF antagonist, TXA2 inhibitor/antagonists,and nitroglycerin"Transplantation Proceedings. 32(5). 999-1000 (2000
T.Miyatake、S.Kubota、K.Miyazaki、S.Watanabe、N.Mafune、T.Murashita、K.Yasuda:“超急性排斥反应期间心脏功能的分析:PAF 拮抗剂、TXA2 抑制剂/拮抗剂和硝酸甘油的作用”
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Naoki Mafune, Kunihiko Kobayashi, Mikio Nishioka, Masao Watanabe and Michiyo Sasaki: "Autoantibody to the Liver Arginase Present in Sera of Patients with Autoimmune Hepatitis and Chronic Hepatitis."Autoimmunity. 30(3). 147-155 (1999)
Naoki Mafune、Kunihiko Kobayashi、Mikio Nishioka、Masao Watanabe 和 Michiyo Sasaki:“自身免疫性肝炎和慢性肝炎患者血清中存在的肝精氨酸酶自身抗体。”自身免疫。
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T.Kunihara,S.Sasaki,N.Shiiya,T.Miyatake,N.Mafune,and K.Yasuda: "Proinflammatory cytokines in the cerebrospinual fluid in repair of the thoracoabdominal aorta"Annals of Thoracic Surgery. in press.
T.Kunihara、S.Sasaki、N.Shiiya、T.Miyatake、N.Mafune 和 K.Yasuda:“胸腹主动脉修复中脑脊液中的促炎细胞因子”胸外科年鉴。
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Anti-Liver Arginase Autoantibody in Human Serum : A New Tool for Diagnosis of Silent Chronic Liver Disease
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批准号:08672632
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$0.64万
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财政年份:1996
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负责人:MAFUNE Naoki
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依托单位:
海外基金