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Soluble complement receptor type 1 (CD35) is released from leukocytes by surface cleavage.可溶性1型补体受体(CD35)通过表面裂解从白细胞中释放出来。
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2
Human complement receptor type 1 (CR1) protein levels and genetic variants in chronic Chagas Disease.慢性恰加斯病患者补体受体 1(CR1)蛋白水平和遗传变异。
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本文引用的文献

1
Low expression of erythrocyte complement receptor type 1 in chronic hepatitis C patients.慢性丙型肝炎患者红细胞补体受体1表达降低。
J Med Virol. 1996 Oct;50(2):126-34. doi: 10.1002/(SICI)1096-9071(199610)50:2<126::AID-JMV5>3.0.CO;2-C.
2
Increased levels of soluble complement receptor 1 in serum patients with liver diseases.肝病患者血清中可溶性补体受体1水平升高。
Hepatology. 1996 Jul;24(1):118-22. doi: 10.1002/hep.510240120.
3
Tumor necrosis factor alpha and interleukin 6 plasma levels in infected cirrhotic patients.感染性肝硬化患者血浆中肿瘤坏死因子α和白细胞介素6的水平
Gastroenterology. 1993 May;104(5):1492-7. doi: 10.1016/0016-5085(93)90361-f.
4
Circulating soluble CR1 (CD35). Serum levels in diseases and evidence for its release by human leukocytes.循环可溶性补体受体1(CD35)。疾病中的血清水平及其由人白细胞释放的证据。
J Immunol. 1993 Aug 1;151(3):1702-11.
5
Identification of membrane-bound CR1 (CD35) in human urine: evidence for its release by glomerular podocytes.人尿中膜结合补体受体1(CD35)的鉴定:肾小球足细胞释放该受体的证据
J Exp Med. 1994 Mar 1;179(3):889-99. doi: 10.1084/jem.179.3.889.
6
Soluble complement receptor type 1 (CD35) is released from leukocytes by surface cleavage.可溶性1型补体受体(CD35)通过表面裂解从白细胞中释放出来。
Eur J Immunol. 1994 Nov;24(11):2725-31. doi: 10.1002/eji.1830241123.
7
Leukocyte activation in the peripheral blood of patients with cirrhosis of the liver and SIRS. Correlation with serum interleukin-6 levels and organ dysfunction.肝硬化和全身炎症反应综合征患者外周血中的白细胞活化。与血清白细胞介素-6水平及器官功能障碍的相关性。
JAMA. 1995 Jul 5;274(1):58-65.
8
Unique role of the complement receptor CR1 in the degradation of C3b associated with immune complexes.补体受体CR1在与免疫复合物相关的C3b降解中的独特作用。
J Exp Med. 1982 Dec 1;156(6):1739-54. doi: 10.1084/jem.156.6.1739.
9
Identification of the membrane glycoprotein that is the C3b receptor of the human erythrocyte, polymorphonuclear leukocyte, B lymphocyte, and monocyte.鉴定作为人类红细胞、多形核白细胞、B淋巴细胞和单核细胞C3b受体的膜糖蛋白。
J Exp Med. 1980 Jul 1;152(1):20-30. doi: 10.1084/jem.152.1.20.
10
Characterization of a soluble form of the C3b/C4b receptor (CR1) in human plasma.人血浆中C3b/C4b受体(CR1)可溶性形式的特性研究
J Immunol. 1985 May;134(5):3332-8.

慢性肝病中的可溶性补体受体1(sCR1):不同肝病阶段的血清水平

Soluble complement receptor type 1 (sCR1) in chronic liver diseases: serum levels at different stages of liver diseases.

作者信息

Di Bona D, Montalto G, Clemenza L, Bascone F, Accardo P, Bellavia D, Craxì A, Brai M

机构信息

Cattedra di Immunologia, Istituto di Patologia Generale, Palermo, Italy.

出版信息

Clin Exp Immunol. 1998 Oct;114(1):102-5. doi: 10.1046/j.1365-2249.1998.00707.x.

DOI:10.1046/j.1365-2249.1998.00707.x
PMID:9764610
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1905076/
Abstract

Complement receptor type 1 (CR1) is an integral membrane protein of many haematopoietic cells and plays an important role in the clearance of complement-associated immune complexes, favouring their transport to liver and spleen macrophages. A small amount of soluble CR1 (sCR1) is also found in plasma and might originate directly from release of leucocytes and other circulating cells. In previous studies, an increase in serum sCR1 level has been observed in liver cirrhosis and end-stage renal failure. High levels have also been found in patients with some haematologic malignancies. sCR1 serum levels were measured using a specific double sandwich ELISA assay. The present study demonstrates the correlation between mean serum sCR1 concentrations and disease severity in patients with chronic liver disease. In patients with liver cirrhosis, grouped according to the Child-Pugh classification, sCR1 rose as liver function decreased. The presence of neoplastic growth in the liver apparently does not play a role in the increase of sCR1. Serum sCR1 was not elevated in other solid malignancies. Since sCR1 accumulates in liver diseases, evaluation of its serum levels could be useful as a liver function test.

摘要

1型补体受体(CR1)是许多造血细胞的一种整合膜蛋白,在补体相关免疫复合物的清除中起重要作用,有助于将其转运至肝脏和脾脏巨噬细胞。血浆中也发现少量可溶性CR1(sCR1),可能直接来源于白细胞和其他循环细胞的释放。在先前的研究中,肝硬化和终末期肾衰竭患者血清sCR1水平升高。一些血液系统恶性肿瘤患者中也发现sCR1水平较高。采用特异性双夹心ELISA法检测血清sCR1水平。本研究证实了慢性肝病患者血清sCR1平均浓度与疾病严重程度之间的相关性。在根据Child-Pugh分类法分组的肝硬化患者中,sCR1水平随肝功能下降而升高。肝脏中肿瘤生长的存在显然对sCR1的升高没有作用。其他实体恶性肿瘤患者血清sCR1未升高。由于sCR1在肝脏疾病中蓄积,评估其血清水平可能有助于肝功能检测。