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1
CR1 deficiency in SLE: acquired or genetic?系统性红斑狼疮中CR1缺乏:后天性还是遗传性?
Clin Exp Immunol. 1985 Nov;62(2):329-36.
2
Disease-associated loss of erythrocyte complement receptors (CR1, C3b receptors) in patients with systemic lupus erythematosus and other diseases involving autoantibodies and/or complement activation.系统性红斑狼疮及其他涉及自身抗体和/或补体激活的疾病患者中与疾病相关的红细胞补体受体(CR1,C3b受体)缺失。
J Immunol. 1985 Sep;135(3):2005-14.
3
[Erythrocyte CR1 receptor reactivity in patients with systemic lupus erythematosus].[系统性红斑狼疮患者红细胞CR1受体反应性]
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4
Low number of complement C3b/C4b receptors (CR1) on erythrocytes from patients with essential mixed cryoglobulinemia, systemic lupus erythematosus and rheumatoid arthritis: relationship with disease activity, anticardiolipin antibodies, complement activation and therapy.原发性混合性冷球蛋白血症、系统性红斑狼疮和类风湿关节炎患者红细胞上补体C3b/C4b受体(CR1)数量减少:与疾病活动度、抗心磷脂抗体、补体激活及治疗的关系
J Rheumatol. 1991 Jul;18(7):1021-5.
5
Erythrocyte complement receptor type 1 in patients with systemic lupus erythematosus.系统性红斑狼疮患者的红细胞补体受体1型
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6
CR1 on erythrocytes of Brazilian systemic lupus erythematosus patients: the influence of disease activity on expression and ability of this receptor to bind immune complexes opsonized with complement from normal human serum.巴西系统性红斑狼疮患者红细胞上的CR1:疾病活动对该受体表达及结合经正常人血清补体调理的免疫复合物能力的影响。
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7
Erythrocytes transfused into patients with SLE and haemolytic anaemia lose complement receptor type 1 from their cell surface.输注到系统性红斑狼疮和溶血性贫血患者体内的红细胞会从其细胞表面失去1型补体受体。
Clin Exp Immunol. 1987 Sep;69(3):501-7.
8
Decreased C3b receptors (CR1) on erythrocytes from patients with systemic lupus erythematosus.系统性红斑狼疮患者红细胞上C3b受体(CR1)减少。
Clin Exp Immunol. 1986 Jan;63(1):41-8.
9
Diminished ability of erythrocytes from patients with systemic lupus erythematosus to limit opsonized immune complex deposition on leukocytes and activation of granulocytes.系统性红斑狼疮患者红细胞限制调理素化免疫复合物在白细胞上沉积及粒细胞活化的能力降低。
Arthritis Rheum. 1998 Apr;41(4):613-22. doi: 10.1002/1529-0131(199804)41:4<613::AID-ART8>3.0.CO;2-A.
10
Deficiency of the C3b/C4b receptor (CR1) of erythrocytes in systemic lupus erythematosus: analysis of the stability of the defect and of a restriction fragment length polymorphism of the CR1 gene.系统性红斑狼疮中红细胞C3b/C4b受体(CR1)的缺陷:CR1基因缺陷稳定性及限制性片段长度多态性分析
J Immunol. 1987 Apr 15;138(8):2708-10.

引用本文的文献

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Ann Rheum Dis. 2008 Jun;67(6):849-54. doi: 10.1136/ard.2007.075044. Epub 2007 Sep 18.
2
Serum C4 concentration in the monitoring of systemic lupus erythematosus: requirement for C4 allotyping.
Rheumatol Int. 1986;6(3):111-4. doi: 10.1007/BF00270346.
3
Mechanisms of immune deposit formation in renal glomeruli.肾小球中免疫沉积物形成的机制。
Springer Semin Immunopathol. 1986;9(2-3):219-35. doi: 10.1007/BF02099023.
4
The rate of loss of CR1 from ageing erythrocytes in vivo in normal subjects and SLE patients: no correlation with structural or numerical polymorphisms.正常受试者和系统性红斑狼疮患者体内衰老红细胞CR1的丢失率:与结构或数量多态性无关。
Clin Exp Immunol. 1988 Apr;72(1):74-8.
5
Erythrocyte complement receptor type 1 in non-SLE rheumatic diseases.非系统性红斑狼疮风湿性疾病中的红细胞补体受体1
Rheumatol Int. 1990;10(2):71-3. doi: 10.1007/BF02274786.

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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。
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Mode of inheritance of decreased C3b receptors on erythrocytes of patients with systemic lupus erythematosus.系统性红斑狼疮患者红细胞上C3b受体减少的遗传方式。
N Engl J Med. 1982 Oct 14;307(16):981-6. doi: 10.1056/NEJM198210143071604.
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Inherited structural polymorphism of the fourth component of human complement.人类补体第四成分的遗传性结构多态性。
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Primate erythrocyte-immune complex-clearing mechanism.灵长类动物红细胞免疫复合物清除机制。
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Clinical applications of immunofixation: detection and quantitation of complement activation.免疫固定法的临床应用:补体激活的检测与定量分析
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6
The molecular basis for the difference in immune hemolysis activity of the Chido and Rodgers isotypes of human complement component C4.人类补体成分C4的Chido和Rodgers同种型免疫溶血活性差异的分子基础。
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7
Complement allotyping in SLE: association with C4A null.系统性红斑狼疮中的补体同种异型分型:与C4A基因缺失的关联。
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8
Low C3b receptor reactivity on erythrocytes from patients with systemic lupus erythematosus detected by immune adherence hemagglutination and radioimmunoassays with monoclonal antibody.通过免疫粘附血凝和单克隆抗体放射免疫测定法检测系统性红斑狼疮患者红细胞上低C3b受体反应性。
Arthritis Rheum. 1984 Dec;27(12):1329-35. doi: 10.1002/art.1780271202.
9
Studies on immune adherence (C3b) receptor activity of human erythrocytes: relationship between receptor activity and presence of immune complexes in serum.人红细胞免疫黏附(C3b)受体活性的研究:受体活性与血清中免疫复合物存在之间的关系。
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系统性红斑狼疮中CR1缺乏:后天性还是遗传性?

CR1 deficiency in SLE: acquired or genetic?

作者信息

Uko G, Dawkins R L, Kay P, Christiansen F T, Hollingsworth P N

出版信息

Clin Exp Immunol. 1985 Nov;62(2):329-36.

PMID:2935336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1577435/
Abstract

Erythrocytes from 30 patients suffering from systemic lupus erythematosus (SLE) were tested for CR1 activity by an immune adherence haemagglutination technique. Defective CR1 activity (CR1D) was found in 11 (37%) of the patients on initial testing. On repeat testings, however, CR1 activity often varied from time to time and was shown to be inversely related to serum anti-DNA binding and apparent complement activation in vivo. Two of the 19 patients with normal CR1 activity acquired CR1D during the study. One patient with previously defective CR1 attained normal activity in the course of the study. The increased occurrence of CR1D in patients with SLE is largely or wholly acquired rather than genetically determined.

摘要

采用免疫黏附血凝技术对30例系统性红斑狼疮(SLE)患者的红细胞进行CR1活性检测。初次检测时,11例(37%)患者发现存在CR1活性缺陷(CR1D)。然而,在重复检测时,CR1活性常常随时间变化,且显示出与血清抗DNA结合及体内明显的补体激活呈负相关。19例CR1活性正常的患者中有2例在研究期间出现了CR1D。1例先前CR1有缺陷的患者在研究过程中CR1活性恢复正常。SLE患者中CR1D发生率增加很大程度上或完全是后天获得的,而非由遗传决定。