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[抗着丝点抗体。67份阳性血清的研究]

[Anti-centromere antibodies. Study of 67 positive sera].

作者信息

Renier G, Le Normand I, Chevailler A, Verret J L, Renier J C, Hurez D

机构信息

Laboratoire d'Immunopathologie, CHRU, Angers.

出版信息

Rev Med Interne. 1992 Nov;13(6):413-4, 417-8.

PMID:1344922
Abstract

From a series of 67 sera containing anticentromere antibodies we endeavoured to determine the principal clinical or biological peculiarities of these antibodies. The titers of anticentromere antibodies were usually high, with few differences between patients. Humoral immunity was frequently perturbed, with antinuclear autoantibodies (without anti-Scl 70), anti-mitochondria antibodies, rheumatoid factors, circulating immune complexes, etc. The disease predominated in women (97%) whose age and duration of symptoms varied considerably. The most frequent clinical manifestation noted in the 47 reports analyzed was Raynaud's phenomenon (93%) which in most cases (90%) was part of a complete or incomplete CREST syndrome. Telangiectasias, calcinosis and acrosclerosis were the main witnesses to the duration of these sclerodermas. Our findings were concordant with those of previous studies. However, the frequency of sicca syndrome (76%) was unexpected, and must be related to 2 laboratory results: the quasi-absence of anti-SSA and anti-SSB antibodies in our patients and the presence of two monoclonal immunoglobulins (IgM kappa and IgG lambda). There may be some degree of independence between the sicca syndrome and the sclerodermal manifestations.

摘要

我们从一系列67份含有抗着丝点抗体的血清中,努力确定这些抗体的主要临床或生物学特性。抗着丝点抗体的滴度通常较高,患者之间差异不大。体液免疫经常受到干扰,存在抗核自身抗体(无抗Scl 70)、抗线粒体抗体、类风湿因子、循环免疫复合物等。该疾病在女性中占主导(97%),其年龄和症状持续时间差异很大。在分析的47份报告中,最常见的临床表现是雷诺现象(93%),在大多数情况下(90%)是完全或不完全CREST综合征的一部分。毛细血管扩张、钙质沉着和肢端硬化是这些硬皮病病程的主要见证。我们的研究结果与先前的研究一致。然而,干燥综合征的发生率(76%)出人意料,这一定与两个实验室结果有关:我们的患者中几乎没有抗SSA和抗SSB抗体,以及存在两种单克隆免疫球蛋白(IgM κ和IgG λ)。干燥综合征和硬皮病表现之间可能存在一定程度的独立性。

相似文献

1
[Anti-centromere antibodies. Study of 67 positive sera].[抗着丝点抗体。67份阳性血清的研究]
Rev Med Interne. 1992 Nov;13(6):413-4, 417-8.
2
Clinical and serological heterogeneity in patients with anticentromere antibodies.抗着丝点抗体患者的临床和血清学异质性
J Rheumatol. 2005 Aug;32(8):1488-94.
3
Anticentromere antibody positive Sjögren's Syndrome: a retrospective descriptive analysis.抗着丝点抗体阳性干燥综合征:回顾性描述性分析。
Arthritis Res Ther. 2010;12(2):R47. doi: 10.1186/ar2958. Epub 2010 Mar 13.
4
The CREST syndrome: a distinct serologic entity with anticentromere antibodies.CREST综合征:一种具有抗着丝点抗体的独特血清学实体。
Am J Med. 1980 Oct;69(4):520-6. doi: 10.1016/0002-9343(80)90462-3.
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Anticentromere antibody--clinical associations. A study of 44 patients.抗着丝点抗体——临床关联。44例患者的研究。
Rheumatol Int. 1995;14(6):253-5. doi: 10.1007/BF00262092.
6
Nailfold capillaroscopic findings in primary Sjögren's syndrome with and without Raynaud's phenomenon and/or positive anti-SSA/Ro and anti-SSB/La antibodies.原发性干燥综合征伴或不伴雷诺现象及抗SSA/Ro和抗SSB/La抗体阳性时的甲襞毛细血管镜检查结果
Rheumatol Int. 2016 Mar;36(3):365-9. doi: 10.1007/s00296-015-3396-9. Epub 2015 Nov 23.
7
A long-term longitudinal study of anticentromere antibodies.一项关于抗着丝粒抗体的长期纵向研究。
Arthritis Rheum. 1984 Feb;27(2):121-4. doi: 10.1002/art.1780270201.
8
[Anticentromere antibodies in rheumatoid polyarthritis with Sjögren syndrome, without the elements of the CREST syndrome].[类风湿性多关节炎合并干燥综合征且无CREST综合征要素患者中的抗着丝点抗体]
Rev Rhum Mal Osteoartic. 1988 Mar 15;55(4):291-2.
9
Anti-centromere autoantibody in a patient evolving from a lupus/Sjögren's overlap to the CREST variant of scleroderma.
J Rheumatol. 1998 Jul;25(7):1419-24.
10
Anticentromere antibodies in rheumatologic practice are not consistently associated with scleroderma.在风湿病临床实践中,抗着丝点抗体与硬皮病之间并无始终如一的关联。
Rev Rhum Engl Ed. 1997 Jun;64(6):362-7.

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Prognostic value of Sjögren's syndrome autoantibodies.干燥综合征自身抗体的预后价值。
J Lab Precis Med. 2018 Oct;3. doi: 10.21037/jlpm.2018.08.05. Epub 2018 Oct 30.
2
Autoantibodies in Sjögren's Syndrome.干燥综合征中的自身抗体。
Rheum Dis Clin North Am. 2016 Aug;42(3):419-34. doi: 10.1016/j.rdc.2016.03.002. Epub 2016 Jun 21.
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Coexistence of antitopoisomerase I and anticentromere antibodies in patients with systemic sclerosis.系统性硬化症患者中抗拓扑异构酶I抗体与抗着丝粒抗体的共存。
Ann Rheum Dis. 2002 Feb;61(2):121-7. doi: 10.1136/ard.61.2.121.