• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

终末补体成分(C9)缺乏症中的系统性红斑狼疮样症状和干燥症状

SLE-like and sicca symptoms in late component (C9) complement deficiency.

作者信息

Sugimoto M, Nishikai M, Sato A, Suzuki Y, Nihei M, Uchida J, Mimura N

出版信息

Ann Rheum Dis. 1987 Feb;46(2):153-5. doi: 10.1136/ard.46.2.153.

DOI:10.1136/ard.46.2.153
PMID:3827337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1002082/
Abstract

Hereditary deficiencies in early and late complement components are well known to predispose to SLE-like syndromes or recurrent infection. Hitherto reported C9 deficient cases have usually been healthy subjects, however, and it is not considered that C9 deficiency is associated with any specific disease. We describe a completely C9 deficient patient with possible Sjögren's syndrome and discuss the relationship.

摘要

众所周知,早期和晚期补体成分的遗传性缺陷易引发系统性红斑狼疮样综合征或反复感染。然而,迄今为止报道的C9缺陷病例通常为健康受试者,且人们认为C9缺陷与任何特定疾病均无关联。我们描述了一名可能患有干燥综合征的完全C9缺陷患者,并讨论了二者之间的关系。

相似文献

1
SLE-like and sicca symptoms in late component (C9) complement deficiency.终末补体成分(C9)缺乏症中的系统性红斑狼疮样症状和干燥症状
Ann Rheum Dis. 1987 Feb;46(2):153-5. doi: 10.1136/ard.46.2.153.
2
Autoimmune thyroid disease is associated with a diagnosis of secondary Sjögren's syndrome in familial systemic lupus.自身免疫性甲状腺疾病与家族性系统性红斑狼疮继发干燥综合征的诊断相关。
Ann Rheum Dis. 2007 Mar;66(3):410-3. doi: 10.1136/ard.2006.055103. Epub 2006 Sep 19.
3
Inherited deficiencies of the late-acting complement components other than C9 found among healthy blood donors.在健康献血者中发现除C9外的晚期补体成分的遗传性缺陷。
Int Arch Allergy Appl Immunol. 1989;90(3):274-9. doi: 10.1159/000235037.
4
[Sjögren's syndrome: immunologic aspects and treatment].[干燥综合征:免疫学方面及治疗]
Wiad Lek. 1983 Jul 1;36(13):1077-81.
5
Recurrent meningitis in a patient with congenital deficiency of the C9 component of complement. First case of C9 deficiency in Europe.一名患有补体C9成分先天性缺陷的患者反复发生脑膜炎。欧洲首例C9缺陷病例。
Arch Intern Med. 1990 Nov;150(11):2395-9.
6
[Hypereosinophilia in Sjögren's syndrome].[干燥综合征中的嗜酸性粒细胞增多症]
Klin Med (Mosk). 1987 Jun;65(6):126-8.
7
Deficiency of the 9th component of complement (C9) in a patient with systemic lupus erythematosus.一名系统性红斑狼疮患者体内补体第九成分(C9)缺乏。
J Rheumatol. 1989 Apr;16(4):542-3.
8
Genetic detection of the silent allele (*Q0) in hereditary deficiencies of the human complement C6, C7, and C9 components.人类补体C6、C7和C9成分遗传性缺陷中沉默等位基因(*Q0)的基因检测。
Am J Med Genet. 1995 Feb 13;55(4):408-13. doi: 10.1002/ajmg.1320550405.
9
A high incidence of C9 deficiency among healthy blood donors in Osaka, Japan.日本大阪健康献血者中C9缺乏症的高发病率。
Int Immunol. 1989;1(1):85-9. doi: 10.1093/intimm/1.1.85.
10
[Chronic hepatitis C and Gougerot-Sjogren syndrome. Apropos of a case].[慢性丙型肝炎与古热罗-舍格伦综合征。附病例报告]
Rev Rhum Ed Fr. 1993 Apr;60(4):305-7.

引用本文的文献

1
A Case of Pediatric Subcutaneous Panniculitis-like T-Cell Lymphoma Successfully Treated with Immunosuppressive Therapy.1例采用免疫抑制疗法成功治疗的儿童皮下脂膜炎样T细胞淋巴瘤
Children (Basel). 2025 Aug 5;12(8):1029. doi: 10.3390/children12081029.
2
Monogenic systemic lupus erythematosus: insights in pathophysiology.单基因系统性红斑狼疮:发病机制的新认识。
Rheumatol Int. 2018 Oct;38(10):1763-1775. doi: 10.1007/s00296-018-4048-7. Epub 2018 May 15.
3
Infectious diseases associated with complement deficiencies.与补体缺陷相关的传染病。
Clin Microbiol Rev. 1991 Jul;4(3):359-95. doi: 10.1128/CMR.4.3.359.

本文引用的文献

1
Deficiency of C7 with systemic lupus erythematosus: solubilization of immune complexes in complement-deficient sera.C7缺乏与系统性红斑狼疮:补体缺陷血清中免疫复合物的溶解
Arthritis Rheum. 1981 Jan;24(1):87-93. doi: 10.1002/art.1780240114.
2
Inherited deficiency of the ninth component of complement in man.人类补体第九成分的遗传性缺陷。
J Immunol. 1980 Nov;125(5):2252-7.
3
Further studies on C9 deficiency.关于C9缺陷的进一步研究。
J Clin Lab Immunol. 1981 Jul;6(1):7-11.
4
Identification of the alpha-gamma subunit of the eighth component of complement (C8) in a patient with systemic lupus erythematosus and absent C8 activity: patients and family studies.系统性红斑狼疮且缺乏补体第八成分(C8)活性患者中补体第八成分(C8)α-γ亚基的鉴定:患者及家系研究
Clin Immunol Immunopathol. 1982 May;23(2):323-34. doi: 10.1016/0090-1229(82)90118-0.
5
HLA antigens and Bf allotypes in SLE: evidence for the association being with specific haplotypes.系统性红斑狼疮中的HLA抗原和Bf同种异型:与特定单倍型相关联的证据。
Tissue Antigens. 1982 Feb;19(2):115-20. doi: 10.1111/j.1399-0039.1982.tb01426.x.
6
HLA antigens of patients with systemic lupus erythematosus in Japan.日本系统性红斑狼疮患者的人类白细胞抗原
Tissue Antigens. 1982 Sep;20(3):221-2. doi: 10.1111/j.1399-0039.1982.tb00348.x.
7
Serologic studies in a family with heterozygous C2 deficiency.对一个患有杂合子C2缺乏症的家族进行的血清学研究。
Am J Med. 1981 Dec;71(6):945-8. doi: 10.1016/0002-9343(81)90311-9.
8
The role of C9 in complement-mediated killing of Neisseria.C9在补体介导的奈瑟菌杀伤中的作用。
J Immunol. 1981 Dec;127(6):2386-90.
9
Evidence for linkage between HL-A histocompatibility genes and those involved in the synthesis of the second component of complement.HL-A组织相容性基因与补体第二成分合成相关基因之间存在连锁关系的证据。
J Exp Med. 1974 Oct 1;140(4):1108-11. doi: 10.1084/jem.140.4.1108.
10
Hereditary deficiency of the fifth component of complement in man. I. Clinical, immunochemical, and family studies.人类补体第五成分的遗传性缺陷。I. 临床、免疫化学及家系研究。
J Clin Invest. 1976 Jun;57(6):1626-34. doi: 10.1172/JCI108433.