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[Hereditary C5 deficiency and recurrent Neisseria meningitidis meningitis].

作者信息

Ducret F, Decoux M, Pointet P, Lambert C, Grosperrin E, Sédaillan A

机构信息

Unité de néphrologie et de médecine interne, Centre Hospitalier, Annecy.

出版信息

Rev Med Interne. 1988 Nov-Dec;9(5):534-7. doi: 10.1016/s0248-8663(88)80021-3.

DOI:10.1016/s0248-8663(88)80021-3
PMID:3067301
Abstract

Deficiencies of the terminal C fragments of the complement system are known to be associated with a remarkable increase in the frequency of Neisseria infections. The correlation is even closer between deficiency of C5 and recurrent N. meningitidis meningitis. The reasons for this bacterial specificity and the immunopathological mechanisms involved have not been clearly established. However, it is known that only adult subjects with homozygous deficiency are affected and that the deficiency is transmitted as an autosomal recessive trait unrelated to the HLA system.

摘要

相似文献

1
[Hereditary C5 deficiency and recurrent Neisseria meningitidis meningitis].
Rev Med Interne. 1988 Nov-Dec;9(5):534-7. doi: 10.1016/s0248-8663(88)80021-3.
2
[Recurring meningococcal meningitis in hereditary C 5 deficiency].遗传性C5缺乏症中的复发性脑膜炎球菌性脑膜炎
Dtsch Med Wochenschr. 1985 Sep 27;110(39):1498-501. doi: 10.1055/s-2008-1069035.
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[Homozygotic C5 deficiency disclosed by purulent Neisseria meningitidis meningitis].[由化脓性脑膜炎奈瑟菌脑膜炎揭示的纯合子C5缺乏症]
Presse Med. 1985 Dec 21;14(45):2287-9.
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A complement C5 gene mutation, c.754G>A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases.一个补体 C5 基因突变,c.754G>A:p.A252T,在南非西开普省很常见,在 7%的黑人非洲脑膜炎球菌病病例中发现为纯合子。
Mol Immunol. 2015 Mar;64(1):170-6. doi: 10.1016/j.molimm.2014.11.010. Epub 2014 Dec 19.
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Recurrent bacterial meningitis due to genetic deficiencies of terminal complement components (C5 and C6).由于终末补体成分(C5和C6)基因缺陷导致的复发性细菌性脑膜炎。
Immunobiology. 1980;158(1-2):101-6. doi: 10.1016/S0171-2985(80)80048-9.
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Recurrent bacterial meningitis in patients with genetic defects of terminal complement components.终末补体成分基因缺陷患者的复发性细菌性脑膜炎
Clin Exp Immunol. 1980 Apr;40(1):16-24.
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Meningococcal disease in congenital absence of the fifth component of complement.先天性补体第五成分缺乏症中的脑膜炎球菌病
Scand J Infect Dis. 1987;19(6):635-9. doi: 10.3109/00365548709117198.
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Phenotypically similar clones of serogroup B Neisseria meningitidis causing recurrent meningitis in a patient with total C5 deficiency.B群脑膜炎奈瑟菌的表型相似克隆株在一名C5完全缺乏的患者中引发复发性脑膜炎。
J Infect. 1994 Sep;29(2):236-8. doi: 10.1016/s0163-4453(94)91010-3.
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Invasive Meningococcal Disease Unraveling a Novel Mutation in the C5 Gene in a Portuguese Family.侵袭性脑膜炎球菌病:葡萄牙一家庭中 C5 基因新型突变的解析。
Pediatr Infect Dis J. 2019 Apr;38(4):416-418. doi: 10.1097/INF.0000000000002149.
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[The association between deficiency of terminal complement components and the occurrence of meningococcal meningitis].[终末补体成分缺乏与脑膜炎球菌性脑膜炎发生之间的关联]
Fukuoka Igaku Zasshi. 1992 May;83(5):201-8.

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Cells. 2021 Jan 13;10(1):148. doi: 10.3390/cells10010148.
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Structure of complement C6 suggests a mechanism for initiation and unidirectional, sequential assembly of membrane attack complex (MAC).补体 C6 的结构提示了膜攻击复合物(MAC)起始和单向、顺序组装的机制。
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