备解素缺乏与脑膜炎球菌病——识别高危人群。 - Suppr

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超能文献

Properdin deficiency and meningococcal disease--identifying those most at risk.

作者信息

Linton S M, Morgan B P

机构信息

Complement Biology Group, Department of Medical Biochemistry, UWCM, Cardiff, UK.

出版信息

Clin Exp Immunol. 1999 Nov;118(2):189-91. doi: 10.1046/j.1365-2249.1999.01057.x.

DOI:10.1046/j.1365-2249.1999.01057.x

PMID:10540177

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1905414/

Abstract

摘要

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本文引用的文献

Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n).

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Assessment of complement deficiency in patients with meningococcal disease in The Netherlands.

Clin Infect Dis. 1999 Jan;28(1):98-105. doi: 10.1086/515075.

Protection against meningococcal serogroup ACYW disease in complement-deficient individuals vaccinated with the tetravalent meningococcal capsular polysaccharide vaccine.

Clin Exp Immunol. 1998 Dec;114(3):362-9. doi: 10.1046/j.1365-2249.1998.00738.x.

Vaccination against meningococcus in complement-deficient individuals.

Clin Exp Immunol. 1998 Dec;114(3):327-9. doi: 10.1046/j.1365-2249.1998.00734.x.

Human properdin deficiency has a heterogeneous genetic background.

Immunopharmacology. 1997 Dec;38(1-2):203-6. doi: 10.1016/s0162-3109(97)00087-8.

Carrier detection by microsatellite haplotyping in 10 properdin type 1-deficient families.

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