Atypical Hemolytic Uremic Syndrome Associated With Complement Factor H Autoantibodies and CFHR1/CFHR3 Deficiency View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2009-09

AUTHORS

BEOM HEE LEE, SOO HEON KWAK, JAE IL SHIN, SO HEE LEE, HYUN JIN CHOI, HEE GYUNG KANG, IL SOO HA, JAE SEUNG LEE, MARIE-AGNÈS DRAGON-DUREY, YONG CHOI, HAE IL CHEONG

ABSTRACT

Although genetic defect of complement factor H (CFH) is a common cause of atypical hemolytic uremic syndrome (aHUS), development of autoantibodies to CFH (CFH-Ab) is also known to be an acquired cause of aHUS. Recently, a correlation between the development of CFH-Ab and the deficiency of the CFH-related proteins, CFHR1 and CFHR3, was identified. In this study, plasma complement profiles were measured and genetic analysis of the CFH, CFI, MCP, CFHR1, and CFHR3 genes were performed in three female patients diagnosed with aHUS with positive CFH-Ab. Acute stage plasmas of all the three patients revealed low C3, low or low-normal CFH antigenic levels, and high titers of CFH-Ab. All the patients also showed complete plasma CFHR1 deficiency and homozygous genomic deletion of CFHR1/CFHR3, but none had CFH, CFI, or MCP mutations. All the patients were treated with plasmapheresis, and two patients required additional immunosuppressive therapy. These patients had a novel subgroup of aHUS characterized by a combination of genetic (a homozygous deletion of CFHR1/CFHR3) and acquired (development of CFH-Ab) factors. Patients with this disease may need intensive immunosuppressive therapy in addition to plasmapheresis. Screening for CFH-Ab and the CFHR1/CFHR3 deficiency should be included in the diagnostic tests for patients with aHUS. More... »

PAGES

336-340

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1203/pdr.0b013e3181b1bd4a

DOI

http://dx.doi.org/10.1203/pdr.0b013e3181b1bd4a

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1032718562

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/19531976


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