C1 inhibitor gene expression in patients with hereditary angioedema: quantitative evaluation by means of real-time RT-PCR

J Allergy Clin Immunol. 2004 Sep;114(3):638-44. doi: 10.1016/j.jaci.2004.06.021.

Abstract

Background: Hereditary angioedema (HAE) is caused by heterozygous defects in the C1 inhibitor (C1-INH) gene (SERPING1/C1NH). In patients' plasma C1-INH levels range between 5% and 30% of normal levels (ie, far from the 50% expected for an autosomal dominant defect). Most patients have antigenic and functional deficiency (type I HAE), and 15% have reduced C1-INH function but normal to increased antigen because of the presence of a dysfunctional protein (type II HAE).

Objective: We sought to contribute to the understanding of the pattern of C1-INH gene expression in patients with HAE.

Methods: We used real-time quantitative RT-PCR to measure C1-INH mRNA levels in PBMCs of 57 patients with HAE typed for mutations in the SERPING1/C1NH gene.

Results: Thirty-six different mutations were identified in genomic DNA. Compared with healthy control subjects, C1-INH mRNA was significantly and similarly reduced in patients with type I and type II HAE (40% and 47%, respectively; P <.0001). By means of direct sequencing of cDNAs, we found that 74% of patients with type I HAE carrying small mutations presented significant amounts of mutated transcripts at the mRNA level, suggesting that both allelic mRNA products were reduced to approximately 50%. In 4 patients carrying large deletions expected to fully inactivate expression from the mutant allele, C1-INH mRNA was 23% on average compared with that seen in control subjects, confirming that normal mRNA was strongly underexpressed.

Conclusions: These new findings, combined with previous evidence of increased C1-INH consumption, might explain the plasma levels of normal C1-INH that are markedly less than the expected 50%.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angioedema / genetics
  • Angioedema / metabolism*
  • Complement C1 Inactivator Proteins / genetics*
  • Complement C1 Inactivator Proteins / metabolism*
  • Complement C1 Inhibitor Protein
  • Down-Regulation
  • Female
  • Humans
  • Leukocytes, Mononuclear / metabolism
  • Male
  • Mutation
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction / methods*
  • Taq Polymerase

Substances

  • Complement C1 Inactivator Proteins
  • Complement C1 Inhibitor Protein
  • RNA, Messenger
  • Taq Polymerase