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The tandem-repeat polymorphism of the DC-SIGNR gene in HCV infection

  • J. Nattermann
  • , G. Ahlenstiel
  • , T. Berg
  • , G. Feldmann
  • , H. D. Nischalke
  • , T. Müller
  • , J. Rockstroh
  • , R. Woitas
  • , T. Sauerbruch
  • , U. Spengler

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)

Abstract

The C-type lectin DC-SIGNR has been shown to bind hepatitis C virus (HCV). Here, we analysed the tandem-repeat polymorphism of the DC-SIGNR gene with respect to intraindividual HCV replication. In a cross-sectional comparison HCV-infected patients (n = 430) and healthy subjects (n = 100) were genotyped for the DC-SIGNR polymorphism using PCR. The distribution of DC-SIGNR alleles did not differ significantly between the two groups. However, HCV-infected patients with 5-, 6-, and 7-repeat alleles had higher HCV-RNA levels when compared with carriers of 4- and 9-repeat alleles (P < 0.05). Thus, the DC-SIGNR polymorphism might affect HCV loads supporting the concept that DC-SIGNR contributes to HCV replication efficacy.

Original languageEnglish
Pages (from-to)42-46
Number of pages5
JournalJournal of Viral Hepatitis
Volume13
Issue number1
DOIs
Publication statusPublished - Jan 2006
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • CD209L
  • DC-SIGNR
  • Genetic polymorphisms
  • HCV
  • L-SIGN

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