Fc gamma RIIa polymorphism in systemic lupus erythematosus

L J Smyth, N Snowden, D Carthy, C. Papasteriades, A Hajeer, William Ollier

    Research output: Contribution to journalArticlepeer-review

    Abstract

    OBJECTIVES: Polymorphism of the phagocyte IgG receptor Fc gamma RIIa may modulate immune complex mediated inflammation, particularly when immune complexes contain IgG2. Previous studies suggest that this polymorphism may be an important risk factor for lupus nephritis. Fc gamma RIIa is biallelic, the alleles R and H each having a gene frequency of about 50%. Nephritis has been associated with an increased frequency of the R allele. The frequency of common Fc gamma RIIa alleles was examined in white subjects from the United Kingdom and Greek subjects with systemic lupus erythematosus (SLE) and healthy controls. METHODS: Fc gamma RIIa genotyping was performed using a single step polymerase chain reaction technique, which differentiates the two major alleles, R and H. Two study populations were examined: (a) white subjects from the United Kingdom: 66 controls and 81 with SLE (19 of whom had renal disease) and (b) Greek: 52 controls and 42 with SLE (19 with renal disease). RESULTS: No significant relation was observed between Fc gamma RIIa genotype and susceptibility to SLE or SLE nephritis. CONCLUSIONS: The Fc gamma RIIa R allele does not seem to be associated with SLE (with or without renal disease) in our United Kingdom white or Greek populations
    Original languageEnglish
    Pages (from-to)744-746
    Number of pages3
    JournalAnnals of the rheumatic diseases
    Volume56, 12
    Publication statusPublished - 1997

    Keywords

    • ACADEMIC JOURNAL PAPERS
    • ORIGINAL ARTICLES

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