Invisible Illness Awareness Week 2016: Our Voices Need to Be Heard
Never heard of Invisible Illness Awareness Week? You're not alone. Jody Smith sheds a little light to make it more visible
Discuss the article on the Forums.

Impaired interferon gamma-mediated immunity.

Discussion in 'Genetic Testing and SNPs' started by Ema, Apr 8, 2014.

  1. Ema

    Ema Senior Member

    Midwest USA

    Have you seen any abnormalities in these genes in your research in our population?

    Thanks, Ema

    Pediatr Res. 2001 Jul;50(1):8-13.
    Impaired interferon gamma-mediated immunity and susceptibility to mycobacterial infection in childhood.
    Remus N1, Reichenbach J, Picard C, Rietschel C, Wood P, Lammas D, Kumararatne DS, Casanova JL.
    Author information

    Mendelian susceptibility to poorly virulent mycobacteria such as bacillus Calmette-Guerin (BCG) and environmental nontuberculous mycobacteria is a clinically heterogeneous syndrome. The clinical features of affected children cover a continuous spectrum from disseminated lethal bacillus Calmette-Guerin infection to local recurrent nontuberculous mycobacterial infection.

    Different types of mutations in four genes (IFNGR1, IFNGR2, IL12B, IL12RB1) have revealed both allelic and nonallelic heterogeneity and result in eight different disorders whose common pathogenic pathway is impaired interferon gamma (IFNgamma) mediated immunity.

    The severity of the clinical phenotype depends on the genotype. Complete IL-12 p40 and IL-12 receptor beta1 deficiencies and partial IFNgamma receptor 1 (IFNgammaR1) and IFNgammaR2 deficiencies generally lead to curable infections at various ages, and antibiotics supplemented with IFNgamma if required are likely to be effective. Complete IFNgammaR1 and IFNgammaR2 deficiencies predispose to overwhelming infection in early childhood, which may respond to antibiotics but relapse when antibiotics are discontinued. Rapid discrimination between complete IFNgammaR1 and IFNgammaR2 deficiency and other defects, therefore, is an important diagnostic step for planning clinical management.



    [PubMed - indexed for MEDLINE]
    SOC and Valentijn like this.
  2. Valentijn

    Valentijn Senior Member

    I'll look into it ... might take a bit, depending on how many SNPs are tested on each gene :p But a brief search in my directory brings up a few matches from patients' 1% and/or 10% result, so there are definitely some abnormalities.
    Ema likes this.
  3. Valentijn

    Valentijn Senior Member

    @Ema - Compared to controls, we come out looking pretty normal:

    SOC and Ema like this.

See more popular forum discussions.

Share This Page