A potential role for monoallelic expression in penetrance of autosomal dominant inborn errors of immunity
In this article, we discuss a recent study, where autosomal monoallelic expression of genes underlying Inborn Errors of Immunity were investigated. About 2-10% of genes are predominantly transcribed from a single allele leading to autosomal random monoallelic expression (I). If this is skewed in a cell population from an individual with an autosomal dominant inborn error of immunity, this can lead to a mild to no phenotype (incomplete penetrance) if the wildtype allele is favored (II), or to more severe disease presentation if the variant allele is favored (III).
Authors
- Emily S.J. Edwards (ORCID: https://orcid.org/0000-0002-0240-4370)
- Menno C. van Zelm (ORCID: https://orcid.org/0000-0003-4161-1919)
Institutions
- Erasmus MC (NL)
- Jeffrey Modell Foundation (AU)
- Alfred Health (AU)
- Monash University (AU)
Publication Details
- Journal
- Immunology and Cell Biology
- Published
- 2025-02-05
- DOI
- https://doi.org/10.1111/imcb.12856
- Primary Topic
- Immunodeficiency and Autoimmune Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- CSL Behring
- Grifols
- Agenzia Italiana del Farmaco, Ministero della Salute