Novel IL2RB gene defect associated with severe eczema, recurrent infections, lymphoproliferation, and IgA nephropathy
Author:
Affiliation:
1. Department of Pediatrics, Allergy Immunology unit Postgraduate Institute of Medical Education and Research Chandigarh India
2. Consultant Pediatric Nephrology Fortis Hospital New Delhi India
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/pai.14160
Reference5 articles.
1. Cutting Edge: Antibody-Dependent Memory-like NK Cells Distinguished by FcRγ Deficiency
2. lnterleukin-2 programs mouse αβ T lymphocytes for apoptosis
3. Defective expression of the interleukin-2/interleukin-15 receptor β subunit leads to a natural killer cell–deficient form of severe combined immunodeficiency
4. Human interleukin-2 receptor β mutations associated with defects in immunity and peripheral tolerance
5. A novel human IL2RB mutation results in T and NK cell–driven immune dysregulation
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