HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Late Onset Hypomorphic RAG2 Deficiency Presentation with Fatal Vaccine-Strain VZV Infection.

AbstractPURPOSE:
Hypomorphic mutations in RAG1 and RAG2 are associated with significant clinical heterogeneity and symptoms of immunodeficiency or autoimmunity may be late in appearance. As a result, immunosuppressive medications may be introduced that can have life-threatening consequences. We describe a previously healthy 13-month-old girl presenting with rash and autoimmune hemolytic anemia, while highlighting the importance of vigilance and consideration of an underlying severe immunodeficiency disease prior to instituting immunosuppressive therapy.
METHODS:
Given clinical deterioration of the patient and a temporal association with recently administered vaccinations, virus genotyping was carried out via 4 real-time Forster Resonance Energy Transfer PCR protocols targeting vaccine-associated single nucleotide polymorphisms. Genomic DNA was extracted from whole blood and analyzed via the next-generation sequencing method of sequencing-by-synthesis. Immune function studies included immunophenotyping of peripheral blood lymphocytes, mitogen-induced proliferation and TLR ligand-induced production of TNFα. Analysis of recombination activity of wild-type and mutant RAG2 constructs was performed.
RESULTS:
Virus genotyping revealed vaccine-strain VZV, mumps, and rubella. Next-generation sequencing identified heterozygosity for RAG2 R73H and P180H mutations. Profound lymphopenia was associated with intense corticosteroid therapy, with some recovery after steroid reduction. Residual, albeit low, RAG2 protein activity was demonstrated.
CONCLUSIONS:
Because of the association of RAG deficiency with late-onset presentation and autoimmunity, live virus vaccination and immunosuppressive therapies are often initiated and can result in negative consequences. Here, hypomorphic RAG2 mutations were linked to disseminated vaccine-strain virus infections following institution of corticosteroid therapy for autoimmune hemolytic anemia.
AuthorsCullen M Dutmer, Edwin J Asturias, Christiana Smith, Megan K Dishop, D Scott Schmid, William J Bellini, Irit Tirosh, Yu Nee Lee, Luigi D Notarangelo, Erwin W Gelfand
JournalJournal of clinical immunology (J Clin Immunol) Vol. 35 Issue 8 Pg. 754-60 (Nov 2015) ISSN: 1573-2592 [Electronic] Netherlands
PMID26515615 (Publication Type: Case Reports, Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • Adrenal Cortex Hormones
  • DNA-Binding Proteins
  • Nuclear Proteins
  • RAG2 protein, human
  • Viral Vaccines
Topics
  • Adolescent
  • Adrenal Cortex Hormones (administration & dosage, adverse effects)
  • Anemia, Hemolytic, Autoimmune (complications, diagnosis, drug therapy)
  • Cells, Cultured
  • DNA-Binding Proteins (genetics)
  • Female
  • Herpes Zoster (complications, diagnosis, drug therapy)
  • Herpesvirus 3, Human (physiology)
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Immunologic Deficiency Syndromes (complications, diagnosis, drug therapy)
  • Immunosuppression Therapy
  • Lymphocyte Activation (drug effects)
  • Nuclear Proteins (genetics)
  • Pedigree
  • Viral Vaccines (immunology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: