Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Whole-Exome Sequencing to Identify Undiagnosed Primary Immunodeficiency Disorders in Children With Community-Acquired Sepsis, Admitted in the Pediatric Intensive Care Unit Publisher Pubmed



Rayzan E1, 2 ; Mirbeyk M3 ; Pezeshki PS3, 4 ; Mohammadpour M5 ; Yaghmaie B5 ; Hassani SA5 ; Sharifzadeh M5 ; Tahernia L5 ; Rezaei N3, 6, 7
Authors
Show Affiliations
Authors Affiliations
  1. 1. Division of Pediatric Hematology/Oncology, Boston Children's Hospital, Boston, MA, United States
  2. 2. International Hematology/Oncology of Pediatrics Experts (IHOPE), Universal Scientific Education and Research Network (USERN), Boston, MA, United States
  3. 3. Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. International Hematology/Oncology of Pediatrics Experts (IHOPE), Universal Scientific Education and Research Network (USERN), Tehran, Iran
  5. 5. Division of Pediatric Intensive Care Unit, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran

Source: Pediatric Allergy and Immunology Published:2023


Abstract

Background: Whole-exome sequencing (WES) provides a powerful diagnostic tool for identifying primary immunodeficiency diseases (PIDs). This study explores the utility of this approach in uncovering previously undiagnosed PIDs in children with community-acquired sepsis (CAS), with a medical history of recurrent infections or a family history of PIDs. Methods: We performed WES on DNA samples extracted from the blood of the 34 enrolled patients, followed by bioinformatic analysis for variant calling, annotation, and prioritization. We also performed a segregation analysis in available family members to confirm the inheritance patterns and assessed the potential impact of the identified variants on protein function. Results: From 34 patients enrolled in the study, 29 patients (85%) with previously undiagnosed genetic diseases, including 28 patients with PIDs and one patient with interstitial lung and liver disease, were identified. We identified two patients with severe combined immunodeficiency (SCID), patients with combined immunodeficiency (CID), six patients with combined immunodeficiency with syndromic features (CID-SF), four patients with defects in intrinsic and innate immunity, four patients with congenital defects of phagocyte function (CPDF), and six patients with the disease of immune dysregulation. Autoinflammatory disorders and predominantly antibody deficiency were diagnosed in one patient each. Conclusion: Our findings demonstrate the potential of WES in identifying undiagnosed PIDs in children with CAS. Implementing WES in the clinical evaluation of CAS patients with a warning sign for PIDs can aid in their timely diagnosis and potentially lead to improved patient care. © 2023 European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.
Other Related Docs
9. Autoimmunity in Primary T-Cell Immunodeficiencies, Expert Review of Clinical Immunology (2016)
23. Approach to the Management of Autoimmunity in Primary Immunodeficiency, Scandinavian Journal of Immunology (2017)
25. Global Systematic Review of Primary Immunodeficiency Registries, Expert Review of Clinical Immunology (2020)
26. Costs of Hospital Admission on Primary Immunodeficiency Diseases, Iranian Journal of Public Health (2017)