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Patterns of Immune Dysregulation in Primary Immunodeficiencies: A Systematic Review

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ELSEVIER
DOI: 10.1016/j.jaip.2020.10.057

关键词

Inborn errors of immunity; Primary immunodefi-ciencies; Immune dysregulation; Autoimmunity; Inflammation; Disease pattern; Eczema

资金

  1. Children's Research Center at the University children's Hospital of Zurich
  2. University of Zurich's Clinical Research Priority Program CYTIMM-Z, Promedica
  3. Beatrice Ederer-Weber foundation (Zurich, Switzerland)
  4. University of Zurich's Cancer Research Center Funding program

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Immune dysregulation is crucial in defining primary immunodeficiencies, and identifying patterns of immune dysregulation can help clinicians recognize specific PIDs. This systematic review provides an overview for clinicians to better assess patients with immune dysregulation symptoms.
BACKGROUND: Immune dysregulation is as important as susceptibility to infection in defining primary immunodeficiencies (PIDs). Because of the variability and nonspecificity of the symptoms of PIDs, diagnosis can be delayed-especially if a patient presents with immune dysregulation. Diagnosis is then based on certain combinations of symptoms and relies on the clinician's ability to recognize a pattern. So far there is no large report linking patterns of immune dysregulations to the underlying genetic defects. OBJECTIVE: To identify immune dysregulatory patterns associated with PIDs and to help clinicians to detect an underlying PID in certain patients with noninfectious inflammatory diseases. METHOD: A systematic literature review was performed. RESULTS: We included 186 articles that reported on n = 745 patients. The most common immune dysregulation category was autoimmunity (62%, n = 463), followed by intestinal disease (38%, n = 283) and lymphoproliferation (36%, n = 268). Most patients (67%) had 1 or more symptoms of immune dysregulation. Autoimmune hemolytic anemia, the most common autoimmune phenotype, was most frequently reported in patients with LPS responsive beige-like anchor protein deficiency (when combined with hypogammaglobulin-emia or gastrointestinal symptoms), activation-induced cytidine deaminase deficiency (when combined with autoimmune hepa-titis), or RAG1 deficiency (when it was the only symptom of immune dysregulation). Eczema, allergies, and asthma were reported in 34%, 4%, and 4% of the patients, respectively. CONCLUSION: Patterns of immune dysregulation may help the physician to recognize specific PIDs. This systematic review provides clinicians with an overview to better assess patients with immune dysregulation. (C) 2020 Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology.

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