Risk factors of clinical dysimmune manifestations in a cohort of 86 children with 22q11.2 deletion syndrome: A retrospective study in France

Am J Med Genet A. 2019 Nov;179(11):2207-2213. doi: 10.1002/ajmg.a.61336. Epub 2019 Aug 30.

Abstract

In this study, we describe the biological immune profiles and clinical dysimmune manifestations (infections, autoimmune diseases, and allergies) of patients with 22q11.2 deletion syndrome with the aim of determining risk factors for clinical events. This retrospective study concerned all the patients with 22q11 deletion syndrome attending the Montpellier University Hospital from January 1, 1992, to December 31, 2014 who had at least one immune investigation before the age of 18. We analyzed the clinical features, biological tests and the course of infections, autoimmunity, and allergy of 86 children. Among these 86 children, 48 (59%) had a low T lymphocyte level. Twenty-nine patients (34%) had a severe infection. The only risk factor for severe infection was the low level of CD4+ T-cells (OR: 3.3; 95% confidence interval (CI) [1.020-11.108]). Eleven patients (13%) developed an autoimmune disease; the only risk factor was an antecedent of severe infection (OR: 4.1; 95% CI [1.099-15.573]). Twenty-three patients (27%) had allergic episodes. A low level of CD8+ T-cells (OR: 3.2; 95% CI [1.07-9.409]) was significantly associated with allergy manifestations. Patients with 22q11 deletion syndrome have a high rate of dysimmune manifestations. We found statistic correlations among CD4+ T-cell count, infectious manifestations, and autoimmunity.

Keywords: 22q11 deletion syndrome; autoimmunity; dysimmunity; infections; lymphocytes.

MeSH terms

  • Autoimmune Diseases / genetics
  • Autoimmune Diseases / immunology
  • Autoimmunity*
  • Child
  • Child, Preschool
  • DiGeorge Syndrome / diagnosis
  • DiGeorge Syndrome / epidemiology*
  • DiGeorge Syndrome / immunology
  • Disease Susceptibility* / immunology
  • Female
  • France / epidemiology
  • Humans
  • Hypersensitivity / genetics
  • Hypersensitivity / immunology
  • Immunoglobulin Isotypes / blood
  • Immunoglobulin Isotypes / immunology
  • Infant
  • Infections / etiology
  • Male
  • Phenotype*
  • Prevalence
  • Severity of Illness Index
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism

Substances

  • Immunoglobulin Isotypes