4.6 Article

Patients with Chromosome 11q Deletions Are Characterized by Inborn Errors of Immunity Involving both B and T Lymphocytes

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JOURNAL OF CLINICAL IMMUNOLOGY
卷 42, 期 7, 页码 1521-1534

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SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10875-022-01303-8

关键词

Chromosome 11q; Jacobsen syndrome; Primary immunodeficiency; Inborn errors of immunity; B lymphocyte function; T lymphocyte function; Granulocyte function; Hypogammaglobulinemia; Children

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Patients with disorders of the long arm of chromosome 11 (11q) often experience immunodeficiency and are susceptible to various infections. This study found that these patients had a high prevalence of respiratory tract infections, varicella infections, chronic eczema, warts, and fungal infections. Immunological screening and treatment are of great importance for this patient group.
Disorders of the long arm of chromosome 11 (11q) are rare and involve various chromosomal regions. Patients with 11q disorders, including Jacobsen syndrome, often present with a susceptibility for bacterial and prolonged viral and fungal infections partially explained by hypogammaglobulinemia. Additional T lymphocyte or granular neutrophil dysfunction may also be present. In order to evaluate infectious burden and immunological function in patients with 11q disorders, we studied a cohort of 14 patients with 11q deletions and duplications. Clinically, 12 patients exhibited prolonged and repetitive respiratory tract infections, frequently requiring (prophylactic) antibiotic treatment (n = 7), ear-tube placement (n = 9), or use of inhalers (n = 5). Complicated varicella infections (n = 5), chronic eczema (n = 6), warts (n = 2), and chronic fungal infections (n = 4) were reported. Six patients were on immunoglobulin replacement therapy. We observed a high prevalence of low B lymphocyte counts (n = 8), decreased T lymphocyte counts (n = 5) and abnormal T lymphocyte function (n = 12). Granulocyte function was abnormal in 29% without a clinical phenotype. Immunodeficiency was found in patients with terminal and interstitial 11q deletions and in one patient with terminal 11q duplication. Genetically, FLI1 and ETS1 are seen as causative for the immunodeficiency, but these genes were deleted nor duplicated in 4 of our 14 patients. Alternative candidate genes on 11q may have a role in immune dysregulation. In conclusion, we present evidence that inborn errors of immunity are present in patients with 11q disorders leading to clinically relevant infections. Therefore, broad immunological screening and necessary treatment is of importance in this patient group.

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