European Society for Immunodeficiencies guidelines for the management of patients with congenital athymia
Language English Country United States Media print-electronic
Document type Journal Article, Review, Practice Guideline
PubMed
39303894
DOI
10.1016/j.jaci.2024.07.031
PII: S0091-6749(24)00980-1
Knihovny.cz E-resources
- Keywords
- 22q11.2 deletion syndrome, Congenital athymia, DiGeorge syndrome, immunology guidelines, thymus transplantation,
- MeSH
- Humans MeSH
- Disease Management MeSH
- Infant, Newborn MeSH
- Immunologic Deficiency Syndromes * therapy diagnosis immunology MeSH
- Thymus Gland immunology MeSH
- Check Tag
- Humans MeSH
- Infant, Newborn MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Practice Guideline MeSH
- Geographicals
- Europe MeSH
Congenital athymia is a life-limiting disorder due to rare inborn errors of immunity causing impaired thymus organogenesis or abnormal thymic stromal cell development and function. Athymic infants have a T-lymphocyte-negative, B-lymphocyte-positive, natural killer cell-positive immunophenotype with profound T-lymphocyte deficiency and are susceptible to severe infections and autoimmunity. Patients variably display syndromic features. Expanding access to newborn screening for severe combined immunodeficiency and T lymphocytopenia and broad genetic testing, including next-generation sequencing technologies, increasingly facilitate their timely identification. The recommended first-line treatment is allogeneic thymus transplantation, which is a specialized procedure available in Europe and the United States. Outcomes for athymic patients are best with early diagnosis and thymus transplantation before the development of infectious and inflammatory complications. These guidelines on behalf of the European Society for Immunodeficiencies provide a comprehensive review for clinicians who manage patients with inborn thymic stromal cell defects; they offer clinical practice recommendations focused on the diagnosis, investigation, risk stratification, and management of congenital athymia with the aim of improving patient outcomes.
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