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CD25 deficiency

Diseases of the Blood and Immune Mechanism

CD25 deficiency, also called interleukin 2 receptor alpha deficiency, is an immunodeficiency disorder associated with mutations in the IL2RA gene, which encodes the CD25 chain of the high-affinity interleukin-2 receptor. The mutations lead to a defective chain or none at all, and the resulting syndrome is described as IPEX-like or as a form of severe combined immunodeficiency. In one patient, CD4 lymphocytes lacking CD25 responded poorly to interleukin-2, with greatly reduced secretion of the anti-inflammatory cytokine interleukin-10. The source adds that the deficiency raises susceptibility to viral infections and possibly fungal and bacterial infections, and may impair the expansion of CD8 and CD4 lymphocytes and natural killer cells. This entry records what the source reports and is not medical advice.

Facts
Classification
Body System
Lymphatic or Immune System 1
ICD-10 Chapter
III: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism 2
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
Sources
1. CD25 deficiency (Wikipedia)
Lead sentence
Quote, Lead sentence
CD25 deficiency or interleukin 2 receptor alpha deficiency is an immunodeficiency disorder associated with mutations in the interleukin 2 receptor alpha (CD25) (IL2RA) gene.
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2. World Health Organization: ICD-10 Version:2019, Chapter III, D80-D89
World Health OrganizationCategory D81.2
Quote, Category D81.2
D81.2 Severe combined immunodeficiency [SCID] with low
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