Cited by 465Down syndrome and intellectual disability researchImmunodeficiency and Autoimmune DisordersT-cell and B-cell Immunology

Infections and immunodeficiency in Down syndrome

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Ram, G, Chinen, J·2011·Clinical and Experimental Immunology

Abstract

Down syndrome (DS) is the most common genetic disease and presents with cognitive impairment, cardiac and gastrointestinal abnormalities, in addition to other miscellaneous clinical conditions. DS individuals may have a high frequency of infections, usually of the upper respiratory tract, characterized by increased severity and prolonged course of disease, which are partially attributed to defects of the immune system. The abnormalities of the immune system associated with DS include: mild to moderate T and B cell lymphopenia, with marked decrease of naive lymphocytes, impaired mitogen-induced T cell proliferation, reduced specific antibody responses to immunizations and defects of neutrophil chemotaxis. Limited evidence of genetic abnormalities secondary to trisomy of chromosome 21 and affecting the immune system is available, such as the potential consequences of gene over-expression, most significantly SOD1 and RCAN1. Secondary immunodeficiency due to metabolic or nutritional factors in DS, particularly zinc deficiency, has been postulated. Non-immunological factors, including abnormal anatomical structures (e.g. small ear canal, tracheomalacia) and gastro-oesophageal reflux, may play a role in the increased frequency of respiratory tract infections. The molecular mechanisms leading to the immune defects observed in DS individuals and the contribution of these immunological abnormalities to the increased risk of infections require further investigation. Addressing immunolo…

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Crossref · 10.1111/j.1365-2249.2011.04335.x

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  • Several factors inhibit insulin signaling including oxidative stress, which occurs in DS due to the triplication of the SOD1 and APP genes on Hsa21, and mTORC1-mediated phosphorylation of the IRS-1 protein.

    “Several factors inhibit insulin signaling including oxidative stress, which occurs in DS due to the triplication of the SOD1 and APP genes on Hsa21, 68 and mTORC1‐mediated phosphorylation of the IRS‐1 protein 69 .”
  • Hypocomplementia could contribute to the increased risk of bacterial lung pneumonia and otitis media in Down syndrome, as complement depletion prevents proper clearance of Streptococcus pneumoniae.

    “Hypocomplementia could clearly contribute to the observed increased risk of bacterial lung pneumonia and otitis media in the population with DS68, as complement depletion prevents proper clearance of Streptococcus pneumoniae 69.”

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Authors
Ram, G., & Chinen, J.
Affiliations
Baylor College of Medicine (US)
Corresponding author
Chinen, J
Venue
Clinical and Experimental Immunology
Published
2011-02-24
Volume
164
Issue
1
Pages
9-16
ISSN
  • 0009-9104 (ISSN-L)
  • 1365-2249
OpenAlex
W1536916194
Cited by
465
References
0
Citations by year
2026: 24 · 2025: 30 · 2024: 42 · 2023: 32 · 2022: 35 · 2021: 43 · 2020: 50 · 2019: 33 · 2018: 32 · 2017: 26 · 2016: 26 · 2015: 17 · 2014: 23 · 2013: 27 · 2012: 12
FWCI
3.59
Type
journal article
Language
en
Open access
Locations
  • Clinical & Experimental Immunology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Down syndrome and intellectual disability research
  • Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
Keywords
Down syndrome, immunodeficiency, respiratory infections, T-cell lymphopenia, B-cell lymphopenia, naive lymphocytes, T cell proliferation, neutrophil chemotaxis, SOD1, RCAN1, zinc deficiency, gastroesophageal reflux, tracheomalacia, infection susceptibility
MeSH terms
Child, Down Syndrome, Humans, Hypersensitivity, Immunologic Deficiency Syndromes, Lymphopenia, Respiratory Tract Infections, Models, Immunological

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