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|Title:||Quantitative, Phenotypical, and Functional Characterization of Cellular Immunity in Children and Adolescents With Down Syndrome|
Rohrer, Tilman R.
|Title:||The Journal of Infectious Diseases|
|Publisher/Platform:||Oxford University Press|
|Year of Publication:||2017|
|Publikation type:||Journal Article|
|Abstract:||Background: Infections and autoimmune disorders are more frequent in Down syndrome, suggesting abnormality of adaptive immunity. Although the role of B cells and antibodies is well characterized, knowledge regarding T cells is limited. Methods: Lymphocyte subpopulations of 40 children and adolescents with Down syndrome and 51 controls were quantified, and phenotype and functionality of antigen-specific effector T cells were analyzed with flow cytometry after polyclonal and pathogen-specific stimulation (with varicella-zoster virus [VZV] and cytomegalovirus [CMV]). Results were correlated with immunoglobulin (Ig) G responses. Results: Apart from general alterations in the percentage of lymphocytes, regulatory T cells, and T-helper 1 and 17 cells, all major T-cell subpopulations showed higher expression of the inhibitory receptor PD-1. Polyclonally stimulated effector CD4+ T-cell frequencies were significantly higher in subjects with Down syndrome, whereas their inhibitory receptor expression (programmed cell death 1 [PD-1] and cytotoxic T-lymphocyte antigen 4 [CTLA-4]) was similar to that of controls and cytokine expression profiles were only marginally altered. Pathogen-specific immunity showed age-appropriate levels of endemic infection, with correlation of CMV-specific cellular and humoral immunity in all subjects. Among VZV IgG-positive individuals, a higher percentage of VZV-specific T-cell-positive subjects was seen in those with Down syndrome. Conclusions: Despite alterations in lymphocyte subpopulations, individuals with Down syndrome can mount effector T-cell responses with similar phenotype and functionality as controls but may require higher effector T-cell frequencies to ensure pathogen control.|
|DOI of the first publication:||10.1093/infdis/jix168|
|URL of the first publication:||https://www.ncbi.nlm.nih.gov/pubmed/28379413|
|Link to this record:||hdl:20.500.11880/27529|
|Date of registration:||13-Jul-2019|
|Third-party funds sponsorship:||HOMFOR|
|Faculty:||M - Medizinische Fakultät|
|Department:||M - Infektionsmedizin|
|Collections:||UniBib – Die Universitätsbibliographie|
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