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Defective inhibition of B-cell proliferation by Wiskott-Aldrich syndrome protein-deficient regulatory T cells

Wiskott-Aldrich syndrome (WAS) is an inherited immunodeficiency characterized by high incidence of autoantibody-mediated autoimmune complications. Such a feature has been associated with defective suppressor activity of WAS protein-deficient, naturally occurring CD4(+)CD25(+)Foxp3(+) regulatory T ce...

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Hlavní autoři: Adriani, Marsilio, Jones, Krysten A., Uchiyama, Toru, Kirby, Martha R., Silvin, Christopher, Anderson, Stacie M., Candotti, Fabio
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society of Hematology 2011
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3123025/
https://ncbi.nlm.nih.gov/pubmed/21515824
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2010-12-322834
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