Expansion of T helper type 17 lymphocytes in patients with chronic granulomatous disease
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064203%3A_____%2F11%3A7091" target="_blank" >RIV/00064203:_____/11:7091 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11130/11:7091
Result on the web
<a href="http://www.ncbi.nlm.nih.gov/pubmed/21910722" target="_blank" >http://www.ncbi.nlm.nih.gov/pubmed/21910722</a>
DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Expansion of T helper type 17 lymphocytes in patients with chronic granulomatous disease
Original language description
Hyper-immunoglobulin (Ig) E syndrome (HIES) is a primary immunodeficiency associated with mutations in STAT3 resulting in impaired development of T helper type 17 (Th17) lymphocytes. HIES patients with a reduced frequency of Th17 cells present with infections caused by Staphylococcus aureus and/or Candida strains. The same spectrum of pathogens is present in patients with chronic granulomatous disease (CGD). We analysed the characteristics of the Th17 compartment in HIES and CGD. HIES patients showed very low numbers of Th17 cells. By contrast, the frequency of Th17 cells and production of Th17-derived cytokines was significantly higher among CGD patients when compared to both control samples and HIES. Naive CD4(+) cells in CGD patients had a normal capacity to differentiate into IL-17-producing cells and the numbers of Th17 cells in the CGD patients normalized following successful bone marrow transplantation. Our findings complement recent data on the importance of Th17 cells for elim
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
EC - Immunology
OECD FORD branch
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Result continuities
Project
<a href="/en/project/NS10489" target="_blank" >NS10489: Functional characteristics of circulating dendritic cells in patients with X-linked agammaglobulinemia</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Clinical and Experimental Immunology
ISSN
0009-9104
e-ISSN
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Volume of the periodical
166
Issue of the periodical within the volume
1
Country of publishing house
GB - UNITED KINGDOM
Number of pages
8
Pages from-to
26-33
UT code for WoS article
000294913700003
EID of the result in the Scopus database
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