pubmed-article:19386512 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19386512 | lifeskim:mentions | umls-concept:C0384648 | lld:lifeskim |
pubmed-article:19386512 | lifeskim:mentions | umls-concept:C0020964 | lld:lifeskim |
pubmed-article:19386512 | lifeskim:mentions | umls-concept:C0173022 | lld:lifeskim |
pubmed-article:19386512 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:19386512 | pubmed:dateCreated | 2009-6-1 | lld:pubmed |
pubmed-article:19386512 | pubmed:abstractText | CD4+ T(H)17 cells display a featured role in barrier immunity. This effector population of T cells is important for clearance of microorganisms but can also promote autoimmunity at barrier sites. Recent work has indicated that these effector cells share a pathway with CD4+ regulatory T cells (T(R) cells) that also have a critical function in barrier protection and immune regulation. The development and function of T(H)17 cells, and their relationship with T(R) cells are discussed. | lld:pubmed |
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