| pubmed-article:20603023 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20603023 | lifeskim:mentions | umls-concept:C0035820 | lld:lifeskim |
| pubmed-article:20603023 | lifeskim:mentions | umls-concept:C1524059 | lld:lifeskim |
| pubmed-article:20603023 | lifeskim:mentions | umls-concept:C0039194 | lld:lifeskim |
| pubmed-article:20603023 | lifeskim:mentions | umls-concept:C0031327 | lld:lifeskim |
| pubmed-article:20603023 | lifeskim:mentions | umls-concept:C0009498 | lld:lifeskim |
| pubmed-article:20603023 | lifeskim:mentions | umls-concept:C0020964 | lld:lifeskim |
| pubmed-article:20603023 | lifeskim:mentions | umls-concept:C1998811 | lld:lifeskim |
| pubmed-article:20603023 | pubmed:issue | 13 | lld:pubmed |
| pubmed-article:20603023 | pubmed:dateCreated | 2010-7-6 | lld:pubmed |
| pubmed-article:20603023 | pubmed:abstractText | Complement is a part of the innate immune system that contributes to first-line host defense. It is also implicated in a number of human inflammatory conditions and has attracted interest as a potential therapeutic target. Understanding the basic biology of complement and its mechanism(s) of action is imperative for developing complement-based treatments for infectious and autoimmune diseases. One of the exciting new developments in this regard is the revelation that complement plays an important role in T cell immunity. In this review, we highlight recent published studies implicating complement in models of CD4+ and CD8+ T cell immune responses, and discuss its potential mechanism(s) action in these processes. We also comment on issues that may impact data interpretation and draw attention to their consideration in future studies. | lld:pubmed |
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