pubmed-article:20065638 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20065638 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
pubmed-article:20065638 | lifeskim:mentions | umls-concept:C0004096 | lld:lifeskim |
pubmed-article:20065638 | lifeskim:mentions | umls-concept:C0003250 | lld:lifeskim |
pubmed-article:20065638 | lifeskim:mentions | umls-concept:C0450442 | lld:lifeskim |
pubmed-article:20065638 | lifeskim:mentions | umls-concept:C0205460 | lld:lifeskim |
pubmed-article:20065638 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:20065638 | pubmed:dateCreated | 2010-1-12 | lld:pubmed |
pubmed-article:20065638 | pubmed:abstractText | Asthma represents a syndrome of airway inflammatory diseases with complex pathology. The immunologic pathogenesis is being increasingly revealed and provides opportunity for targeted biological intervention. Current experience with immunomodulators as targeted therapy in asthma is described in this literature review. Targeted therapies have included strategies to activate dendritic cells through the TLR-9 receptors, to interrupt the action of T(H)2 cytokines with cytokine blockers and monoclonal antibodies, to promote development of T(H)1 responses, to block IgE mediated pathways and to block TNFalpha. Omalizumab is the only biological therapy that has an approved indication in asthma at this time. An improved understanding of the heterogeneity of asthma should allow for specific targeting of different disease phenotypes specific therapies including immunomodulators. | lld:pubmed |
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