Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3410370 | The Lancet Infectious Diseases | 2011 | 11 Pages |
SummaryToll-like receptors (TLRs) recognise highly conserved molecular structures, collectively known as pathogen-associated molecular patterns. In the past two decades, development and clinical implementation of TLR ligands—ie, chemically modified synthetic derivatives of naturally occurring ligands and fully synthetic small molecules—have been topics of intense research. Targeted manipulation of TLR signalling has been applied clinically to boost vaccine effectiveness, promote a robust T helper 1-predominant immune response against viral infection, or dampen the exaggerated inflammatory response to bacterial infection. Use of these new therapeutic molecules as adjuncts to conventional pharmacotherapy or stand-alone treatments might offer solutions to unmet clinical needs or could replace existing partly effective therapeutic strategies.