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Single nucleotide polymorphisms in toll-like receptor 6 are associated with altered lipopeptide- and mycobacteria-induced IL-6 secretion

Toll-like receptors (TLRs) are critical mediators of the immune response to pathogens. The influence of human TLR6 polymorphisms on susceptibility to infection is only partially understood. Most microbes contain lipopeptides recognized by TLR2/1 or TLR2/6 heterodimers. Our aim was to determine wheth...

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Autores principales: Shehu Shey, Muki, Randhawa, April Kaur, Bowmaker, Mark, Smith, Elizabeth, Jens Scriba, Thomas, de Kock, Marwou, Mahomed, Hassan, Hussey, Gregory, Richard Hawn, Thomas, Albert Hanekom, Willem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518443/
https://www.ncbi.nlm.nih.gov/pubmed/20445564
http://dx.doi.org/10.1038/gene.2010.14
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author Shehu Shey, Muki
Randhawa, April Kaur
Bowmaker, Mark
Smith, Elizabeth
Jens Scriba, Thomas
de Kock, Marwou
Mahomed, Hassan
Hussey, Gregory
Richard Hawn, Thomas
Albert Hanekom, Willem
author_facet Shehu Shey, Muki
Randhawa, April Kaur
Bowmaker, Mark
Smith, Elizabeth
Jens Scriba, Thomas
de Kock, Marwou
Mahomed, Hassan
Hussey, Gregory
Richard Hawn, Thomas
Albert Hanekom, Willem
author_sort Shehu Shey, Muki
collection PubMed
description Toll-like receptors (TLRs) are critical mediators of the immune response to pathogens. The influence of human TLR6 polymorphisms on susceptibility to infection is only partially understood. Most microbes contain lipopeptides recognized by TLR2/1 or TLR2/6 heterodimers. Our aim was to determine whether single nucleotide polymorphisms (SNPs) in TLR6 are associated with altered immune responses to lipopeptides and whole mycobacteria. We sequenced the TLR6 coding region in 100 healthy South African adults to assess genetic variation and determined associations between polymorphisms and lipopeptide- and mycobacteria-induced IL-6 production in whole blood. We found 2 polymorphisms, C745T and G1083C that were associated with altered IL-6 secretion. G1083C was associated with altered IL-6 levels in response to lipopeptides, Mycobacterium tuberculosis lysate (Mtb, P = 0.018) and BCG (P = 0.039). The 745T allele was also associated with lower NF-κB signaling in response to di-acylated lipopeptide, PAM2 (P = 0.019) or Mtb (P = 0.026) in a HEK293 cell line reconstitution assay, compared with the 745C allele. We conclude that TLR6 polymorphisms may be associated with altered lipopeptide-induced cytokine responses and recognition of Mtb. These studies provide new insight into the role of TLR6 variation and the innate immune response to human infection.
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spelling pubmed-35184432012-12-10 Single nucleotide polymorphisms in toll-like receptor 6 are associated with altered lipopeptide- and mycobacteria-induced IL-6 secretion Shehu Shey, Muki Randhawa, April Kaur Bowmaker, Mark Smith, Elizabeth Jens Scriba, Thomas de Kock, Marwou Mahomed, Hassan Hussey, Gregory Richard Hawn, Thomas Albert Hanekom, Willem Genes Immun Article Toll-like receptors (TLRs) are critical mediators of the immune response to pathogens. The influence of human TLR6 polymorphisms on susceptibility to infection is only partially understood. Most microbes contain lipopeptides recognized by TLR2/1 or TLR2/6 heterodimers. Our aim was to determine whether single nucleotide polymorphisms (SNPs) in TLR6 are associated with altered immune responses to lipopeptides and whole mycobacteria. We sequenced the TLR6 coding region in 100 healthy South African adults to assess genetic variation and determined associations between polymorphisms and lipopeptide- and mycobacteria-induced IL-6 production in whole blood. We found 2 polymorphisms, C745T and G1083C that were associated with altered IL-6 secretion. G1083C was associated with altered IL-6 levels in response to lipopeptides, Mycobacterium tuberculosis lysate (Mtb, P = 0.018) and BCG (P = 0.039). The 745T allele was also associated with lower NF-κB signaling in response to di-acylated lipopeptide, PAM2 (P = 0.019) or Mtb (P = 0.026) in a HEK293 cell line reconstitution assay, compared with the 745C allele. We conclude that TLR6 polymorphisms may be associated with altered lipopeptide-induced cytokine responses and recognition of Mtb. These studies provide new insight into the role of TLR6 variation and the innate immune response to human infection. 2010-05-06 2010-10 /pmc/articles/PMC3518443/ /pubmed/20445564 http://dx.doi.org/10.1038/gene.2010.14 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Shehu Shey, Muki
Randhawa, April Kaur
Bowmaker, Mark
Smith, Elizabeth
Jens Scriba, Thomas
de Kock, Marwou
Mahomed, Hassan
Hussey, Gregory
Richard Hawn, Thomas
Albert Hanekom, Willem
Single nucleotide polymorphisms in toll-like receptor 6 are associated with altered lipopeptide- and mycobacteria-induced IL-6 secretion
title Single nucleotide polymorphisms in toll-like receptor 6 are associated with altered lipopeptide- and mycobacteria-induced IL-6 secretion
title_full Single nucleotide polymorphisms in toll-like receptor 6 are associated with altered lipopeptide- and mycobacteria-induced IL-6 secretion
title_fullStr Single nucleotide polymorphisms in toll-like receptor 6 are associated with altered lipopeptide- and mycobacteria-induced IL-6 secretion
title_full_unstemmed Single nucleotide polymorphisms in toll-like receptor 6 are associated with altered lipopeptide- and mycobacteria-induced IL-6 secretion
title_short Single nucleotide polymorphisms in toll-like receptor 6 are associated with altered lipopeptide- and mycobacteria-induced IL-6 secretion
title_sort single nucleotide polymorphisms in toll-like receptor 6 are associated with altered lipopeptide- and mycobacteria-induced il-6 secretion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518443/
https://www.ncbi.nlm.nih.gov/pubmed/20445564
http://dx.doi.org/10.1038/gene.2010.14
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