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Cutting edge: A common polymorphism impairs cell surface trafficking and functional responses of TLR1 but protects against leprosy.

Authors: Johnson, CM  Lyle, EA  Omueti, KO  Stepensky, VA  Yegin, O  Alpsoy, E  Hamann, L  Schumann, RR  Tapping, RI 
Citation: Johnson CM, etal., J Immunol. 2007 Jun 15;178(12):7520-4.
Pubmed: (View Article at PubMed) PMID:17548585

TLRs constitute an essential family of pattern recognition molecules that, through direct recognition of conserved microbial components, initiate inflammatory responses following infection. In this role, TLR1 enables host responses to a variety of bacteria, including pathogenic species of mycobacteria. In this study, we report that I602S, a common single nucleotide polymorphism within TLR1, is associated with aberrant trafficking of the receptor to the cell surface and diminished responses of blood monocytes to bacterial agonists. When expressed in heterologous systems, the TLR1 602S variant, but not the TLR1 602I variant, exhibits the expected deficiencies in trafficking and responsiveness. Among white Europeans, the 602S allele represents the most common single nucleotide polymorphism affecting TLR function identified to date. Surprisingly, the 602S allele is associated with a decreased incidence of leprosy, suggesting that Mycobacterium leprae subverts the TLR system as a mechanism of immune evasion.

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CRRD Object Information
CRRD ID: 7246917
Created: 2013-06-24
Species: All species
Last Modified: 2013-06-24
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.