Collectin CL-LK Is a Novel Soluble Pattern Recognition Receptor for Mycobacterium tuberculosis.

Understanding the molecular components of immune recognition of the tuberculosis (TB) bacillus, Mycobacterium tuberculosis, can help designing novel strategies to combat TB. Here, we identify collectin CL-LK as a novel soluble C-type lectin able to bind M. tuberculosis, and characterize mycobacteria...

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Main Authors: Anthony Troegeler, Geanncarlo Lugo-Villarino, Søren Hansen, Voahangy Rasolofo, Maiken Lumby Henriksen, Kenichiro Mori, Katsuki Ohtani, Carine Duval, Ingrid Mercier, Alan Bénard, Jérome Nigou, Denis Hudrisier, Nobutaka Wakamiya, Olivier Neyrolles
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4501752?pdf=render
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spelling doaj-8152964fa72949a1be1c199f8cf0faea2020-11-24T21:55:12ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01107e013269210.1371/journal.pone.0132692Collectin CL-LK Is a Novel Soluble Pattern Recognition Receptor for Mycobacterium tuberculosis.Anthony TroegelerGeanncarlo Lugo-VillarinoSøren HansenVoahangy RasolofoMaiken Lumby HenriksenKenichiro MoriKatsuki OhtaniCarine DuvalIngrid MercierAlan BénardJérome NigouDenis HudrisierNobutaka WakamiyaOlivier NeyrollesUnderstanding the molecular components of immune recognition of the tuberculosis (TB) bacillus, Mycobacterium tuberculosis, can help designing novel strategies to combat TB. Here, we identify collectin CL-LK as a novel soluble C-type lectin able to bind M. tuberculosis, and characterize mycobacterial mannose-capped lipoarabinomannan as a primary ligand for CL-LK. Mice deficient in CL-K1, one of the CL-LK subunits, do not display altered susceptibility to M. tuberculosis. However, we found that the amount of CL-LK in the serum of patients with active TB is reduced, compared to that in controls, and correlates inversely to the magnitude of the immune response to the pathogen. These findings indicate that CL-LK might be of interest for future diagnostic and treatment monitoring purposes.http://europepmc.org/articles/PMC4501752?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Anthony Troegeler
Geanncarlo Lugo-Villarino
Søren Hansen
Voahangy Rasolofo
Maiken Lumby Henriksen
Kenichiro Mori
Katsuki Ohtani
Carine Duval
Ingrid Mercier
Alan Bénard
Jérome Nigou
Denis Hudrisier
Nobutaka Wakamiya
Olivier Neyrolles
spellingShingle Anthony Troegeler
Geanncarlo Lugo-Villarino
Søren Hansen
Voahangy Rasolofo
Maiken Lumby Henriksen
Kenichiro Mori
Katsuki Ohtani
Carine Duval
Ingrid Mercier
Alan Bénard
Jérome Nigou
Denis Hudrisier
Nobutaka Wakamiya
Olivier Neyrolles
Collectin CL-LK Is a Novel Soluble Pattern Recognition Receptor for Mycobacterium tuberculosis.
PLoS ONE
author_facet Anthony Troegeler
Geanncarlo Lugo-Villarino
Søren Hansen
Voahangy Rasolofo
Maiken Lumby Henriksen
Kenichiro Mori
Katsuki Ohtani
Carine Duval
Ingrid Mercier
Alan Bénard
Jérome Nigou
Denis Hudrisier
Nobutaka Wakamiya
Olivier Neyrolles
author_sort Anthony Troegeler
title Collectin CL-LK Is a Novel Soluble Pattern Recognition Receptor for Mycobacterium tuberculosis.
title_short Collectin CL-LK Is a Novel Soluble Pattern Recognition Receptor for Mycobacterium tuberculosis.
title_full Collectin CL-LK Is a Novel Soluble Pattern Recognition Receptor for Mycobacterium tuberculosis.
title_fullStr Collectin CL-LK Is a Novel Soluble Pattern Recognition Receptor for Mycobacterium tuberculosis.
title_full_unstemmed Collectin CL-LK Is a Novel Soluble Pattern Recognition Receptor for Mycobacterium tuberculosis.
title_sort collectin cl-lk is a novel soluble pattern recognition receptor for mycobacterium tuberculosis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Understanding the molecular components of immune recognition of the tuberculosis (TB) bacillus, Mycobacterium tuberculosis, can help designing novel strategies to combat TB. Here, we identify collectin CL-LK as a novel soluble C-type lectin able to bind M. tuberculosis, and characterize mycobacterial mannose-capped lipoarabinomannan as a primary ligand for CL-LK. Mice deficient in CL-K1, one of the CL-LK subunits, do not display altered susceptibility to M. tuberculosis. However, we found that the amount of CL-LK in the serum of patients with active TB is reduced, compared to that in controls, and correlates inversely to the magnitude of the immune response to the pathogen. These findings indicate that CL-LK might be of interest for future diagnostic and treatment monitoring purposes.
url http://europepmc.org/articles/PMC4501752?pdf=render
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