Toll-like receptor activation during cutaneous allergen sensitization blocks development of asthma through IFN-gamma-dependent mechanisms

Toll-like receptors (TLRs) are pattern-recognition receptors that have a pivotal role as primary sensors of microbial products and as initiators of innate and adaptive immune responses. We investigated the role of TLR2, TLR3, and TLR4 activation during cutaneous allergen sensitization in the modulat...

Full description

Bibliographic Details
Main Authors: Haapakoski, R, Karisola, P, Fyhrquist, N, Savinko, T, Lehtimäki, S, Wolff, H, Lauerma, A, Alenius, H
Format: Journal article
Language:English
Published: 2013
_version_ 1797064560157392896
author Haapakoski, R
Karisola, P
Fyhrquist, N
Savinko, T
Lehtimäki, S
Wolff, H
Lauerma, A
Alenius, H
author_facet Haapakoski, R
Karisola, P
Fyhrquist, N
Savinko, T
Lehtimäki, S
Wolff, H
Lauerma, A
Alenius, H
author_sort Haapakoski, R
collection OXFORD
description Toll-like receptors (TLRs) are pattern-recognition receptors that have a pivotal role as primary sensors of microbial products and as initiators of innate and adaptive immune responses. We investigated the role of TLR2, TLR3, and TLR4 activation during cutaneous allergen sensitization in the modulation of allergic asthma. The results show that dermal exposure to TLR4 ligand lipopolysaccharide (LPS) or TLR2 ligand Pam 3 Cys suppresses asthmatic responses by reducing airway hyperreactivity, mucus production, Th2-type inflammation in the lungs, and IgE antibodies in serum in a dose-dependent manner. In contrast, TLR3 ligand Poly(I:C) did not protect the mice from asthmatic symptoms but reduced IgE and induced IgG2a in serum. LPS (especially) and Pam 3 Cys enhanced the activation of dermal dendritic cell (DCs) by increasing the expression of CD80 and CD86 but decreased DC numbers in draining lymph nodes at early time points. Later, these changes in DCs led to an increased number of CD8 + T cells and enhanced the production of IFN-γ in bronchoalveolar lavage fluid. In conclusion, dermal exposure to LPS during sensitization modulates the asthmatic response by skewing the Th1/Th2 balance toward Th1 by stimulating the production of IFN-γ. These findings support the hygiene hypothesis and pinpoint the importance of dermal microbiome in the development of allergy and asthma. © 2013 The Society for Investigative Dermatology.
first_indexed 2024-03-06T21:16:06Z
format Journal article
id oxford-uuid:3fd735a2-c4b0-4413-912c-c1761803070a
institution University of Oxford
language English
last_indexed 2024-03-06T21:16:06Z
publishDate 2013
record_format dspace
spelling oxford-uuid:3fd735a2-c4b0-4413-912c-c1761803070a2022-03-26T14:34:27ZToll-like receptor activation during cutaneous allergen sensitization blocks development of asthma through IFN-gamma-dependent mechanismsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:3fd735a2-c4b0-4413-912c-c1761803070aEnglishSymplectic Elements at Oxford2013Haapakoski, RKarisola, PFyhrquist, NSavinko, TLehtimäki, SWolff, HLauerma, AAlenius, HToll-like receptors (TLRs) are pattern-recognition receptors that have a pivotal role as primary sensors of microbial products and as initiators of innate and adaptive immune responses. We investigated the role of TLR2, TLR3, and TLR4 activation during cutaneous allergen sensitization in the modulation of allergic asthma. The results show that dermal exposure to TLR4 ligand lipopolysaccharide (LPS) or TLR2 ligand Pam 3 Cys suppresses asthmatic responses by reducing airway hyperreactivity, mucus production, Th2-type inflammation in the lungs, and IgE antibodies in serum in a dose-dependent manner. In contrast, TLR3 ligand Poly(I:C) did not protect the mice from asthmatic symptoms but reduced IgE and induced IgG2a in serum. LPS (especially) and Pam 3 Cys enhanced the activation of dermal dendritic cell (DCs) by increasing the expression of CD80 and CD86 but decreased DC numbers in draining lymph nodes at early time points. Later, these changes in DCs led to an increased number of CD8 + T cells and enhanced the production of IFN-γ in bronchoalveolar lavage fluid. In conclusion, dermal exposure to LPS during sensitization modulates the asthmatic response by skewing the Th1/Th2 balance toward Th1 by stimulating the production of IFN-γ. These findings support the hygiene hypothesis and pinpoint the importance of dermal microbiome in the development of allergy and asthma. © 2013 The Society for Investigative Dermatology.
spellingShingle Haapakoski, R
Karisola, P
Fyhrquist, N
Savinko, T
Lehtimäki, S
Wolff, H
Lauerma, A
Alenius, H
Toll-like receptor activation during cutaneous allergen sensitization blocks development of asthma through IFN-gamma-dependent mechanisms
title Toll-like receptor activation during cutaneous allergen sensitization blocks development of asthma through IFN-gamma-dependent mechanisms
title_full Toll-like receptor activation during cutaneous allergen sensitization blocks development of asthma through IFN-gamma-dependent mechanisms
title_fullStr Toll-like receptor activation during cutaneous allergen sensitization blocks development of asthma through IFN-gamma-dependent mechanisms
title_full_unstemmed Toll-like receptor activation during cutaneous allergen sensitization blocks development of asthma through IFN-gamma-dependent mechanisms
title_short Toll-like receptor activation during cutaneous allergen sensitization blocks development of asthma through IFN-gamma-dependent mechanisms
title_sort toll like receptor activation during cutaneous allergen sensitization blocks development of asthma through ifn gamma dependent mechanisms
work_keys_str_mv AT haapakoskir tolllikereceptoractivationduringcutaneousallergensensitizationblocksdevelopmentofasthmathroughifngammadependentmechanisms
AT karisolap tolllikereceptoractivationduringcutaneousallergensensitizationblocksdevelopmentofasthmathroughifngammadependentmechanisms
AT fyhrquistn tolllikereceptoractivationduringcutaneousallergensensitizationblocksdevelopmentofasthmathroughifngammadependentmechanisms
AT savinkot tolllikereceptoractivationduringcutaneousallergensensitizationblocksdevelopmentofasthmathroughifngammadependentmechanisms
AT lehtimakis tolllikereceptoractivationduringcutaneousallergensensitizationblocksdevelopmentofasthmathroughifngammadependentmechanisms
AT wolffh tolllikereceptoractivationduringcutaneousallergensensitizationblocksdevelopmentofasthmathroughifngammadependentmechanisms
AT lauermaa tolllikereceptoractivationduringcutaneousallergensensitizationblocksdevelopmentofasthmathroughifngammadependentmechanisms
AT aleniush tolllikereceptoractivationduringcutaneousallergensensitizationblocksdevelopmentofasthmathroughifngammadependentmechanisms