Bacillus-derived poly-γ-glutamic acid attenuates allergic airway inflammation through a Toll-like receptor-4-dependent pathway in a murine model of asthma
Summary Background Asthma is an inflammatory disease of the airways that is mediated by Th2 responses. Poly‐γ‐glutamic acid (γ‐PGA) is an extracellular polymeric compound that is synthesized by Bacillus cells. Previously, we found that γ‐PGA promoted Th1 cell development in a manner dependent on ant...
Gespeichert in:
Veröffentlicht in: | Clinical and experimental allergy 2011-08, Vol.41 (8), p.1143-1156 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1156 |
---|---|
container_issue | 8 |
container_start_page | 1143 |
container_title | Clinical and experimental allergy |
container_volume | 41 |
creator | Lee, K. Kim, S.-H. Yoon, H. J. Paik, D. J. Kim, J. M. Youn, J. |
description | Summary
Background
Asthma is an inflammatory disease of the airways that is mediated by Th2 responses. Poly‐γ‐glutamic acid (γ‐PGA) is an extracellular polymeric compound that is synthesized by Bacillus cells. Previously, we found that γ‐PGA promoted Th1 cell development in a manner dependent on antigen‐presenting cells, but inhibited Th2 cell development.
Objective
To investigate the effect of γ‐PGA on dendritic cells (DCs), and its potential for treating Th2‐mediated allergic asthma.
Methods
Wild‐type, Toll‐like receptor (TLR)‐2 deficient, and TLR‐4‐defective mice were used. DCs derived from the bone marrow and extracted from the lung were stimulated with γ‐PGA and assayed for the expression of signalling molecules, costimulatory molecules, and cytokines. Mice were sensitized and challenged with ovalbumin (OVA) to induce asthma. They were repeatedly injected intranasally with γ‐PGA before and during the challenge period, and inflammation and structural remodelling of the airways were examined.
Results
γ‐PGA selectively signalled conventional DCs to activate NF‐κB and mitogen‐activated protein kinase, leading to the up‐regulation of CD86, CD40, and IL‐12, but not IL‐10 and IL‐6. These effects of γ‐PGA were dependent on TLR‐4 and independent of TLR‐2. Importantly, the intranasal administration of γ‐PGA to OVA‐sensitized/challenged mice reduced the airway hyperresponsiveness and allergic inflammation such as leucocyte influx, goblet cell hyperplasia, eosinophilia, and Th2 cytokine production. In addition to lowered IgE titres, the treatment of mice with γ‐PGA significantly reduced the multiplication and Th2 polarization of mediastinal lymph node T cells upon allergen‐specific restimulation. These anti‐asthmatic effects of γ‐PGA were also abolished in TLR‐4‐defective mice.
Conclusions and Clinical Relevance
Our data indicate that γ‐PGA activates DCs to favour Th1 cell induction through a TLR‐4‐dependent pathway and alleviates pathologic symptoms in a Th2‐biased asthmatic model. These findings highlight the potential of γ‐PGA for the treatment of asthma and other allergic disease in which Th2 polarization plays an important role.
Cite this as: K. Lee, S.‐H. Kim, H. J. Yoon, D. J. Paik, J. M. Kim and J. Youn, Clinical & Experimental Allergy, 2011 (41) 1143–1156. |
doi_str_mv | 10.1111/j.1365-2222.2011.03792.x |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_888108953</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>888108953</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4692-f84f13a9952e41759923c6f406a31d62bc60be34859e186ce43aea6712fc2faf3</originalsourceid><addsrcrecordid>eNqFksuO0zAUhiMEYsrAKyBvEKsUXxInXrCYqeYCGg0gDWJpnTonrTvOBdth2mfhMeY9eCYSWsqS44WP9H-_LZ3zJwlhdM7GereZMyHzlI8155SxORWF4vPtk2R2FJ4mM6ryLC1KlZ0kL0LYUEpFrsrnyQlnsuA0z2fJz3Mw1rkhpBV6-wMr0ndul_56TFduiNBYQ0agIhAjtgNEDAScQ7-aBOsfYEdsWztoGoi2a0lc-25YrQmQu8651Nl7JB4N9rHzaTZ-0mNbYRtJD3G9d49sM3jbImm6Ch3pagIhrht4mTyrwQV8dbhPk6-XF3eL6_Tm09WHxdlNajKpeFqXWc0EKJVzzFiRK8WFkXVGJQhWSb40ki5RZGWukJXSYCYAQRaM14bXUIvT5O3-3d533wcMUTc2GHQOWuyGoMuyZLRUufg_WRQZLTiXI_n6QA7LBivde9uA3-m_kx-BNwcAggFXe2iNDf-4THA5npF7v-cerMPdUWdUT0nQGz0tXE8L11MS9J8k6K1eXJxN3ehP934bIm6PfvD3WhaiyPW32yutLml5_vHzrf4ifgPGMLgb</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>877407226</pqid></control><display><type>article</type><title>Bacillus-derived poly-γ-glutamic acid attenuates allergic airway inflammation through a Toll-like receptor-4-dependent pathway in a murine model of asthma</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Lee, K. ; Kim, S.-H. ; Yoon, H. J. ; Paik, D. J. ; Kim, J. M. ; Youn, J.</creator><creatorcontrib>Lee, K. ; Kim, S.-H. ; Yoon, H. J. ; Paik, D. J. ; Kim, J. M. ; Youn, J.</creatorcontrib><description>Summary
Background
Asthma is an inflammatory disease of the airways that is mediated by Th2 responses. Poly‐γ‐glutamic acid (γ‐PGA) is an extracellular polymeric compound that is synthesized by Bacillus cells. Previously, we found that γ‐PGA promoted Th1 cell development in a manner dependent on antigen‐presenting cells, but inhibited Th2 cell development.
Objective
To investigate the effect of γ‐PGA on dendritic cells (DCs), and its potential for treating Th2‐mediated allergic asthma.
Methods
Wild‐type, Toll‐like receptor (TLR)‐2 deficient, and TLR‐4‐defective mice were used. DCs derived from the bone marrow and extracted from the lung were stimulated with γ‐PGA and assayed for the expression of signalling molecules, costimulatory molecules, and cytokines. Mice were sensitized and challenged with ovalbumin (OVA) to induce asthma. They were repeatedly injected intranasally with γ‐PGA before and during the challenge period, and inflammation and structural remodelling of the airways were examined.
Results
γ‐PGA selectively signalled conventional DCs to activate NF‐κB and mitogen‐activated protein kinase, leading to the up‐regulation of CD86, CD40, and IL‐12, but not IL‐10 and IL‐6. These effects of γ‐PGA were dependent on TLR‐4 and independent of TLR‐2. Importantly, the intranasal administration of γ‐PGA to OVA‐sensitized/challenged mice reduced the airway hyperresponsiveness and allergic inflammation such as leucocyte influx, goblet cell hyperplasia, eosinophilia, and Th2 cytokine production. In addition to lowered IgE titres, the treatment of mice with γ‐PGA significantly reduced the multiplication and Th2 polarization of mediastinal lymph node T cells upon allergen‐specific restimulation. These anti‐asthmatic effects of γ‐PGA were also abolished in TLR‐4‐defective mice.
Conclusions and Clinical Relevance
Our data indicate that γ‐PGA activates DCs to favour Th1 cell induction through a TLR‐4‐dependent pathway and alleviates pathologic symptoms in a Th2‐biased asthmatic model. These findings highlight the potential of γ‐PGA for the treatment of asthma and other allergic disease in which Th2 polarization plays an important role.
Cite this as: K. Lee, S.‐H. Kim, H. J. Yoon, D. J. Paik, J. M. Kim and J. Youn, Clinical & Experimental Allergy, 2011 (41) 1143–1156.</description><identifier>ISSN: 0954-7894</identifier><identifier>EISSN: 1365-2222</identifier><identifier>DOI: 10.1111/j.1365-2222.2011.03792.x</identifier><identifier>PMID: 21672055</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>airway inflammation ; Allergic diseases ; Animal models ; Animals ; Antigen-presenting cells ; Asthma ; Asthma - drug therapy ; Asthma - immunology ; Bacillus ; Bacillus - chemistry ; Biological and medical sciences ; Bone marrow ; Bronchial Hyperreactivity - drug therapy ; Bronchial Hyperreactivity - immunology ; CD86 antigen ; Chronic obstructive pulmonary disease, asthma ; Costimulator ; Cytokines ; Data processing ; Dendritic cells ; Dendritic Cells - drug effects ; Dendritic Cells - immunology ; Development ; Disease Models, Animal ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Goblet cells ; Helper cells ; Hypersensitivity ; Immunoglobulin E ; Inflammation ; Inflammation - drug therapy ; Inflammation - immunology ; Inflammatory diseases ; Interleukin 10 ; Interleukin 12 ; Intranasal administration ; Lung ; Lymphocytes T ; Medical sciences ; Mice ; Mice, Congenic ; Mice, Inbred BALB C ; Mice, Inbred C3H ; Mice, Inbred C57BL ; Mice, Inbred NOD ; Ovalbumin ; Pneumology ; Polarization ; Poly( gamma -glutamic acid) ; poly-γ-glutamic acid ; Polyglutamic Acid - pharmacology ; Respiratory tract ; Respiratory tract diseases ; Signal transduction ; Th2 Cells - drug effects ; Th2 Cells - immunology ; Th2 responses ; TLR2 protein ; Toll-Like Receptor 4 - immunology ; Toll-like receptor-4 ; Toll-like receptors</subject><ispartof>Clinical and experimental allergy, 2011-08, Vol.41 (8), p.1143-1156</ispartof><rights>2011 Blackwell Publishing Ltd</rights><rights>2015 INIST-CNRS</rights><rights>2011 Blackwell Publishing Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4692-f84f13a9952e41759923c6f406a31d62bc60be34859e186ce43aea6712fc2faf3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2222.2011.03792.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2222.2011.03792.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24326262$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21672055$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, K.</creatorcontrib><creatorcontrib>Kim, S.-H.</creatorcontrib><creatorcontrib>Yoon, H. J.</creatorcontrib><creatorcontrib>Paik, D. J.</creatorcontrib><creatorcontrib>Kim, J. M.</creatorcontrib><creatorcontrib>Youn, J.</creatorcontrib><title>Bacillus-derived poly-γ-glutamic acid attenuates allergic airway inflammation through a Toll-like receptor-4-dependent pathway in a murine model of asthma</title><title>Clinical and experimental allergy</title><addtitle>Clin Exp Allergy</addtitle><description>Summary
Background
Asthma is an inflammatory disease of the airways that is mediated by Th2 responses. Poly‐γ‐glutamic acid (γ‐PGA) is an extracellular polymeric compound that is synthesized by Bacillus cells. Previously, we found that γ‐PGA promoted Th1 cell development in a manner dependent on antigen‐presenting cells, but inhibited Th2 cell development.
Objective
To investigate the effect of γ‐PGA on dendritic cells (DCs), and its potential for treating Th2‐mediated allergic asthma.
Methods
Wild‐type, Toll‐like receptor (TLR)‐2 deficient, and TLR‐4‐defective mice were used. DCs derived from the bone marrow and extracted from the lung were stimulated with γ‐PGA and assayed for the expression of signalling molecules, costimulatory molecules, and cytokines. Mice were sensitized and challenged with ovalbumin (OVA) to induce asthma. They were repeatedly injected intranasally with γ‐PGA before and during the challenge period, and inflammation and structural remodelling of the airways were examined.
Results
γ‐PGA selectively signalled conventional DCs to activate NF‐κB and mitogen‐activated protein kinase, leading to the up‐regulation of CD86, CD40, and IL‐12, but not IL‐10 and IL‐6. These effects of γ‐PGA were dependent on TLR‐4 and independent of TLR‐2. Importantly, the intranasal administration of γ‐PGA to OVA‐sensitized/challenged mice reduced the airway hyperresponsiveness and allergic inflammation such as leucocyte influx, goblet cell hyperplasia, eosinophilia, and Th2 cytokine production. In addition to lowered IgE titres, the treatment of mice with γ‐PGA significantly reduced the multiplication and Th2 polarization of mediastinal lymph node T cells upon allergen‐specific restimulation. These anti‐asthmatic effects of γ‐PGA were also abolished in TLR‐4‐defective mice.
Conclusions and Clinical Relevance
Our data indicate that γ‐PGA activates DCs to favour Th1 cell induction through a TLR‐4‐dependent pathway and alleviates pathologic symptoms in a Th2‐biased asthmatic model. These findings highlight the potential of γ‐PGA for the treatment of asthma and other allergic disease in which Th2 polarization plays an important role.
Cite this as: K. Lee, S.‐H. Kim, H. J. Yoon, D. J. Paik, J. M. Kim and J. Youn, Clinical & Experimental Allergy, 2011 (41) 1143–1156.</description><subject>airway inflammation</subject><subject>Allergic diseases</subject><subject>Animal models</subject><subject>Animals</subject><subject>Antigen-presenting cells</subject><subject>Asthma</subject><subject>Asthma - drug therapy</subject><subject>Asthma - immunology</subject><subject>Bacillus</subject><subject>Bacillus - chemistry</subject><subject>Biological and medical sciences</subject><subject>Bone marrow</subject><subject>Bronchial Hyperreactivity - drug therapy</subject><subject>Bronchial Hyperreactivity - immunology</subject><subject>CD86 antigen</subject><subject>Chronic obstructive pulmonary disease, asthma</subject><subject>Costimulator</subject><subject>Cytokines</subject><subject>Data processing</subject><subject>Dendritic cells</subject><subject>Dendritic Cells - drug effects</subject><subject>Dendritic Cells - immunology</subject><subject>Development</subject><subject>Disease Models, Animal</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Goblet cells</subject><subject>Helper cells</subject><subject>Hypersensitivity</subject><subject>Immunoglobulin E</subject><subject>Inflammation</subject><subject>Inflammation - drug therapy</subject><subject>Inflammation - immunology</subject><subject>Inflammatory diseases</subject><subject>Interleukin 10</subject><subject>Interleukin 12</subject><subject>Intranasal administration</subject><subject>Lung</subject><subject>Lymphocytes T</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Congenic</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C3H</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred NOD</subject><subject>Ovalbumin</subject><subject>Pneumology</subject><subject>Polarization</subject><subject>Poly( gamma -glutamic acid)</subject><subject>poly-γ-glutamic acid</subject><subject>Polyglutamic Acid - pharmacology</subject><subject>Respiratory tract</subject><subject>Respiratory tract diseases</subject><subject>Signal transduction</subject><subject>Th2 Cells - drug effects</subject><subject>Th2 Cells - immunology</subject><subject>Th2 responses</subject><subject>TLR2 protein</subject><subject>Toll-Like Receptor 4 - immunology</subject><subject>Toll-like receptor-4</subject><subject>Toll-like receptors</subject><issn>0954-7894</issn><issn>1365-2222</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFksuO0zAUhiMEYsrAKyBvEKsUXxInXrCYqeYCGg0gDWJpnTonrTvOBdth2mfhMeY9eCYSWsqS44WP9H-_LZ3zJwlhdM7GereZMyHzlI8155SxORWF4vPtk2R2FJ4mM6ryLC1KlZ0kL0LYUEpFrsrnyQlnsuA0z2fJz3Mw1rkhpBV6-wMr0ndul_56TFduiNBYQ0agIhAjtgNEDAScQ7-aBOsfYEdsWztoGoi2a0lc-25YrQmQu8651Nl7JB4N9rHzaTZ-0mNbYRtJD3G9d49sM3jbImm6Ch3pagIhrht4mTyrwQV8dbhPk6-XF3eL6_Tm09WHxdlNajKpeFqXWc0EKJVzzFiRK8WFkXVGJQhWSb40ki5RZGWukJXSYCYAQRaM14bXUIvT5O3-3d533wcMUTc2GHQOWuyGoMuyZLRUufg_WRQZLTiXI_n6QA7LBivde9uA3-m_kx-BNwcAggFXe2iNDf-4THA5npF7v-cerMPdUWdUT0nQGz0tXE8L11MS9J8k6K1eXJxN3ehP934bIm6PfvD3WhaiyPW32yutLml5_vHzrf4ifgPGMLgb</recordid><startdate>201108</startdate><enddate>201108</enddate><creator>Lee, K.</creator><creator>Kim, S.-H.</creator><creator>Yoon, H. J.</creator><creator>Paik, D. J.</creator><creator>Kim, J. M.</creator><creator>Youn, J.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>201108</creationdate><title>Bacillus-derived poly-γ-glutamic acid attenuates allergic airway inflammation through a Toll-like receptor-4-dependent pathway in a murine model of asthma</title><author>Lee, K. ; Kim, S.-H. ; Yoon, H. J. ; Paik, D. J. ; Kim, J. M. ; Youn, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4692-f84f13a9952e41759923c6f406a31d62bc60be34859e186ce43aea6712fc2faf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>airway inflammation</topic><topic>Allergic diseases</topic><topic>Animal models</topic><topic>Animals</topic><topic>Antigen-presenting cells</topic><topic>Asthma</topic><topic>Asthma - drug therapy</topic><topic>Asthma - immunology</topic><topic>Bacillus</topic><topic>Bacillus - chemistry</topic><topic>Biological and medical sciences</topic><topic>Bone marrow</topic><topic>Bronchial Hyperreactivity - drug therapy</topic><topic>Bronchial Hyperreactivity - immunology</topic><topic>CD86 antigen</topic><topic>Chronic obstructive pulmonary disease, asthma</topic><topic>Costimulator</topic><topic>Cytokines</topic><topic>Data processing</topic><topic>Dendritic cells</topic><topic>Dendritic Cells - drug effects</topic><topic>Dendritic Cells - immunology</topic><topic>Development</topic><topic>Disease Models, Animal</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Goblet cells</topic><topic>Helper cells</topic><topic>Hypersensitivity</topic><topic>Immunoglobulin E</topic><topic>Inflammation</topic><topic>Inflammation - drug therapy</topic><topic>Inflammation - immunology</topic><topic>Inflammatory diseases</topic><topic>Interleukin 10</topic><topic>Interleukin 12</topic><topic>Intranasal administration</topic><topic>Lung</topic><topic>Lymphocytes T</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Congenic</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C3H</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred NOD</topic><topic>Ovalbumin</topic><topic>Pneumology</topic><topic>Polarization</topic><topic>Poly( gamma -glutamic acid)</topic><topic>poly-γ-glutamic acid</topic><topic>Polyglutamic Acid - pharmacology</topic><topic>Respiratory tract</topic><topic>Respiratory tract diseases</topic><topic>Signal transduction</topic><topic>Th2 Cells - drug effects</topic><topic>Th2 Cells - immunology</topic><topic>Th2 responses</topic><topic>TLR2 protein</topic><topic>Toll-Like Receptor 4 - immunology</topic><topic>Toll-like receptor-4</topic><topic>Toll-like receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, K.</creatorcontrib><creatorcontrib>Kim, S.-H.</creatorcontrib><creatorcontrib>Yoon, H. J.</creatorcontrib><creatorcontrib>Paik, D. J.</creatorcontrib><creatorcontrib>Kim, J. M.</creatorcontrib><creatorcontrib>Youn, J.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Clinical and experimental allergy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, K.</au><au>Kim, S.-H.</au><au>Yoon, H. J.</au><au>Paik, D. J.</au><au>Kim, J. M.</au><au>Youn, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bacillus-derived poly-γ-glutamic acid attenuates allergic airway inflammation through a Toll-like receptor-4-dependent pathway in a murine model of asthma</atitle><jtitle>Clinical and experimental allergy</jtitle><addtitle>Clin Exp Allergy</addtitle><date>2011-08</date><risdate>2011</risdate><volume>41</volume><issue>8</issue><spage>1143</spage><epage>1156</epage><pages>1143-1156</pages><issn>0954-7894</issn><eissn>1365-2222</eissn><abstract>Summary
Background
Asthma is an inflammatory disease of the airways that is mediated by Th2 responses. Poly‐γ‐glutamic acid (γ‐PGA) is an extracellular polymeric compound that is synthesized by Bacillus cells. Previously, we found that γ‐PGA promoted Th1 cell development in a manner dependent on antigen‐presenting cells, but inhibited Th2 cell development.
Objective
To investigate the effect of γ‐PGA on dendritic cells (DCs), and its potential for treating Th2‐mediated allergic asthma.
Methods
Wild‐type, Toll‐like receptor (TLR)‐2 deficient, and TLR‐4‐defective mice were used. DCs derived from the bone marrow and extracted from the lung were stimulated with γ‐PGA and assayed for the expression of signalling molecules, costimulatory molecules, and cytokines. Mice were sensitized and challenged with ovalbumin (OVA) to induce asthma. They were repeatedly injected intranasally with γ‐PGA before and during the challenge period, and inflammation and structural remodelling of the airways were examined.
Results
γ‐PGA selectively signalled conventional DCs to activate NF‐κB and mitogen‐activated protein kinase, leading to the up‐regulation of CD86, CD40, and IL‐12, but not IL‐10 and IL‐6. These effects of γ‐PGA were dependent on TLR‐4 and independent of TLR‐2. Importantly, the intranasal administration of γ‐PGA to OVA‐sensitized/challenged mice reduced the airway hyperresponsiveness and allergic inflammation such as leucocyte influx, goblet cell hyperplasia, eosinophilia, and Th2 cytokine production. In addition to lowered IgE titres, the treatment of mice with γ‐PGA significantly reduced the multiplication and Th2 polarization of mediastinal lymph node T cells upon allergen‐specific restimulation. These anti‐asthmatic effects of γ‐PGA were also abolished in TLR‐4‐defective mice.
Conclusions and Clinical Relevance
Our data indicate that γ‐PGA activates DCs to favour Th1 cell induction through a TLR‐4‐dependent pathway and alleviates pathologic symptoms in a Th2‐biased asthmatic model. These findings highlight the potential of γ‐PGA for the treatment of asthma and other allergic disease in which Th2 polarization plays an important role.
Cite this as: K. Lee, S.‐H. Kim, H. J. Yoon, D. J. Paik, J. M. Kim and J. Youn, Clinical & Experimental Allergy, 2011 (41) 1143–1156.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21672055</pmid><doi>10.1111/j.1365-2222.2011.03792.x</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0954-7894 |
ispartof | Clinical and experimental allergy, 2011-08, Vol.41 (8), p.1143-1156 |
issn | 0954-7894 1365-2222 |
language | eng |
recordid | cdi_proquest_miscellaneous_888108953 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | airway inflammation Allergic diseases Animal models Animals Antigen-presenting cells Asthma Asthma - drug therapy Asthma - immunology Bacillus Bacillus - chemistry Biological and medical sciences Bone marrow Bronchial Hyperreactivity - drug therapy Bronchial Hyperreactivity - immunology CD86 antigen Chronic obstructive pulmonary disease, asthma Costimulator Cytokines Data processing Dendritic cells Dendritic Cells - drug effects Dendritic Cells - immunology Development Disease Models, Animal Fundamental and applied biological sciences. Psychology Fundamental immunology Goblet cells Helper cells Hypersensitivity Immunoglobulin E Inflammation Inflammation - drug therapy Inflammation - immunology Inflammatory diseases Interleukin 10 Interleukin 12 Intranasal administration Lung Lymphocytes T Medical sciences Mice Mice, Congenic Mice, Inbred BALB C Mice, Inbred C3H Mice, Inbred C57BL Mice, Inbred NOD Ovalbumin Pneumology Polarization Poly( gamma -glutamic acid) poly-γ-glutamic acid Polyglutamic Acid - pharmacology Respiratory tract Respiratory tract diseases Signal transduction Th2 Cells - drug effects Th2 Cells - immunology Th2 responses TLR2 protein Toll-Like Receptor 4 - immunology Toll-like receptor-4 Toll-like receptors |
title | Bacillus-derived poly-γ-glutamic acid attenuates allergic airway inflammation through a Toll-like receptor-4-dependent pathway in a murine model of asthma |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T04%3A11%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Bacillus-derived%20poly-%CE%B3-glutamic%20acid%20attenuates%20allergic%20airway%20inflammation%20through%20a%20Toll-like%20receptor-4-dependent%20pathway%20in%20a%20murine%20model%20of%20asthma&rft.jtitle=Clinical%20and%20experimental%20allergy&rft.au=Lee,%20K.&rft.date=2011-08&rft.volume=41&rft.issue=8&rft.spage=1143&rft.epage=1156&rft.pages=1143-1156&rft.issn=0954-7894&rft.eissn=1365-2222&rft_id=info:doi/10.1111/j.1365-2222.2011.03792.x&rft_dat=%3Cproquest_pubme%3E888108953%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=877407226&rft_id=info:pmid/21672055&rfr_iscdi=true |