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...

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Veröffentlicht in:Clinical and experimental allergy 2011-08, Vol.41 (8), p.1143-1156
Hauptverfasser: Lee, K., Kim, S.-H., Yoon, H. J., Paik, D. J., Kim, J. M., Youn, J.
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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.
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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 &amp; 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&amp;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 &amp; 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 &amp; 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>
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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
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