Intralymphatic treatment of flagellin–ovalbumin mixture reduced allergic inflammation in murine model of allergic rhinitis

Background Bacterial flagellin, a Toll‐like receptor 5 agonist, is used as an adjuvant for immunomodulation. In this study, we aimed to evaluate the effect and its mechanism following intralymphatic administration of OVA‐flagellin (FlaB) mixture in the mouse model of allergic rhinitis. Materials and...

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Veröffentlicht in:Allergy (Copenhagen) 2016-05, Vol.71 (5), p.629-639
Hauptverfasser: Kim, E. H., Kim, J. H., Samivel, R., Bae, J.‐S., Chung, Y.‐J., Chung, P.‐S., Lee, S. E., Mo, J.‐H.
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container_end_page 639
container_issue 5
container_start_page 629
container_title Allergy (Copenhagen)
container_volume 71
creator Kim, E. H.
Kim, J. H.
Samivel, R.
Bae, J.‐S.
Chung, Y.‐J.
Chung, P.‐S.
Lee, S. E.
Mo, J.‐H.
description Background Bacterial flagellin, a Toll‐like receptor 5 agonist, is used as an adjuvant for immunomodulation. In this study, we aimed to evaluate the effect and its mechanism following intralymphatic administration of OVA‐flagellin (FlaB) mixture in the mouse model of allergic rhinitis. Materials and Methods BALB/c mice were sensitized with OVA and treated with an OVA‐FlaB mixture via intranasal, sublingual, and intralymphatic routes to evaluate the effect of each treatment. Several parameters for allergic inflammation and its underlying mechanisms were then evaluated. Results Intralymphatic injection of the OVA‐FlaB mixture reduced symptom scores, eosinophil infiltration in the nasal mucosa, and total and OVA‐specific IgE levels more significantly than intranasal and sublingual administration. Systemic cytokine (IL‐4, IL‐5, IL‐6, IL‐17, and IFN‐γ) production and local cytokine (IL‐4 and IL‐5) production were also reduced significantly after intralymphatic injection with OVA‐FlaB. Double intralymphatic injection of the mixture was more effective than single injection. Moreover, the expression of innate cytokines such as IL‐25 and IL‐33 in nasal epithelial cells was reduced, and the expression of chemokines such as CCL24 (eotaxin‐2), CXCL1, and CXCL2 was decreased in the nasal mucosa, suggesting the underlying mechanism for intralymphatic administration of the OVA‐FlaB mixture. Conclusion Intralymphatic administration of an OVA‐FlaB mixture was more effective in alleviating allergic inflammation than intranasal and sublingual administration in a mouse model of allergic rhinitis. This effect may be attributed to the reduced expression of innate cytokines and chemokines. This treatment modality can be considered as a new therapeutic method and agent.
doi_str_mv 10.1111/all.12839
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H. ; Kim, J. H. ; Samivel, R. ; Bae, J.‐S. ; Chung, Y.‐J. ; Chung, P.‐S. ; Lee, S. E. ; Mo, J.‐H.</creator><creatorcontrib>Kim, E. H. ; Kim, J. H. ; Samivel, R. ; Bae, J.‐S. ; Chung, Y.‐J. ; Chung, P.‐S. ; Lee, S. E. ; Mo, J.‐H.</creatorcontrib><description>Background Bacterial flagellin, a Toll‐like receptor 5 agonist, is used as an adjuvant for immunomodulation. In this study, we aimed to evaluate the effect and its mechanism following intralymphatic administration of OVA‐flagellin (FlaB) mixture in the mouse model of allergic rhinitis. Materials and Methods BALB/c mice were sensitized with OVA and treated with an OVA‐FlaB mixture via intranasal, sublingual, and intralymphatic routes to evaluate the effect of each treatment. Several parameters for allergic inflammation and its underlying mechanisms were then evaluated. Results Intralymphatic injection of the OVA‐FlaB mixture reduced symptom scores, eosinophil infiltration in the nasal mucosa, and total and OVA‐specific IgE levels more significantly than intranasal and sublingual administration. Systemic cytokine (IL‐4, IL‐5, IL‐6, IL‐17, and IFN‐γ) production and local cytokine (IL‐4 and IL‐5) production were also reduced significantly after intralymphatic injection with OVA‐FlaB. Double intralymphatic injection of the mixture was more effective than single injection. Moreover, the expression of innate cytokines such as IL‐25 and IL‐33 in nasal epithelial cells was reduced, and the expression of chemokines such as CCL24 (eotaxin‐2), CXCL1, and CXCL2 was decreased in the nasal mucosa, suggesting the underlying mechanism for intralymphatic administration of the OVA‐FlaB mixture. Conclusion Intralymphatic administration of an OVA‐FlaB mixture was more effective in alleviating allergic inflammation than intranasal and sublingual administration in a mouse model of allergic rhinitis. This effect may be attributed to the reduced expression of innate cytokines and chemokines. This treatment modality can be considered as a new therapeutic method and agent.</description><identifier>ISSN: 0105-4538</identifier><identifier>EISSN: 1398-9995</identifier><identifier>DOI: 10.1111/all.12839</identifier><identifier>PMID: 26752101</identifier><language>eng</language><publisher>Denmark: Blackwell Publishing Ltd</publisher><subject>Allergens - administration &amp; dosage ; Allergens - immunology ; allergic rhinitis ; Allergies ; Animals ; Antibody Specificity - immunology ; Chemokines ; Cytokines ; Cytokines - genetics ; Cytokines - metabolism ; Disease Models, Animal ; Eosinophils - immunology ; Eosinophils - metabolism ; Eosinophils - pathology ; Female ; flagellin ; Flagellin - administration &amp; dosage ; Flagellin - immunology ; Immunization - methods ; Immunoglobulin E - immunology ; Immunohistochemistry ; Inflammation ; innate cytokine ; intralymphatic injection ; Mice ; mouse model ; Nasal Mucosa - immunology ; Nasal Mucosa - metabolism ; Nasal Mucosa - pathology ; Neutrophil Infiltration - immunology ; Nose ; Ovalbumin - administration &amp; dosage ; Ovalbumin - immunology ; Rhinitis, Allergic - diagnosis ; Rhinitis, Allergic - immunology ; Rhinitis, Allergic - metabolism ; Rhinitis, Allergic - therapy ; Severity of Illness Index ; Spleen - cytology ; Spleen - immunology ; Spleen - metabolism</subject><ispartof>Allergy (Copenhagen), 2016-05, Vol.71 (5), p.629-639</ispartof><rights>2016 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2016 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2016 John Wiley &amp; Sons A/S</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4529-6a5b4c5d2167e7b5725ad9d5bc17a524135720a7b4a97fcf18aa2c984f20eb4d3</citedby><cites>FETCH-LOGICAL-c4529-6a5b4c5d2167e7b5725ad9d5bc17a524135720a7b4a97fcf18aa2c984f20eb4d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fall.12839$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fall.12839$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26752101$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, E. H.</creatorcontrib><creatorcontrib>Kim, J. H.</creatorcontrib><creatorcontrib>Samivel, R.</creatorcontrib><creatorcontrib>Bae, J.‐S.</creatorcontrib><creatorcontrib>Chung, Y.‐J.</creatorcontrib><creatorcontrib>Chung, P.‐S.</creatorcontrib><creatorcontrib>Lee, S. E.</creatorcontrib><creatorcontrib>Mo, J.‐H.</creatorcontrib><title>Intralymphatic treatment of flagellin–ovalbumin mixture reduced allergic inflammation in murine model of allergic rhinitis</title><title>Allergy (Copenhagen)</title><addtitle>Allergy</addtitle><description>Background Bacterial flagellin, a Toll‐like receptor 5 agonist, is used as an adjuvant for immunomodulation. In this study, we aimed to evaluate the effect and its mechanism following intralymphatic administration of OVA‐flagellin (FlaB) mixture in the mouse model of allergic rhinitis. Materials and Methods BALB/c mice were sensitized with OVA and treated with an OVA‐FlaB mixture via intranasal, sublingual, and intralymphatic routes to evaluate the effect of each treatment. Several parameters for allergic inflammation and its underlying mechanisms were then evaluated. Results Intralymphatic injection of the OVA‐FlaB mixture reduced symptom scores, eosinophil infiltration in the nasal mucosa, and total and OVA‐specific IgE levels more significantly than intranasal and sublingual administration. Systemic cytokine (IL‐4, IL‐5, IL‐6, IL‐17, and IFN‐γ) production and local cytokine (IL‐4 and IL‐5) production were also reduced significantly after intralymphatic injection with OVA‐FlaB. Double intralymphatic injection of the mixture was more effective than single injection. Moreover, the expression of innate cytokines such as IL‐25 and IL‐33 in nasal epithelial cells was reduced, and the expression of chemokines such as CCL24 (eotaxin‐2), CXCL1, and CXCL2 was decreased in the nasal mucosa, suggesting the underlying mechanism for intralymphatic administration of the OVA‐FlaB mixture. Conclusion Intralymphatic administration of an OVA‐FlaB mixture was more effective in alleviating allergic inflammation than intranasal and sublingual administration in a mouse model of allergic rhinitis. This effect may be attributed to the reduced expression of innate cytokines and chemokines. This treatment modality can be considered as a new therapeutic method and agent.</description><subject>Allergens - administration &amp; dosage</subject><subject>Allergens - immunology</subject><subject>allergic rhinitis</subject><subject>Allergies</subject><subject>Animals</subject><subject>Antibody Specificity - immunology</subject><subject>Chemokines</subject><subject>Cytokines</subject><subject>Cytokines - genetics</subject><subject>Cytokines - metabolism</subject><subject>Disease Models, Animal</subject><subject>Eosinophils - immunology</subject><subject>Eosinophils - metabolism</subject><subject>Eosinophils - pathology</subject><subject>Female</subject><subject>flagellin</subject><subject>Flagellin - administration &amp; dosage</subject><subject>Flagellin - immunology</subject><subject>Immunization - methods</subject><subject>Immunoglobulin E - immunology</subject><subject>Immunohistochemistry</subject><subject>Inflammation</subject><subject>innate cytokine</subject><subject>intralymphatic injection</subject><subject>Mice</subject><subject>mouse model</subject><subject>Nasal Mucosa - immunology</subject><subject>Nasal Mucosa - metabolism</subject><subject>Nasal Mucosa - pathology</subject><subject>Neutrophil Infiltration - immunology</subject><subject>Nose</subject><subject>Ovalbumin - administration &amp; dosage</subject><subject>Ovalbumin - immunology</subject><subject>Rhinitis, Allergic - diagnosis</subject><subject>Rhinitis, Allergic - immunology</subject><subject>Rhinitis, Allergic - metabolism</subject><subject>Rhinitis, Allergic - therapy</subject><subject>Severity of Illness Index</subject><subject>Spleen - cytology</subject><subject>Spleen - immunology</subject><subject>Spleen - metabolism</subject><issn>0105-4538</issn><issn>1398-9995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0UFr2zAUB3AxWpa026FfoBh6WQ9OJFmKrGMIW1cI9LKdjSw_twqSnEp2u8AO_Q79hvsklZesh0GhugjE7_3Few-hM4JnJJ25snZGaFnID2hKClnmUkp-hKaYYJ4zXpQTdBLjBmMsqMQf0YQuBKcEkyn6fe37oOzObe9Ub3TWB1C9A99nXZu1Vt2Ctcb_eXruHpStB2d85syvfgiQBWgGDU2Wfodwm2qNTwXOpZzOZyMcgvGQua4BO8a9wnBnvOlN_ISOW2UjfD7cp-jnt68_Vt_z9c3V9Wq5zjXjVOYLxWumeUPJQoCouaBcNbLhtSZCccpIkZ6wEjVTUrS6JaVSVMuStRRDzZriFH3Z525Ddz9A7Ctnok6dKQ_dECsiSiGF5Fi-hzLBhGAjvfiPbroh-NTIqApZYCF4Upd7pUMXY4C22gbjVNhVBFfj9qo0lurv9pI9PyQOtYPmVf5bVwLzPXg0FnZvJ1XL9Xof-QKXpKZu</recordid><startdate>201605</startdate><enddate>201605</enddate><creator>Kim, E. H.</creator><creator>Kim, J. H.</creator><creator>Samivel, R.</creator><creator>Bae, J.‐S.</creator><creator>Chung, Y.‐J.</creator><creator>Chung, P.‐S.</creator><creator>Lee, S. E.</creator><creator>Mo, J.‐H.</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201605</creationdate><title>Intralymphatic treatment of flagellin–ovalbumin mixture reduced allergic inflammation in murine model of allergic rhinitis</title><author>Kim, E. H. ; Kim, J. H. ; Samivel, R. ; Bae, J.‐S. ; Chung, Y.‐J. ; Chung, P.‐S. ; Lee, S. 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H.</creatorcontrib><creatorcontrib>Kim, J. H.</creatorcontrib><creatorcontrib>Samivel, R.</creatorcontrib><creatorcontrib>Bae, J.‐S.</creatorcontrib><creatorcontrib>Chung, Y.‐J.</creatorcontrib><creatorcontrib>Chung, P.‐S.</creatorcontrib><creatorcontrib>Lee, S. E.</creatorcontrib><creatorcontrib>Mo, J.‐H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Allergy (Copenhagen)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, E. H.</au><au>Kim, J. H.</au><au>Samivel, R.</au><au>Bae, J.‐S.</au><au>Chung, Y.‐J.</au><au>Chung, P.‐S.</au><au>Lee, S. E.</au><au>Mo, J.‐H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intralymphatic treatment of flagellin–ovalbumin mixture reduced allergic inflammation in murine model of allergic rhinitis</atitle><jtitle>Allergy (Copenhagen)</jtitle><addtitle>Allergy</addtitle><date>2016-05</date><risdate>2016</risdate><volume>71</volume><issue>5</issue><spage>629</spage><epage>639</epage><pages>629-639</pages><issn>0105-4538</issn><eissn>1398-9995</eissn><abstract>Background Bacterial flagellin, a Toll‐like receptor 5 agonist, is used as an adjuvant for immunomodulation. In this study, we aimed to evaluate the effect and its mechanism following intralymphatic administration of OVA‐flagellin (FlaB) mixture in the mouse model of allergic rhinitis. Materials and Methods BALB/c mice were sensitized with OVA and treated with an OVA‐FlaB mixture via intranasal, sublingual, and intralymphatic routes to evaluate the effect of each treatment. Several parameters for allergic inflammation and its underlying mechanisms were then evaluated. Results Intralymphatic injection of the OVA‐FlaB mixture reduced symptom scores, eosinophil infiltration in the nasal mucosa, and total and OVA‐specific IgE levels more significantly than intranasal and sublingual administration. Systemic cytokine (IL‐4, IL‐5, IL‐6, IL‐17, and IFN‐γ) production and local cytokine (IL‐4 and IL‐5) production were also reduced significantly after intralymphatic injection with OVA‐FlaB. Double intralymphatic injection of the mixture was more effective than single injection. Moreover, the expression of innate cytokines such as IL‐25 and IL‐33 in nasal epithelial cells was reduced, and the expression of chemokines such as CCL24 (eotaxin‐2), CXCL1, and CXCL2 was decreased in the nasal mucosa, suggesting the underlying mechanism for intralymphatic administration of the OVA‐FlaB mixture. Conclusion Intralymphatic administration of an OVA‐FlaB mixture was more effective in alleviating allergic inflammation than intranasal and sublingual administration in a mouse model of allergic rhinitis. This effect may be attributed to the reduced expression of innate cytokines and chemokines. This treatment modality can be considered as a new therapeutic method and agent.</abstract><cop>Denmark</cop><pub>Blackwell Publishing Ltd</pub><pmid>26752101</pmid><doi>10.1111/all.12839</doi><tpages>11</tpages></addata></record>
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subjects Allergens - administration & dosage
Allergens - immunology
allergic rhinitis
Allergies
Animals
Antibody Specificity - immunology
Chemokines
Cytokines
Cytokines - genetics
Cytokines - metabolism
Disease Models, Animal
Eosinophils - immunology
Eosinophils - metabolism
Eosinophils - pathology
Female
flagellin
Flagellin - administration & dosage
Flagellin - immunology
Immunization - methods
Immunoglobulin E - immunology
Immunohistochemistry
Inflammation
innate cytokine
intralymphatic injection
Mice
mouse model
Nasal Mucosa - immunology
Nasal Mucosa - metabolism
Nasal Mucosa - pathology
Neutrophil Infiltration - immunology
Nose
Ovalbumin - administration & dosage
Ovalbumin - immunology
Rhinitis, Allergic - diagnosis
Rhinitis, Allergic - immunology
Rhinitis, Allergic - metabolism
Rhinitis, Allergic - therapy
Severity of Illness Index
Spleen - cytology
Spleen - immunology
Spleen - metabolism
title Intralymphatic treatment of flagellin–ovalbumin mixture reduced allergic inflammation in murine model of allergic rhinitis
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