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...
Gespeichert in:
Veröffentlicht in: | Allergy (Copenhagen) 2016-05, Vol.71 (5), p.629-639 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1787979509</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4033716521</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4529-6a5b4c5d2167e7b5725ad9d5bc17a524135720a7b4a97fcf18aa2c984f20eb4d3</originalsourceid><addsrcrecordid>eNqN0UFr2zAUB3AxWpa026FfoBh6WQ9OJFmKrGMIW1cI9LKdjSw_twqSnEp2u8AO_Q79hvsklZesh0GhugjE7_3Few-hM4JnJJ25snZGaFnID2hKClnmUkp-hKaYYJ4zXpQTdBLjBmMsqMQf0YQuBKcEkyn6fe37oOzObe9Ub3TWB1C9A99nXZu1Vt2Ctcb_eXruHpStB2d85syvfgiQBWgGDU2Wfodwm2qNTwXOpZzOZyMcgvGQua4BO8a9wnBnvOlN_ISOW2UjfD7cp-jnt68_Vt_z9c3V9Wq5zjXjVOYLxWumeUPJQoCouaBcNbLhtSZCccpIkZ6wEjVTUrS6JaVSVMuStRRDzZriFH3Z525Ddz9A7Ctnok6dKQ_dECsiSiGF5Fi-hzLBhGAjvfiPbroh-NTIqApZYCF4Upd7pUMXY4C22gbjVNhVBFfj9qo0lurv9pI9PyQOtYPmVf5bVwLzPXg0FnZvJ1XL9Xof-QKXpKZu</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1783930775</pqid></control><display><type>article</type><title>Intralymphatic treatment of flagellin–ovalbumin mixture reduced allergic inflammation in murine model of allergic rhinitis</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Wiley Online Library Free Content</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Kim, E. 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 & 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</subject><ispartof>Allergy (Copenhagen), 2016-05, Vol.71 (5), p.629-639</ispartof><rights>2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2016 John Wiley & 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 & 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 & 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 & 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. E. ; Mo, J.‐H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4529-6a5b4c5d2167e7b5725ad9d5bc17a524135720a7b4a97fcf18aa2c984f20eb4d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Allergens - administration & dosage</topic><topic>Allergens - immunology</topic><topic>allergic rhinitis</topic><topic>Allergies</topic><topic>Animals</topic><topic>Antibody Specificity - immunology</topic><topic>Chemokines</topic><topic>Cytokines</topic><topic>Cytokines - genetics</topic><topic>Cytokines - metabolism</topic><topic>Disease Models, Animal</topic><topic>Eosinophils - immunology</topic><topic>Eosinophils - metabolism</topic><topic>Eosinophils - pathology</topic><topic>Female</topic><topic>flagellin</topic><topic>Flagellin - administration & dosage</topic><topic>Flagellin - immunology</topic><topic>Immunization - methods</topic><topic>Immunoglobulin E - immunology</topic><topic>Immunohistochemistry</topic><topic>Inflammation</topic><topic>innate cytokine</topic><topic>intralymphatic injection</topic><topic>Mice</topic><topic>mouse model</topic><topic>Nasal Mucosa - immunology</topic><topic>Nasal Mucosa - metabolism</topic><topic>Nasal Mucosa - pathology</topic><topic>Neutrophil Infiltration - immunology</topic><topic>Nose</topic><topic>Ovalbumin - administration & dosage</topic><topic>Ovalbumin - immunology</topic><topic>Rhinitis, Allergic - diagnosis</topic><topic>Rhinitis, Allergic - immunology</topic><topic>Rhinitis, Allergic - metabolism</topic><topic>Rhinitis, Allergic - therapy</topic><topic>Severity of Illness Index</topic><topic>Spleen - cytology</topic><topic>Spleen - immunology</topic><topic>Spleen - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><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 & 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> |
fulltext | fulltext |
identifier | ISSN: 0105-4538 |
ispartof | Allergy (Copenhagen), 2016-05, Vol.71 (5), p.629-639 |
issn | 0105-4538 1398-9995 |
language | eng |
recordid | cdi_proquest_miscellaneous_1787979509 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete; Wiley Online Library Free Content; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-14T12%3A08%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Intralymphatic%20treatment%20of%20flagellin%E2%80%93ovalbumin%20mixture%20reduced%20allergic%20inflammation%20in%20murine%20model%20of%20allergic%20rhinitis&rft.jtitle=Allergy%20(Copenhagen)&rft.au=Kim,%20E.%20H.&rft.date=2016-05&rft.volume=71&rft.issue=5&rft.spage=629&rft.epage=639&rft.pages=629-639&rft.issn=0105-4538&rft.eissn=1398-9995&rft_id=info:doi/10.1111/all.12839&rft_dat=%3Cproquest_cross%3E4033716521%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1783930775&rft_id=info:pmid/26752101&rfr_iscdi=true |