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Anti-Interleukin-1 Beta/Tumor Necrosis Factor-Alpha IgY Antibodies Reduce Pathological Allergic Responses in Guinea Pigs with Allergic Rhinitis
This study aims to determine whether the combined blockade of IL-1β and TNF-α can alleviate the pathological allergic inflammatory reaction in the nasal mucosa and lung tissues in allergic rhinitis (AR) guinea pigs. Healthy guinea pigs treated with saline were used as the healthy controls. The AR gu...
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Published in: | Mediators of Inflammation 2016-01, Vol.2016 (2016), p.920-930-085 |
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container_end_page | 930-085 |
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container_title | Mediators of Inflammation |
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creator | Qin, Xiang Guo-zhu, Hu Dan, He Hui-ping, Wei Xiao-mu, Wu Li-hua, Wu Zhu, Wen Xi-ling, Zhu Wen-yun, Zhou Wei-xu, Hu Wen-ding, Wang |
description | This study aims to determine whether the combined blockade of IL-1β and TNF-α can alleviate the pathological allergic inflammatory reaction in the nasal mucosa and lung tissues in allergic rhinitis (AR) guinea pigs. Healthy guinea pigs treated with saline were used as the healthy controls. The AR guinea pigs were randomly divided into (1) the AR model group treated with intranasal saline; (2) the 0.1% nonspecific IgY treatment group; (3) the 0.1% anti-TNF-α IgY treatment group; (4) the 0.1% anti-IL-1β IgY treatment group; (5) the 0.1% combined anti-IL-1β and TNF-α IgY treatment group; and (6) the fluticasone propionate treatment group. The inflammatory cells were evaluated using Wright’s staining. Histopathology was examined using hematoxylin-eosin staining. The results showed that the number of eosinophils was significantly decreased in the peripheral blood, nasal lavage fluid, and bronchoalveolar lavage fluid ( P < 0.05 ), and eosinophil, neutrophil, and lymphocyte infiltration and edema were significantly reduced or absent in the nasal mucosa and lung tissues ( P < 0.05 ) in the combined 0.1% anti-IL-1β- and TNF-α IgY-treated guinea pigs. The data suggest that topical blockade of IL-1β and TNF-α could reduce pathological allergic inflammation in the nasal mucosa and lung tissues in AR guinea pigs. |
doi_str_mv | 10.1155/2016/3128182 |
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Healthy guinea pigs treated with saline were used as the healthy controls. The AR guinea pigs were randomly divided into (1) the AR model group treated with intranasal saline; (2) the 0.1% nonspecific IgY treatment group; (3) the 0.1% anti-TNF-α IgY treatment group; (4) the 0.1% anti-IL-1β IgY treatment group; (5) the 0.1% combined anti-IL-1β and TNF-α IgY treatment group; and (6) the fluticasone propionate treatment group. The inflammatory cells were evaluated using Wright’s staining. Histopathology was examined using hematoxylin-eosin staining. The results showed that the number of eosinophils was significantly decreased in the peripheral blood, nasal lavage fluid, and bronchoalveolar lavage fluid ( P < 0.05 ), and eosinophil, neutrophil, and lymphocyte infiltration and edema were significantly reduced or absent in the nasal mucosa and lung tissues ( P < 0.05 ) in the combined 0.1% anti-IL-1β- and TNF-α IgY-treated guinea pigs. The data suggest that topical blockade of IL-1β and TNF-α could reduce pathological allergic inflammation in the nasal mucosa and lung tissues in AR guinea pigs.</description><identifier>ISSN: 0962-9351</identifier><identifier>EISSN: 1466-1861</identifier><identifier>DOI: 10.1155/2016/3128182</identifier><identifier>PMID: 27046957</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Limiteds</publisher><subject>Allergies ; Analysis ; Animals ; Antibodies ; Asthma ; Cytokines ; Disease Models, Animal ; Fluticasone ; Gangrene ; Guinea Pigs ; Immunoglobulins ; Immunoglobulins - therapeutic use ; Inflammation ; Interleukin-1beta - antagonists & inhibitors ; Interleukin-1beta - immunology ; Interleukins ; Laboratories ; Lung - drug effects ; Lung - immunology ; Lung - metabolism ; Male ; Medical research ; Nasal Mucosa - drug effects ; Nasal Mucosa - immunology ; Nasal Mucosa - metabolism ; Nose ; Pathology ; Rhinitis ; Rhinitis, Allergic - drug therapy ; Rhinitis, Allergic - immunology ; Science ; Tumor necrosis factor ; Tumor Necrosis Factor-alpha - antagonists & inhibitors ; Tumor Necrosis Factor-alpha - immunology ; Tumor necrosis factor-TNF ; Viral antibodies</subject><ispartof>Mediators of Inflammation, 2016-01, Vol.2016 (2016), p.920-930-085</ispartof><rights>Copyright © 2016 Hu Wei-xu et al.</rights><rights>COPYRIGHT 2016 John Wiley & Sons, Inc.</rights><rights>Copyright © 2016 Hu Wei-xu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2016 Hu Wei-xu et al. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a677t-c79bde4f4ff943dd49870deb866a69aed2bb37ddd5011e9aff9d735a7d7045cf3</citedby><cites>FETCH-LOGICAL-a677t-c79bde4f4ff943dd49870deb866a69aed2bb37ddd5011e9aff9d735a7d7045cf3</cites><orcidid>0000-0003-1525-353X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1774492992/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1774492992?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771,74872</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27046957$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Oliveira, Sandra Helena Penha</contributor><creatorcontrib>Qin, Xiang</creatorcontrib><creatorcontrib>Guo-zhu, Hu</creatorcontrib><creatorcontrib>Dan, He</creatorcontrib><creatorcontrib>Hui-ping, Wei</creatorcontrib><creatorcontrib>Xiao-mu, Wu</creatorcontrib><creatorcontrib>Li-hua, Wu</creatorcontrib><creatorcontrib>Zhu, Wen</creatorcontrib><creatorcontrib>Xi-ling, Zhu</creatorcontrib><creatorcontrib>Wen-yun, Zhou</creatorcontrib><creatorcontrib>Wei-xu, Hu</creatorcontrib><creatorcontrib>Wen-ding, Wang</creatorcontrib><title>Anti-Interleukin-1 Beta/Tumor Necrosis Factor-Alpha IgY Antibodies Reduce Pathological Allergic Responses in Guinea Pigs with Allergic Rhinitis</title><title>Mediators of Inflammation</title><addtitle>Mediators Inflamm</addtitle><description>This study aims to determine whether the combined blockade of IL-1β and TNF-α can alleviate the pathological allergic inflammatory reaction in the nasal mucosa and lung tissues in allergic rhinitis (AR) guinea pigs. 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The data suggest that topical blockade of IL-1β and TNF-α could reduce pathological allergic inflammation in the nasal mucosa and lung tissues in AR guinea pigs.</description><subject>Allergies</subject><subject>Analysis</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Asthma</subject><subject>Cytokines</subject><subject>Disease Models, Animal</subject><subject>Fluticasone</subject><subject>Gangrene</subject><subject>Guinea Pigs</subject><subject>Immunoglobulins</subject><subject>Immunoglobulins - therapeutic use</subject><subject>Inflammation</subject><subject>Interleukin-1beta - antagonists & inhibitors</subject><subject>Interleukin-1beta - immunology</subject><subject>Interleukins</subject><subject>Laboratories</subject><subject>Lung - drug effects</subject><subject>Lung - immunology</subject><subject>Lung - metabolism</subject><subject>Male</subject><subject>Medical research</subject><subject>Nasal Mucosa - drug effects</subject><subject>Nasal Mucosa - immunology</subject><subject>Nasal Mucosa - metabolism</subject><subject>Nose</subject><subject>Pathology</subject><subject>Rhinitis</subject><subject>Rhinitis, Allergic - drug therapy</subject><subject>Rhinitis, Allergic - immunology</subject><subject>Science</subject><subject>Tumor necrosis factor</subject><subject>Tumor Necrosis Factor-alpha - antagonists & inhibitors</subject><subject>Tumor Necrosis Factor-alpha - immunology</subject><subject>Tumor necrosis factor-TNF</subject><subject>Viral antibodies</subject><issn>0962-9351</issn><issn>1466-1861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkk9v0zAYhyMEYmVw44wicUGCrP4XO74glYmNShNUaBw4WU78pnVJ7WInTHwKvjLOWtYVcSA52LGf97H85pdlzzE6w7gspwRhPqWYVLgiD7IJZpwXuOL4YTZBkpNC0hKfZE9iXCOESsaqx9kJEYhxWYpJ9mvmelvMXQ-hg-GbdQXO30Gvp9fDxof8IzTBRxvzC930PhSzbrvS-Xz5NR_ram8sxPwzmKGBfKH7le_80ja6y2ddByFN02bcehcTZl1-OVgHOl_YZcxvbL-6h62ss72NT7NHre4iPNuPp9mXi_fX5x-Kq0-X8_PZVaG5EH3RCFkbYC1rW8moMUxWAhmoK841lxoMqWsqjDElwhikTpgRtNTCpJuXTUtPs_nOa7xeq22wGx1-Kq-tul3wYal06G3TgaoINFQwwasSMUxBU8Y0CCKgRi1CdXK93bm2Q70B04Drg-6OpMc7zq7U0v9QrEIII5YEr_aC4L8PEHu1sbGBrtMO_BAVFkIyLBGqEvryL3Tth-BSq0aKMUmkJAdqqdMFrGt9OrcZpWpWYsoZoWKkzv5BpdfAxjbeQWvT-lHBm13BGIoYoL27I0ZqDKMaw6j2YUz4i_t9uYP_pC8Br3dA-vlG39j_1EFioNUHOj2pkQlY7ABtQ8rSoTOL0YPKdC6it05MxkFgTFIhYccfkiAlKVKoKulvU9gFxg</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Qin, Xiang</creator><creator>Guo-zhu, Hu</creator><creator>Dan, He</creator><creator>Hui-ping, Wei</creator><creator>Xiao-mu, Wu</creator><creator>Li-hua, Wu</creator><creator>Zhu, Wen</creator><creator>Xi-ling, Zhu</creator><creator>Wen-yun, Zhou</creator><creator>Wei-xu, Hu</creator><creator>Wen-ding, Wang</creator><general>Hindawi Limiteds</general><general>Hindawi Publishing Corporation</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>188</scope><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1525-353X</orcidid></search><sort><creationdate>20160101</creationdate><title>Anti-Interleukin-1 Beta/Tumor Necrosis Factor-Alpha IgY Antibodies Reduce Pathological Allergic Responses in Guinea Pigs with Allergic Rhinitis</title><author>Qin, Xiang ; Guo-zhu, Hu ; Dan, He ; Hui-ping, Wei ; Xiao-mu, Wu ; Li-hua, Wu ; Zhu, Wen ; Xi-ling, Zhu ; Wen-yun, Zhou ; Wei-xu, Hu ; Wen-ding, Wang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a677t-c79bde4f4ff943dd49870deb866a69aed2bb37ddd5011e9aff9d735a7d7045cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Allergies</topic><topic>Analysis</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Asthma</topic><topic>Cytokines</topic><topic>Disease Models, Animal</topic><topic>Fluticasone</topic><topic>Gangrene</topic><topic>Guinea Pigs</topic><topic>Immunoglobulins</topic><topic>Immunoglobulins - 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Healthy guinea pigs treated with saline were used as the healthy controls. The AR guinea pigs were randomly divided into (1) the AR model group treated with intranasal saline; (2) the 0.1% nonspecific IgY treatment group; (3) the 0.1% anti-TNF-α IgY treatment group; (4) the 0.1% anti-IL-1β IgY treatment group; (5) the 0.1% combined anti-IL-1β and TNF-α IgY treatment group; and (6) the fluticasone propionate treatment group. The inflammatory cells were evaluated using Wright’s staining. Histopathology was examined using hematoxylin-eosin staining. The results showed that the number of eosinophils was significantly decreased in the peripheral blood, nasal lavage fluid, and bronchoalveolar lavage fluid ( P < 0.05 ), and eosinophil, neutrophil, and lymphocyte infiltration and edema were significantly reduced or absent in the nasal mucosa and lung tissues ( P < 0.05 ) in the combined 0.1% anti-IL-1β- and TNF-α IgY-treated guinea pigs. The data suggest that topical blockade of IL-1β and TNF-α could reduce pathological allergic inflammation in the nasal mucosa and lung tissues in AR guinea pigs.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Limiteds</pub><pmid>27046957</pmid><doi>10.1155/2016/3128182</doi><orcidid>https://orcid.org/0000-0003-1525-353X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Allergies Analysis Animals Antibodies Asthma Cytokines Disease Models, Animal Fluticasone Gangrene Guinea Pigs Immunoglobulins Immunoglobulins - therapeutic use Inflammation Interleukin-1beta - antagonists & inhibitors Interleukin-1beta - immunology Interleukins Laboratories Lung - drug effects Lung - immunology Lung - metabolism Male Medical research Nasal Mucosa - drug effects Nasal Mucosa - immunology Nasal Mucosa - metabolism Nose Pathology Rhinitis Rhinitis, Allergic - drug therapy Rhinitis, Allergic - immunology Science Tumor necrosis factor Tumor Necrosis Factor-alpha - antagonists & inhibitors Tumor Necrosis Factor-alpha - immunology Tumor necrosis factor-TNF Viral antibodies |
title | Anti-Interleukin-1 Beta/Tumor Necrosis Factor-Alpha IgY Antibodies Reduce Pathological Allergic Responses in Guinea Pigs with Allergic Rhinitis |
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