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Intranasal delivery of a truncated recombinant human SP‐D is effective at down‐regulating allergic hypersensitivity in mice sensitized to allergens of Aspergillus fumigatus
Summary C57BL/6 mice were sensitized to Aspergillus fumigatus 1‐week culture filtrate, which is rich in the non‐glycosylated allergen Asp f1, a major allergen in allergic bronchopulmonary aspergillosis (ABPA). A comparison of the effect of treatment of allergen challenged mice by intranasal administ...
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Published in: | Clinical and experimental immunology 2002-10, Vol.130 (1), p.19-24 |
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C57BL/6 mice were sensitized to Aspergillus fumigatus 1‐week culture filtrate, which is rich in the non‐glycosylated allergen Asp f1, a major allergen in allergic bronchopulmonary aspergillosis (ABPA). A comparison of the effect of treatment of allergen challenged mice by intranasal administration of a 60‐kDa truncated recombinant form of human SP‐D (rfhSP‐D) or recombinant full length SP‐A (rhSP‐A) was undertaken. Treatment with rfhSP‐D produced significant reduction in IgE, IgG1 and peripheral blood eosinophilia and treatment with rfhSP‐D, but not rhSP‐A resulted in a significant reduction in airway hyperresponsiveness as measured by whole body plethysmography. Lung histology revealed less peribronchial lymphocytic infiltration in mice treated with rfhSP‐D. Intracellular cytokine staining of spleen homogenates showed increases in IL‐12 and IFN‐γ and decrease in IL‐4. The level of endogenous mouse SP‐D was elevated sixfold in the lungs of sensitized mice and was not affected by treatment with rfhSP‐D. Taken with our previous studies, with a BALB/c mouse model of ABPA using a 3‐week A. fumigatus culture filtrate, the present results show that rfhSP‐D can suppress the development of allergic symptoms in sensitized mice independent of genetic background and using a different preparation of A. fumigatus allergens. |
doi_str_mv | 10.1046/j.1365-2249.2002.01968.x |
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C57BL/6 mice were sensitized to Aspergillus fumigatus 1‐week culture filtrate, which is rich in the non‐glycosylated allergen Asp f1, a major allergen in allergic bronchopulmonary aspergillosis (ABPA). A comparison of the effect of treatment of allergen challenged mice by intranasal administration of a 60‐kDa truncated recombinant form of human SP‐D (rfhSP‐D) or recombinant full length SP‐A (rhSP‐A) was undertaken. Treatment with rfhSP‐D produced significant reduction in IgE, IgG1 and peripheral blood eosinophilia and treatment with rfhSP‐D, but not rhSP‐A resulted in a significant reduction in airway hyperresponsiveness as measured by whole body plethysmography. Lung histology revealed less peribronchial lymphocytic infiltration in mice treated with rfhSP‐D. Intracellular cytokine staining of spleen homogenates showed increases in IL‐12 and IFN‐γ and decrease in IL‐4. The level of endogenous mouse SP‐D was elevated sixfold in the lungs of sensitized mice and was not affected by treatment with rfhSP‐D. Taken with our previous studies, with a BALB/c mouse model of ABPA using a 3‐week A. fumigatus culture filtrate, the present results show that rfhSP‐D can suppress the development of allergic symptoms in sensitized mice independent of genetic background and using a different preparation of A. fumigatus allergens.</description><identifier>ISSN: 0009-9104</identifier><identifier>EISSN: 1365-2249</identifier><identifier>DOI: 10.1046/j.1365-2249.2002.01968.x</identifier><identifier>PMID: 12296848</identifier><identifier>CODEN: CEXIAL</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science, Ltd</publisher><subject>ABPA allergy IL‐12 plethysmography SP‐D ; Administration, Intranasal ; Allergens - immunology ; Allergens - toxicity ; Animal Studies ; Animals ; Antibodies, Fungal - biosynthesis ; Antibodies, Fungal - immunology ; Antigens, Fungal - immunology ; Antigens, Fungal - toxicity ; Antigens, Plant ; Aspergillosis, Allergic Bronchopulmonary - chemically induced ; Aspergillosis, Allergic Bronchopulmonary - drug therapy ; Aspergillosis, Allergic Bronchopulmonary - pathology ; Aspergillus fumigatus - immunology ; Biological and medical sciences ; Bronchial Hyperreactivity - chemically induced ; Bronchial Hyperreactivity - drug therapy ; Drug Evaluation, Preclinical ; Eosinophilia - chemically induced ; Eosinophilia - drug therapy ; Female ; Fungal Proteins - immunology ; Fungal Proteins - toxicity ; Histamine and antagonists. Allergy ; Humans ; Immunization ; Interferon-gamma - analysis ; Interleukin-12 - analysis ; Interleukin-4 - analysis ; Lung - pathology ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Peptide Fragments - administration & dosage ; Peptide Fragments - pharmacology ; Peptide Fragments - therapeutic use ; Pharmacology. Drug treatments ; Plethysmography, Whole Body ; Pulmonary Surfactant-Associated Protein A - analysis ; Pulmonary Surfactant-Associated Protein A - pharmacology ; Pulmonary Surfactant-Associated Protein A - therapeutic use ; Pulmonary Surfactant-Associated Protein D - administration & dosage ; Pulmonary Surfactant-Associated Protein D - analysis ; Pulmonary Surfactant-Associated Protein D - chemistry ; Pulmonary Surfactant-Associated Protein D - pharmacology ; Pulmonary Surfactant-Associated Protein D - therapeutic use ; Recombinant Fusion Proteins - administration & dosage ; Recombinant Fusion Proteins - pharmacology ; Recombinant Fusion Proteins - therapeutic use ; Species Specificity ; Spleen - chemistry ; Spleen - immunology ; Spleen - pathology</subject><ispartof>Clinical and experimental immunology, 2002-10, Vol.130 (1), p.19-24</ispartof><rights>2003 INIST-CNRS</rights><rights>Copyright Blackwell Scientific Publications Ltd. Oct 2002</rights><rights>2002 Blackwell Publishing Ltd 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5088-737b89af105452992127406a43e0f34d9d27c9d4edaf7d9cf85ea3a283510de53</citedby><cites>FETCH-LOGICAL-c5088-737b89af105452992127406a43e0f34d9d27c9d4edaf7d9cf85ea3a283510de53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1906502/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1906502/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13912881$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12296848$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>STRONG, P.</creatorcontrib><creatorcontrib>REID, K. B. M.</creatorcontrib><creatorcontrib>CLARK, H.</creatorcontrib><title>Intranasal delivery of a truncated recombinant human SP‐D is effective at down‐regulating allergic hypersensitivity in mice sensitized to allergens of Aspergillus fumigatus</title><title>Clinical and experimental immunology</title><addtitle>Clin Exp Immunol</addtitle><description>Summary
C57BL/6 mice were sensitized to Aspergillus fumigatus 1‐week culture filtrate, which is rich in the non‐glycosylated allergen Asp f1, a major allergen in allergic bronchopulmonary aspergillosis (ABPA). A comparison of the effect of treatment of allergen challenged mice by intranasal administration of a 60‐kDa truncated recombinant form of human SP‐D (rfhSP‐D) or recombinant full length SP‐A (rhSP‐A) was undertaken. Treatment with rfhSP‐D produced significant reduction in IgE, IgG1 and peripheral blood eosinophilia and treatment with rfhSP‐D, but not rhSP‐A resulted in a significant reduction in airway hyperresponsiveness as measured by whole body plethysmography. Lung histology revealed less peribronchial lymphocytic infiltration in mice treated with rfhSP‐D. Intracellular cytokine staining of spleen homogenates showed increases in IL‐12 and IFN‐γ and decrease in IL‐4. The level of endogenous mouse SP‐D was elevated sixfold in the lungs of sensitized mice and was not affected by treatment with rfhSP‐D. Taken with our previous studies, with a BALB/c mouse model of ABPA using a 3‐week A. fumigatus culture filtrate, the present results show that rfhSP‐D can suppress the development of allergic symptoms in sensitized mice independent of genetic background and using a different preparation of A. fumigatus allergens.</description><subject>ABPA allergy IL‐12 plethysmography SP‐D</subject><subject>Administration, Intranasal</subject><subject>Allergens - immunology</subject><subject>Allergens - toxicity</subject><subject>Animal Studies</subject><subject>Animals</subject><subject>Antibodies, Fungal - biosynthesis</subject><subject>Antibodies, Fungal - immunology</subject><subject>Antigens, Fungal - immunology</subject><subject>Antigens, Fungal - toxicity</subject><subject>Antigens, Plant</subject><subject>Aspergillosis, Allergic Bronchopulmonary - chemically induced</subject><subject>Aspergillosis, Allergic Bronchopulmonary - drug therapy</subject><subject>Aspergillosis, Allergic Bronchopulmonary - pathology</subject><subject>Aspergillus fumigatus - immunology</subject><subject>Biological and medical sciences</subject><subject>Bronchial Hyperreactivity - chemically induced</subject><subject>Bronchial Hyperreactivity - drug therapy</subject><subject>Drug Evaluation, Preclinical</subject><subject>Eosinophilia - chemically induced</subject><subject>Eosinophilia - drug therapy</subject><subject>Female</subject><subject>Fungal Proteins - immunology</subject><subject>Fungal Proteins - toxicity</subject><subject>Histamine and antagonists. Allergy</subject><subject>Humans</subject><subject>Immunization</subject><subject>Interferon-gamma - analysis</subject><subject>Interleukin-12 - analysis</subject><subject>Interleukin-4 - analysis</subject><subject>Lung - pathology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Peptide Fragments - administration & dosage</subject><subject>Peptide Fragments - pharmacology</subject><subject>Peptide Fragments - therapeutic use</subject><subject>Pharmacology. Drug treatments</subject><subject>Plethysmography, Whole Body</subject><subject>Pulmonary Surfactant-Associated Protein A - analysis</subject><subject>Pulmonary Surfactant-Associated Protein A - pharmacology</subject><subject>Pulmonary Surfactant-Associated Protein A - therapeutic use</subject><subject>Pulmonary Surfactant-Associated Protein D - administration & dosage</subject><subject>Pulmonary Surfactant-Associated Protein D - analysis</subject><subject>Pulmonary Surfactant-Associated Protein D - chemistry</subject><subject>Pulmonary Surfactant-Associated Protein D - pharmacology</subject><subject>Pulmonary Surfactant-Associated Protein D - therapeutic use</subject><subject>Recombinant Fusion Proteins - administration & dosage</subject><subject>Recombinant Fusion Proteins - pharmacology</subject><subject>Recombinant Fusion Proteins - therapeutic use</subject><subject>Species Specificity</subject><subject>Spleen - chemistry</subject><subject>Spleen - immunology</subject><subject>Spleen - pathology</subject><issn>0009-9104</issn><issn>1365-2249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqNks1uEzEQx1cIREPhFZCFRG8JtvfLPoBUhQKRKoEEnK2Jd5w48nqDvds2nHgEHoVn4knwklULnDj5Y37_mbHnn2WE0QWjRfVit2B5Vc45L-SCU8oXlMlKLG7uZbPbwP1sRimVc5kUJ9mjGHfpWFUVf5idMM4TX4hZ9mPl-wAeIjjSoLNXGA6kMwRIHwavoceGBNRdu7YefE-2QwuefPzw89v318RGgsag7pOMQE-a7tqnQMDN4KC3fkPAOQwbq8n2sMcQ0UebYNsfiPWktRrJdPc11em7iU9XYw_ncT-KnRsiMUNrN9AP8XH2wICL-GRaT7PPby4-Ld_NL9-_XS3PL-e6pELM67xeCwmG0bIouZSc8bqgFRQ5UpMXjWx4rWVTYAOmbqQ2okTIgYu8ZLTBMj_NXh3z7od1i43G8Z-c2gfbQjioDqz6O-LtVm26K8UkrUrKU4KzKUHovgwYe9XaqNE58NgNUTFRSFGXY6Vn_4C7bgg-PU6NUxVVJWWCxBHSoYsxoLnthFE1ekLt1Dh6NY5ejZ5Qvz2hbpL06Z8vuRNOJkjA8wmAqMGZ5Adt4x2XS8aFYIl7eeSurcPDfzeglhercZf_AtQq2aA</recordid><startdate>200210</startdate><enddate>200210</enddate><creator>STRONG, P.</creator><creator>REID, K. B. M.</creator><creator>CLARK, H.</creator><general>Blackwell Science, Ltd</general><general>Blackwell</general><general>Oxford University Press</general><general>Blackwell Science Inc</general><scope>IQODW</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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>M7N</scope><scope>5PM</scope></search><sort><creationdate>200210</creationdate><title>Intranasal delivery of a truncated recombinant human SP‐D is effective at down‐regulating allergic hypersensitivity in mice sensitized to allergens of Aspergillus fumigatus</title><author>STRONG, P. ; REID, K. B. M. ; CLARK, H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5088-737b89af105452992127406a43e0f34d9d27c9d4edaf7d9cf85ea3a283510de53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>ABPA allergy IL‐12 plethysmography SP‐D</topic><topic>Administration, Intranasal</topic><topic>Allergens - immunology</topic><topic>Allergens - toxicity</topic><topic>Animal Studies</topic><topic>Animals</topic><topic>Antibodies, Fungal - biosynthesis</topic><topic>Antibodies, Fungal - immunology</topic><topic>Antigens, Fungal - immunology</topic><topic>Antigens, Fungal - toxicity</topic><topic>Antigens, Plant</topic><topic>Aspergillosis, Allergic Bronchopulmonary - chemically induced</topic><topic>Aspergillosis, Allergic Bronchopulmonary - drug therapy</topic><topic>Aspergillosis, Allergic Bronchopulmonary - pathology</topic><topic>Aspergillus fumigatus - immunology</topic><topic>Biological and medical sciences</topic><topic>Bronchial Hyperreactivity - chemically induced</topic><topic>Bronchial Hyperreactivity - drug therapy</topic><topic>Drug Evaluation, Preclinical</topic><topic>Eosinophilia - chemically induced</topic><topic>Eosinophilia - drug therapy</topic><topic>Female</topic><topic>Fungal Proteins - immunology</topic><topic>Fungal Proteins - toxicity</topic><topic>Histamine and antagonists. Allergy</topic><topic>Humans</topic><topic>Immunization</topic><topic>Interferon-gamma - analysis</topic><topic>Interleukin-12 - analysis</topic><topic>Interleukin-4 - analysis</topic><topic>Lung - pathology</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Peptide Fragments - administration & dosage</topic><topic>Peptide Fragments - pharmacology</topic><topic>Peptide Fragments - therapeutic use</topic><topic>Pharmacology. Drug treatments</topic><topic>Plethysmography, Whole Body</topic><topic>Pulmonary Surfactant-Associated Protein A - analysis</topic><topic>Pulmonary Surfactant-Associated Protein A - pharmacology</topic><topic>Pulmonary Surfactant-Associated Protein A - therapeutic use</topic><topic>Pulmonary Surfactant-Associated Protein D - administration & dosage</topic><topic>Pulmonary Surfactant-Associated Protein D - analysis</topic><topic>Pulmonary Surfactant-Associated Protein D - chemistry</topic><topic>Pulmonary Surfactant-Associated Protein D - pharmacology</topic><topic>Pulmonary Surfactant-Associated Protein D - therapeutic use</topic><topic>Recombinant Fusion Proteins - administration & dosage</topic><topic>Recombinant Fusion Proteins - pharmacology</topic><topic>Recombinant Fusion Proteins - therapeutic use</topic><topic>Species Specificity</topic><topic>Spleen - chemistry</topic><topic>Spleen - immunology</topic><topic>Spleen - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>STRONG, P.</creatorcontrib><creatorcontrib>REID, K. B. M.</creatorcontrib><creatorcontrib>CLARK, H.</creatorcontrib><collection>Pascal-Francis</collection><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>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical and experimental immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>STRONG, P.</au><au>REID, K. B. M.</au><au>CLARK, H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intranasal delivery of a truncated recombinant human SP‐D is effective at down‐regulating allergic hypersensitivity in mice sensitized to allergens of Aspergillus fumigatus</atitle><jtitle>Clinical and experimental immunology</jtitle><addtitle>Clin Exp Immunol</addtitle><date>2002-10</date><risdate>2002</risdate><volume>130</volume><issue>1</issue><spage>19</spage><epage>24</epage><pages>19-24</pages><issn>0009-9104</issn><eissn>1365-2249</eissn><coden>CEXIAL</coden><abstract>Summary
C57BL/6 mice were sensitized to Aspergillus fumigatus 1‐week culture filtrate, which is rich in the non‐glycosylated allergen Asp f1, a major allergen in allergic bronchopulmonary aspergillosis (ABPA). A comparison of the effect of treatment of allergen challenged mice by intranasal administration of a 60‐kDa truncated recombinant form of human SP‐D (rfhSP‐D) or recombinant full length SP‐A (rhSP‐A) was undertaken. Treatment with rfhSP‐D produced significant reduction in IgE, IgG1 and peripheral blood eosinophilia and treatment with rfhSP‐D, but not rhSP‐A resulted in a significant reduction in airway hyperresponsiveness as measured by whole body plethysmography. Lung histology revealed less peribronchial lymphocytic infiltration in mice treated with rfhSP‐D. Intracellular cytokine staining of spleen homogenates showed increases in IL‐12 and IFN‐γ and decrease in IL‐4. The level of endogenous mouse SP‐D was elevated sixfold in the lungs of sensitized mice and was not affected by treatment with rfhSP‐D. Taken with our previous studies, with a BALB/c mouse model of ABPA using a 3‐week A. fumigatus culture filtrate, the present results show that rfhSP‐D can suppress the development of allergic symptoms in sensitized mice independent of genetic background and using a different preparation of A. fumigatus allergens.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science, Ltd</pub><pmid>12296848</pmid><doi>10.1046/j.1365-2249.2002.01968.x</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ABPA allergy IL‐12 plethysmography SP‐D Administration, Intranasal Allergens - immunology Allergens - toxicity Animal Studies Animals Antibodies, Fungal - biosynthesis Antibodies, Fungal - immunology Antigens, Fungal - immunology Antigens, Fungal - toxicity Antigens, Plant Aspergillosis, Allergic Bronchopulmonary - chemically induced Aspergillosis, Allergic Bronchopulmonary - drug therapy Aspergillosis, Allergic Bronchopulmonary - pathology Aspergillus fumigatus - immunology Biological and medical sciences Bronchial Hyperreactivity - chemically induced Bronchial Hyperreactivity - drug therapy Drug Evaluation, Preclinical Eosinophilia - chemically induced Eosinophilia - drug therapy Female Fungal Proteins - immunology Fungal Proteins - toxicity Histamine and antagonists. Allergy Humans Immunization Interferon-gamma - analysis Interleukin-12 - analysis Interleukin-4 - analysis Lung - pathology Medical sciences Mice Mice, Inbred BALB C Mice, Inbred C57BL Peptide Fragments - administration & dosage Peptide Fragments - pharmacology Peptide Fragments - therapeutic use Pharmacology. Drug treatments Plethysmography, Whole Body Pulmonary Surfactant-Associated Protein A - analysis Pulmonary Surfactant-Associated Protein A - pharmacology Pulmonary Surfactant-Associated Protein A - therapeutic use Pulmonary Surfactant-Associated Protein D - administration & dosage Pulmonary Surfactant-Associated Protein D - analysis Pulmonary Surfactant-Associated Protein D - chemistry Pulmonary Surfactant-Associated Protein D - pharmacology Pulmonary Surfactant-Associated Protein D - therapeutic use Recombinant Fusion Proteins - administration & dosage Recombinant Fusion Proteins - pharmacology Recombinant Fusion Proteins - therapeutic use Species Specificity Spleen - chemistry Spleen - immunology Spleen - pathology |
title | Intranasal delivery of a truncated recombinant human SP‐D is effective at down‐regulating allergic hypersensitivity in mice sensitized to allergens of Aspergillus fumigatus |
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