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Allergenicity and immunogenicity of the major mugwort pollen allergen Art v 1 chemically modified by acetylation

Summary Background Treating allergies with modified allergens is an approach to make the treatment safer and more efficient. Art v 1 is the most prominent allergen of mugwort pollen and a significant cause of hayfever around Europe. The aim of this study was to reduce the allergenicity of Art v 1 by...

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Published in:Clinical and experimental allergy 2009-03, Vol.39 (3), p.435-446
Main Authors: Perovic, I., Milovanovic, M., Stanic, D., Burazer, L., Petrovic, D., Milcic-Matic, N., Gafvelin, G., Van Hage, M., Jankov, R., Velickovic, T. Cirkovic
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cited_by cdi_FETCH-LOGICAL-c5668-1fbc29e3b65be454e546c94069b05385710eaa71131689406ed11901b13e2ec63
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container_issue 3
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container_title Clinical and experimental allergy
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creator Perovic, I.
Milovanovic, M.
Stanic, D.
Burazer, L.
Petrovic, D.
Milcic-Matic, N.
Gafvelin, G.
Van Hage, M.
Jankov, R.
Velickovic, T. Cirkovic
description Summary Background Treating allergies with modified allergens is an approach to make the treatment safer and more efficient. Art v 1 is the most prominent allergen of mugwort pollen and a significant cause of hayfever around Europe. The aim of this study was to reduce the allergenicity of Art v 1 by acetylation, and to investigate the capacity of the modified protein to generate blocking antibodies. Methods The reduction of allergenicity of Art v 1 following acetylation was monitored by immunoblot, ELISA inhibition using a pool of sera from mugwort pollen allergic patients, basophil activation assay and by skin prick testing of mugwort‐allergic patients. Rabbits were immunized against Art v 1 and acetylated Art v 1 (acArt v 1) and the rabbit antisera were tested for their capacity to block human IgE binding in ELISA. Human T cell proliferation against Art v 1 and acArt v 1 was examined in peripheral blood mononuclear cells (PBMCs) of mugwort pollen allergic patients and cytokine release in PBMC cultures was monitored. Results Acetylation of Art v 1 gave a derivative of reduced allergenicity in the in vitro and ex vivo tests applied. The skin test reactivity to acArt v 1 was significantly reduced in 19 patients when compared with the reactivity to Art v 1. Rabbit antibodies to acArt v 1 and Art v 1 showed similar capacity to block human IgE binding to Art v 1 in inhibition ELISA. Both proteins were able to induce proliferation of PBMCs and CD3/CD4+ cells of mugwort‐allergic patients. Release of IL‐5 was significantly reduced in cultures stimulated with acArt v 1. Conclusions Art v 1 modified by acetylation had a significantly reduced allergenicity in vitro and in vivo, while its immunogenicity was retained. Modification of allergens by acetylation could be a new strategy for allergen‐specific immunotherapy.
doi_str_mv 10.1111/j.1365-2222.2008.03158.x
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Cirkovic</creator><creatorcontrib>Perovic, I. ; Milovanovic, M. ; Stanic, D. ; Burazer, L. ; Petrovic, D. ; Milcic-Matic, N. ; Gafvelin, G. ; Van Hage, M. ; Jankov, R. ; Velickovic, T. Cirkovic</creatorcontrib><description>Summary Background Treating allergies with modified allergens is an approach to make the treatment safer and more efficient. Art v 1 is the most prominent allergen of mugwort pollen and a significant cause of hayfever around Europe. The aim of this study was to reduce the allergenicity of Art v 1 by acetylation, and to investigate the capacity of the modified protein to generate blocking antibodies. Methods The reduction of allergenicity of Art v 1 following acetylation was monitored by immunoblot, ELISA inhibition using a pool of sera from mugwort pollen allergic patients, basophil activation assay and by skin prick testing of mugwort‐allergic patients. Rabbits were immunized against Art v 1 and acetylated Art v 1 (acArt v 1) and the rabbit antisera were tested for their capacity to block human IgE binding in ELISA. Human T cell proliferation against Art v 1 and acArt v 1 was examined in peripheral blood mononuclear cells (PBMCs) of mugwort pollen allergic patients and cytokine release in PBMC cultures was monitored. Results Acetylation of Art v 1 gave a derivative of reduced allergenicity in the in vitro and ex vivo tests applied. The skin test reactivity to acArt v 1 was significantly reduced in 19 patients when compared with the reactivity to Art v 1. Rabbit antibodies to acArt v 1 and Art v 1 showed similar capacity to block human IgE binding to Art v 1 in inhibition ELISA. Both proteins were able to induce proliferation of PBMCs and CD3/CD4+ cells of mugwort‐allergic patients. Release of IL‐5 was significantly reduced in cultures stimulated with acArt v 1. Conclusions Art v 1 modified by acetylation had a significantly reduced allergenicity in vitro and in vivo, while its immunogenicity was retained. Modification of allergens by acetylation could be a new strategy for allergen‐specific immunotherapy.</description><identifier>ISSN: 0954-7894</identifier><identifier>EISSN: 1365-2222</identifier><identifier>DOI: 10.1111/j.1365-2222.2008.03158.x</identifier><identifier>PMID: 19178539</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Acetylation ; Adolescent ; Adult ; allergen-specific immunotherapy ; Allergens - chemistry ; Allergens - immunology ; allergoid ; Animals ; Antibody Formation - immunology ; Antigen-Antibody Reactions - immunology ; Antigens, Plant ; Art v 1 ; Basophil Degranulation Test ; Basophils - immunology ; Binding, Competitive - immunology ; Biological and medical sciences ; blocking antibodies ; Cytokines - metabolism ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Humans ; Hypersensitivity - immunology ; Immunization ; Immunoglobulin E - immunology ; Immunoglobulin G - blood ; Immunoglobulin G - immunology ; Isoelectric Point ; Leukocytes, Mononuclear - cytology ; Leukocytes, Mononuclear - immunology ; Leukocytes, Mononuclear - metabolism ; Male ; Middle Aged ; Molecular Weight ; mugwort pollen allergy ; Plant Proteins - chemistry ; Plant Proteins - immunology ; Pollen - chemistry ; Pollen - immunology ; Rabbits ; Young Adult</subject><ispartof>Clinical and experimental allergy, 2009-03, Vol.39 (3), p.435-446</ispartof><rights>2009 The Authors. Journal compilation © 2009 Blackwell Publishing Ltd</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5668-1fbc29e3b65be454e546c94069b05385710eaa71131689406ed11901b13e2ec63</citedby><cites>FETCH-LOGICAL-c5668-1fbc29e3b65be454e546c94069b05385710eaa71131689406ed11901b13e2ec63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=21119291$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19178539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:118212825$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Perovic, I.</creatorcontrib><creatorcontrib>Milovanovic, M.</creatorcontrib><creatorcontrib>Stanic, D.</creatorcontrib><creatorcontrib>Burazer, L.</creatorcontrib><creatorcontrib>Petrovic, D.</creatorcontrib><creatorcontrib>Milcic-Matic, N.</creatorcontrib><creatorcontrib>Gafvelin, G.</creatorcontrib><creatorcontrib>Van Hage, M.</creatorcontrib><creatorcontrib>Jankov, R.</creatorcontrib><creatorcontrib>Velickovic, T. Cirkovic</creatorcontrib><title>Allergenicity and immunogenicity of the major mugwort pollen allergen Art v 1 chemically modified by acetylation</title><title>Clinical and experimental allergy</title><addtitle>Clin Exp Allergy</addtitle><description>Summary Background Treating allergies with modified allergens is an approach to make the treatment safer and more efficient. Art v 1 is the most prominent allergen of mugwort pollen and a significant cause of hayfever around Europe. The aim of this study was to reduce the allergenicity of Art v 1 by acetylation, and to investigate the capacity of the modified protein to generate blocking antibodies. Methods The reduction of allergenicity of Art v 1 following acetylation was monitored by immunoblot, ELISA inhibition using a pool of sera from mugwort pollen allergic patients, basophil activation assay and by skin prick testing of mugwort‐allergic patients. Rabbits were immunized against Art v 1 and acetylated Art v 1 (acArt v 1) and the rabbit antisera were tested for their capacity to block human IgE binding in ELISA. Human T cell proliferation against Art v 1 and acArt v 1 was examined in peripheral blood mononuclear cells (PBMCs) of mugwort pollen allergic patients and cytokine release in PBMC cultures was monitored. Results Acetylation of Art v 1 gave a derivative of reduced allergenicity in the in vitro and ex vivo tests applied. The skin test reactivity to acArt v 1 was significantly reduced in 19 patients when compared with the reactivity to Art v 1. Rabbit antibodies to acArt v 1 and Art v 1 showed similar capacity to block human IgE binding to Art v 1 in inhibition ELISA. Both proteins were able to induce proliferation of PBMCs and CD3/CD4+ cells of mugwort‐allergic patients. Release of IL‐5 was significantly reduced in cultures stimulated with acArt v 1. Conclusions Art v 1 modified by acetylation had a significantly reduced allergenicity in vitro and in vivo, while its immunogenicity was retained. Modification of allergens by acetylation could be a new strategy for allergen‐specific immunotherapy.</description><subject>Acetylation</subject><subject>Adolescent</subject><subject>Adult</subject><subject>allergen-specific immunotherapy</subject><subject>Allergens - chemistry</subject><subject>Allergens - immunology</subject><subject>allergoid</subject><subject>Animals</subject><subject>Antibody Formation - immunology</subject><subject>Antigen-Antibody Reactions - immunology</subject><subject>Antigens, Plant</subject><subject>Art v 1</subject><subject>Basophil Degranulation Test</subject><subject>Basophils - immunology</subject><subject>Binding, Competitive - immunology</subject><subject>Biological and medical sciences</subject><subject>blocking antibodies</subject><subject>Cytokines - metabolism</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Humans</subject><subject>Hypersensitivity - immunology</subject><subject>Immunization</subject><subject>Immunoglobulin E - immunology</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulin G - immunology</subject><subject>Isoelectric Point</subject><subject>Leukocytes, Mononuclear - cytology</subject><subject>Leukocytes, Mononuclear - immunology</subject><subject>Leukocytes, Mononuclear - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Molecular Weight</subject><subject>mugwort pollen allergy</subject><subject>Plant Proteins - chemistry</subject><subject>Plant Proteins - immunology</subject><subject>Pollen - chemistry</subject><subject>Pollen - immunology</subject><subject>Rabbits</subject><subject>Young Adult</subject><issn>0954-7894</issn><issn>1365-2222</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqNkk1v1DAQhiMEokvhLyBf4JbFH7FjHzisVmUpquBSQOrFcpxJ620SL3HC7v77OmyUHllfPHr9vOOxZ5IEEbwkcX3aLgkTPKVxLSnGcokZ4XJ5eJEs5oOXyQIrnqW5VNlF8iaELcaYcSVfJxdEkVxyphbJblXX0N1D66zrj8i0JXJNM7R-lnyF-gdAjdn6DjXD_d53Pdr5aGuRmcxoFbW_iCD7AI2zUT6ixpeuclCiIqa10B9r0zvfvk1eVaYO8G7aL5OfX65u11_Tmx-b6_XqJrVcCJmSqrBUASsELyDjGfBMWJVhoQrMmeQ5wWBMTggjQo46lIQoTArCgIIV7DJJT3nDHnZDoXeda0x31N44PUmPMQLNRfyXPPIfT_yu838GCL1uXLBQ16YFPwQdi5IYU_FfkOIMUyXoGSBTLGP8DBALyrmMoDyBtvMhdFDNryJYj4Oht3rsvx77P9qk_jcY-hCt76c7hqKB8tk4TUIEPkyACbGBVWda68LM0ZhdUUUi9_nE7V0Nx7ML0Our1Rg998WFHg6z33SPWuQs5_r3942-Vd_u7ta_pN6wJ9LH4sM</recordid><startdate>200903</startdate><enddate>200903</enddate><creator>Perovic, I.</creator><creator>Milovanovic, M.</creator><creator>Stanic, D.</creator><creator>Burazer, L.</creator><creator>Petrovic, D.</creator><creator>Milcic-Matic, N.</creator><creator>Gafvelin, G.</creator><creator>Van Hage, M.</creator><creator>Jankov, R.</creator><creator>Velickovic, T. Cirkovic</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>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope><scope>ADTPV</scope><scope>AOWAS</scope></search><sort><creationdate>200903</creationdate><title>Allergenicity and immunogenicity of the major mugwort pollen allergen Art v 1 chemically modified by acetylation</title><author>Perovic, I. ; Milovanovic, M. ; Stanic, D. ; Burazer, L. ; Petrovic, D. ; Milcic-Matic, N. ; Gafvelin, G. ; Van Hage, M. ; Jankov, R. ; Velickovic, T. Cirkovic</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5668-1fbc29e3b65be454e546c94069b05385710eaa71131689406ed11901b13e2ec63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acetylation</topic><topic>Adolescent</topic><topic>Adult</topic><topic>allergen-specific immunotherapy</topic><topic>Allergens - chemistry</topic><topic>Allergens - immunology</topic><topic>allergoid</topic><topic>Animals</topic><topic>Antibody Formation - immunology</topic><topic>Antigen-Antibody Reactions - immunology</topic><topic>Antigens, Plant</topic><topic>Art v 1</topic><topic>Basophil Degranulation Test</topic><topic>Basophils - immunology</topic><topic>Binding, Competitive - immunology</topic><topic>Biological and medical sciences</topic><topic>blocking antibodies</topic><topic>Cytokines - metabolism</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Humans</topic><topic>Hypersensitivity - immunology</topic><topic>Immunization</topic><topic>Immunoglobulin E - immunology</topic><topic>Immunoglobulin G - blood</topic><topic>Immunoglobulin G - immunology</topic><topic>Isoelectric Point</topic><topic>Leukocytes, Mononuclear - cytology</topic><topic>Leukocytes, Mononuclear - immunology</topic><topic>Leukocytes, Mononuclear - metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Molecular Weight</topic><topic>mugwort pollen allergy</topic><topic>Plant Proteins - chemistry</topic><topic>Plant Proteins - immunology</topic><topic>Pollen - chemistry</topic><topic>Pollen - immunology</topic><topic>Rabbits</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Perovic, I.</creatorcontrib><creatorcontrib>Milovanovic, M.</creatorcontrib><creatorcontrib>Stanic, D.</creatorcontrib><creatorcontrib>Burazer, L.</creatorcontrib><creatorcontrib>Petrovic, D.</creatorcontrib><creatorcontrib>Milcic-Matic, N.</creatorcontrib><creatorcontrib>Gafvelin, G.</creatorcontrib><creatorcontrib>Van Hage, M.</creatorcontrib><creatorcontrib>Jankov, R.</creatorcontrib><creatorcontrib>Velickovic, T. Cirkovic</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>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><jtitle>Clinical and experimental allergy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Perovic, I.</au><au>Milovanovic, M.</au><au>Stanic, D.</au><au>Burazer, L.</au><au>Petrovic, D.</au><au>Milcic-Matic, N.</au><au>Gafvelin, G.</au><au>Van Hage, M.</au><au>Jankov, R.</au><au>Velickovic, T. Cirkovic</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Allergenicity and immunogenicity of the major mugwort pollen allergen Art v 1 chemically modified by acetylation</atitle><jtitle>Clinical and experimental allergy</jtitle><addtitle>Clin Exp Allergy</addtitle><date>2009-03</date><risdate>2009</risdate><volume>39</volume><issue>3</issue><spage>435</spage><epage>446</epage><pages>435-446</pages><issn>0954-7894</issn><eissn>1365-2222</eissn><abstract>Summary Background Treating allergies with modified allergens is an approach to make the treatment safer and more efficient. Art v 1 is the most prominent allergen of mugwort pollen and a significant cause of hayfever around Europe. The aim of this study was to reduce the allergenicity of Art v 1 by acetylation, and to investigate the capacity of the modified protein to generate blocking antibodies. Methods The reduction of allergenicity of Art v 1 following acetylation was monitored by immunoblot, ELISA inhibition using a pool of sera from mugwort pollen allergic patients, basophil activation assay and by skin prick testing of mugwort‐allergic patients. Rabbits were immunized against Art v 1 and acetylated Art v 1 (acArt v 1) and the rabbit antisera were tested for their capacity to block human IgE binding in ELISA. Human T cell proliferation against Art v 1 and acArt v 1 was examined in peripheral blood mononuclear cells (PBMCs) of mugwort pollen allergic patients and cytokine release in PBMC cultures was monitored. Results Acetylation of Art v 1 gave a derivative of reduced allergenicity in the in vitro and ex vivo tests applied. The skin test reactivity to acArt v 1 was significantly reduced in 19 patients when compared with the reactivity to Art v 1. Rabbit antibodies to acArt v 1 and Art v 1 showed similar capacity to block human IgE binding to Art v 1 in inhibition ELISA. Both proteins were able to induce proliferation of PBMCs and CD3/CD4+ cells of mugwort‐allergic patients. Release of IL‐5 was significantly reduced in cultures stimulated with acArt v 1. Conclusions Art v 1 modified by acetylation had a significantly reduced allergenicity in vitro and in vivo, while its immunogenicity was retained. Modification of allergens by acetylation could be a new strategy for allergen‐specific immunotherapy.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19178539</pmid><doi>10.1111/j.1365-2222.2008.03158.x</doi><tpages>12</tpages></addata></record>
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subjects Acetylation
Adolescent
Adult
allergen-specific immunotherapy
Allergens - chemistry
Allergens - immunology
allergoid
Animals
Antibody Formation - immunology
Antigen-Antibody Reactions - immunology
Antigens, Plant
Art v 1
Basophil Degranulation Test
Basophils - immunology
Binding, Competitive - immunology
Biological and medical sciences
blocking antibodies
Cytokines - metabolism
Female
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Humans
Hypersensitivity - immunology
Immunization
Immunoglobulin E - immunology
Immunoglobulin G - blood
Immunoglobulin G - immunology
Isoelectric Point
Leukocytes, Mononuclear - cytology
Leukocytes, Mononuclear - immunology
Leukocytes, Mononuclear - metabolism
Male
Middle Aged
Molecular Weight
mugwort pollen allergy
Plant Proteins - chemistry
Plant Proteins - immunology
Pollen - chemistry
Pollen - immunology
Rabbits
Young Adult
title Allergenicity and immunogenicity of the major mugwort pollen allergen Art v 1 chemically modified by acetylation
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