Avian glycan-specific IgM monoclonal antibodies for the detection and quantitation of type A and B haemagglutinins in egg-derived influenza vaccines
► Two Mabs which are of particular interest to detect and quantify HA in egg influenza vaccines were characterised. ► Two ELISAs were set up, one is strain specific, the other is a universal influenza ELISA. ► These ELISAs are of particular interest for the quantitation of HA in egg-grown pandemic a...
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creator | Legastelois, Isabelle Chevalier, Michel Bernard, Marie-Clotilde de Montfort, Aymeric Fouque, Martine Pilloud, Alexandra Serraille, Christelle Devard, Nicolas Engel, Olivier Sodoyer, Régis Moste, Catherine |
description | ► Two Mabs which are of particular interest to detect and quantify HA in egg influenza vaccines were characterised. ► Two ELISAs were set up, one is strain specific, the other is a universal influenza ELISA. ► These ELISAs are of particular interest for the quantitation of HA in egg-grown pandemic and seasonal vaccines.
Two IgM monoclonal antibodies (MAbs), Y6F5 and Y13F9, were selected during a screening of clones obtained immunising BALB/c mice with purified envelop proteins of the A/Sydney/5/97 (H3N2) IVR108 influenza strain. These MAbs recognised avian glycans on the haemagglutinin (HA) of the virus. This broad recognition allowed these MAbs to be used as enzyme-labelled secondary antibody reagents in a strain specific enzyme-linked immunosorbent assay (ELISA) in combination with a capture MAb that recognised and allowed the quantitation of the strain specific HA protein present in an egg-produced influenza vaccine. Advantage was taken of these MAbs to develop a universal ELISA in which the MAbs were used both as capture antibody and as enzyme-labelled secondary antibody to detect and quantify the HA protein of any egg-derived influenza vaccine. These avian-glycan specific IgM MAbs may prove to be particularly useful for determining the HA concentration in monovalent egg-derived pandemic influenza vaccines, in which the HA concentration may be lower than 5μg/ml. The HA detection limit in the ELISA assays developed in this study was 1.9μg/ml, as opposed to the 5μg/ml quantitation limit generally accepted for the standard single-radial-immunodiffusion (SRID) assay, the approved technique for quantifying HA content in influenza vaccines. These ELISAs can also be used to quantify influenza HA formulated with emulsion-based or mineral salt adjuvants that could interfere with HA measurement by the SRID assay. |
doi_str_mv | 10.1016/j.jviromet.2011.08.027 |
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Two IgM monoclonal antibodies (MAbs), Y6F5 and Y13F9, were selected during a screening of clones obtained immunising BALB/c mice with purified envelop proteins of the A/Sydney/5/97 (H3N2) IVR108 influenza strain. These MAbs recognised avian glycans on the haemagglutinin (HA) of the virus. This broad recognition allowed these MAbs to be used as enzyme-labelled secondary antibody reagents in a strain specific enzyme-linked immunosorbent assay (ELISA) in combination with a capture MAb that recognised and allowed the quantitation of the strain specific HA protein present in an egg-produced influenza vaccine. Advantage was taken of these MAbs to develop a universal ELISA in which the MAbs were used both as capture antibody and as enzyme-labelled secondary antibody to detect and quantify the HA protein of any egg-derived influenza vaccine. These avian-glycan specific IgM MAbs may prove to be particularly useful for determining the HA concentration in monovalent egg-derived pandemic influenza vaccines, in which the HA concentration may be lower than 5μg/ml. The HA detection limit in the ELISA assays developed in this study was 1.9μg/ml, as opposed to the 5μg/ml quantitation limit generally accepted for the standard single-radial-immunodiffusion (SRID) assay, the approved technique for quantifying HA content in influenza vaccines. These ELISAs can also be used to quantify influenza HA formulated with emulsion-based or mineral salt adjuvants that could interfere with HA measurement by the SRID assay.</description><identifier>ISSN: 0166-0934</identifier><identifier>EISSN: 1879-0984</identifier><identifier>DOI: 10.1016/j.jviromet.2011.08.027</identifier><identifier>PMID: 21907241</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>adjuvants ; Animals ; Antibodies, Monoclonal ; Antigens, Viral - analysis ; Antigens, Viral - immunology ; birds ; clones ; detection limit ; ELISA ; enzyme-linked immunosorbent assay ; Enzyme-Linked Immunosorbent Assay - methods ; Hemagglutinin Glycoproteins, Influenza Virus - analysis ; Hemagglutinin Glycoproteins, Influenza Virus - immunology ; hemagglutinins ; IgM ; Immunodiffusion - methods ; Immunoglobulin M ; Influenza ; Influenza A virus - growth & development ; Influenza A virus - immunology ; Influenza Vaccines - chemistry ; Influenza Vaccines - immunology ; Mice ; Mice, Inbred BALB C ; Monoclonal antibodies ; pandemic ; polysaccharides ; Polysaccharides - immunology ; screening ; SRID ; Universal influenza reagent ; vaccines ; viruses</subject><ispartof>Journal of virological methods, 2011-12, Vol.178 (1-2), p.129-136</ispartof><rights>2011 Elsevier B.V.</rights><rights>Copyright © 2011 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-c42c2af55870fe8835328ba61b91e11e0da739903b54ce4450befc0e18b82c033</citedby><cites>FETCH-LOGICAL-c423t-c42c2af55870fe8835328ba61b91e11e0da739903b54ce4450befc0e18b82c033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jviromet.2011.08.027$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21907241$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Legastelois, Isabelle</creatorcontrib><creatorcontrib>Chevalier, Michel</creatorcontrib><creatorcontrib>Bernard, Marie-Clotilde</creatorcontrib><creatorcontrib>de Montfort, Aymeric</creatorcontrib><creatorcontrib>Fouque, Martine</creatorcontrib><creatorcontrib>Pilloud, Alexandra</creatorcontrib><creatorcontrib>Serraille, Christelle</creatorcontrib><creatorcontrib>Devard, Nicolas</creatorcontrib><creatorcontrib>Engel, Olivier</creatorcontrib><creatorcontrib>Sodoyer, Régis</creatorcontrib><creatorcontrib>Moste, Catherine</creatorcontrib><title>Avian glycan-specific IgM monoclonal antibodies for the detection and quantitation of type A and B haemagglutinins in egg-derived influenza vaccines</title><title>Journal of virological methods</title><addtitle>J Virol Methods</addtitle><description>► Two Mabs which are of particular interest to detect and quantify HA in egg influenza vaccines were characterised. ► Two ELISAs were set up, one is strain specific, the other is a universal influenza ELISA. ► These ELISAs are of particular interest for the quantitation of HA in egg-grown pandemic and seasonal vaccines.
Two IgM monoclonal antibodies (MAbs), Y6F5 and Y13F9, were selected during a screening of clones obtained immunising BALB/c mice with purified envelop proteins of the A/Sydney/5/97 (H3N2) IVR108 influenza strain. These MAbs recognised avian glycans on the haemagglutinin (HA) of the virus. This broad recognition allowed these MAbs to be used as enzyme-labelled secondary antibody reagents in a strain specific enzyme-linked immunosorbent assay (ELISA) in combination with a capture MAb that recognised and allowed the quantitation of the strain specific HA protein present in an egg-produced influenza vaccine. Advantage was taken of these MAbs to develop a universal ELISA in which the MAbs were used both as capture antibody and as enzyme-labelled secondary antibody to detect and quantify the HA protein of any egg-derived influenza vaccine. These avian-glycan specific IgM MAbs may prove to be particularly useful for determining the HA concentration in monovalent egg-derived pandemic influenza vaccines, in which the HA concentration may be lower than 5μg/ml. The HA detection limit in the ELISA assays developed in this study was 1.9μg/ml, as opposed to the 5μg/ml quantitation limit generally accepted for the standard single-radial-immunodiffusion (SRID) assay, the approved technique for quantifying HA content in influenza vaccines. These ELISAs can also be used to quantify influenza HA formulated with emulsion-based or mineral salt adjuvants that could interfere with HA measurement by the SRID assay.</description><subject>adjuvants</subject><subject>Animals</subject><subject>Antibodies, Monoclonal</subject><subject>Antigens, Viral - analysis</subject><subject>Antigens, Viral - immunology</subject><subject>birds</subject><subject>clones</subject><subject>detection limit</subject><subject>ELISA</subject><subject>enzyme-linked immunosorbent assay</subject><subject>Enzyme-Linked Immunosorbent Assay - methods</subject><subject>Hemagglutinin Glycoproteins, Influenza Virus - analysis</subject><subject>Hemagglutinin Glycoproteins, Influenza Virus - immunology</subject><subject>hemagglutinins</subject><subject>IgM</subject><subject>Immunodiffusion - methods</subject><subject>Immunoglobulin M</subject><subject>Influenza</subject><subject>Influenza A virus - growth & development</subject><subject>Influenza A virus - immunology</subject><subject>Influenza Vaccines - chemistry</subject><subject>Influenza Vaccines - immunology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Monoclonal antibodies</subject><subject>pandemic</subject><subject>polysaccharides</subject><subject>Polysaccharides - immunology</subject><subject>screening</subject><subject>SRID</subject><subject>Universal influenza reagent</subject><subject>vaccines</subject><subject>viruses</subject><issn>0166-0934</issn><issn>1879-0984</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAQgC0EosvCXyi-cUoYx3k4N5aKR6UiDtCz5TiT1KvE3trOSsvv4AfjdFuuvfg138xY8xFyySBnwOqP-3x_NN7NGPMCGMtB5FA0L8iGiabNoBXlS7JJYJ3OvLwgb0LYA0DVcP6aXBSshaYo2Yb83R2NsnScTlrZLBxQm8Foej3-oLOzTk_OqokqG03neoOBDs7TeIe0x4g6GmdTsKf3y4pE9fDgBhpPB6S7h9BneqdwVuM4LdFYYwM1luI4Zj16c8Q-XYdpQftH0aPS2lgMb8mrQU0B3z3uW3L79cvvq-_Zzc9v11e7m0yXBY_rqgs1VJVoYEAheMUL0amadS1DxhB61fC2Bd5VpcayrKDDQQMy0YlCA-db8uFc9-Dd_YIhytkEjdOkLLolyJYxVkEL8DwJUPO2TrPekvpMau9C8DjIgzez8ifJQK7q5F4-qZOrOglCJnUp8fKxxdLN2P9Pe3KVgPdnYFBOqtGbIG9_pQp18rp2rhLx6UxgGtrRoJdBG7Qae-OTLNk789wv_gF2L7lM</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Legastelois, Isabelle</creator><creator>Chevalier, Michel</creator><creator>Bernard, Marie-Clotilde</creator><creator>de Montfort, Aymeric</creator><creator>Fouque, Martine</creator><creator>Pilloud, Alexandra</creator><creator>Serraille, Christelle</creator><creator>Devard, Nicolas</creator><creator>Engel, Olivier</creator><creator>Sodoyer, Régis</creator><creator>Moste, Catherine</creator><general>Elsevier B.V</general><scope>FBQ</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>7X8</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>20111201</creationdate><title>Avian glycan-specific IgM monoclonal antibodies for the detection and quantitation of type A and B haemagglutinins in egg-derived influenza vaccines</title><author>Legastelois, Isabelle ; Chevalier, Michel ; Bernard, Marie-Clotilde ; de Montfort, Aymeric ; Fouque, Martine ; Pilloud, Alexandra ; Serraille, Christelle ; Devard, Nicolas ; Engel, Olivier ; Sodoyer, Régis ; Moste, Catherine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-c42c2af55870fe8835328ba61b91e11e0da739903b54ce4450befc0e18b82c033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>adjuvants</topic><topic>Animals</topic><topic>Antibodies, Monoclonal</topic><topic>Antigens, Viral - analysis</topic><topic>Antigens, Viral - immunology</topic><topic>birds</topic><topic>clones</topic><topic>detection limit</topic><topic>ELISA</topic><topic>enzyme-linked immunosorbent assay</topic><topic>Enzyme-Linked Immunosorbent Assay - methods</topic><topic>Hemagglutinin Glycoproteins, Influenza Virus - analysis</topic><topic>Hemagglutinin Glycoproteins, Influenza Virus - immunology</topic><topic>hemagglutinins</topic><topic>IgM</topic><topic>Immunodiffusion - methods</topic><topic>Immunoglobulin M</topic><topic>Influenza</topic><topic>Influenza A virus - growth & development</topic><topic>Influenza A virus - immunology</topic><topic>Influenza Vaccines - chemistry</topic><topic>Influenza Vaccines - immunology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Monoclonal antibodies</topic><topic>pandemic</topic><topic>polysaccharides</topic><topic>Polysaccharides - immunology</topic><topic>screening</topic><topic>SRID</topic><topic>Universal influenza reagent</topic><topic>vaccines</topic><topic>viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Legastelois, Isabelle</creatorcontrib><creatorcontrib>Chevalier, Michel</creatorcontrib><creatorcontrib>Bernard, Marie-Clotilde</creatorcontrib><creatorcontrib>de Montfort, Aymeric</creatorcontrib><creatorcontrib>Fouque, Martine</creatorcontrib><creatorcontrib>Pilloud, Alexandra</creatorcontrib><creatorcontrib>Serraille, Christelle</creatorcontrib><creatorcontrib>Devard, Nicolas</creatorcontrib><creatorcontrib>Engel, Olivier</creatorcontrib><creatorcontrib>Sodoyer, Régis</creatorcontrib><creatorcontrib>Moste, Catherine</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal of virological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Legastelois, Isabelle</au><au>Chevalier, Michel</au><au>Bernard, Marie-Clotilde</au><au>de Montfort, Aymeric</au><au>Fouque, Martine</au><au>Pilloud, Alexandra</au><au>Serraille, Christelle</au><au>Devard, Nicolas</au><au>Engel, Olivier</au><au>Sodoyer, Régis</au><au>Moste, Catherine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Avian glycan-specific IgM monoclonal antibodies for the detection and quantitation of type A and B haemagglutinins in egg-derived influenza vaccines</atitle><jtitle>Journal of virological methods</jtitle><addtitle>J Virol Methods</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>178</volume><issue>1-2</issue><spage>129</spage><epage>136</epage><pages>129-136</pages><issn>0166-0934</issn><eissn>1879-0984</eissn><abstract>► Two Mabs which are of particular interest to detect and quantify HA in egg influenza vaccines were characterised. ► Two ELISAs were set up, one is strain specific, the other is a universal influenza ELISA. ► These ELISAs are of particular interest for the quantitation of HA in egg-grown pandemic and seasonal vaccines.
Two IgM monoclonal antibodies (MAbs), Y6F5 and Y13F9, were selected during a screening of clones obtained immunising BALB/c mice with purified envelop proteins of the A/Sydney/5/97 (H3N2) IVR108 influenza strain. These MAbs recognised avian glycans on the haemagglutinin (HA) of the virus. This broad recognition allowed these MAbs to be used as enzyme-labelled secondary antibody reagents in a strain specific enzyme-linked immunosorbent assay (ELISA) in combination with a capture MAb that recognised and allowed the quantitation of the strain specific HA protein present in an egg-produced influenza vaccine. Advantage was taken of these MAbs to develop a universal ELISA in which the MAbs were used both as capture antibody and as enzyme-labelled secondary antibody to detect and quantify the HA protein of any egg-derived influenza vaccine. These avian-glycan specific IgM MAbs may prove to be particularly useful for determining the HA concentration in monovalent egg-derived pandemic influenza vaccines, in which the HA concentration may be lower than 5μg/ml. The HA detection limit in the ELISA assays developed in this study was 1.9μg/ml, as opposed to the 5μg/ml quantitation limit generally accepted for the standard single-radial-immunodiffusion (SRID) assay, the approved technique for quantifying HA content in influenza vaccines. These ELISAs can also be used to quantify influenza HA formulated with emulsion-based or mineral salt adjuvants that could interfere with HA measurement by the SRID assay.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>21907241</pmid><doi>10.1016/j.jviromet.2011.08.027</doi><tpages>8</tpages></addata></record> |
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subjects | adjuvants Animals Antibodies, Monoclonal Antigens, Viral - analysis Antigens, Viral - immunology birds clones detection limit ELISA enzyme-linked immunosorbent assay Enzyme-Linked Immunosorbent Assay - methods Hemagglutinin Glycoproteins, Influenza Virus - analysis Hemagglutinin Glycoproteins, Influenza Virus - immunology hemagglutinins IgM Immunodiffusion - methods Immunoglobulin M Influenza Influenza A virus - growth & development Influenza A virus - immunology Influenza Vaccines - chemistry Influenza Vaccines - immunology Mice Mice, Inbred BALB C Monoclonal antibodies pandemic polysaccharides Polysaccharides - immunology screening SRID Universal influenza reagent vaccines viruses |
title | Avian glycan-specific IgM monoclonal antibodies for the detection and quantitation of type A and B haemagglutinins in egg-derived influenza vaccines |
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