Loading…
A live‐attenuated pneumococcal vaccine elicits CD 4 + T ‐cell dependent class switching and provides serotype independent protection against acute otitis media
Acute otitis media ( AOM ) caused by Streptococcus pneumoniae remains one of the most common infectious diseases worldwide despite widespread vaccination. A major limitation of the currently licensed pneumococcal vaccines is the lack of efficacy against mucosal disease manifestations such as AOM , a...
Saved in:
Published in: | EMBO molecular medicine 2014-01, Vol.6 (1), p.141-154 |
---|---|
Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c671-88922f956a91d3351abf6a7432f5e1a0d0a2ce19af57fdfc9f81de46cae4b6fc3 |
container_end_page | 154 |
container_issue | 1 |
container_start_page | 141 |
container_title | EMBO molecular medicine |
container_volume | 6 |
creator | Rosch, Jason W Iverson, Amy R Humann, Jessica Mann, Beth Gao, Geli Vogel, Peter Mina, Michael Murrah, Kyle A Perez, Antonia C Edward Swords, W Tuomanen, Elaine I McCullers, Jonathan A |
description | Acute otitis media (
AOM
) caused by
Streptococcus pneumoniae
remains one of the most common infectious diseases worldwide despite widespread vaccination. A major limitation of the currently licensed pneumococcal vaccines is the lack of efficacy against mucosal disease manifestations such as
AOM
, acute bacterial sinusitis and pneumonia. We sought to generate a novel class of live vaccines that (1) retain all major antigenic virulence proteins yet are fully attenuated and (2) protect against otitis media. A live vaccine candidate based on deletion of the signal recognition pathway component
ftsY
induced potent, serotype‐independent protection against otitis media, sinusitis, pneumonia and invasive pneumococcal disease. Protection was maintained in animals coinfected with influenza virus, but was lost if mice were depleted of
CD
4
+
T cells at the time of vaccination. The live vaccine induced a strong serum IgG2a and IgG2b response that correlated with
CD
4
+
T‐cell mediated class switching. Deletion of genes required for microbial adaptation to the host environment is a novel live attenuated vaccine strategy yielding the first experimental vaccine effective against pneumococcal otitis media.
image
Pneumococcal vaccines prevent sepsis and meningitis‐induced diseases but not otitis media, sinusitis, or pneumonia. A novel live genetically attenuated pneumococcal vaccine is shown protective against mucosal infections in mice and chinchilla models.
A novel, live attenuated pneumococcal vaccine was generated by targeting genes required for microbial adaptation to the host environment
The live attenuated vaccine was able to confer effective serotype‐independent protection against pneumococcal acute otitis media in the murine model
The live attenuated vaccine was able to confer effective protection in the chinchilla model of pneumococcal acute otitis media
The live attenuated vaccine induced potent serotype‐independent antibody responses and conferred serotype independent protection against pneumococcal colonization and invasive disease
The live attenuated vaccine induced antibody subtypes distinct from the current conjugate vaccine and these antibody subtypes were dependent upon
CD4
+ T‐cells during vaccination |
doi_str_mv | 10.1002/emmm.201202150 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2289918281</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2289918281</sourcerecordid><originalsourceid>FETCH-LOGICAL-c671-88922f956a91d3351abf6a7432f5e1a0d0a2ce19af57fdfc9f81de46cae4b6fc3</originalsourceid><addsrcrecordid>eNpFkc9OwzAMxisEEjC4crbEEW0kaZu2x2n8lZC47F55jgNBbTqadIgbj8A78GY8CUVD42TL_r7Pln5JcibFTAqhLrlt25kSUgklc7GXHMkiL6aZLrP9XV_ow-Q4hBchdK5leZR8zaFxG_7--MQY2Q8Y2cDa89B21BFhAxskcp6BG0cuBlhcQQYXsITRQ9w0YHjN3rCPQA2GAOHNRXp2_gnQj1l9t3GGxzH3XXxfMzj_7xi3kSm6zgM-ofMhAtIQGbroogvQsnF4khxYbAKf_tVJsry5Xi7upg-Pt_eL-cOUdCGnZVkpZatcYyVNmuYSV1ZjkaXK5ixRGIGKWFZo88IaS5UtpeFME3K20pbSSXK-jR2feh04xPqlG3o_XqyVKqtKlqqUo2q2VVHfhdCzrde9a7F_r6WofznUvxzqHYf0B66pgY8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2289918281</pqid></control><display><type>article</type><title>A live‐attenuated pneumococcal vaccine elicits CD 4 + T ‐cell dependent class switching and provides serotype independent protection against acute otitis media</title><source>PubMed (Medline)</source><source>Wiley-Blackwell Open Access Collection</source><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><creator>Rosch, Jason W ; Iverson, Amy R ; Humann, Jessica ; Mann, Beth ; Gao, Geli ; Vogel, Peter ; Mina, Michael ; Murrah, Kyle A ; Perez, Antonia C ; Edward Swords, W ; Tuomanen, Elaine I ; McCullers, Jonathan A</creator><creatorcontrib>Rosch, Jason W ; Iverson, Amy R ; Humann, Jessica ; Mann, Beth ; Gao, Geli ; Vogel, Peter ; Mina, Michael ; Murrah, Kyle A ; Perez, Antonia C ; Edward Swords, W ; Tuomanen, Elaine I ; McCullers, Jonathan A</creatorcontrib><description>Acute otitis media (
AOM
) caused by
Streptococcus pneumoniae
remains one of the most common infectious diseases worldwide despite widespread vaccination. A major limitation of the currently licensed pneumococcal vaccines is the lack of efficacy against mucosal disease manifestations such as
AOM
, acute bacterial sinusitis and pneumonia. We sought to generate a novel class of live vaccines that (1) retain all major antigenic virulence proteins yet are fully attenuated and (2) protect against otitis media. A live vaccine candidate based on deletion of the signal recognition pathway component
ftsY
induced potent, serotype‐independent protection against otitis media, sinusitis, pneumonia and invasive pneumococcal disease. Protection was maintained in animals coinfected with influenza virus, but was lost if mice were depleted of
CD
4
+
T cells at the time of vaccination. The live vaccine induced a strong serum IgG2a and IgG2b response that correlated with
CD
4
+
T‐cell mediated class switching. Deletion of genes required for microbial adaptation to the host environment is a novel live attenuated vaccine strategy yielding the first experimental vaccine effective against pneumococcal otitis media.
image
Pneumococcal vaccines prevent sepsis and meningitis‐induced diseases but not otitis media, sinusitis, or pneumonia. A novel live genetically attenuated pneumococcal vaccine is shown protective against mucosal infections in mice and chinchilla models.
A novel, live attenuated pneumococcal vaccine was generated by targeting genes required for microbial adaptation to the host environment
The live attenuated vaccine was able to confer effective serotype‐independent protection against pneumococcal acute otitis media in the murine model
The live attenuated vaccine was able to confer effective protection in the chinchilla model of pneumococcal acute otitis media
The live attenuated vaccine induced potent serotype‐independent antibody responses and conferred serotype independent protection against pneumococcal colonization and invasive disease
The live attenuated vaccine induced antibody subtypes distinct from the current conjugate vaccine and these antibody subtypes were dependent upon
CD4
+ T‐cells during vaccination</description><identifier>ISSN: 1757-4676</identifier><identifier>EISSN: 1757-4684</identifier><identifier>DOI: 10.1002/emmm.201202150</identifier><language>eng</language><publisher>Frankfurt: EMBO Press</publisher><subject>Candidates ; CD4 antigen ; Class switching ; Clonal deletion ; Ear diseases ; Experiments ; Gene deletion ; Immunoglobulin G ; Immunoglobulins ; Infectious diseases ; Influenza ; Lymphocytes ; Lymphocytes T ; Meningitis ; Mucosa ; Otitis media ; Pneumonia ; Sepsis ; Sinusitis ; Streptococcus infections ; Vaccines ; Variance analysis ; Virulence</subject><ispartof>EMBO molecular medicine, 2014-01, Vol.6 (1), p.141-154</ispartof><rights>2014. This work is published under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c671-88922f956a91d3351abf6a7432f5e1a0d0a2ce19af57fdfc9f81de46cae4b6fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2289918281/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2289918281?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25731,27901,27902,36989,44566,74869</link.rule.ids></links><search><creatorcontrib>Rosch, Jason W</creatorcontrib><creatorcontrib>Iverson, Amy R</creatorcontrib><creatorcontrib>Humann, Jessica</creatorcontrib><creatorcontrib>Mann, Beth</creatorcontrib><creatorcontrib>Gao, Geli</creatorcontrib><creatorcontrib>Vogel, Peter</creatorcontrib><creatorcontrib>Mina, Michael</creatorcontrib><creatorcontrib>Murrah, Kyle A</creatorcontrib><creatorcontrib>Perez, Antonia C</creatorcontrib><creatorcontrib>Edward Swords, W</creatorcontrib><creatorcontrib>Tuomanen, Elaine I</creatorcontrib><creatorcontrib>McCullers, Jonathan A</creatorcontrib><title>A live‐attenuated pneumococcal vaccine elicits CD 4 + T ‐cell dependent class switching and provides serotype independent protection against acute otitis media</title><title>EMBO molecular medicine</title><description>Acute otitis media (
AOM
) caused by
Streptococcus pneumoniae
remains one of the most common infectious diseases worldwide despite widespread vaccination. A major limitation of the currently licensed pneumococcal vaccines is the lack of efficacy against mucosal disease manifestations such as
AOM
, acute bacterial sinusitis and pneumonia. We sought to generate a novel class of live vaccines that (1) retain all major antigenic virulence proteins yet are fully attenuated and (2) protect against otitis media. A live vaccine candidate based on deletion of the signal recognition pathway component
ftsY
induced potent, serotype‐independent protection against otitis media, sinusitis, pneumonia and invasive pneumococcal disease. Protection was maintained in animals coinfected with influenza virus, but was lost if mice were depleted of
CD
4
+
T cells at the time of vaccination. The live vaccine induced a strong serum IgG2a and IgG2b response that correlated with
CD
4
+
T‐cell mediated class switching. Deletion of genes required for microbial adaptation to the host environment is a novel live attenuated vaccine strategy yielding the first experimental vaccine effective against pneumococcal otitis media.
image
Pneumococcal vaccines prevent sepsis and meningitis‐induced diseases but not otitis media, sinusitis, or pneumonia. A novel live genetically attenuated pneumococcal vaccine is shown protective against mucosal infections in mice and chinchilla models.
A novel, live attenuated pneumococcal vaccine was generated by targeting genes required for microbial adaptation to the host environment
The live attenuated vaccine was able to confer effective serotype‐independent protection against pneumococcal acute otitis media in the murine model
The live attenuated vaccine was able to confer effective protection in the chinchilla model of pneumococcal acute otitis media
The live attenuated vaccine induced potent serotype‐independent antibody responses and conferred serotype independent protection against pneumococcal colonization and invasive disease
The live attenuated vaccine induced antibody subtypes distinct from the current conjugate vaccine and these antibody subtypes were dependent upon
CD4
+ T‐cells during vaccination</description><subject>Candidates</subject><subject>CD4 antigen</subject><subject>Class switching</subject><subject>Clonal deletion</subject><subject>Ear diseases</subject><subject>Experiments</subject><subject>Gene deletion</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulins</subject><subject>Infectious diseases</subject><subject>Influenza</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Meningitis</subject><subject>Mucosa</subject><subject>Otitis media</subject><subject>Pneumonia</subject><subject>Sepsis</subject><subject>Sinusitis</subject><subject>Streptococcus infections</subject><subject>Vaccines</subject><subject>Variance analysis</subject><subject>Virulence</subject><issn>1757-4676</issn><issn>1757-4684</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpFkc9OwzAMxisEEjC4crbEEW0kaZu2x2n8lZC47F55jgNBbTqadIgbj8A78GY8CUVD42TL_r7Pln5JcibFTAqhLrlt25kSUgklc7GXHMkiL6aZLrP9XV_ow-Q4hBchdK5leZR8zaFxG_7--MQY2Q8Y2cDa89B21BFhAxskcp6BG0cuBlhcQQYXsITRQ9w0YHjN3rCPQA2GAOHNRXp2_gnQj1l9t3GGxzH3XXxfMzj_7xi3kSm6zgM-ofMhAtIQGbroogvQsnF4khxYbAKf_tVJsry5Xi7upg-Pt_eL-cOUdCGnZVkpZatcYyVNmuYSV1ZjkaXK5ixRGIGKWFZo88IaS5UtpeFME3K20pbSSXK-jR2feh04xPqlG3o_XqyVKqtKlqqUo2q2VVHfhdCzrde9a7F_r6WofznUvxzqHYf0B66pgY8</recordid><startdate>201401</startdate><enddate>201401</enddate><creator>Rosch, Jason W</creator><creator>Iverson, Amy R</creator><creator>Humann, Jessica</creator><creator>Mann, Beth</creator><creator>Gao, Geli</creator><creator>Vogel, Peter</creator><creator>Mina, Michael</creator><creator>Murrah, Kyle A</creator><creator>Perez, Antonia C</creator><creator>Edward Swords, W</creator><creator>Tuomanen, Elaine I</creator><creator>McCullers, Jonathan A</creator><general>EMBO Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>201401</creationdate><title>A live‐attenuated pneumococcal vaccine elicits CD 4 + T ‐cell dependent class switching and provides serotype independent protection against acute otitis media</title><author>Rosch, Jason W ; Iverson, Amy R ; Humann, Jessica ; Mann, Beth ; Gao, Geli ; Vogel, Peter ; Mina, Michael ; Murrah, Kyle A ; Perez, Antonia C ; Edward Swords, W ; Tuomanen, Elaine I ; McCullers, Jonathan A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c671-88922f956a91d3351abf6a7432f5e1a0d0a2ce19af57fdfc9f81de46cae4b6fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Candidates</topic><topic>CD4 antigen</topic><topic>Class switching</topic><topic>Clonal deletion</topic><topic>Ear diseases</topic><topic>Experiments</topic><topic>Gene deletion</topic><topic>Immunoglobulin G</topic><topic>Immunoglobulins</topic><topic>Infectious diseases</topic><topic>Influenza</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Meningitis</topic><topic>Mucosa</topic><topic>Otitis media</topic><topic>Pneumonia</topic><topic>Sepsis</topic><topic>Sinusitis</topic><topic>Streptococcus infections</topic><topic>Vaccines</topic><topic>Variance analysis</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rosch, Jason W</creatorcontrib><creatorcontrib>Iverson, Amy R</creatorcontrib><creatorcontrib>Humann, Jessica</creatorcontrib><creatorcontrib>Mann, Beth</creatorcontrib><creatorcontrib>Gao, Geli</creatorcontrib><creatorcontrib>Vogel, Peter</creatorcontrib><creatorcontrib>Mina, Michael</creatorcontrib><creatorcontrib>Murrah, Kyle A</creatorcontrib><creatorcontrib>Perez, Antonia C</creatorcontrib><creatorcontrib>Edward Swords, W</creatorcontrib><creatorcontrib>Tuomanen, Elaine I</creatorcontrib><creatorcontrib>McCullers, Jonathan A</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>EMBO molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rosch, Jason W</au><au>Iverson, Amy R</au><au>Humann, Jessica</au><au>Mann, Beth</au><au>Gao, Geli</au><au>Vogel, Peter</au><au>Mina, Michael</au><au>Murrah, Kyle A</au><au>Perez, Antonia C</au><au>Edward Swords, W</au><au>Tuomanen, Elaine I</au><au>McCullers, Jonathan A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A live‐attenuated pneumococcal vaccine elicits CD 4 + T ‐cell dependent class switching and provides serotype independent protection against acute otitis media</atitle><jtitle>EMBO molecular medicine</jtitle><date>2014-01</date><risdate>2014</risdate><volume>6</volume><issue>1</issue><spage>141</spage><epage>154</epage><pages>141-154</pages><issn>1757-4676</issn><eissn>1757-4684</eissn><abstract>Acute otitis media (
AOM
) caused by
Streptococcus pneumoniae
remains one of the most common infectious diseases worldwide despite widespread vaccination. A major limitation of the currently licensed pneumococcal vaccines is the lack of efficacy against mucosal disease manifestations such as
AOM
, acute bacterial sinusitis and pneumonia. We sought to generate a novel class of live vaccines that (1) retain all major antigenic virulence proteins yet are fully attenuated and (2) protect against otitis media. A live vaccine candidate based on deletion of the signal recognition pathway component
ftsY
induced potent, serotype‐independent protection against otitis media, sinusitis, pneumonia and invasive pneumococcal disease. Protection was maintained in animals coinfected with influenza virus, but was lost if mice were depleted of
CD
4
+
T cells at the time of vaccination. The live vaccine induced a strong serum IgG2a and IgG2b response that correlated with
CD
4
+
T‐cell mediated class switching. Deletion of genes required for microbial adaptation to the host environment is a novel live attenuated vaccine strategy yielding the first experimental vaccine effective against pneumococcal otitis media.
image
Pneumococcal vaccines prevent sepsis and meningitis‐induced diseases but not otitis media, sinusitis, or pneumonia. A novel live genetically attenuated pneumococcal vaccine is shown protective against mucosal infections in mice and chinchilla models.
A novel, live attenuated pneumococcal vaccine was generated by targeting genes required for microbial adaptation to the host environment
The live attenuated vaccine was able to confer effective serotype‐independent protection against pneumococcal acute otitis media in the murine model
The live attenuated vaccine was able to confer effective protection in the chinchilla model of pneumococcal acute otitis media
The live attenuated vaccine induced potent serotype‐independent antibody responses and conferred serotype independent protection against pneumococcal colonization and invasive disease
The live attenuated vaccine induced antibody subtypes distinct from the current conjugate vaccine and these antibody subtypes were dependent upon
CD4
+ T‐cells during vaccination</abstract><cop>Frankfurt</cop><pub>EMBO Press</pub><doi>10.1002/emmm.201202150</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1757-4676 |
ispartof | EMBO molecular medicine, 2014-01, Vol.6 (1), p.141-154 |
issn | 1757-4676 1757-4684 |
language | eng |
recordid | cdi_proquest_journals_2289918281 |
source | PubMed (Medline); Wiley-Blackwell Open Access Collection; Publicly Available Content Database (Proquest) (PQ_SDU_P3) |
subjects | Candidates CD4 antigen Class switching Clonal deletion Ear diseases Experiments Gene deletion Immunoglobulin G Immunoglobulins Infectious diseases Influenza Lymphocytes Lymphocytes T Meningitis Mucosa Otitis media Pneumonia Sepsis Sinusitis Streptococcus infections Vaccines Variance analysis Virulence |
title | A live‐attenuated pneumococcal vaccine elicits CD 4 + T ‐cell dependent class switching and provides serotype independent protection against acute otitis media |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T08%3A27%3A21IST&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=A%20live%E2%80%90attenuated%20pneumococcal%20vaccine%20elicits%20CD%204%20+%20T%20%E2%80%90cell%20dependent%20class%20switching%20and%20provides%20serotype%20independent%20protection%20against%20acute%20otitis%20media&rft.jtitle=EMBO%20molecular%20medicine&rft.au=Rosch,%20Jason%20W&rft.date=2014-01&rft.volume=6&rft.issue=1&rft.spage=141&rft.epage=154&rft.pages=141-154&rft.issn=1757-4676&rft.eissn=1757-4684&rft_id=info:doi/10.1002/emmm.201202150&rft_dat=%3Cproquest_cross%3E2289918281%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c671-88922f956a91d3351abf6a7432f5e1a0d0a2ce19af57fdfc9f81de46cae4b6fc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2289918281&rft_id=info:pmid/&rfr_iscdi=true |