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An evaluation of the emerging vaccines and immunotherapy against staphylococcal pneumonia in children
Staphylococcus aureus is a commensal of human skin and nares. It is also one of the leading nosocomial pathogens in both developed and developing countries and is responsible for a wide range of life threatening infections, especially in patients who are immunocompromised, post-surgery, undergoing h...
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Published in: | BMC public health 2011-04, Vol.11 Suppl 3 (S3), p.S27-S27, Article S27 |
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description | Staphylococcus aureus is a commensal of human skin and nares. It is also one of the leading nosocomial pathogens in both developed and developing countries and is responsible for a wide range of life threatening infections, especially in patients who are immunocompromised, post-surgery, undergoing haemodialysis and those who are treated with catheters and ventilators. Over the past two decades, the incidence of nosocomial staphylococcal infections has increased dramatically. Currently there are at least seven vaccine and immunotherapy candidates against S. aureus in the developmental phase targeting both active and passive immunization.
We used a modified CHNRI methodology for setting priorities in health research investments. This was done in two stages. In Stage I, we systematically reviewed the literature related to emerging vaccines against Staphylococcus aureus relevant to several criteria of interest: answerability; cost of development, production and implementation; efficacy and effectiveness; deliverability, affordability and sustainability; maximum potential impact on disease burden reduction; acceptability to the end users and health workers; and effect on equity. In Stage II, we conducted an expert opinion exercise by inviting 20 experts (leading basic scientists, international public health researchers, international policy makers and representatives of pharmaceutical companies) to participate. The policy makers and industry representatives accepted our invitation on the condition of anonymity, due to sensitive nature of their involvement in such exercises. They answered questions from CHNRI framework and their "collective optimism" towards each criterion was documented on a scale from 0 to 100%.
The panel of experts expressed low levels of optimism (score around or below 50%) on the criteria of answerability, efficacy, maximum disease burden reduction potential, low cost of production, low cost of implementation and affordability; moderate levels of optimism (scores around 60 to 80%) that these vaccines could be developed at a low cost, and thus on the deliverability, sustainability and impact on equity; and high levels of optimism (scores above 80%) regarding acceptable of such a product to both the end-users and health workers. While assessing the candidates for passive immunization against S.aureus, the experts were poorly optimistic regarding low production cost, low implementation cost, efficacy, deliverability, sustainability, affordabil |
doi_str_mv | 10.1186/1471-2458-11-S3-S27 |
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We used a modified CHNRI methodology for setting priorities in health research investments. This was done in two stages. In Stage I, we systematically reviewed the literature related to emerging vaccines against Staphylococcus aureus relevant to several criteria of interest: answerability; cost of development, production and implementation; efficacy and effectiveness; deliverability, affordability and sustainability; maximum potential impact on disease burden reduction; acceptability to the end users and health workers; and effect on equity. In Stage II, we conducted an expert opinion exercise by inviting 20 experts (leading basic scientists, international public health researchers, international policy makers and representatives of pharmaceutical companies) to participate. The policy makers and industry representatives accepted our invitation on the condition of anonymity, due to sensitive nature of their involvement in such exercises. They answered questions from CHNRI framework and their "collective optimism" towards each criterion was documented on a scale from 0 to 100%.
The panel of experts expressed low levels of optimism (score around or below 50%) on the criteria of answerability, efficacy, maximum disease burden reduction potential, low cost of production, low cost of implementation and affordability; moderate levels of optimism (scores around 60 to 80%) that these vaccines could be developed at a low cost, and thus on the deliverability, sustainability and impact on equity; and high levels of optimism (scores above 80%) regarding acceptable of such a product to both the end-users and health workers. While assessing the candidates for passive immunization against S.aureus, the experts were poorly optimistic regarding low production cost, low implementation cost, efficacy, deliverability, sustainability, affordability and equity; moderately optimistic regarding answerability and acceptability to health workers and end-users. They were of the opinion that these interventions would have only a modest impact (3 to 5%) on the burden of childhood pneumonia. .
In order to provide an effective vaccine against S. aureus, a number of unresolved issues in vaccine development relating to optimal antigenic target identification, criteria for acceptable efficacy, identification of target population, commercial development limitations, optimal timing of immunization strategy, storage, cold chain requirements and cost need to be addressed properly. There is still a great deal unknown about the complex interaction between S. aureus and the human host. However, given the nature of S. aureus and the lessons learned from the recent failure of two emerging vaccines, it is clear that a multi-component vaccine is essential. Combating only one virulence factor is not sufficient in the human host but finding the right combination of factors will be very challenging.</description><identifier>ISSN: 1471-2458</identifier><identifier>EISSN: 1471-2458</identifier><identifier>DOI: 10.1186/1471-2458-11-S3-S27</identifier><identifier>PMID: 21501445</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Bacteria ; Child ; Humans ; Immunization ; Immunotherapy ; Medical research ; Pneumonia, Staphylococcal - prevention & control ; Pneumonia, Staphylococcal - therapy ; Randomized Controlled Trials as Topic ; Staphylococcal Vaccines - supply & distribution ; Staphylococcus aureus - immunology ; Staphylococcus infections ; Streptococcus infections ; Treatment Outcome ; Vaccines</subject><ispartof>BMC public health, 2011-04, Vol.11 Suppl 3 (S3), p.S27-S27, Article S27</ispartof><rights>2011 Huda et al; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright ©2011 Huda et al; licensee BioMed Central Ltd. 2011 Huda et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b560t-858319d23f61270e40000cffa7f1b0a4c473167d39723967bb7a233261ee46b03</citedby><cites>FETCH-LOGICAL-b560t-858319d23f61270e40000cffa7f1b0a4c473167d39723967bb7a233261ee46b03</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/PMC3239838/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/902199134?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21501445$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huda, Tanvir</creatorcontrib><creatorcontrib>Nair, Harish</creatorcontrib><creatorcontrib>Theodoratou, Evropi</creatorcontrib><creatorcontrib>Zgaga, Lina</creatorcontrib><creatorcontrib>Fattom, Ali</creatorcontrib><creatorcontrib>El Arifeen, Shams</creatorcontrib><creatorcontrib>Rubens, Craig</creatorcontrib><creatorcontrib>Campbell, Harry</creatorcontrib><creatorcontrib>Rudan, Igor</creatorcontrib><title>An evaluation of the emerging vaccines and immunotherapy against staphylococcal pneumonia in children</title><title>BMC public health</title><addtitle>BMC Public Health</addtitle><description>Staphylococcus aureus is a commensal of human skin and nares. It is also one of the leading nosocomial pathogens in both developed and developing countries and is responsible for a wide range of life threatening infections, especially in patients who are immunocompromised, post-surgery, undergoing haemodialysis and those who are treated with catheters and ventilators. Over the past two decades, the incidence of nosocomial staphylococcal infections has increased dramatically. Currently there are at least seven vaccine and immunotherapy candidates against S. aureus in the developmental phase targeting both active and passive immunization.
We used a modified CHNRI methodology for setting priorities in health research investments. This was done in two stages. In Stage I, we systematically reviewed the literature related to emerging vaccines against Staphylococcus aureus relevant to several criteria of interest: answerability; cost of development, production and implementation; efficacy and effectiveness; deliverability, affordability and sustainability; maximum potential impact on disease burden reduction; acceptability to the end users and health workers; and effect on equity. In Stage II, we conducted an expert opinion exercise by inviting 20 experts (leading basic scientists, international public health researchers, international policy makers and representatives of pharmaceutical companies) to participate. The policy makers and industry representatives accepted our invitation on the condition of anonymity, due to sensitive nature of their involvement in such exercises. They answered questions from CHNRI framework and their "collective optimism" towards each criterion was documented on a scale from 0 to 100%.
The panel of experts expressed low levels of optimism (score around or below 50%) on the criteria of answerability, efficacy, maximum disease burden reduction potential, low cost of production, low cost of implementation and affordability; moderate levels of optimism (scores around 60 to 80%) that these vaccines could be developed at a low cost, and thus on the deliverability, sustainability and impact on equity; and high levels of optimism (scores above 80%) regarding acceptable of such a product to both the end-users and health workers. While assessing the candidates for passive immunization against S.aureus, the experts were poorly optimistic regarding low production cost, low implementation cost, efficacy, deliverability, sustainability, affordability and equity; moderately optimistic regarding answerability and acceptability to health workers and end-users. They were of the opinion that these interventions would have only a modest impact (3 to 5%) on the burden of childhood pneumonia. .
In order to provide an effective vaccine against S. aureus, a number of unresolved issues in vaccine development relating to optimal antigenic target identification, criteria for acceptable efficacy, identification of target population, commercial development limitations, optimal timing of immunization strategy, storage, cold chain requirements and cost need to be addressed properly. There is still a great deal unknown about the complex interaction between S. aureus and the human host. However, given the nature of S. aureus and the lessons learned from the recent failure of two emerging vaccines, it is clear that a multi-component vaccine is essential. Combating only one virulence factor is not sufficient in the human host but finding the right combination of factors will be very challenging.</description><subject>Bacteria</subject><subject>Child</subject><subject>Humans</subject><subject>Immunization</subject><subject>Immunotherapy</subject><subject>Medical research</subject><subject>Pneumonia, Staphylococcal - prevention & control</subject><subject>Pneumonia, Staphylococcal - therapy</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Staphylococcal Vaccines - supply & distribution</subject><subject>Staphylococcus aureus - immunology</subject><subject>Staphylococcus infections</subject><subject>Streptococcus infections</subject><subject>Treatment Outcome</subject><subject>Vaccines</subject><issn>1471-2458</issn><issn>1471-2458</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kl2L1DAUhoso7rr6CwQJ3nhVzUnSpLkRlsXVhQUvRq_DaZp2MrTJmLQD8--346zDjrC5STjnzcN7PoriPdDPALX8AkJByURVlwDlipcrpl4Ul6foyyfvi-JNzhtKQdUVe11cMKgoCFFdFu46ELfDYcbJx0BiR6a1I250qfehJzu01geXCYaW-HGcQ1zyCbd7gj36kCeSJ9yu90O00VocyDa4eYzBI_GB2LUf2uTC2-JVh0N27x7vq-L37bdfNz_K-5_f726u78umknQq66rmoFvGOwlMUSfocmzXoeqgoSisUBykarlWjGupmkYh45xJcE7IhvKr4u7IbSNuzDb5EdPeRPTmbyCm3mCavB2cqVXHZNXSptONECg1gkMJVNhaMa3dwvp6ZG3nZnStdWFKOJxBzzPBr00fd4Yv3mpeL4DbI6Dx8RnAecbG0RxGZg4jMwBmxc0y1AX06dFJin9mlycz-mzdMGBwcc6mlgI0cH2o_-N_yk2cU1habjRloBeVWET8KLIp5pxcd7IE1Bw26xkTH5624_Tn3yrxB3yoyrc</recordid><startdate>20110413</startdate><enddate>20110413</enddate><creator>Huda, Tanvir</creator><creator>Nair, Harish</creator><creator>Theodoratou, Evropi</creator><creator>Zgaga, Lina</creator><creator>Fattom, Ali</creator><creator>El Arifeen, Shams</creator><creator>Rubens, Craig</creator><creator>Campbell, Harry</creator><creator>Rudan, Igor</creator><general>BioMed Central</general><general>BioMed Central Ltd</general><general>BMC</general><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>7T2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>M0S</scope><scope>M1P</scope><scope>M7S</scope><scope>PATMY</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20110413</creationdate><title>An evaluation of the emerging vaccines and immunotherapy against staphylococcal pneumonia in children</title><author>Huda, Tanvir ; Nair, Harish ; Theodoratou, Evropi ; Zgaga, Lina ; Fattom, Ali ; El Arifeen, Shams ; Rubens, Craig ; Campbell, Harry ; Rudan, Igor</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b560t-858319d23f61270e40000cffa7f1b0a4c473167d39723967bb7a233261ee46b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Bacteria</topic><topic>Child</topic><topic>Humans</topic><topic>Immunization</topic><topic>Immunotherapy</topic><topic>Medical research</topic><topic>Pneumonia, Staphylococcal - prevention & control</topic><topic>Pneumonia, Staphylococcal - therapy</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Staphylococcal Vaccines - supply & distribution</topic><topic>Staphylococcus aureus - immunology</topic><topic>Staphylococcus infections</topic><topic>Streptococcus infections</topic><topic>Treatment Outcome</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huda, Tanvir</creatorcontrib><creatorcontrib>Nair, Harish</creatorcontrib><creatorcontrib>Theodoratou, Evropi</creatorcontrib><creatorcontrib>Zgaga, Lina</creatorcontrib><creatorcontrib>Fattom, Ali</creatorcontrib><creatorcontrib>El Arifeen, Shams</creatorcontrib><creatorcontrib>Rubens, Craig</creatorcontrib><creatorcontrib>Campbell, Harry</creatorcontrib><creatorcontrib>Rudan, Igor</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>British Nursing Database</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</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 (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Engineering Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Engineering Database</collection><collection>Environmental Science Database</collection><collection>ProQuest - Publicly Available Content Database</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><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC public health</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huda, Tanvir</au><au>Nair, Harish</au><au>Theodoratou, Evropi</au><au>Zgaga, Lina</au><au>Fattom, Ali</au><au>El Arifeen, Shams</au><au>Rubens, Craig</au><au>Campbell, Harry</au><au>Rudan, Igor</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An evaluation of the emerging vaccines and immunotherapy against staphylococcal pneumonia in children</atitle><jtitle>BMC public health</jtitle><addtitle>BMC Public Health</addtitle><date>2011-04-13</date><risdate>2011</risdate><volume>11 Suppl 3</volume><issue>S3</issue><spage>S27</spage><epage>S27</epage><pages>S27-S27</pages><artnum>S27</artnum><issn>1471-2458</issn><eissn>1471-2458</eissn><abstract>Staphylococcus aureus is a commensal of human skin and nares. It is also one of the leading nosocomial pathogens in both developed and developing countries and is responsible for a wide range of life threatening infections, especially in patients who are immunocompromised, post-surgery, undergoing haemodialysis and those who are treated with catheters and ventilators. Over the past two decades, the incidence of nosocomial staphylococcal infections has increased dramatically. Currently there are at least seven vaccine and immunotherapy candidates against S. aureus in the developmental phase targeting both active and passive immunization.
We used a modified CHNRI methodology for setting priorities in health research investments. This was done in two stages. In Stage I, we systematically reviewed the literature related to emerging vaccines against Staphylococcus aureus relevant to several criteria of interest: answerability; cost of development, production and implementation; efficacy and effectiveness; deliverability, affordability and sustainability; maximum potential impact on disease burden reduction; acceptability to the end users and health workers; and effect on equity. In Stage II, we conducted an expert opinion exercise by inviting 20 experts (leading basic scientists, international public health researchers, international policy makers and representatives of pharmaceutical companies) to participate. The policy makers and industry representatives accepted our invitation on the condition of anonymity, due to sensitive nature of their involvement in such exercises. They answered questions from CHNRI framework and their "collective optimism" towards each criterion was documented on a scale from 0 to 100%.
The panel of experts expressed low levels of optimism (score around or below 50%) on the criteria of answerability, efficacy, maximum disease burden reduction potential, low cost of production, low cost of implementation and affordability; moderate levels of optimism (scores around 60 to 80%) that these vaccines could be developed at a low cost, and thus on the deliverability, sustainability and impact on equity; and high levels of optimism (scores above 80%) regarding acceptable of such a product to both the end-users and health workers. While assessing the candidates for passive immunization against S.aureus, the experts were poorly optimistic regarding low production cost, low implementation cost, efficacy, deliverability, sustainability, affordability and equity; moderately optimistic regarding answerability and acceptability to health workers and end-users. They were of the opinion that these interventions would have only a modest impact (3 to 5%) on the burden of childhood pneumonia. .
In order to provide an effective vaccine against S. aureus, a number of unresolved issues in vaccine development relating to optimal antigenic target identification, criteria for acceptable efficacy, identification of target population, commercial development limitations, optimal timing of immunization strategy, storage, cold chain requirements and cost need to be addressed properly. There is still a great deal unknown about the complex interaction between S. aureus and the human host. However, given the nature of S. aureus and the lessons learned from the recent failure of two emerging vaccines, it is clear that a multi-component vaccine is essential. Combating only one virulence factor is not sufficient in the human host but finding the right combination of factors will be very challenging.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>21501445</pmid><doi>10.1186/1471-2458-11-S3-S27</doi><oa>free_for_read</oa></addata></record> |
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subjects | Bacteria Child Humans Immunization Immunotherapy Medical research Pneumonia, Staphylococcal - prevention & control Pneumonia, Staphylococcal - therapy Randomized Controlled Trials as Topic Staphylococcal Vaccines - supply & distribution Staphylococcus aureus - immunology Staphylococcus infections Streptococcus infections Treatment Outcome Vaccines |
title | An evaluation of the emerging vaccines and immunotherapy against staphylococcal pneumonia in children |
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