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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">First clinical trial of a MERS coronavirus DNA vaccine</title><author><name sortKey="Yoon, In Kyu" sort="Yoon, In Kyu" uniqKey="Yoon I" first="In-Kyu" last="Yoon">In-Kyu Yoon</name><affiliation><nlm:aff id="aff1">International Vaccine Institute, Gwanak-gu, Seoul, 08826, South Korea</nlm:aff></affiliation></author><author><name sortKey="Kim, Jerome H" sort="Kim, Jerome H" uniqKey="Kim J" first="Jerome H" last="Kim">Jerome H. Kim</name><affiliation><nlm:aff id="aff1">International Vaccine Institute, Gwanak-gu, Seoul, 08826, South Korea</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">31351923</idno><idno type="pmc">7128141</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128141</idno><idno type="RBID">PMC:7128141</idno><idno type="doi">10.1016/S1473-3099(19)30397-4</idno><date when="2019">2019</date><idno type="wicri:Area/Pmc/Corpus">000805</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000805</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">First clinical trial of a MERS coronavirus DNA vaccine</title><author><name sortKey="Yoon, In Kyu" sort="Yoon, In Kyu" uniqKey="Yoon I" first="In-Kyu" last="Yoon">In-Kyu Yoon</name><affiliation><nlm:aff id="aff1">International Vaccine Institute, Gwanak-gu, Seoul, 08826, South Korea</nlm:aff></affiliation></author><author><name sortKey="Kim, Jerome H" sort="Kim, Jerome H" uniqKey="Kim J" first="Jerome H" last="Kim">Jerome H. Kim</name><affiliation><nlm:aff id="aff1">International Vaccine Institute, Gwanak-gu, Seoul, 08826, South Korea</nlm:aff></affiliation></author></analytic><series><title level="j">The Lancet. Infectious Diseases</title><idno type="ISSN">1473-3099</idno><idno type="eISSN">1474-4457</idno><imprint><date when="2019">2019</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><back><div1 type="bibliography"><listBibl><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Dighe, A" uniqKey="Dighe A">A Dighe</name></author><author><name sortKey="Jombart, T" uniqKey="Jombart T">T Jombart</name></author><author><name sortKey="Van Kerkhove, Md" uniqKey="Van Kerkhove M">MD Van Kerkhove</name></author><author><name sortKey="Ferguson, N" uniqKey="Ferguson N">N Ferguson</name></author></analytic></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Modjarrad, K" uniqKey="Modjarrad K">K Modjarrad</name></author><author><name sortKey="Roberts, Cc" uniqKey="Roberts C">CC Roberts</name></author><author><name sortKey="Mills, Kt" uniqKey="Mills K">KT Mills</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Skariyachan, S" uniqKey="Skariyachan S">S Skariyachan</name></author><author><name sortKey="Challapilli, Sb" uniqKey="Challapilli S">SB Challapilli</name></author><author><name sortKey="Packirisamy, S" uniqKey="Packirisamy S">S Packirisamy</name></author><author><name sortKey="Kumargowda, St" uniqKey="Kumargowda S">ST Kumargowda</name></author><author><name sortKey="Sridhar, Vs" uniqKey="Sridhar V">VS Sridhar</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zhao, J" uniqKey="Zhao J">J Zhao</name></author><author><name sortKey="Li, K" uniqKey="Li K">K Li</name></author><author><name sortKey="Wohlford Lenane, C" uniqKey="Wohlford Lenane C">C Wohlford-Lenane</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Agrawal, As" uniqKey="Agrawal A">AS Agrawal</name></author><author><name sortKey="Tao, X" uniqKey="Tao X">X Tao</name></author><author><name sortKey="Algaissi, A" uniqKey="Algaissi A">A Algaissi</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Muthumani, K" uniqKey="Muthumani K">K Muthumani</name></author><author><name sortKey="Falzarano, D" uniqKey="Falzarano D">D Falzarano</name></author><author><name sortKey="Reuschel, El" uniqKey="Reuschel E">EL Reuschel</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="discussion"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Lancet Infect Dis</journal-id><journal-id journal-id-type="iso-abbrev">Lancet Infect Dis</journal-id><journal-title-group><journal-title>The Lancet. Infectious Diseases</journal-title></journal-title-group><issn pub-type="ppub">1473-3099</issn><issn pub-type="epub">1474-4457</issn><publisher><publisher-name>Elsevier Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">31351923</article-id><article-id pub-id-type="pmc">7128141</article-id><article-id pub-id-type="publisher-id">S1473-3099(19)30397-4</article-id><article-id pub-id-type="doi">10.1016/S1473-3099(19)30397-4</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>First clinical trial of a MERS coronavirus DNA vaccine</article-title></title-group><contrib-group><contrib contrib-type="author" id="au10"><name><surname>Yoon</surname><given-names>In-Kyu</given-names></name><xref rid="aff1" ref-type="aff">a</xref></contrib><contrib contrib-type="author" id="au20"><name><surname>Kim</surname><given-names>Jerome H</given-names></name><email>jerome.kim@ivi.int</email><xref rid="aff1" ref-type="aff">a</xref></contrib></contrib-group><aff id="aff1"><label>a</label>International Vaccine Institute, Gwanak-gu, Seoul, 08826, South Korea</aff><pub-date pub-type="pmc-release"><day>24</day><month>7</month><year>2019</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><month>9</month><year>2019</year></pub-date><pub-date pub-type="epub"><day>24</day><month>7</month><year>2019</year></pub-date><volume>19</volume><issue>9</issue><fpage>924</fpage><lpage>925</lpage><permissions><copyright-statement>© 2019 Elsevier Ltd. All rights reserved.</copyright-statement><copyright-year>2019</copyright-year><copyright-holder>Elsevier Ltd</copyright-holder><license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p></license></permissions><related-article related-article-type="article-reference" id="d32e272" ext-link-type="doi" xlink:href="10.1016/S1473-3099(19)30266-X"></related-article></article-meta></front><body><p id="para10">Middle East respiratory syndrome (MERS) coronavirus is an emerging pathogen with pandemic potential that continues to cause sporadic human disease 7 years after the first case in a human was detected in 2012.<xref rid="bib1" ref-type="bibr"><sup>1</sup></xref> Zoonotic transmission with consequent risk of human epidemics will probably continue into the future, given that MERS coronavirus appears to be highly endemic among dromedary camels from geographically widespread areas of the Middle East and Africa.<xref rid="bib2" ref-type="bibr"><sup>2</sup></xref> In light of this potential threat to global public health, WHO along with the Coalition for Epidemic Preparedness Innovations have prioritised research and development of countermeasures against MERS coronavirus,<xref rid="bib3" ref-type="bibr">3</xref>, <xref rid="bib4" ref-type="bibr">4</xref> and WHO has developed a target product profile for both preventive and reactive use of MERS coronavirus vaccines.<xref rid="bib5" ref-type="bibr"><sup>5</sup></xref></p><p id="para20">In <italic>The Lancet Infectious Diseases</italic>, Kayvon Modjarrad and colleagues<xref rid="bib6" ref-type="bibr"><sup>6</sup></xref> report results from their phase 1, open-label, dose-ranging study of GLS-5300, the first DNA vaccine candidate against MERS coronavirus to enter clinical trials. In the study, 75 adults aged 18–50 years at one site in the USA were enrolled sequentially using a dose-escalation protocol to receive 0·67 mg, 2 mg, or 6 mg GLS-5300 intramuscular injection at baseline, week 4, and week 12 followed immediately by co-localised intramuscular electroporation. The primary outcome of the study was safety, assessed during the vaccination period up to 48 weeks after dose 3.</p><p id="para30">There were no vaccine-associated serious adverse events. The most common adverse events were injection-site reactions (in 93% of participants), the most common solicited symptom was administration-site pain (92%), and the most common unsolicited adverse events were infections (36%). Seroconversion measured by MERS coronavirus spike glycoprotein subunit 1 (S1)-ELISA was detected in 66% and 86% of participants after the first and second injections, respectively, and in 79% at week 60. Neutralising antibodies were detected in 27 (43%) of 63 participants at week 14, 25 (39%) of 65 at week 24, and two (3%) of 66 at week 60. MERS coronavirus S-specific IFNγ-ELISPOT responses were detected in 47 (71%) of 66 participants after the second injection and in 44 (76%) of 58 after the third vaccination.</p><p id="para40">No licensed MERS coronavirus vaccine is currently available, and substantial challenges exist to the development of such a vaccine. These include: (1) available animal models (eg, transduced mice, and transgenic mice, rabbits, rhesus macaques, marmosets, alpacas, and camels) might not mimic human disease;<xref rid="bib7" ref-type="bibr"><sup>7</sup></xref> (2) an immune correlate of protection has not been defined, and the protective immune response in natural infection is poorly understood, although both humoral and cellular responses are probably necessary for viral clearance;<xref rid="bib8" ref-type="bibr"><sup>8</sup></xref> (3) there is a theoretical risk of immune enhancement during MERS coronavirus infection after vaccination, possibly leading to immunopathological pulmonary eosinophilic infiltration;<xref rid="bib9" ref-type="bibr"><sup>9</sup></xref> (4) demonstration of efficacy in the field will probably not be possible, necessitating alternative regulatory pathways for licensure; and (5) if MERS shifts from a pattern of sporadic outbreaks to pandemic spread, it is not known whether vaccines based on current MERS coronavirus isolates will offer protection against pandemic strains.</p><p id="para50">The results of Modjarrad and colleagues' study illustrate the challenges and promise in developing a vaccine against a novel pathogen with episodic outbreaks and little available knowledge. Despite preclinical demonstration of protection by GLS-5300 against radiological and histopathological pneumonia after MERS coronavirus challenge in rhesus macaques,<xref rid="bib10" ref-type="bibr"><sup>10</sup></xref> it remains difficult to interpret the relevance of the immunogenicity parameters that were assessed in humans in the phase 1 trial given our poor understanding of protective natural immune responses. Modjarrad and colleagues sought to bridge this gap in a post-hoc analysis by obtaining samples from ten individuals who had recovered from natural MERS coronavirus infection during the 2015 outbreak in South Korea (convalescent serum and peripheral blood mononuclear cell samples were obtained at a mean of 19·8 months [SD 0·7] after the original MERS diagnosis). Anti-S1 and neutralising antibody titres following natural infection were significantly higher than vaccine-induced responses in the acute phase, but were not different to vaccine in late convalescent samples and at similar post-vaccination timepoints.</p><p id="para60">Given the differences between S1-ELISA and neutralising antibody responses to GLS-5300, the comparison of post-natural infection versus post-vaccination responses will have an important role in the development of vaccines against sporadically occurring pathogens such as MERS coronavirus. Despite many challenges for development, the platform technologies on which vaccines such as GLS-5300 are based hold promise against novel pathogen threats because of the rapidity with which they can be formulated and manufactured; four MERS coronavirus vaccine candidates that have started phase 1 trials are based on different platform technologies.<xref rid="bib6" ref-type="bibr"><sup>6</sup></xref> Completion of the phase 1 trial of GLS-5300 represents an incremental but important step in the development of vaccines against emerging viral global threats.</p><p id="para70"><fig id="f10"><graphic xlink:href="fx1_lrg"></graphic><permissions><copyright-statement>© 2019 CDC/Science Photo Library</copyright-statement><copyright-year>2019</copyright-year><license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p></license></permissions></fig></p></body><back><ref-list id="bibl10"><title>References</title><ref id="bib1"><label>1</label><element-citation publication-type="journal" id="sbref10"><person-group person-group-type="author"><collab>FAO-OIE-WHO MERS Technical Working Group</collab></person-group><article-title>MERS: progress on the global response, remaining challenges and the way forward</article-title><source>Antiviral Res</source><volume>159</volume><year>2018</year><fpage>35</fpage><lpage>44</lpage><pub-id pub-id-type="pmid">30236531</pub-id></element-citation></ref><ref id="bib2"><label>2</label><element-citation publication-type="journal" id="sbref20"><person-group person-group-type="author"><name><surname>Dighe</surname><given-names>A</given-names></name><name><surname>Jombart</surname><given-names>T</given-names></name><name><surname>Van Kerkhove</surname><given-names>MD</given-names></name><name><surname>Ferguson</surname><given-names>N</given-names></name></person-group><article-title>A systematic review of MERS-CoV seroprevalence and RNA prevalence in dromedary camels: implications for animal vaccination</article-title><source>Epidemics</source><year>2019</year><comment>published online June 5.</comment><pub-id pub-id-type="doi">10.1016/j.epidem.2019.100350</pub-id></element-citation></ref><ref id="bib3"><label>3</label><element-citation publication-type="other" id="sbref30"><person-group person-group-type="author"><collab>Coalition for Epidemic Preparedness Initiatives</collab></person-group><article-title>Targeting diseases with epidemic potential</article-title><ext-link ext-link-type="uri" xlink:href="https://cepi.net/research_dev/priority-diseases" id="interrefs20">https://cepi.net/research_dev/priority-diseases</ext-link><year>2019</year></element-citation></ref><ref id="bib4"><label>4</label><element-citation 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on challenge with live virus</article-title><source>Hum Vaccin Immunother</source><volume>12</volume><year>2016</year><fpage>2351</fpage><lpage>2356</lpage><pub-id pub-id-type="pmid">27269431</pub-id></element-citation></ref><ref id="bib10"><label>10</label><element-citation publication-type="journal" id="sbref100"><person-group person-group-type="author"><name><surname>Muthumani</surname><given-names>K</given-names></name><name><surname>Falzarano</surname><given-names>D</given-names></name><name><surname>Reuschel</surname><given-names>EL</given-names></name></person-group><article-title>A synthetic consensus anti-spike protein DNA vaccine induces protective immunity against Middle East respiratory syndrome coronavirus in nonhuman primates</article-title><source>Sci Transl Med</source><volume>7</volume><year>2015</year><object-id pub-id-type="publisher-id">301ra132</object-id></element-citation></ref></ref-list><ack><p>I-KY and JHK's institution is collaborating with GeneOne Life Science on a Middle East respiratory syndrome coronavirus vaccine trial in South Korea.</p></ack></back></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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