Cytokine profile in plasma of severe COVID-19 does not differ from ARDS and sepsis.
Identifieur interne : 000646 ( Main/Exploration ); précédent : 000645; suivant : 000647Cytokine profile in plasma of severe COVID-19 does not differ from ARDS and sepsis.
Auteurs : Jennifer G. Wilson ; Laura J. Simpson [États-Unis] ; Anne-Maud Ferreira [États-Unis] ; Arjun Rustagi [États-Unis] ; Jonasel Roque [États-Unis] ; Adijat Asuni [États-Unis] ; Thanmayi Ranganath [États-Unis] ; Philip M. Grant [États-Unis] ; Aruna Subramanian [États-Unis] ; Yael Rosenberg-Hasson [États-Unis] ; Holden T. Maecker [États-Unis] ; Susan P. Holmes [États-Unis] ; Joseph E. Levitt [États-Unis] ; Catherine A. Blish [États-Unis] ; Angela J. Rogers [États-Unis]Source :
- JCI insight [ 2379-3708 ] ; 2020.
Descripteurs français
- KwdFr :
- Adulte (MeSH), Adulte d'âge moyen (MeSH), Antagoniste du récepteur à l'interleukine-1 (immunologie), Antagoniste du récepteur à l'interleukine-1 (sang), Cytokines (immunologie), Cytokines (sang), Facteur de nécrose tumorale alpha (immunologie), Facteur de nécrose tumorale alpha (sang), Femelle (MeSH), Humains (MeSH), Indice de gravité de la maladie (MeSH), Infections à coronavirus (immunologie), Infections à coronavirus (sang), Interleukine-1 bêta (immunologie), Interleukine-1 bêta (sang), Interleukine-18 (immunologie), Interleukine-18 (sang), Interleukine-6 (immunologie), Interleukine-6 (sang), Interleukine-8 (immunologie), Interleukine-8 (sang), Mâle (MeSH), Pandémies (MeSH), Pneumopathie virale (immunologie), Pneumopathie virale (sang), Sepsie (immunologie), Sepsie (sang), Sujet âgé (MeSH), Études cas-témoins (MeSH).
- MESH :
- immunologie : Antagoniste du récepteur à l'interleukine-1, Cytokines, Facteur de nécrose tumorale alpha, Infections à coronavirus, Interleukine-1 bêta, Interleukine-18, Interleukine-6, Interleukine-8, Pneumopathie virale, Sepsie.
- sang : Antagoniste du récepteur à l'interleukine-1, Cytokines, Facteur de nécrose tumorale alpha, Infections à coronavirus, Interleukine-1 bêta, Interleukine-18, Interleukine-6, Interleukine-8, Pneumopathie virale, Sepsie.
- Adulte, Adulte d'âge moyen, Femelle, Humains, Indice de gravité de la maladie, Mâle, Pandémies, Sujet âgé, Études cas-témoins.
English descriptors
- KwdEn :
- Adult (MeSH), Aged (MeSH), COVID-19 (MeSH), Case-Control Studies (MeSH), Coronavirus Infections (blood), Coronavirus Infections (immunology), Cytokine Release Syndrome (blood), Cytokine Release Syndrome (immunology), Cytokines (blood), Cytokines (immunology), Female (MeSH), Humans (MeSH), Interleukin 1 Receptor Antagonist Protein (blood), Interleukin 1 Receptor Antagonist Protein (immunology), Interleukin-18 (blood), Interleukin-18 (immunology), Interleukin-1beta (blood), Interleukin-1beta (immunology), Interleukin-6 (blood), Interleukin-6 (immunology), Interleukin-8 (blood), Interleukin-8 (immunology), Male (MeSH), Middle Aged (MeSH), Pandemics (MeSH), Pneumonia, Viral (blood), Pneumonia, Viral (immunology), Respiratory Distress Syndrome (blood), Respiratory Distress Syndrome (immunology), Sepsis (blood), Sepsis (immunology), Severity of Illness Index (MeSH), Tumor Necrosis Factor-alpha (blood), Tumor Necrosis Factor-alpha (immunology).
- MESH :
- chemical , blood : Cytokines, Interleukin 1 Receptor Antagonist Protein, Interleukin-18, Interleukin-1beta, Interleukin-6, Interleukin-8, Tumor Necrosis Factor-alpha.
- blood : Coronavirus Infections, Cytokine Release Syndrome, Pneumonia, Viral, Respiratory Distress Syndrome, Sepsis.
- immunology : Coronavirus Infections, Cytokine Release Syndrome, Cytokines, Interleukin 1 Receptor Antagonist Protein, Interleukin-18, Interleukin-1beta, Interleukin-6, Interleukin-8, Pneumonia, Viral, Respiratory Distress Syndrome, Sepsis, Tumor Necrosis Factor-alpha.
- Adult, Aged, COVID-19, Case-Control Studies, Female, Humans, Male, Middle Aged, Pandemics, Severity of Illness Index.
Abstract
BACKGROUNDElevated levels of inflammatory cytokines have been associated with poor outcomes among COVID-19 patients. It is unknown, however, how these levels compare with those observed in critically ill patients with acute respiratory distress syndrome (ARDS) or sepsis due to other causes.METHODSWe used a Luminex assay to determine expression of 76 cytokines from plasma of hospitalized COVID-19 patients and banked plasma samples from ARDS and sepsis patients. Our analysis focused on detecting statistical differences in levels of 6 cytokines associated with cytokine storm (IL-1β, IL-1RA, IL-6, IL-8, IL-18, and TNF-α) between patients with moderate COVID-19, severe COVID-19, and ARDS or sepsis.RESULTSFifteen hospitalized COVID-19 patients, 9 of whom were critically ill, were compared with critically ill patients with ARDS (n = 12) or sepsis (n = 16). There were no statistically significant differences in baseline levels of IL-1β, IL-1RA, IL-6, IL-8, IL-18, and TNF-α between patients with COVID-19 and critically ill controls with ARDS or sepsis.CONCLUSIONLevels of inflammatory cytokines were not higher in severe COVID-19 patients than in moderate COVID-19 or critically ill patients with ARDS or sepsis in this small cohort. Broad use of immunosuppressive therapies in ARDS has failed in numerous Phase 3 studies; use of these therapies in unselected patients with COVID-19 may be unwarranted.FUNDINGFunding was received from NHLBI K23 HL125663 (AJR); The Bill and Melinda Gates Foundation OPP1113682 (AJR and CAB); Burroughs Wellcome Fund Investigators in the Pathogenesis of Infectious Diseases #1016687 NIH/NIAID U19AI057229-16; Stanford Maternal Child Health Research Institute; and Chan Zuckerberg Biohub (CAB).
DOI: 10.1172/jci.insight.140289
PubMed: 32706339
PubMed Central: PMC7526438
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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<author><name sortKey="Ranganath, Thanmayi" sort="Ranganath, Thanmayi" uniqKey="Ranganath T" first="Thanmayi" last="Ranganath">Thanmayi Ranganath</name>
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<author><name sortKey="Grant, Philip M" sort="Grant, Philip M" uniqKey="Grant P" first="Philip M" last="Grant">Philip M. Grant</name>
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<author><name sortKey="Subramanian, Aruna" sort="Subramanian, Aruna" uniqKey="Subramanian A" first="Aruna" last="Subramanian">Aruna Subramanian</name>
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<author><name sortKey="Rosenberg Hasson, Yael" sort="Rosenberg Hasson, Yael" uniqKey="Rosenberg Hasson Y" first="Yael" last="Rosenberg-Hasson">Yael Rosenberg-Hasson</name>
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<author><name sortKey="Maecker, Holden T" sort="Maecker, Holden T" uniqKey="Maecker H" first="Holden T" last="Maecker">Holden T. Maecker</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult (MeSH)</term>
<term>Aged (MeSH)</term>
<term>COVID-19 (MeSH)</term>
<term>Case-Control Studies (MeSH)</term>
<term>Coronavirus Infections (blood)</term>
<term>Coronavirus Infections (immunology)</term>
<term>Cytokine Release Syndrome (blood)</term>
<term>Cytokine Release Syndrome (immunology)</term>
<term>Cytokines (blood)</term>
<term>Cytokines (immunology)</term>
<term>Female (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Interleukin 1 Receptor Antagonist Protein (blood)</term>
<term>Interleukin 1 Receptor Antagonist Protein (immunology)</term>
<term>Interleukin-18 (blood)</term>
<term>Interleukin-18 (immunology)</term>
<term>Interleukin-1beta (blood)</term>
<term>Interleukin-1beta (immunology)</term>
<term>Interleukin-6 (blood)</term>
<term>Interleukin-6 (immunology)</term>
<term>Interleukin-8 (blood)</term>
<term>Interleukin-8 (immunology)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Pandemics (MeSH)</term>
<term>Pneumonia, Viral (blood)</term>
<term>Pneumonia, Viral (immunology)</term>
<term>Respiratory Distress Syndrome (blood)</term>
<term>Respiratory Distress Syndrome (immunology)</term>
<term>Sepsis (blood)</term>
<term>Sepsis (immunology)</term>
<term>Severity of Illness Index (MeSH)</term>
<term>Tumor Necrosis Factor-alpha (blood)</term>
<term>Tumor Necrosis Factor-alpha (immunology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte (MeSH)</term>
<term>Adulte d'âge moyen (MeSH)</term>
<term>Antagoniste du récepteur à l'interleukine-1 (immunologie)</term>
<term>Antagoniste du récepteur à l'interleukine-1 (sang)</term>
<term>Cytokines (immunologie)</term>
<term>Cytokines (sang)</term>
<term>Facteur de nécrose tumorale alpha (immunologie)</term>
<term>Facteur de nécrose tumorale alpha (sang)</term>
<term>Femelle (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Indice de gravité de la maladie (MeSH)</term>
<term>Infections à coronavirus (immunologie)</term>
<term>Infections à coronavirus (sang)</term>
<term>Interleukine-1 bêta (immunologie)</term>
<term>Interleukine-1 bêta (sang)</term>
<term>Interleukine-18 (immunologie)</term>
<term>Interleukine-18 (sang)</term>
<term>Interleukine-6 (immunologie)</term>
<term>Interleukine-6 (sang)</term>
<term>Interleukine-8 (immunologie)</term>
<term>Interleukine-8 (sang)</term>
<term>Mâle (MeSH)</term>
<term>Pandémies (MeSH)</term>
<term>Pneumopathie virale (immunologie)</term>
<term>Pneumopathie virale (sang)</term>
<term>Sepsie (immunologie)</term>
<term>Sepsie (sang)</term>
<term>Sujet âgé (MeSH)</term>
<term>Études cas-témoins (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en"><term>Cytokines</term>
<term>Interleukin 1 Receptor Antagonist Protein</term>
<term>Interleukin-18</term>
<term>Interleukin-1beta</term>
<term>Interleukin-6</term>
<term>Interleukin-8</term>
<term>Tumor Necrosis Factor-alpha</term>
</keywords>
<keywords scheme="MESH" qualifier="blood" xml:lang="en"><term>Coronavirus Infections</term>
<term>Cytokine Release Syndrome</term>
<term>Pneumonia, Viral</term>
<term>Respiratory Distress Syndrome</term>
<term>Sepsis</term>
</keywords>
<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Antagoniste du récepteur à l'interleukine-1</term>
<term>Cytokines</term>
<term>Facteur de nécrose tumorale alpha</term>
<term>Infections à coronavirus</term>
<term>Interleukine-1 bêta</term>
<term>Interleukine-18</term>
<term>Interleukine-6</term>
<term>Interleukine-8</term>
<term>Pneumopathie virale</term>
<term>Sepsie</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Coronavirus Infections</term>
<term>Cytokine Release Syndrome</term>
<term>Cytokines</term>
<term>Interleukin 1 Receptor Antagonist Protein</term>
<term>Interleukin-18</term>
<term>Interleukin-1beta</term>
<term>Interleukin-6</term>
<term>Interleukin-8</term>
<term>Pneumonia, Viral</term>
<term>Respiratory Distress Syndrome</term>
<term>Sepsis</term>
<term>Tumor Necrosis Factor-alpha</term>
</keywords>
<keywords scheme="MESH" qualifier="sang" xml:lang="fr"><term>Antagoniste du récepteur à l'interleukine-1</term>
<term>Cytokines</term>
<term>Facteur de nécrose tumorale alpha</term>
<term>Infections à coronavirus</term>
<term>Interleukine-1 bêta</term>
<term>Interleukine-18</term>
<term>Interleukine-6</term>
<term>Interleukine-8</term>
<term>Pneumopathie virale</term>
<term>Sepsie</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>COVID-19</term>
<term>Case-Control Studies</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Pandemics</term>
<term>Severity of Illness Index</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Femelle</term>
<term>Humains</term>
<term>Indice de gravité de la maladie</term>
<term>Mâle</term>
<term>Pandémies</term>
<term>Sujet âgé</term>
<term>Études cas-témoins</term>
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<front><div type="abstract" xml:lang="en">BACKGROUNDElevated levels of inflammatory cytokines have been associated with poor outcomes among COVID-19 patients. It is unknown, however, how these levels compare with those observed in critically ill patients with acute respiratory distress syndrome (ARDS) or sepsis due to other causes.METHODSWe used a Luminex assay to determine expression of 76 cytokines from plasma of hospitalized COVID-19 patients and banked plasma samples from ARDS and sepsis patients. Our analysis focused on detecting statistical differences in levels of 6 cytokines associated with cytokine storm (IL-1β, IL-1RA, IL-6, IL-8, IL-18, and TNF-α) between patients with moderate COVID-19, severe COVID-19, and ARDS or sepsis.RESULTSFifteen hospitalized COVID-19 patients, 9 of whom were critically ill, were compared with critically ill patients with ARDS (n = 12) or sepsis (n = 16). There were no statistically significant differences in baseline levels of IL-1β, IL-1RA, IL-6, IL-8, IL-18, and TNF-α between patients with COVID-19 and critically ill controls with ARDS or sepsis.CONCLUSIONLevels of inflammatory cytokines were not higher in severe COVID-19 patients than in moderate COVID-19 or critically ill patients with ARDS or sepsis in this small cohort. Broad use of immunosuppressive therapies in ARDS has failed in numerous Phase 3 studies; use of these therapies in unselected patients with COVID-19 may be unwarranted.FUNDINGFunding was received from NHLBI K23 HL125663 (AJR); The Bill and Melinda Gates Foundation OPP1113682 (AJR and CAB); Burroughs Wellcome Fund Investigators in the Pathogenesis of Infectious Diseases #1016687 NIH/NIAID U19AI057229-16; Stanford Maternal Child Health Research Institute; and Chan Zuckerberg Biohub (CAB).</div>
</front>
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<DateCompleted><Year>2020</Year>
<Month>09</Month>
<Day>17</Day>
</DateCompleted>
<DateRevised><Year>2020</Year>
<Month>12</Month>
<Day>18</Day>
</DateRevised>
<Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">2379-3708</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>5</Volume>
<Issue>17</Issue>
<PubDate><Year>2020</Year>
<Month>09</Month>
<Day>03</Day>
</PubDate>
</JournalIssue>
<Title>JCI insight</Title>
<ISOAbbreviation>JCI Insight</ISOAbbreviation>
</Journal>
<ArticleTitle>Cytokine profile in plasma of severe COVID-19 does not differ from ARDS and sepsis.</ArticleTitle>
<ELocationID EIdType="doi" ValidYN="Y">10.1172/jci.insight.140289</ELocationID>
<ELocationID EIdType="pii" ValidYN="Y">140289</ELocationID>
<Abstract><AbstractText>BACKGROUNDElevated levels of inflammatory cytokines have been associated with poor outcomes among COVID-19 patients. It is unknown, however, how these levels compare with those observed in critically ill patients with acute respiratory distress syndrome (ARDS) or sepsis due to other causes.METHODSWe used a Luminex assay to determine expression of 76 cytokines from plasma of hospitalized COVID-19 patients and banked plasma samples from ARDS and sepsis patients. Our analysis focused on detecting statistical differences in levels of 6 cytokines associated with cytokine storm (IL-1β, IL-1RA, IL-6, IL-8, IL-18, and TNF-α) between patients with moderate COVID-19, severe COVID-19, and ARDS or sepsis.RESULTSFifteen hospitalized COVID-19 patients, 9 of whom were critically ill, were compared with critically ill patients with ARDS (n = 12) or sepsis (n = 16). There were no statistically significant differences in baseline levels of IL-1β, IL-1RA, IL-6, IL-8, IL-18, and TNF-α between patients with COVID-19 and critically ill controls with ARDS or sepsis.CONCLUSIONLevels of inflammatory cytokines were not higher in severe COVID-19 patients than in moderate COVID-19 or critically ill patients with ARDS or sepsis in this small cohort. Broad use of immunosuppressive therapies in ARDS has failed in numerous Phase 3 studies; use of these therapies in unselected patients with COVID-19 may be unwarranted.FUNDINGFunding was received from NHLBI K23 HL125663 (AJR); The Bill and Melinda Gates Foundation OPP1113682 (AJR and CAB); Burroughs Wellcome Fund Investigators in the Pathogenesis of Infectious Diseases #1016687 NIH/NIAID U19AI057229-16; Stanford Maternal Child Health Research Institute; and Chan Zuckerberg Biohub (CAB).</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Wilson</LastName>
<ForeName>Jennifer G</ForeName>
<Initials>JG</Initials>
<AffiliationInfo><Affiliation>Department of Emergency Medicine and.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Simpson</LastName>
<ForeName>Laura J</ForeName>
<Initials>LJ</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Ferreira</LastName>
<ForeName>Anne-Maud</ForeName>
<Initials>AM</Initials>
<AffiliationInfo><Affiliation>Department of Statistics, Stanford University, California, USA.</Affiliation>
</AffiliationInfo>
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<ForeName>Arjun</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Roque</LastName>
<ForeName>Jonasel</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
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<ForeName>Adijat</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Ranganath</LastName>
<ForeName>Thanmayi</ForeName>
<Initials>T</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<ForeName>Philip M</ForeName>
<Initials>PM</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Subramanian</LastName>
<ForeName>Aruna</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Rosenberg-Hasson</LastName>
<ForeName>Yael</ForeName>
<Initials>Y</Initials>
<AffiliationInfo><Affiliation>Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Maecker</LastName>
<ForeName>Holden T</ForeName>
<Initials>HT</Initials>
<AffiliationInfo><Affiliation>Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Holmes</LastName>
<ForeName>Susan P</ForeName>
<Initials>SP</Initials>
<AffiliationInfo><Affiliation>Department of Statistics, Stanford University, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Levitt</LastName>
<ForeName>Joseph E</ForeName>
<Initials>JE</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Blish</LastName>
<ForeName>Catherine A</ForeName>
<Initials>CA</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Chan Zuckerberg Biohub, San Francisco, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Rogers</LastName>
<ForeName>Angela J</ForeName>
<Initials>AJ</Initials>
<AffiliationInfo><Affiliation>Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>K23 HL125663</GrantID>
<Acronym>HL</Acronym>
<Agency>NHLBI NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant><GrantID>T32 AI007502</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant><GrantID>U19 AI057229</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
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<PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType>
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<ArticleDate DateType="Electronic"><Year>2020</Year>
<Month>09</Month>
<Day>03</Day>
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<MeshHeading><DescriptorName UI="D000080424" MajorTopicYN="N">Cytokine Release Syndrome</DescriptorName>
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<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
</MeshHeading>
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</MeshHeading>
<MeshHeading><DescriptorName UI="D012128" MajorTopicYN="N">Respiratory Distress Syndrome</DescriptorName>
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<QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName>
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<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="Y">COVID-19</Keyword>
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<region><li>Californie</li>
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<settlement><li>Stanford (Californie)</li>
</settlement>
<orgName><li>Université Stanford</li>
</orgName>
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<tree><noCountry><name sortKey="Wilson, Jennifer G" sort="Wilson, Jennifer G" uniqKey="Wilson J" first="Jennifer G" last="Wilson">Jennifer G. Wilson</name>
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<country name="États-Unis"><region name="Californie"><name sortKey="Simpson, Laura J" sort="Simpson, Laura J" uniqKey="Simpson L" first="Laura J" last="Simpson">Laura J. Simpson</name>
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<name sortKey="Blish, Catherine A" sort="Blish, Catherine A" uniqKey="Blish C" first="Catherine A" last="Blish">Catherine A. Blish</name>
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<name sortKey="Ranganath, Thanmayi" sort="Ranganath, Thanmayi" uniqKey="Ranganath T" first="Thanmayi" last="Ranganath">Thanmayi Ranganath</name>
<name sortKey="Rogers, Angela J" sort="Rogers, Angela J" uniqKey="Rogers A" first="Angela J" last="Rogers">Angela J. Rogers</name>
<name sortKey="Roque, Jonasel" sort="Roque, Jonasel" uniqKey="Roque J" first="Jonasel" last="Roque">Jonasel Roque</name>
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<name sortKey="Subramanian, Aruna" sort="Subramanian, Aruna" uniqKey="Subramanian A" first="Aruna" last="Subramanian">Aruna Subramanian</name>
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