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Treatment of immunocompromised COVID-19 patients with convalescent plasma.

Identifieur interne : 000187 ( Main/Exploration ); précédent : 000186; suivant : 000188

Treatment of immunocompromised COVID-19 patients with convalescent plasma.

Auteurs : Monica Fung [États-Unis] ; Ashok Nambiar [États-Unis] ; Suchi Pandey [États-Unis] ; J Matthew Aldrich [États-Unis] ; Justin Teraoka [États-Unis] ; Christopher Freise [États-Unis] ; John Roberts [États-Unis] ; Sindhu Chandran [États-Unis] ; Steven R. Hays [États-Unis] ; Emma Bainbridge [États-Unis] ; Catherine Devoe [États-Unis] ; Annelys Roque Gardner [États-Unis] ; Deborah Yokoe [États-Unis] ; Timothy J. Henrich [États-Unis] ; Jennifer M. Babik [États-Unis] ; Peter Chin-Hong [États-Unis]

Source :

RBID : pubmed:32989856

Abstract

Immunosuppressed patients such as solid organ transplant and hematologic malignancy patients appear to be at increased risk for morbidity and mortality due to coronavirus disease 2019 (COVID-19) caused by SARS coronavirus 2 (SARS-CoV-2). Convalescent plasma, a method of passive immunization that has been applied to prior viral pandemics, holds promise as a potential treatment for COVID-19. Immunocompromised patients may experience more benefit from convalescent plasma given underlying deficits in B and T cell immunity as well as contraindications to antiviral and immunomodulatory therapy. We describe our institutional experience with four immunosuppressed patients (two kidney transplant recipients, one lung transplant recipient, and one chronic myelogenous leukemia patient) treated with COVID-19 convalescent plasma through the Expanded Access Program (NCT04338360). All patients clinically improved after administration (two fully recovered and two discharged to skilled nursing facilities) and none experienced a transfusion reaction. We also report the characteristics of convalescent plasma product from a local blood center including positive SARS-CoV-2 IgG and negative SARS-CoV-2 PCR in all samples tested. This preliminary evidence suggest that convalescent plasma may be safe among immunosuppressed patients with COVID-19 and emphasizes the need for further data on the efficacy of convalescent plasma as either primary or adjunctive therapy for COVID-19.

DOI: 10.1111/tid.13477
PubMed: 32989856
PubMed Central: PMC7537112


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">Immunosuppressed patients such as solid organ transplant and hematologic malignancy patients appear to be at increased risk for morbidity and mortality due to coronavirus disease 2019 (COVID-19) caused by SARS coronavirus 2 (SARS-CoV-2). Convalescent plasma, a method of passive immunization that has been applied to prior viral pandemics, holds promise as a potential treatment for COVID-19. Immunocompromised patients may experience more benefit from convalescent plasma given underlying deficits in B and T cell immunity as well as contraindications to antiviral and immunomodulatory therapy. We describe our institutional experience with four immunosuppressed patients (two kidney transplant recipients, one lung transplant recipient, and one chronic myelogenous leukemia patient) treated with COVID-19 convalescent plasma through the Expanded Access Program (NCT04338360). All patients clinically improved after administration (two fully recovered and two discharged to skilled nursing facilities) and none experienced a transfusion reaction. We also report the characteristics of convalescent plasma product from a local blood center including positive SARS-CoV-2 IgG and negative SARS-CoV-2 PCR in all samples tested. This preliminary evidence suggest that convalescent plasma may be safe among immunosuppressed patients with COVID-19 and emphasizes the need for further data on the efficacy of convalescent plasma as either primary or adjunctive therapy for COVID-19.</div>
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<AbstractText>Immunosuppressed patients such as solid organ transplant and hematologic malignancy patients appear to be at increased risk for morbidity and mortality due to coronavirus disease 2019 (COVID-19) caused by SARS coronavirus 2 (SARS-CoV-2). Convalescent plasma, a method of passive immunization that has been applied to prior viral pandemics, holds promise as a potential treatment for COVID-19. Immunocompromised patients may experience more benefit from convalescent plasma given underlying deficits in B and T cell immunity as well as contraindications to antiviral and immunomodulatory therapy. We describe our institutional experience with four immunosuppressed patients (two kidney transplant recipients, one lung transplant recipient, and one chronic myelogenous leukemia patient) treated with COVID-19 convalescent plasma through the Expanded Access Program (NCT04338360). All patients clinically improved after administration (two fully recovered and two discharged to skilled nursing facilities) and none experienced a transfusion reaction. We also report the characteristics of convalescent plasma product from a local blood center including positive SARS-CoV-2 IgG and negative SARS-CoV-2 PCR in all samples tested. This preliminary evidence suggest that convalescent plasma may be safe among immunosuppressed patients with COVID-19 and emphasizes the need for further data on the efficacy of convalescent plasma as either primary or adjunctive therapy for COVID-19.</AbstractText>
<CopyrightInformation>© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</CopyrightInformation>
</Abstract>
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<Author ValidYN="Y">
<LastName>Fung</LastName>
<ForeName>Monica</ForeName>
<Initials>M</Initials>
<Identifier Source="ORCID">https://orcid.org/0000-0002-1725-5259</Identifier>
<AffiliationInfo>
<Affiliation>Division of Infectious Disease, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Nambiar</LastName>
<ForeName>Ashok</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Department of Laboratory Medicine, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Pandey</LastName>
<ForeName>Suchi</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Department of Pathology, Stanford University School of Medicine, Palo Alto, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Aldrich</LastName>
<ForeName>J Matthew</ForeName>
<Initials>JM</Initials>
<AffiliationInfo>
<Affiliation>Department of Anesthesia and Perioperative Care, University of California San Francisco, San Francisco, C,, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Teraoka</LastName>
<ForeName>Justin</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Disease, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Freise</LastName>
<ForeName>Christopher</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Division of Transplant Surgery, Department of Surgery, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Roberts</LastName>
<ForeName>John</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Division of Transplant Surgery, Department of Surgery, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Chandran</LastName>
<ForeName>Sindhu</ForeName>
<Initials>S</Initials>
<Identifier Source="ORCID">https://orcid.org/0000-0003-4547-3381</Identifier>
<AffiliationInfo>
<Affiliation>Division of Nephrology, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Hays</LastName>
<ForeName>Steven R</ForeName>
<Initials>SR</Initials>
<AffiliationInfo>
<Affiliation>Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Bainbridge</LastName>
<ForeName>Emma</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Disease, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>DeVoe</LastName>
<ForeName>Catherine</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Disease, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Roque Gardner</LastName>
<ForeName>Annelys</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Disease, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Yokoe</LastName>
<ForeName>Deborah</ForeName>
<Initials>D</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Disease, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Henrich</LastName>
<ForeName>Timothy J</ForeName>
<Initials>TJ</Initials>
<Identifier Source="ORCID">https://orcid.org/0000-0002-6684-0622</Identifier>
<AffiliationInfo>
<Affiliation>Division of Infectious Disease, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
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<LastName>Babik</LastName>
<ForeName>Jennifer M</ForeName>
<Initials>JM</Initials>
<Identifier Source="ORCID">https://orcid.org/0000-0001-6914-4959</Identifier>
<AffiliationInfo>
<Affiliation>Division of Infectious Disease, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Chin-Hong</LastName>
<ForeName>Peter</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Disease, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
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<Grant>
<GrantID>T32 AI060530</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>75A50120C00096</GrantID>
<Agency>US Department of Health and Human Services</Agency>
<Country></Country>
</Grant>
</GrantList>
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<PublicationType UI="D002363">Case Reports</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2020</Year>
<Month>09</Month>
<Day>29</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>Denmark</Country>
<MedlineTA>Transpl Infect Dis</MedlineTA>
<NlmUniqueID>100883688</NlmUniqueID>
<ISSNLinking>1398-2273</ISSNLinking>
</MedlineJournalInfo>
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<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="Y">COVID-19</Keyword>
<Keyword MajorTopicYN="Y">convalescent plasma</Keyword>
<Keyword MajorTopicYN="Y">immunocompromised</Keyword>
<Keyword MajorTopicYN="Y">transplant</Keyword>
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<name sortKey="Aldrich, J Matthew" sort="Aldrich, J Matthew" uniqKey="Aldrich J" first="J Matthew" last="Aldrich">J Matthew Aldrich</name>
<name sortKey="Babik, Jennifer M" sort="Babik, Jennifer M" uniqKey="Babik J" first="Jennifer M" last="Babik">Jennifer M. Babik</name>
<name sortKey="Bainbridge, Emma" sort="Bainbridge, Emma" uniqKey="Bainbridge E" first="Emma" last="Bainbridge">Emma Bainbridge</name>
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<name sortKey="Chin Hong, Peter" sort="Chin Hong, Peter" uniqKey="Chin Hong P" first="Peter" last="Chin-Hong">Peter Chin-Hong</name>
<name sortKey="Devoe, Catherine" sort="Devoe, Catherine" uniqKey="Devoe C" first="Catherine" last="Devoe">Catherine Devoe</name>
<name sortKey="Freise, Christopher" sort="Freise, Christopher" uniqKey="Freise C" first="Christopher" last="Freise">Christopher Freise</name>
<name sortKey="Hays, Steven R" sort="Hays, Steven R" uniqKey="Hays S" first="Steven R" last="Hays">Steven R. Hays</name>
<name sortKey="Henrich, Timothy J" sort="Henrich, Timothy J" uniqKey="Henrich T" first="Timothy J" last="Henrich">Timothy J. Henrich</name>
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